We are grateful to Kiona Parker (UCI) for providing images of transgenic An. stephensi larvae, and to Fraser Colman (LSTM) and Beth Poulton (LSTM) for providing transgenic An. gambiae larvae. Beth Poulton (LSTM) also provided precious assistance during the imaging of An. gambiae larvae. This work was funded by the Tata Institute for Genetics and Society (TIGS) and the LSTM&#39;s Director Catalyst Fund awarded to A.A. (DCF2014AA). A.A.J. is a Donald Bren Professor at the University of California,Irvine.

NOTE: A schematic workflow of the illustrated protocol is shown in Figure 2.
1. Design of &#966;C31 attB -tagged plasmids (Figure 3)
<ol>
	<li>Create attB donor plasmids carrying the following essential components
	<ol>
		<li>Dominant fluorescent marker
		<ol>
			<li>Choose a promoter to drive the expression of the fluorescent marker. 
			&#8203;NOTE: For Anopheles transgenesis, fluorescent markers are usually under the regulation of the 3xP3 promoter39, which drives expression in the eyes and nerve cord. Alternatively, the PUBc promoter5 can be used when expression in multiple tissues is desired. Donor plasmids and docking lines used as examples in this protocol are marked using the 3xP3 promoter.</li>
			<li>Choose a fluorescent protein (FP) that is compatible with that of the receiving docking line so that they are readily distinguishable. 
			&#8203;NOTE: Do not use the same marker that is already present in the docking line and avoid the simultaneous use of GFP (green)/YFP (yellow) and GFP (green)/CFP (cyan) as they are very difficult to reliably differentiate. Donor plasmids used as examples in this protocol are marked with either DsRed or YFP as they are to be integrated in a docking line marked with CFP.</li>
		</ol>
		</li>
		<li>attB recombination site(s)
		<ol>
			<li>Use a single attB site for integration of a transgenic cassette (single-attB design) (Figure 3A).</li>
			<li>Use two inverted attB sites for RMCE (double-attB design) where the sites lay inverted in respect to one another and enclose the donor DNA template (Figure 3B). 
			NOTE: The orientation of the attB site(s) must be compatible with that of the attP site(s) present in the docking line.</li>
		</ol>
		</li>
		<li>Desired transgene cargo
		<ol>
			<li>Use any other desired features to be integrated in the mosquito genome based on the specific purpose of the experiment. Here, we describe the integration of an antimalarial effector molecule into the genome of An. stephensi and the integration of the components of the GAL4/UAS system into An. gambiae mosquitoes.</li>
		</ol>
		</li>
		<li>Plasmid backbone components
		<ol>
			<li>Include, amongst other essential components for plasmid replication in bacteria, a marker for plasmid selection in vitro (i.e., an antibiotic resistance gene). 
			NOTE: The plasmid backbone will be integrated in the mosquito genome in the single-attB design for integration (Figure 3A), while it will not be inserted in the double-attB design for RMCE (Figure 3B).</li>
		</ol>
		</li>
	</ol>
	</li>
</ol>
2. Preparation of plasmids for the microinjection mix
NOTE: The protocol illustrated here involves the use of two plasmids: an attB-tagged donor plasmid carrying the transgene of interest, and a helper plasmid that expresses the &#966;C31 integrase under the regulation of the Drosophila Hsp70 promoter40.
<ol>
	<li>Purify donor and helper plasmids using an endotoxin-free plasmid purification kit. 
	NOTE: Sequence the final plasmid preparation used for injection to verify the integrity of all components.</li>
	<li>Combine appropriate amounts of the two plasmids to obtain a mix with a final concentration of 350 ng/&#181;L of the donor plasmid and 150 ng/&#181;L of the helper plasmid when resuspended in injection buffer. 
	NOTE: When calculating the necessary volume of mix, consider that 10-15 &#181;L are sufficient for each day of planned injections and DNA can be prepared in advance and stored at -20 &#176;C. Integrase helper plasmid concentrations of 60-500 ng/&#181;L and donor plasmid concentrations of 85-200 ng/&#181;L have also been reported21,22,26,41.</li>
	<li>Precipitate the DNA by adding 0.1 volumes of 3 M sodium acetate (pH 5.2) and 2.5 volumes of ice-cold 100% EtOH and vortex. A white precipitate should be immediately visible. Having highly concentrated initial plasmid preparations (i.e., ~1 &#181;g/&#181;L) improves precipitation efficiency. 
	NOTE: Stopping point - The precipitate can be stored at -20 &#176;C overnight.</li>
	<li>Centrifuge at 15,000 x g for 20 min at 4 &#176;C, discard the supernatant, and wash the pellet with 1 mL of ice-cold 70% EtOH.</li>
	<li>Wash the pellet with 1 mL of ice-cold 70% EtOH and centrifuge at 15,000 x g for 5 min at room temperature.</li>
	<li>Discard the supernatant without disturbing the pellet and air dry.</li>
	<li>Resuspend the pellet in 1x injection buffer (0.1 mM Na3PO4, 5 mM KCl, pH 7.2, 0.22 &#181;m filter sterilized) to reach a total final concentration of 500 ng/&#181;L. 
	NOTE: Assume that some DNA will be lost during the precipitation process; therefore, add a smaller volume of injection buffer first, check the concentration on a spectrophotometer (e.g., Nanodrop), and then add an appropriate remaining volume to reach 500 ng/&#181;L.</li>
	<li>Ensure that the DNA is thoroughly resuspended, prepare aliquots of 10-15 &#181;L each and store them at -20 &#176;C.</li>
	<li>On the day of injection, thaw one aliquot and centrifuge at 15,000 x g for 5 min to remove any particulate residues. 
	&#8203;NOTE: An alternative method for particulate removal is to filter the solution through a 0.22 &#181;m filter. Avoid the presence of particulate residues in the injection mix as they lead to needle blockage during embryo microinjection.</li>
</ol>
3. Microinjection of embryos from an Anopheles docking line
<ol>
	<li>Blood feed 4-7-day-old mosquitoes from the desired docking line 72 h prior to microinjection (i.e., for injection on Monday and Tuesday feed females on the previous Friday; for injection on Thursday and Friday feed females on Monday of the same week).</li>
	<li>Blood feed wild-type (WT) mosquitoes (i.e., mosquitoes with the same genomic background of the docking line) on the same day; these will be needed for outcrossing. 
	NOTE: The size and quality of the blood meal affect egg quality, so it is recommended to always use fresh blood (i.e., blood drawn within the previous 7 days). Arm feeding or feeding on mice may increase the quality and quantity of eggs, however these methods are not encouraged. Specific approved protocols will be necessary for human and animal use.</li>
	<li>Perform embryo microinjections
	<ol>
		<li>Perform An. gambiae embryo microinjections in 25 mM NaCl42 by targeting the posterior pole of the embryo at a 45-degree angle. For a detailed protocol for embryo collection, alignment, and microinjection refer to Pondeville et al.43 and Lobo et al.44.</li>
		<li>Perform An. stephensi embryo microinjections in halocarbon oil 700:27 (2:1) by targeting the posterior pole of the embryo at a 30-degree angle. A detailed protocol for embryo collection, alignment, and microinjection can be found in Terenius et al.45 and Lobo et al.44.</li>
		<li>Transfer eggs immediately after injection in a Petri dish filled with sterile distilled water (pH 7.2) and return them to insectary conditions.</li>
	</ol>
	</li>
	<li>Upon hatching, transfer G0 larvae into a tray with salted distilled water (0.1% tonic salt) daily and rear to pupae.</li>
	<li>Record hatching rate (i.e., number of larvae hatched/number of embryos injected). 
	&#8203;NOTE: Embryo movement aids hatching, so gentle swirling is desirable. Hatching should start ~48 h after injection. Since injection may cause a slight developmental delay it is advisable to keep monitoring for late-hatching larvae for 3-4 days.</li>
</ol>
4. Crossing and screening of transformed individuals
<ol>
	<li>[OPTIONAL STEP] Screen G0 (injected) 1st or 2nd instar larvae (L1-L2) for transient expression of the fluorescent marker.
	<ol>
		<li>Use a fine-tip glass pipette to transfer G0 L1-L2 larvae to a microscope slides with wells. Place one larva in each well.</li>
		<li>Use a fluorescence stereoscope with the appropriate filter to screen for the presence of transient expression of the fluorescent marker. 
		NOTE: The pattern of transient expression is dictated by the promoter used. When using the 3xP3 promoter, transient expression of the fluorescent marker is visible in the anal papillae (see Figure 6 in Pondeville et al.43)</li>
		<li>Rear G0 positive individuals separately.</li>
	</ol>
	</li>
	<li>Sort G0 pupae by sex under a stereoscope52.</li>
	<li>Let males emerge in separate cages in groups of 3-5 (founder families) and add a 10-fold excess of age-matched WT females. 
	NOTE: Since males mate multiple times, it is important to provide an excess of WT females to maximize the mating chances of each male.</li>
	<li>Let females emerge in separate cages in groups of 10-15 (founder families) and add an equal number of age-matched WT males. 
	NOTE: If there is limited space in the insectary, females can emerge all together in a single cage. The female to male ratio can be as low as 1 male to 3 females.</li>
	<li>Allow adults to mate for 4-5 days and provide females with a blood meal. 
	&#8203;NOTE: Blood feed and collect eggs from G0 females multiple times to maximize the chances of getting transformants from multiple gonotrophic cycles.</li>
	<li>Blood feed WT individuals at the same time for outcrossing.</li>
	<li>Collect eggs and rear emerging next generation G1s.</li>
	<li>Screen G1 L3-L4 larvae for appropriate fluorescence to identify transformants.
	<ol>
		<li>Collect larvae in a Petri dish lined with filter paper or on a microscope slide and screen using a fluorescent stereoscope with appropriate filters for the presence of the marker introduced with the attB-tagged cargo. 
		&#8203;NOTE: Fluorescence driven by the 3xP3 promoter is visible in all postembryonic stages and the screening may be performed on younger larvae, however these are more fragile and must be handled relatively carefully. Pupae can also be screened.
		<ol>
			<li>For single-attB designs for integration screen for the presence of the new and pre-existing marker; they should both be present since the new cassette is inserted next to the original one (Figure 3A,&#160;Figure 4). 
			&#8203;NOTE: Screening exception for single attB designs: When using marker-less docking lines22, screen for the presence of the new marker only. When using docking lines where integration results in the inactivation of the pre-existing marker21, screen for the presence of the new marker and the loss of the pre-existing one.</li>
			<li>For double-attB designs for RMCE, screen for the presence of the new marker and the loss of the pre-existing one, only the newly introduced marker should be present since the new cassette replaces the original one (Figure 3B, Figure 5). 
			&#8203;NOTE: Occasional integration events can be recovered in RMCE experiments where only a single attP recombined and thus both markers will be present. The screening of G1 individuals can be carried out also at the pupa stage following the same procedure52.</li>
		</ol>
		</li>
	</ol>
	</li>
	<li>Transfer transformed G1 individuals into a larval tray and rear to pupae. Discard non-fluorescent individuals and individuals with an unexpected marker expression pattern.</li>
	<li>Sort transformed G1 pupae by sex and cross them en masse with opposite-sex age-matched WT individuals.</li>
	<li>Allow adults to mate for 4-5 days, provide a blood meal, collect the eggs, and rear the next generation G2 progeny.
	<ol>
		<li>For single integration experiments, collect eggs directly from the en masse cross as the integration site is identical in all individuals.</li>
		<li>For RMCE experiments, collect eggs from single females and maintain progeny separate until molecular assessment is complete due to the potential presence of two alternative cassette orientations (Figure 3B).</li>
	</ol>
	</li>
	<li>Screen the G2 progeny (at either the larva or pupa stage) for the presence of the fluorescent marker (50% of the individuals are expected to be positive), discard non-fluorescent progeny.</li>
	<li>Set aside a subset of G2 positive individuals for molecular analysis, rear the rest to adulthood. 
	NOTE: If all G2 individuals must be kept alive, molecular analysis can be conducted on single adult&#39;s legs46 or pupal case DNA extractions (L. Grigoraki personal communication). Alternatively, molecular analysis can be performed after all the G2 individuals have oviposited and eggs have hatched.</li>
	<li>Allow adult males and females to intercross in the same cage to establish the new transgenic line. 
	&#8203;NOTE: For RMCE experiments, adult intercross must occur between siblings deriving from a single female until orientation of insertion is determined via molecular analysis.</li>
</ol>
5. Molecular validation of the insertion site by DNA amplification (PCR)
<ol>
	<li>Prepare a map of the predicted insertion site in the genome of the docking line after transformation.
	<ol>
		<li>Single integration: Ensure that the predicted insertion site carries the original docking construct plus the whole sequence of the donor plasmid between the two hybrid sites attL and attR (Figure 3A).</li>
		<li>RMCE: Ensure that the predicted insertion site is identical to that of the docking line where hybrid inverted attL sites replace the original inverted attP sites and the exchange template replaces the cassette originally present between them (Figure 3B).</li>
	</ol>
	</li>
	<li>Design oligonucleotide primers to amplify the insertional junction at either side of the integration locus.
	<ol>
		<li>Single integration: Design oligonucleotide primer pairs that span across the attR and/or attL sites. One primer must bind to the previously integrated docking construct and the other to the newly integrated transgene (Figure 3A).</li>
		<li>RMCE: Cassette replacement can occur in two different orientations with respect to the chromosome (designated A and B). Design alternative combinations of 4 oligonucleotide primers to give a discrete product in only one of the orientations, with one pair being diagnostic for orientation A, and the other for orientation B (Figure 3B, Figure 6).</li>
	</ol>
	</li>
	<li>Extract genomic DNA from G2 positive individuals and perform the diagnostic PCR and gel electrophoresis to visualize the presence of expected diagnostic amplicons from the predicted integration site maps. 
	NOTE: DNA may alternatively be extracted from single adult&#39;s legs46 or pupal cases (L. Grigoraki personal communication).</li>
	<li>Sequence PCR products to confirm expected sequences.</li>
</ol>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/62146/62146fig02.jpg" /> 
Figure 2. Workflow diagram for site-directed &#966;C31 genome modification in Anopheles mosquitoes. <a href="https://www.jove.com/files/ftp_upload/62146/62146fig02large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" class="xfigimg" src="/files/ftp_upload/62146/62146fig03.jpg" /> 
Figure 3. Molecular basis of &#966;C31-mediated single integration (A) and RMCE (B). A) Schematic maps of the genomic insertion in an An. stephensi docking line (80.9, Table 1) carrying a single attP site and marked with CFP (top), a single-attB design donor plasmid marked with DsRed (middle), and the expected insertion site resulting after successful integration (bottom). B) Schematic maps of the genomic insertion in an An. gambiae docking line (A11, Table 1) carrying two inverted attP sites and marked with CFP (top), a double-attB design donor plasmid marked with YFP (middle), and the expected insertion site resulting after successful RMCE (bottom). Wavy line: mosquito genome; Striped arrows: piggyBac transposon arms; 3xP3: promoter of the fluorescent marker; SV40: viral terminator; Ori: origin of replication; AmpR: ampicillin resistance gene. Crossing lines represent the site(s) of recombination between attP and attB sites. Numbered black arrows represent primer binding sites for the molecular validation of the insertion locus (step 5 of the protocol). Fully annotated single and double attB-tagged plasmids are available from the authors upon request. <a href="https://www.jove.com/files/ftp_upload/62146/62146fig03large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

The authors have nothing to disclose.

The accurate design of attB-tagged plasmids that are compatible with the docking line of choice is paramount for the success of the experiment. Careful consideration must be given to the choice of the marker used for the screening of transformants, including the fluorescence color and its pattern of expression, which will be subject to the pattern already present in the docking line. It is necessary to use fluorescent markers that are easily distinguishable: good marker combinations include RFP (red)/CFP (cyan), RFP (red)/GFP (green), RFP (red)/YFP (yellow), and YFP (yellow)/CFP (cyan), while combinations to avoid are YFP (yellow)/GFP (green) and CFP (cyan)/GFP (green). The 3xP3 promoter39, specific to the eyes and nerve cord, is the most frequently used to drive the expression of fluorescent markers for mosquito transgenesis. Indeed, all the Anopheles docking lines currently available utilize this promoter. Alternative regulatory regions are that of the An. gambiae polyubiquitin gene (PUBc)5 or the viral promoter IE120, which drive expression in multiple tissues. When used along with 3xP3, these promoters would expand the possible color combinations and even the use of the same fluorophore. The indicated promoters are active throughout the mosquito life cycle allowing screening and fluorescence monitoring at all life stages. An additional consideration during plasmid design is the size of the cargo to be integrated or exchanged. While the &#966;C31 system has remarkable carrying capacities18, it should be considered that the size of the donor plasmid generally correlates negatively with transformation efficiency22.
In the described protocol the source of integrase is a helper plasmid expressing the enzyme ubiquitously40. The ubiquitous presence of the integrase may lead to the transformation of somatic cells if microinjections are not precisely directed to the area where the germline forms. While such transformation events will be lost as they are not heritable, somatic effects can decrease the fitness of injected individuals. To avoid this and increase transformation efficiency, integrase expression can be restricted to the germline, for example by using the vasa promoter22,26. Other protocols describe the use of in vitro transcribed messenger RNA (mRNA) as source of &#966;C31 integrase19,24,43. However, this involves the laborious preparation of mRNA and requires careful handling of the injection mix and the use of RNase free reagents to avoid degradation. Plasmid sources of integrase have been demonstrated in both An. gambiae9,21,22,26,33,37 and An. stephensi (A.A. personal communication) to be reliable and lead to efficient transformation, and are thus our preferred option. A further option for integrase delivery is its in vivo production in self-docking helper lines. Such lines were created in An. gambiae that express the &#966;C31 integrase under the regulation of the germline-specific promoter nanos and were found to lead to an improved survival and transformation efficiency20. However, potential fitness loads imposed by the in vivo production of the integrase enzyme on the helper line must be considered.
As with other transgenic techniques, special care must be reserved to the rearing and crossing of individuals deriving from injected embryos to maximize the chances to recover transformants. Individuals that have stably inherited the transgene can be firstly recovered at the G1 progeny. However, early signs of potential transformation can be evaluated by the presence of transient episomal expression of the fluorescent marker in the anal papillae and/or nerve cord of G0 first and second instar larvae when using the 3xP3 promoter43. While the presence of transient fluorescence suggests successful plasmid delivery, it does not guarantee heritable germline transformation. Similarly, the lack of transient expression does not exclude successful transformation. Nevertheless, it has been observed that transiently positive individuals are more likely to yield transgenic progeny compared to transiently negative ones43,48. In expert hands, rearing and crossing of only positive individuals may be an option to reduce mosquito numbers. However, given the importance and fragility of small G0 larvae, the least amount of manipulation is still advisable and the rearing of all G0 individuals is always recommended.
The mating scheme reported in this protocol is designed to maximize the chance of mating and to isolate independent transformation events. However, if insectary space or personnel availability is an issue, G0 adults can be pooled by sex in single cages if enough opposite-sex individuals are provided. Such a setup will not allow discrimination between multiple transformation events occurring in individuals from the same cage. Depending on the experimental setup, the presence of a double (single integration) or single (RMCE) marker is expected during the screening process. In single integration experiments it is important to verify the presence of the original marker from the docking line, while in RMCE is important to verify the loss of the previously integrated marker. Indeed, it is not uncommon in RMCE designs to recover transformants in which single integration instead of exchange occurred due to the recombination of a single attP site9,33. In such individuals both fluorescent markers are present as well as the whole donor plasmid backbone highlighting the importance of conducting a thorough screening for both fluorescent markers.
While the presence of expected fluorescence patterns indicates successful transformation, molecular characterization of the insertion site must be undertaken. To do so, the preparation of accurate maps of the predicted insertion locus, including the flanking genomic regions of the docking line, is crucial for the design of adequate diagnostic oligonucleotide primers for gene amplification analyses. Single integration events result in the formation of attR and attL hybrid sites at the junction between the newly integrated DNA and the previously inserted cassette. These sites can be targeted for insertion site validation. In RMCE designs, the insertion of the donor cassette can occur in two alternative orientations in respect to the genomic locus, thus four primers can be used in alternative PCR combinations to detect which orientation the line carries. As the orientation of cassette insertion may affect transgene expression, in comparative gene expression analysis it is important to use lines carrying the same orientation of insertion.
When working with low numbers of transformants it may not be desirable to sacrifice whole individuals for molecular analysis. An option to this is conducting molecular analysis on DNA extracted from single adult&#39;s legs46 as leg loss does not affect an adult female ability to mate and oviposit49. However, there is a risk of damaging the individual in the process of leg removal. Success has been obtained using discarded pupal cases (L. Grigoraki personal communication), however the safest approach is to perform molecular analysis on G2 parents after obtaining viable G3 progeny.
In recent years, CRISPR/Cas9 has revolutionized the way of performing site-specific genome editing26,41,50,51. Unlike site-directed RMCE, CRISPR/Cas9-mediated gene integrations (knock-ins) are independent of the presence of pre-inserted recombination sites with only a one-step transformation event needed. Nevertheless, the CRISPR/Cas9 system relies on the presence of large known genomic sequences flanking the desired insertion site for successful homology directed repair as well as on the efficient site recognition mediated by guide RNAs. These conditions cannot always be met or may be laborious to troubleshoot and, given the availability of multiple docking lines in An. gambiae and An. stephensi and lines derived from them, the &#966;C31 system remains a very valuable tool to perform direct phenotypic comparisons between transgenes at the same genomic locations.

The ability to modify the genome of mosquito vectors of diseases reliably and reproducibly has bolstered in vivo functional validation of genes and opened the doors to realizable genetic vector control strategies, such as those targeting Anopheles mosquitoes that transmit malaria1.
Early mosquito genome editing relied solely on transposable element (TE)-mediated transformation, with piggyBac being the most commonly used transposon in Anopheles2,3,4. However, the random nature of TE integration can lead to undesirable modifications such as gene knockouts (insertional mutagenesis) and significant position effects on transgene expression5,6,7,8. Multiple insertions are also a common occurrence when using piggyBac5,9, which makes the validation and the isolation of transgenic lines with single insertions laborious. Other drawbacks include their potential remobilization, as observed in the germline of Anopheles stephensi when providing a source of piggyBac transposase10,11,12, and their limited size of DNA cargo (10-15 kb in length) with transformation efficiency declining with increasing size of the donor plasmid13,14.
Site-directed integration approaches were introduced to circumvent these issues. The most common site-directed genome modification in mosquitoes is that mediated by the &#966;C31 system (Figure 1a). This is driven by a viral integrase that catalyzes the recombination between two heterospecific attachment (att) sites occurring naturally in the genome of the bacteriophage &#966;C31 (attP) and in the Streptomyces bacterium host (attB)15. Recombination of the two sites is unidirectional and results in the formation of hybrid sites (attL and attR). The recombination of such hybrid sites (leading to DNA excision) would require not only the presence of an active viral integrase but also another phage-encoded recombination factor16,17. A stable integration site is thus generated that relieves the issue of potential undesired remobilization15. Moreover, the system allows the integration of large cargoes (e.g., integration of &#62;100 kb constructs was reported in D. melanogaster18), significantly increasing carrying capacities. Integration occurs in a single predefined genomic locus which greatly simplifies the validation of insertion and the mating scheme to obtain a stable transgenic line. Finally, the site-directed nature of the integration allows normalization of expression as alternative transgenes are located in the same locus and therefore are regulated within the same neighboring genomic context. Indeed, one of the main applications of the technique is the direct comparison of phenotypes conferred by different transgenes following insertion into an identical locus.
Achieving &#966;C31-mediated integration involves two phases: phase I is the creation of transgenic docking lines carrying attP site(s), and phase II is the site-directed integration of an attB-flanked cargo in the genome of the docking line19. The creation of phase I docking lines has relied on the TE-mediated random integration of attP-tagged constructs and thus involved an initial laborious process (including southern blot and inverse PCR analyses on single-female progeny) to isolate and validate transgenic lines carrying a single integration event in unique, transcriptionally active, and fitness neutral genomic locations. Nevertheless, several docking lines for &#966;C31-mediated single integration have been developed and validated in An. gambiae19,20,21,22 and in An. stephensi23,24,25&#160;(Table 1). Each of these lines varies in terms of the genomic location of the docking site and the strain-specific genetic background and from them a great variety of new transgenic lines can be created. The complex validation of TE-mediated integrations for producing docking lines can now be circumvented by the CRISPR/Cas9 technology26; however this relies on the a priori knowledge of neutral loci to be targeted and their surrounding sequences.
&#966;C31-mediated integration has been applied extensively to insect genome editing from the model organism D. melanogaster27, to the mosquitoes Aedes aegypti13,28, Ae. albopictus29, An. gambiae19, and An. stephensi24, as well as other insects including Ceratitis capitata30 and Bombyx mori31.
A limitation of &#966;C31-mediated integration, especially in view of potential field releases for vector control, is the integration in the mosquito genome of the entire attB-bearing donor plasmid, including undesirable sequences such as antibiotic-resistance gene markers and plasmid backbone components of bacterial origin. To address this, a modification of the standard system, recombinase-mediated cassette exchange (RMCE), was implemented that allows the precise replacement of a previously integrated transgenic cassette with a new donor DNA (Figure 1b). This is achieved by using two inverted att sites flanking the donor and recipient cassettes at each end, which drives two independent recombination events to take place simultaneously resulting in cassette exchange without integration of the plasmid backbone. This improved design circumvents the integration of undesired sequences and expands the application of &#966;C31 systems to include for example the integration of unmarked DNA cargos by screening for the loss of a previously integrated fluorescent marker32.
RMCE was achieved first with D. melanogaster32 and later applied successfully to non-model insects including An. gambiae9,26,33, Ae. aegypti34, Plutella xylostella34, and B. mori35. Several docking lines for RMCE have been developed and validated in An. gambiae5,9,26 (Table 1). To our knowledge, RMCE is yet to be explored in other Anopheles vectors species.
To date, the &#966;C31 system has been used widely in Anopheles mosquitoes to introduce and study a variety of molecules including antimalaria effectors19,24,36, components of the GAL4/UAS system to overexpress and knockdown genes for insecticide resistance studies9,33, regulatory elements, reporter genes5,21,37, and gene-drive elements26,38.
This protocol describes how to perform 1) site-directed integration of an attB-flanked cargo and 2) RMCE of a construct flanked by inverted attB sites into the genome of Anopheles docking lines. This is achieved by using two plasmids: a donor attB-tagged plasmid carrying the transgene of interest, and a helper plasmid expressing the &#966;C31 integrase. The major malaria vectors An. gambiae and An. stephensi are used as specific examples, however these protocols are applicable to other Anopheles species.
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/62146/62146fig01.jpg" /> 
Figure 1. Site-directed genome modifications, single integration and recombinase-mediated cassette exchange (RMCE) , using the&#160;&#966;C31&#160;system.&#160;The&#160;&#966;C31&#160;integrase (INT, grey double arrow) catalyzes the recombination between the&#160;attB&#160;site(s) (purple striped) present in a donor plasmid and the&#160;attP&#160;site(s) (blue striped) present in a receiving docking line, which results in the formation of hybrid sites&#160;attL&#160;and&#160;attR. A) Integration is achieved when single&#160;attB&#160;and&#160;attP&#160;sites recombine and results in the presence of two integrated markers (blue and red). B) RMCE occurs when two&#160;attB/P sites recombine simultaneously and results in the replacement of the cassette between the&#160;att&#160;sites of the docking line (blue marker) with that carried by the donor plasmid (red marker). C) Partial nucleotide sequences of&#160;attP&#160;(blue) and&#160;attB&#160;(purple) and the hybrid sites&#160;attL/R. Recombination occurs between the &#39;TT&#39; core sequences highlighted in bold black.&#160;<a href="https://www.jove.com/files/ftp_upload/62146/62146fig01large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

<table><tbody><tr><td>1.5 mL eppendorf tubes</td><td></td><td></td><td></td></tr><tr><td>8-well microslides</td><td>VWR</td><td>MARI1216690</td><td></td></tr><tr><td>DNeasy Blood &amp;amp; Tissue Kit</td><td>Qiagen</td><td>69504</td><td></td></tr><tr><td>EndoFree&amp;nbsp;Plasmid&amp;nbsp;Maxi&amp;nbsp;Kit (10)</td><td>Qiagen</td><td>12362</td><td></td></tr><tr><td>Ethanol, Absolute, Molecular Biology Grade</td><td></td><td></td><td></td></tr><tr><td>Filter set CFP for Leica MZ FLIII Excitation 436/20 nm, extinction 480/40 nm</td><td>Leica</td><td>10446363</td><td></td></tr><tr><td>Filter set dsRED for Leica MZ FLIII Excitation 545/30 nm, extinction 620/60 nm</td><td>Leica</td><td>10447079</td><td></td></tr><tr><td>Filter set YFP customised for Leica MZ FLIII</td><td>Omega Optical</td><td>500QM25, 500QM35</td><td></td></tr><tr><td>Halocarbon oil 27</td><td>Sigma</td><td>H8773</td><td></td></tr><tr><td>Halocarbon oil 700</td><td>Sigma</td><td>H8898</td><td></td></tr><tr><td>Petri dishes</td><td></td><td></td><td></td></tr><tr><td>Potassium&amp;nbsp;chloride</td><td></td><td></td><td></td></tr><tr><td>Sodium Chloride</td><td></td><td></td><td></td></tr><tr><td>Sodium phosphate dibasic</td><td></td><td></td><td></td></tr><tr><td>Sodium&amp;nbsp;Acetate&amp;nbsp;Solution (3 M),&amp;nbsp;pH&amp;nbsp;5.2</td><td>Thermo Fisher Scientific (Life Technologies)</td><td>R1181</td><td></td></tr><tr><td>Stable brush Size 0</td><td></td><td></td><td></td></tr></tbody></table>

site-directed &#966;c31-mediated integration and cassette exchange in anopheles vectors of malaria

Functional genomic analysis and related strategies for genetic control of malaria rely on validated and reproducible methods to accurately modify the genome of Anopheles mosquitoes. Amongst these methods, the &#966;C31 system allows precise and stable site-directed integration of transgenes, or the substitution of integrated transgenic cassettes via recombinase-mediated cassette exchange (RMCE). This method relies on the action of the Streptomyces &#966;C31 bacteriophage integrase to catalyze recombination between two specific attachment sites designated attP (derived from the phage) and attB (derived from the host bacterium). The system uses one or two attP sites that have been integrated previously into the mosquito genome and attB site(s) in the donor template DNA. Here we illustrate how to stably modify the genome of attP-bearing Anopheles docking lines using two plasmids: an attB-tagged donor carrying the integration or exchange template and a helper plasmid encoding the &#966;C31 integrase. We report two representative results of &#966;C31-mediated site-directed modification: the single integration of a transgenic cassette in An. stephensi and RMCE in An. gambiae mosquitoes. &#966;C31-mediated genome manipulation offers the advantage of reproducible transgene expression from validated, fitness neutral genomic sites, allowing comparative qualitative and quantitative analyses of phenotypes. The site-directed nature of the integration also substantially simplifies the validation of the single insertion site and the mating scheme to obtain a stable transgenic line. These and other characteristics make the &#966;C31 system an essential component of the genetic toolkit for the transgenic manipulation of malaria mosquitoes and other insect vectors.

The protocol illustrated here enables to generate a stable Anopheles transgenic line in ~10 weeks (assuming a 21-day mosquito life cycle).
Post-injection larval hatching rates in An. gambiae are expected to be generally lower than An. stephensi, however hatching rates between 10-50% have been reported9,20,24,26,33,43,47. Given appropriate injection technique, hatching rates of &#8805;20% are generally sufficient to yield transformants. DNA uptake by the embryos can be assessed by screening young larvae for transient expression of the fluorescent marker. In successful RMCE experiments in An. gambiae using the 3xP3 promoter up to 50% of the surviving G0 larvae showed episomal expression of the marker in the anal papillae48.
Generalized estimates of transformation efficiency are difficult to evaluate among laboratories and even among experiments as transformation depends on a complex interplay of variables including purity, concentration, size, and potential toxicity of the injected DNA, quality of eggs, pre- and post-injection handling of eggs, mosquito rearing, and most importantly the experience of the operator. Transformation rates up to 7% have been obtained for RMCE in An. gambiae (calculated as the number of independent transformation events in the total G0 individuals)9,26,33, and up to 2.2% transformation rate for integration in An. stephensi. We suggest injecting at least 500 embryos, which should lead to the hatching of at least 100 G0 larvae and to 2-7 G0 adult founders from which stably transformed progeny can be obtained. If screening for transient expression in G0 larvae, up to 40 positive larvae can be expected.
Examples of phenotypic validation of transformation via the screening of fluorescent markers regulated by the 3xP3 promoter are reported in Figure 4&#160;and&#160;Figure 5. Figure 4 shows a new An. stephensi line obtained by insertion of a DsRed-marked cassette into a docking line marked with CFP (80.9, Table 1), resulting in G1 progeny expressing both markers as indicated by the red and blue fluorescence detected in the eyes.
RMCE designs are instead expected to result in the replacement of the marker originally inserted into the docking line with that of the donor plasmid. Figure 5A and&#160;Figure B illustrate this marker exchange in an An. gambiae docking line marked with CFP (A11, Table 1) where after successful RMCE the CFP marker is lost and the YFP marker is acquired resulting in yellow (but not blue) eye and nerve cord fluorescence33. Occasionally, RMCE can result in a single integration event instead of the exchange of the desired transgenic cassette as illustrated in Figure 5C, where a larva marked with both the original CFP and the new YFP markers is shown. It is reported that up to 50% of the total number of transformation events are single integrations9, 33.
When screening for the presence of a fluorescent marker it is crucial to distinguish its signal from possible background autofluorescence. This is particularly important when using CFP as Anopheles larvae display natural blue autofluorescence (Figure 6A). Increasing the magnification and focusing on the tissues and organs where fluorescence is expected to be driven by the promoter is necessary to identify true CFP-positive individuals as illustrated in Figure 6B using the 3xP3-CFP marker.
Individual transformants are finally assessed molecularly via PCR to confirm the expected insertion site. Figure 7 reports the PCR validation in individuals from an exchange An. gambiae line showing the two potential orientations of insertion in the mosquito genome33.
<img alt="Figure 4" class="xfigimg" src="/files/ftp_upload/62146/62146fig04.jpg" /> 
Figure 4. Validation of &#966;C31 single integration in An. stephensi larvae (dorsal view).&#160;A) The docking line (80.9, Table 1) expresses CFP in the eyes under the regulation of the 3xP3 promoter. B) Successful integration results in the expression of the newly acquired DsRed as well as the original CFP marker in the eyes. <a href="https://www.jove.com/files/ftp_upload/62146/62146fig04large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 5" class="xfigimg" src="/files/ftp_upload/62146/62146fig05.jpg" /> 
Figure 5. Validation of &#966;C31 RMCE in An. gambiae larvae (ventral view).&#160;A) The docking line (A10, Table 1) expresses CFP under the regulation of the 3xP3 promoter in the eyes (e) and the nerve cord (nc)5. B) Successful RMCE results in the swap of fluorescent marker from CFP to YFP33. C) Single integration event occurred during RMCE experiment where the transformant larva expresses both the CFP and YFP markers. This larva carries GAL4/UAS components that cause a broad expression pattern of YFP, particularly strong in the abdominal muscles (am). <a href="https://www.jove.com/files/ftp_upload/62146/62146fig05large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 6" class="xfigimg" src="/files/ftp_upload/62146/62146fig06.jpg" /> 
Figure 6. CFP autofluorescence in An. gambiae larvae (dorsal view). A) Side-by-side image of a positive (CFP+) and a negative (CFP-) L4 larva using the CFP filter. B) Close-up image of the larval eyes that reveals a CFP+ vs CFP- individual. <a href="https://www.jove.com/files/ftp_upload/62146/62146fig06large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 7" class="xfigimg" src="/files/ftp_upload/62146/62146fig07.jpg" /> 
Figure 7. Molecular validation of the orientation of cassette insertion in representative transgenic An. gambiae created by &#966;C31 RMCE. The transgenic cassette can be inserted in one of two alternative orientations (A or B) in respect to the insertion site. Each PCR reaction (I - IV) uses a combination of primers (5-8)33 designed to give a diagnostic amplification fragment for each orientation as indicated in the schematic plasmid maps. T1: representative transgenic individual carrying orientation of insertion A; T2: representative transgenic individual carrying orientation of insertion B; WT: wild type; DL: docking line; -: reaction negative control where water was used as template.This figure has been modified from Adolfi et al. (2019)33.&#160;<a href="https://www.jove.com/files/ftp_upload/62146/62146fig07large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Species</td>
			<td>Strain</td>
			<td>Name</td>
			<td>attP(s)</td>
			<td>Chromo-some</td>
			<td>Promoter-marker</td>
			<td>Institution of origin</td>
			<td>Reference</td>
		</tr>
		<tr>
			<td>An. stephensi</td>
			<td>Indiana</td>
			<td>26.10b</td>
			<td>Single</td>
			<td>2R</td>
			<td>3xP3-eCFP</td>
			<td>Univ. of California Irvine</td>
			<td>25</td>
		</tr>
		<tr>
			<td>An. stephensi</td>
			<td>Indiana</td>
			<td>44Cb</td>
			<td>Single</td>
			<td>X</td>
			<td>3xP3-eCFP</td>
			<td>Univ. of California Irvine</td>
			<td>23, 24</td>
		</tr>
		<tr>
			<td>An. stephensi</td>
			<td>Indiana</td>
			<td>80.9b</td>
			<td>Single</td>
			<td>2L</td>
			<td>3xP3-eCFP</td>
			<td>Univ. of California Irvine</td>
			<td>This study</td>
		</tr>
		<tr>
			<td>An. gambiae</td>
			<td>G3</td>
			<td>113</td>
			<td>Single</td>
			<td>2R</td>
			<td>3xP3-eCFP</td>
			<td>Univ. of California Irvine</td>
			<td>This study</td>
		</tr>
		<tr>
			<td>An. gambiae</td>
			<td>KIL</td>
			<td>Ec</td>
			<td>Single</td>
			<td>3R</td>
			<td>3xP3-eCFP</td>
			<td>Keele Univ.</td>
			<td>19, 43</td>
		</tr>
		<tr>
			<td>An. gambiae</td>
			<td>G3</td>
			<td>X1</td>
			<td>Single</td>
			<td>2L</td>
			<td>No marker</td>
			<td>Univ. of Strasbourg</td>
			<td>22</td>
		</tr>
		<tr>
			<td>An. gambiae</td>
			<td>G3</td>
			<td>YAttP</td>
			<td>Single</td>
			<td>Y</td>
			<td>3xP3-RFP</td>
			<td>Imperial College London</td>
			<td>21</td>
		</tr>
		<tr>
			<td>An. gambiae</td>
			<td>G3</td>
			<td>A10b</td>
			<td>Double</td>
			<td>2R</td>
			<td>3xP3-eCFP</td>
			<td>Liverpool School Trop. Med.</td>
			<td>5</td>
		</tr>
		<tr>
			<td>An. gambiae</td>
			<td>G3</td>
			<td>A11b</td>
			<td>Double</td>
			<td>2R</td>
			<td>3xP3-eCFP</td>
			<td>Liverpool School Trop. Med.</td>
			<td>9</td>
		</tr>
		<tr>
			<td colspan="8">a. Strain from Johns Hopkins University (gift of M. Jacobs-Lorena) and in culture at the Univ. of California Irvine for &#62;20 years.</td>
		</tr>
		<tr>
			<td colspan="8">b. These lines are available from the authors upon reasonable request.</td>
		</tr>
		<tr>
			<td colspan="8">c. This line is available at the BEI repository www.beiresources.org as MRA-1163.</td>
		</tr>
	</tbody>
</table>
Table 1. Anopheles attP docking lines.

Watch this Scientific Journal Video about Site-Directed Ï†C31-Mediated Integration and Cassette Exchange in Anopheles Vectors of Malaria at JoVE.com

Site-Directed &#966;C31-Mediated Integration and Cassette Exchange in Anopheles Vectors of Malaria

The protocol describes how to achieve site-directed modifications in the genome of Anopheles malaria mosquitoes using the &#966;C31 system. Modifications described include both the integration and the exchange of transgenic cassettes in the genome of attP-bearing docking lines.

Functional genomic analysis and related strategies for genetic control of malaria rely on validated and reproducible methods to accurately modify the ...

site-directed-c31-mediated-integration-cassette-exchange-anopheles

Research

JoVE Journal

Genetics

3.8K Views.  Liverpool School of Tropical Medicine. Dit protocol ondersteunt de karakterisering van de rol van muggengenen die betrokken zijn bij een verscheidenheid aan fysiologische routes, waaronder bijvoorbeeld insectenresistentie en de ontwikkeling van malariaparasieten. De methode drijft transgene insertie in enkele vooraf gegekarakteriseerde locaties en maakt het daarom mogelijk om fenotypes die het gevolg zijn van alternatieve transgenen direct te vergelijken, waardoor het probleem van positioneel effect effectief wordt vermeden. Deze ...

Video: Site-Directed φC31-Mediated Integration and Cassette Exchange in Anopheles Vectors of Malaria

Transfection and Mutagenesis of Target Genes in Mosquito Cells by Locked Nucleic Acid-modified Oligonucleotides

Plasmodium parasites, the causative agent of malaria, are transmitted through the bites of infected Anopheles mosquitoes resulting in over 250 million new infections each year. Despite decades of research, there is still no vaccine against malaria, highlighting the need for novel control strategies. One innovative approach is the use of genetically modified mosquitoes to effectively control malaria parasite transmission. Deliberate alterations of cell signaling pathways in the mosquito, via targeted mutagenesis, have been found to regulate parasite development 1. From these studies, we can begin to identify potential gene targets for transformation. Targeted mutagenesis has traditionally relied upon the homologous recombination between a target gene and a large DNA molecule. However, the construction and use of such complex DNA molecules for generation of stably transformed cell lines is costly, time consuming and often inefficient. Therefore, a strategy using locked nucleic acid-modified oligonucleotides (LNA-ONs) provides a useful alternative for introducing artificial single nucleotide substitutions into episomal and chromosomal DNA gene targets (reviewed in 2). LNA-ON-mediated targeted mutagenesis has been used to introduce point mutations into genes of interest in cultured cells of both yeast and mice 3,4. We show here that LNA-ONs can be used to introduce a single nucleotide change in a transfected episomal target that results in a switch from blue fluorescent protein (BFP) expression to green fluorescent protein (GFP) expression in both Anopheles gambiae and Anopheles stephensi cells. This conversion demonstrates for the first time that effective mutagenesis of target genes in mosquito cells can be mediated by LNA-ONs and suggests that this technique may be applicable to mutagenesis of chromosomal targets in vitro and in vivo.

Oligonucleotides can be used to site specifically substitute a single nucleotide of transfected target genes in both Anopheles gambiae and Anopheles stephensi cells.

Plasmodium parasites, the causative agent of malaria, are transmitted through the bites of infected Anopheles mosquitoes resulting in over 250 million new ...

Immunology and Infection

Site-specific Bacterial Chromosome Engineering: &#934;C31 Integrase Mediated Cassette Exchange (IMCE)

The bacterial chromosome may be used to stably maintain foreign DNA in the mega-base range1. Integration into the chromosome circumvents issues such as plasmid replication, plasmid stability, plasmid incompatibility, and plasmid copy number variance. This method uses the site-specific integrase from the Streptomyces phage (&Phi;) C312,3. The &Phi;C31 integrase catalyzes a direct recombination between two specific DNA sites: attB and attP (34 and 39 bp, respectively)4. This recombination is stable and does not revert5. A "landing pad" (LP) sequence consisting of a spectinomycin- resistance gene, aadA (SpR), and the E. coli &szlig;-glucuronidase gene (uidA) flanked by attP sites has been integrated into the chromosomes of Sinorhizobium meliloti, Ochrobactrum anthropi, and Agrobacterium tumefaciens in an intergenic region, the ampC locus, and the tetA locus, respectively. S. meliloti is used in this protocol. Mobilizable donor vectors containing attB sites flanking a stuffer red fluorescent protein (rfp) gene and an antibiotic resistance gene have also been constructed. In this example the gentamicin resistant plasmid pJH110 is used. The rfp gene6 may be replaced with a desired construct using SphI and PstI. Alternatively a synthetic construct flanked by attB sites may be sub-cloned into a mobilizable vector such as pK19mob7. The expression of the &Phi;C31 integrase gene (cloned from pHS628) is driven by the lac promoter, on a mobilizable broad host range plasmid pRK78139.
A tetraparental mating protocol is used to transfer the donor cassette into the LP strain thereby replacing the markers in the LP sequence with the donor cassette. These cells are trans-integrants. Trans-integrants are formed with a typical efficiency of 0.5%. Trans-integrants are typically found within the first 500-1,000 colonies screened by antibiotic sensitivity or blue-white screening using 5-bromo-4-chloro-3-indolyl-beta-D-glucuronic acid (X-gluc). This protocol contains the mating and selection procedures for creating and isolating trans-integrants.

A quick and efficient method to integrate foreign DNA of interest into pre-made acceptor strains, termed landing pad strains, is described. The method allows site-specific integration of a DNA cassette into the engineered landing pad locus of a given strain, through conjugation and expression of the &#934;C31 integrase.

The bacterial chromosome may be used to stably maintain foreign DNA in the mega-base range1. Integration into the chromosome circumvents issues such as ...

Bioengineering

Fluorescent in situ Hybridization on Mitotic Chromosomes of Mosquitoes

Fluorescent in situ hybridization (FISH) is a technique routinely used by many laboratories to determine the chromosomal position of DNA and RNA probes. One important application of this method is the development of high-quality physical maps useful for improving the genome assemblies for various organisms. The natural banding pattern of polytene and mitotic chromosomes provides guidance for the precise ordering and orientation of the genomic supercontigs. Among the three mosquito genera, namely Anopheles, Aedes, and Culex, a well-established chromosome-based mapping technique has been developed only for Anopheles, whose members possess readable polytene chromosomes 1. As a result of genome mapping efforts, 88% of the An. gambiae genome has been placed to precise chromosome positions 2,3 . Two other mosquito genera, Aedes and Culex, have poorly polytenized chromosomes because of significant overrepresentation of transposable elements in their genomes 4, 5, 6. Only 31 and 9% of the genomic supercontings have been assigned without order or orientation to chromosomes of Ae. aegypti 7 and Cx. quinquefasciatus 8, respectively. Mitotic chromosome preparation for these two species had previously been limited to brain ganglia and cell lines. However, chromosome slides prepared from the brain ganglia of mosquitoes usually contain low numbers of metaphase plates 9. Also, although a FISH technique has been developed for mitotic chromosomes from a cell line of Ae. aegypti 10, the accumulation of multiple chromosomal rearrangements in cell line chromosomes 11 makes them useless for genome mapping. Here we describe a simple, robust technique for obtaining high-quality mitotic chromosome preparations from imaginal discs (IDs) of 4th instar larvae which can be used for all three genera of mosquitoes. A standard FISH protocol 12 is optimized for using BAC clones of genomic DNA as a probe on mitotic chromosomes of Ae. aegypti and Cx. quinquefasciatus, and for utilizing an intergenic spacer (IGS) region of ribosomal DNA (rDNA) as a probe on An. gambiae chromosomes. In addition to physical mapping, the developed technique can be applied to population cytogenetics and chromosome taxonomy/systematics of mosquitoes and other insect groups.

Fluorescent in situ Hybridization on Mitotic Chromosomes of Mosquitoes

Among the three mosquito genera, namely Anopheles, Aedes, and Culex, physical genome mapping techniques were established only for Anopheles, whose members possess readable polytene chromosomes. For the genera of Aedes and Culex, however, cytogenetic mapping remains challenging because of the poor quality of polytene chromosomes. Here we present a universal protocol for obtaining high-quality preparations of mitotic chromosomes and an optimized FISH protocol for all three genera of mosquitoes.

Fluorescent in situ hybridization (FISH) is a technique routinely used by many laboratories to determine the chromosomal position of DNA and RNA probes. ...

Using the GAL4-UAS System for Functional Genetics in Anopheles gambiae

The bipartite GAL4-UAS system is a versatile and powerful tool for functional genetic analysis. The essence of the system is to cross transgenic 'driver' lines that express the yeast transcription factor GAL4 in a tissue specific manner, with transgenic 'responder' lines carrying a candidate gene/RNA interference construct whose expression is controlled by Upstream Activation Sequences (UAS) that bind GAL4. In the ensuing progeny, the gene or silencing construct is thus expressed in a prescribed spatiotemporal manner, enabling the resultant phenotypes to be assayed and gene function inferred. The binary system enables flexibility in experimental approaches to screen phenotypes generated by transgene expression in multiple tissue-specific patterns, even if severe fitness costs are induced. We have adapted this system for Anopheles gambiae, the principal malaria vector in Africa.
In this article, we provide some of the common procedures used during GAL4-UAS analysis. We describe the An. gambiae GAL4-UAS lines already generated, as well as the cloning of new responder constructs for upregulation and RNAi knockdown. We specify a step by step guide for sexing of mosquito pupae to establish genetic crosses, that also includes screening progeny to follow inheritance of fluorescent gene markers that tag the driver and responder insertions. We also present a protocol for clearing An. gambiae embryos to study embryonic development. Finally, we introduce potential adaptions of the method to generate driver lines through CRISPR/Cas9 insertion of GAL4 downstream of target genes.

Using the GAL4-UAS System for Functional Genetics in Anopheles gambiae

The bipartite GAL4-UAS system is a versatile tool for modification of gene expression in a controlled spatiotemporal manner which permits functional genetic analysis in Anopheles gambiae. The procedures described for using this system are a semi-standardized cloning strategy, sexing and screening of pupae for fluorescent protein markers and embryo fixation.

The bipartite GAL4-UAS system is a versatile and powerful tool for functional genetic analysis. The essence of the system is to cross transgenic 'driver' ...

Small-Cage Laboratory Trials of Genetically-Engineered Anopheline Mosquitoes

Control of mosquito-borne pathogens using genetically-modified vectors has been proposed as a promising tool to complement conventional control strategies. CRISPR-based homing gene drive systems have made transgenic technologies more accessible within the scientific community. Evaluation of transgenic mosquito performance and comparisons with wild-type counterparts in small laboratory cage trials provide valuable data for the design of subsequent field cage experiments and experimental assessments to refine the strategies for disease prevention. Here, we present three different protocols used in laboratory settings to evaluate transgene spread in anopheline mosquito vectors of malaria. These include inundative releases (no gene-drive system), and gene-drive overlapping and non-overlapping generation trials. The three trials vary in a number of parameters and can be adapted to desired experimental settings. Moreover, insectary studies in small cages are part of the progressive transition of engineered insects from the laboratory to open field releases. Therefore, the protocols described here represent invaluable tools to provide empirical values that will ultimately aid field implementation of new technologies for malaria elimination.

The protocols reported here illustrate three alternative ways to assess the performance of genetically-engineered mosquitoes destined for vector control in laboratory-contained small cage trials. Each protocol is tailored to the specific modification the mosquito strain bears (gene drive or non-gene drive) and the types of parameters measured.

Control of mosquito-borne pathogens using genetically-modified vectors has been proposed as a promising tool to complement conventional control ...

Microinjection Method for Anopheles gambiae Embryos

Embryo microinjection techniques are essential for many molecular and genetic studies of insect species. They provide a means to introduce exogenous DNA fragments encoding genes of interest as well as favorable traits into the insect germline in a stable and heritable manner. The resulting transgenic strains can be studied for phenotypic changes resulting from the expression of the integrated DNA to answer basic questions or used in practical applications. Although the technology is straightforward, it requires of the investigator patience and practice to achieve a level of skill that maximizes efficiency. Shown here is a method for microinjection of embryos of the African malaria mosquito, Anopheles gambiae. The objective is to deliver by microinjection exogenous DNA to the embryo so that it can be taken up in the developing germline (pole) cells. Expression from the injected DNA of transposases, integrases, recombinases, or other nucleases (for example CRISPR-associated proteins, Cas) can trigger events that lead to its covalent insertion into chromosomes. Transgenic An. gambiae generated from these technologies have been used for basic studies of immune system components, genes involved in blood-feeding, and elements of the olfactory system. In addition, these techniques have been used to produce An. gambiae strains with traits that may help control the transmission of malaria parasites.

Microinjection Method for Anopheles gambiae Embryos

Microinjection techniques are essential to introduce exogenous genes into the genomes of mosquitoes. This protocol explains a method used by the James laboratory to microinject DNA constructs into Anopheles gambiae embryos to generate transformed mosquitoes.

Embryo microinjection techniques are essential for many molecular and genetic studies of insect species. They provide a means to introduce exogenous DNA ...

phiC31 Integrase-Mediated Embryo Transgenesis in Drosophila

Embryo Microinjection for Transgenesis in Drosophila

Transgenesis in Drosophila is an essential approach to studying gene function at the organism level. Embryo microinjection is a crucial step for the construction of transgenic flies. Microinjection requires some types of equipment, including a microinjector, a micromanipulator, an inverted microscope, and a stereo microscope.&#160;Plasmids isolated with a plasmid miniprep kit are qualified for microinjection. Embryos at the pre-blastoderm or syncytial blastoderm stage, where nuclei share a common cytoplasm, are subjected to microinjection. A cell strainer eases the process of dechorionating embryos. The optimal time for dechorionation and desiccation of embryos needs to be determined experimentally. To increase the efficiency of embryo microinjection, needles prepared by a puller need to be beveled by a needle grinder. In the process of grinding needles, we utilize a foot air pump with a pressure gauge to avoid the capillary effect of the needle tip. We routinely inject 120-140 embryos for each plasmid and obtain at least one transgenic line for around 85% of plasmids. This article takes the phiC31 integrase-mediated transgenesis in Drosophila as an example and&#160;presents a detailed protocol for embryo microinjection for transgenesis in Drosophila.

Author Spotlight: Optimizing Embryo Microinjection for Transgenesis in Drosophila

This article takes the phiC31 integrase-mediated transgenesis in Drosophila as an example and presents an optimized protocol for embryo microinjection,&#160;a crucial step for creating transgenic flies.

Transgenesis in Drosophila is an essential approach to studying gene function at the organism level. Embryo microinjection is a crucial step for the ...

IR-TEx: An Open Source Data Integration Tool for Big Data Transcriptomics Designed for the Malaria Vector Anopheles gambiae

IR-TEx is an application written in Shiny (an R package) that allows exploration of the expression of (as well as assigning functions to) transcripts whose expression is associated with insecticide resistance phenotypes in Anopheles gambiae mosquitoes. The application can be used online or downloaded and used locally by anyone. The local application can be modified to add new insecticide resistance datasets generated from multiple -omics platforms. This guide demonstrates how to add new datasets and handle missing data. Furthermore, IR-TEx can be completely and easily recoded to use-omics datasets from any experimental data, making it a valuable resource to many researchers. The protocol illustrates the utility of IR-TEx in identifying new insecticide resistance candidates using the the microsomal glutathione transferase, GSTMS1, as an example. This transcript is upregulated in multiple pyrethroid resistant populations from C&#244;te D&#39;Ivoire and Burkina Faso. The identification of co-correlated transcripts provides further insight into the putative roles of this gene.

IR-TEx: An Open Source Data Integration Tool for Big Data Transcriptomics Designed for the Malaria Vector Anopheles gambiae

IR-TEx explores insecticide resistance-related transcriptional profiles in the species Anopheles gambiae. Provided here are full instructions for using the application, modifications for exploring multiple transcriptomic datasets, and using the framework to build an interactive database for collections of transcriptomic data from any organism, generated in any platform.

IR-TEx is an application written in Shiny (an R package) that allows exploration of the expression of (as well as assigning functions to) transcripts ...

Biology

Effective Oral RNA Interference (RNAi) Administration to Adult Anopheles gambiae Mosquitoes

RNA interference has been a heavily utilized tool for reverse genetic analysis for two decades. In adult mosquitoes, double-stranded RNA (dsRNA) administration has been accomplished primarily via injection, which requires significant time and is not suitable for field applications. To overcome these limitations, here we present a more efficient method for robust activation of RNAi by oral delivery of dsRNA to adult Anopheles gambiae. Long dsRNAs were produced in Escherichia coli strain HT115 (DE3), and a concentrated suspension of heat-killed dsRNA-containing bacteria in 10% sucrose was offered on cotton balls ad-libitum to adult mosquitoes. Cotton balls were replaced every 2 days for the duration of the treatment. Use of this method to target doublesex (a gene involved in sex differentiation) or fork head (which encodes a salivary gland transcription factor) resulted in reduced target gene expression and/or protein immunofluorescence signal, as measured by quantitative Real-Time PCR (qRT-PCR) or fluorescence confocal microscopy, respectively. Defects in salivary gland morphology were also observed. This highly flexible, user-friendly, low-cost, time-efficient method of dsRNA delivery could be broadly applicable to target genes important for insect vector physiology and beyond.

Effective Oral RNA Interference RNAi Administration to Adult Anopheles gambiae Mosquitoes

The oral administration of dsRNA produced by bacteria, a delivery method for RNA interference (RNAi) that is routinely used in Caenorhabditis elegans, was successfully applied here to adult mosquitoes. Our method allows for robust reverse genetics studies and transmission-blocking vector studies without the use of injection.

RNA interference has been a heavily utilized tool for reverse genetic analysis for two decades. In adult mosquitoes, double-stranded RNA (dsRNA) ...

Identifying Kinases Rewiring in Malaria Parasite: A Chemical Genetics Approach

Understanding the Development of Compensatory Pathways in a Mutant Malaria Parasite Harbouring Hypomorphic Allele of Plant-Like Kinases

One of the mechanisms for subverting the effect of drugs by&#160;the malaria parasite is through rewiring of its transcriptome. The effect is more pronounced for target genes belonging to the multigene family. Plasmodium falciparum protein kinases belonging to the CDPK family are essential for blood stage development. As such, CDPKs are considered good targets for the development of anti-malarial compounds. The chemical genetics approach has been historically used to elucidate the function of protein kinases in higher eukaryotes. It requires the substitution of gatekeeper residue for another amino acid with a different side chain through genetic manipulation. Amino acid substitution at the gatekeeper position modulates the activity of a protein kinase and changes its susceptibility to a specific class of compounds known as bumped kinase inhibitors (BKIs) that help in the functional identification of the target gene. Here, we have exploited the chemical genetics approach to understand compensatory mechanisms evolved by a mutant parasite harboring a hypomorphic allele of cdpk1. Overall, our approach helps in identifying compensatory pathways that may be simultaneously targeted to prevent the development of drug resistance against individual kinases.

Author Spotlight: Identifying Compensatory Pathways in Malaria Parasites Containing Hypomorphic Allele of Essential Protein Kinases

Chemical genetics involves the substitution of a gatekeeper residue with an amino acid containing a different side chain at the target locus. Here, we have generated a mutant parasite containing a hypomorphic allele of cdpk1 and identified compensatory pathways adopted by the parasite in the mutant background.

Site-Directed φC31-Mediated Integration and Cassette Exchange in Anopheles Vectors of Malaria

Samenvatting

Meer video's verkennen