This work was funded by a grant from the National Science Foundation (grant number MCB-0447750).

1. Prepare Ice-Cap Seedling Plates with Agar Growth Media
Molten growth media (0.5X Murashige and Skoog (MS) basal salt mixture, 2 mM Morpholinoethanesulfonic acid (MES), 0.6% agar (w/v), pH 5.7) is dispensed into autoclaved Seedling Plates using a MicroFill Microplate Dispenser. One liter of media is needed per 18 Seedling Plates.
<ol>
	<li>Prepare growth media in one liter glass bottles with screw top lids and autoclave for 20 minutes.</li>
	<li>Autoclave one liter of distilled water in a glass bottle with screw top lid. At the same time also autoclave empty Seedling Plates wrapped in aluminum foil.</li>
	<li>Transfer the autoclaved media and water to an incubator set at 65&deg;C. This temperature will maintain the growth media in a molten state.</li>
	<li>After autoclaving, remove Seedling Plates from foil and place in laminar flow hood to dry. Plates must be completely dry before proceeding so that the adhesive packing tape can completely seal the holes on the bottom of the wells of the plates.</li>
	<li>Wipe down lab bench with 95% ethanol to sanitize.</li>
	<li>Soak clear plastic lids for the Seedling Plates in 95% ethanol to sanitize. Remove lids from ethanol and air dry in laminar flow hood. Do not autoclave the plastic lids to sterilize them because they will melt in the autoclave.</li>
	<li>Apply packing tape to the bottom of each Seedling Plate and firmly seal using the roller tool.</li>
	<li>Place the bottles of molten growth media and sterilized water in a water bath set at 65&deg;C.</li>
	<li>Attach a bottle containing 70% ethanol at room temperature to the MicroFill machine and run the purge cycle two times to sanitize the plumbing of the MicroFill machine.</li>
	<li>Attach the bottle with sterile water to the MicroFill machine. Run the purge cycle six times to warm the plumbing and clear the ethanol out of the system. The bottle of water should remain in the 65&deg;C bath throughout this procedure.</li>
	<li>After completing the purges with sterile water, immediately attach the bottle of molten growth media to the MicroFill machine. Run the purge cycle two times to clear the distilled water out of the plumbing. The bottle of growth media should remain in the 65&deg;C bath throughout this procedure.</li>
	<li>Dispense 450 microliters of growth media into the wells of each Seedling Plate. Work quickly so that the growth media does not solidify in the plumbing of the MicroFill machine.</li>
	<li>When all of the Seedling Plates have been filled, immediately attach the bottle of 65&deg;C sterile water to the MicroFill machine and run the purge cycle 12 times to clean the plumbing. The bottle of water should remain in the 65&deg;C bath throughout this procedure.</li>
	<li>If a MicroFill machine is not available, Seedling Plates can also be prepared by hand-pipetting molten agar into the sealed plates using a multichannel pipettor.</li>
	<li>Inspect the wells of each Seedling Plates to ensure that the growth media has not leaked out of any wells. Hand pipette additional molten growth media into individual wells as needed.</li>
	<li>Cover each plate with a clear plastic lid, and allow growth media to solidify in the Seedling Plates at room temperature. Stack plates and wrap in aluminum foil for storage at 4&deg;C. Store plates upside down to prevent water accumulation in the wells during storage.</li>
</ol>
2. Sow Seeds into Ice-Cap Seedling Plates and Germinate Seedlings
We have previously described a semi-automated method for dispensing Arabidopsis seeds into Seedling Plates using a seed loading device (2). Although this device can be useful for some batches of seed, we have found that the variability in seed size displayed by different batches of Arabidopsis seeds limits the general utility of this device. We are in the process of developing an alternative automated method for seed dispensing, but at present we have found that the most effective strategy for dispensing seeds into the Seedling Plates is to perform this step by hand as described below.
<ol>
	<li>Sprinkle dry seeds onto Whatman filter paper.</li>
	<li>Dispense 95% ethanol onto seeds so that all of the seeds are covered with ethanol. This treatment will surface sterilize the seeds.</li>
	<li>Allow seeds to air dry.</li>
	<li>Transfer individual seeds into the wells of the Seedling Plates using a modified disposable glass Pasteur pipette. The end of the Pasteur pipette is sealed by flaming the tip. The resulting glass tip is moistened by gently touching to the agar media, which allows a single seeds to be easily picked up and transferred to the surface of the agar in the wells of the Seedling Plate. A double-headed version of this seed plating tool can also be used to increase throughput.</li>
	<li>Cover each Seedling Plate with a clear plastic lid and seal with Micropore surgical tape. Wrap the stacked plates with aluminum foil and store Arabidopsis seeds at 4&deg;C for four days to stratify the seeds and synchronize germination. Tomato seeds should be stored in the dark at 12&deg;C for four days.</li>
	<li>Place the Seedling Plates under fluorescent light at 18&deg; to 20&deg;C to initiate germination.</li>
</ol>
3. Transfer Seedling Plates to Ice-Cap Fountain
After the Seedling Plates have been under light for four days, transfer the Seedling Plates to the Ice-Cap fountain. For Arabidopsis, the seedlings are typically left in the Ice Cap fountain for 10 to 14 days.
<ol>
	<li>Assemble the Ice-Cap Fountain by placing a cookie sheet on top of the custom rack structure which has been placed inside a plastic storage box. Use the leveling nuts to adjust the level of the cookie sheet. Place a submersible pump in the storage box and attach the output hose from the pump to the side of the cookie sheet using a spring loaded clamp. Assemble the Ice-Cap Fountain on a shelf in the plant growth room or growth chamber so that the surface of the Ice-Cap Fountain receives direct fluorescent lighting.</li>
	<li>Fill the Ice-Cap Fountain with a mixture of 3 parts distilled water to 1 part tap water. Water should be added to the fountain until the submersible pump is several centimeters below the water level. Mark the final water level in the plastic storage box using lab tape and a marking pen.</li>
	<li>Prepare Root Plates by adding one 3/32-inch diameter stainless steel ball to each well of a Root Plate.</li>
	<li>The stainless steel balls can be added to the Root Plates using a custom made ball dispensing device 1. This device is made by placing a single sheet of aluminum foil over the surface of a 96-well PCR plate and using a marking pen to mark the locations of the centers of each well on the surface of the foil. This marked sheet of foil is then placed on top of an additional 6 sheets of aluminum foil and wrapped around the smooth surface of a lid from a used pipette tip box. A sharp tool such as a wooden skewer is then used to create a divot large enough to hold a single metal ball at each of the 96 positions. To fill this dispensing device with balls, an excess of metal balls is poured over the device and it is gently shaken to remove excess balls. The Root Plate is then placed over the top of the dispensing device, which is flipped over to drop one ball into each well of the Root Plate.</li>
	<li>Add 340 microliters of a mixture of 3 parts distilled water to 1 part tap water to each well of the Root Plate using the MicroFill machine. Make sure that the steel balls have been added to the Root Plates before dispensing the water.</li>
	<li>Peel the adhesive film off the bottom of the Seedling Plates and remove the clear plastic lids from the plates. Place each Seedling Plate in a Root Plate containing a metal ball and water and secure the two plates together using two elastic hair bands.</li>
	<li>Place the stacked Ice-Cap plates in the Ice-Cap Fountain. The clear plastic lids should not be used when the plates are in the Ice-Cap Fountain. Check to make sure that well A-01 of the Seedling Plate is aligned with well A-01 of the Root Plate.</li>
	<li>The stacked Seedling/Root Plates should be left in the Ice-Cap Fountain until the majority of the seedlings have root tissue that has penetrated into the Root Plates. The ideal growth temperature for Arabidopsis seedlings in the Ice-Cap Fountain is ca. 18&deg;C. The water level in the cookie sheet should be such that water can flow into the wells of the Root Plates, but not so deep that the seedlings in the Seedling Plate are submerged. If the water level is not correct you will need to get a different cookie sheet of the correct depth.</li>
	<li>Add distilled water periodically to the Ice-Cap Fountain to maintain the original water level. By adding pure distilled water to the fountain you will replace the liquid lost due to evaporation without changing the mineral composition of the water in the fountain. Water level should be checked daily in the Ice-Cap Fountain.</li>
</ol>
4. Harvest Root Tissue
Root tissue is harvested by freezing the water in the Root Plate and then peeling the Seedling Plate away from the Root Plate.
<ol>
	<li>The day before harvesting root tissue, remove the stacked Ice-Cap Plates from the Ice-Cap Fountain.</li>
	<li>Insert three wooden skewers between the wells of the stacked Seedling and Root plates. The purpose of the skewers is to raise the nibs of the Seedling Plates out of the wells of the Root Plates in preparation for the freezing process.</li>
	<li>Allow the stacked Ice-Cap Plates with wooden skewers inserted to stand overnight under lights. This incubation allows slight evaporation of the liquid in the Root Plates, which facilitates the subsequent freezing and plate separation processes.</li>
	<li>On the day of tissue harvest, prepare a freezing bath. Place a 96-well metal thermal block in a pyrex dish with mixture of dry ice and 95% ethanol. Allow the thermal block to equilibrate in temperature for ca. 20 minutes. Place the Pyrex dish on top of some type of insulating material such as an autoclave mitten so that the low temperature does not damage the surface of the lab bench.</li>
	<li>Place the stacked Ice-Cap plates with the wooden skewers into the chilled thermal block and incubate for 5 minutes. During this time the water in the Root Plate will freeze solid. The seedlings in the Seedling Plate do not freeze during this treatment and remain fully viable.</li>
	<li>Remove the stacked Ice-Cap plates from the thermal block and place them on the lab bench at room temperature. Remove the elastic bands and the wooden skewers from the stacked plates. Firmly press down on the top of the Seedling Plate to "crack" the plates. Then carefully peel the Root Plate and the Seedling Plate apart.</li>
	<li>Allow the water in the Root Plates to thaw at room temperature. Thawing can be expedited by incubating the Root Plates in a thermal block set at 25&deg;C.</li>
</ol>
5. Store Seedling Plate at Low Temperature in the Dark
Following tissue harvest, the seedling plates can be stored in the dark at low temperature which will maintain the viability of the seedlings while genotype analysis is performed. The seedlings can be stored at these temperatures for several weeks without affecting viability.
<ol>
	<li>Following tissue harvest, seal the lower part of the seedling plate with adhesive tape.</li>
	<li>Place a clear plastic lid on top of the Seedling Plate and secure with micropore tape.</li>
	<li>Stack several Seedling Plates together and wrap in aluminum foil.</li>
	<li>For Arabidopsis seedlings, place the plates at 4&deg;C. For tomato seedlings, place the plates at 12&deg;C. Once genotyping is complete, the seedlings can be removed from this low temperature incubation and transplanted to soil as described below.</li>
</ol>
6. DNA Extraction
DNA suitable for PCR reactions can be easily extracted from the root tissue samples. The yield of total DNA recovered from Arabidopsis root tissue samples is ca. 400 ng on average 2.
<ol>
	<li>Make sure that the water in the Root Plates has completely thawed before performing the DNA extraction procedure. Inspect the plates to determine if any wells have substantially less water than average. Hand pipette distilled water into wells that require additional water.</li>
	<li>Use the MicroFill machine to add 25 microliters of a Tris-EDTA solution (500 mM Tris, pH 8; 50 mM EDTA, pH8) to each well of the Root Plates.</li>
	<li>Seal the wells of the Root Plates using thermal sealing foil and a heat sealing machine.</li>
	<li>Place the sealed root plates on the GenoGrinder machine with the sealed end of the plates facing down. This plate orientation provides optimal bead movement and prevents the beads from sticking in the wells. Shake the plates in the GenoGrinder for 3 &frac12; minutes at 1350 strokes per minute.</li>
	<li>Transfer the plates to a centrifuge with microplate carriers and spin the plates for 10 minutes at 3500 RPM at 4&deg;C to pellet the pulverized root tissue.</li>
	<li>The resulting diluted extract contains genomic DNA that can be directly used in PCR reactions. Typically one will add 2 microliters of this DNA extract to a PCR reaction.</li>
	<li>For storage of DNA samples, seal the microplate using adhesive packing tape and place at minus 20&deg;C. DNA samples can be stored for several months with no apparent reduction in quality.</li>
</ol>
7. Transfer Seedlings with Desired Genotype to Soil
Once genotype analysis is complete, seedlings with the desired genotype can be transferred from the Seedling Plates to soil.
<ol>
	<li>Remove the Seedling Plates from cold storage and prepare pots with water-saturated soil mixture.</li>
	<li>To remove an individual seedling from the Seedling Plate, use a forceps that allows one to grab the agar plug without crushing the seedling. Grab the agar plug with the forceps and gently slide the agar plug out of the Seedling Plate being careful not to damage the seedling. Alternatively, pressurized air can be used to gently shoot the agar plug and seedling out of the well. Apply pressure to the small hole in the bottom of the well until the plug pops out onto the lab bench.</li>
	<li>Prepare a small hole in the soil the size of the agar plug. Place the agar plug in the soil and pack moist soil around the agar plug to secure the seedling in the soil. Do not attempt to remove any of the agar from around the seedling.</li>
	<li>Place the transplanted seedlings in a growth room under standard growth conditions. Cover the pot with a plastic lid for the first two days after transplant. Subsequently remove the lid and continue to grow the plants using standard conditions.</li>
</ol>
8. Representative Results:
An example of Arabidopsis seedlings grown using the Ice-Cap system is shown in Figure 4A. These seedlings had been in the Ice-Cap fountain for two weeks when the picture was taken and were ready for tissue harvest. Root tissue from these same seedling is shown in Figure 4B. The total amount of DNA extracted from one sample of Arabidopsis root tissue is typically in the range of 100 ng to 700 ng 2. This yield calculation is based on the use of only one portion of the crude root extract. Because only ca. 10% of the crude root extract is typically used for the DNA extraction process, it is possible to obtain significantly more genomic DNA for downstream analysis by retaining more of the crude extract. The total amount of genomic DNA obtained using the Ice-Cap procedure is sufficient to perform hundreds of PCR reactions 2.
<img alt="Figure 1" src="/files/ftp_upload/3280/3280fig1.jpg" /> 
Figure 1: Flow chart of the Ice-Cap process. A) Seedling Plate containing agar growth media on which seedlings germinate. Roots penetrate the agar and grow down towards the bottom of the plate. Holes in the bottoms of the wells of the plate are sealed with adhesive film. B) The Seedling Plate is stacked on top of a Root Plate containing water and a metal ball. Roots exit the holes in the bottoms of the wells of the Seedling Plate and grow into the wells of the Root Plate. C) Wooden skewers are inserted between the Seedling Plate and the Root Plate the day before the stacked Ice Cap plates are placed in a thermoblock in a dry ice/ethanol bath. D) Once the water in the Root Plate has frozen solid, the Seedling Plate is peeled away from the Root Plate, yielding a Root Plate with 96 tissue samples and a Seedling Plate with 96 viable seedlings. The wooden skewers facilitate the separation of the two plates during this step.
<img alt="Figure 2" src="/files/ftp_upload/3280/3280fig2.jpg" /> 
Figure 2: Photographs of a Seedling Plate and a Root Plate. A) A Seedling Plate and a Root Plate seen separately. B) A Seedling Plate stacked on top of a Root Plate. The steel balls used for DNA extraction can be seen in the wells of the Root Plate. Elastic bands are used to secure the two plates together.
<img alt="Figure 3" src="/files/ftp_upload/3280/3280fig3.jpg" /> 
Figure 3: The Ice-Cap Fountain. The Ice-Cap Fountain is used to maintain a constant water level at the precise height of the tops of the wells of the Root Plates. This continuous watering system ensures that the water in the wells of the root plates does not become depleted due to evaporation or transpiration. A) A home-made rack that supports the cookie sheet on which the stacked Ice-Cap Plates sit. B) A close-up view of one of the 1" nuts that provides a means for precisely adjusting the level of the cookie sheet so that a uniform water depth is achieved across the surface of the fountain. C) This image displays all of the parts needed to construct the home-made rack for an Ice-Cap Fountain. D) The assembled Ice-Cap Fountain. A submersible fountain pump constantly moves water from the lower reservoir to the cookie sheet, which rests on top of the home-made rack. A spring loaded clamp is used to attach the hose to the edge of the cookie sheet.
<img alt="Figure 4" src="/files/ftp_upload/3280/3280fig4.jpg" /> 
Figure 4: Arabidopsis seedlings grown using the Ice-Cap process. A) Top view looking down into two wells of a Seedling Plate. Each well contains an Arabidopsis seedling. B) Side view of two wells of a Root Plate. Roots can be seen twisting around the inner surface of the wells. The seedlings in this picture had been in the Ice-Cap Fountain for ca. two weeks and are at the growth stage where tissue harvest would normally be performed.

<ol>
	<li>Clark, K. A., Krysan, P. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Protocol:+An+improved+high-throughput+method+for+generating+tissue+samples+in+96-well+format+for+plant+genotyping+(Ice-Cap+2.0).">Protocol: An improved high-throughput method for generating tissue samples in 96-well format for plant genotyping (Ice-Cap 2.0).</a> Plant Methods. 3, 8-8 (2007).</li><li>Krysan, P. I. c. e. -. c. a. p. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+high-throughput+method+for+capturing+plant+tissue+samples+for+genotype+analysis.">A high-throughput method for capturing plant tissue samples for genotype analysis.</a> Plant Physiol. 135, 1162-1169 (2004).</li><li>Jander, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Arabidopsis+map-based+cloning+in+the+post-genome+era.">Arabidopsis map-based cloning in the post-genome era.</a> Plant Physiol. 129, 440-450 (2002).</li><li>Liljegren, S. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=SHATTERPROOF+MADS-box+genes+control+seed+dispersal+in+Arabidopsis.">SHATTERPROOF MADS-box genes control seed dispersal in Arabidopsis.</a> Nature. 404, 766-770 (2000).</li><li>Buechel, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Role+of+A-type+ARABIDOPSIS+RESPONSE+REGULATORS+in+meristem+maintenance+and+regeneration.">Role of A-type ARABIDOPSIS RESPONSE REGULATORS in meristem maintenance and regeneration.</a> Eur. J. Cell. Biol. 89, 279-284 (2010).</li><li>Krysan, P. J., Jester, P. J., Gottwald, J. R., Sussman, M. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=An+Arabidopsis+mitogen-activated+protein+kinase+kinase+kinase+gene+family+encodes+essential+positive+regulators+of+cytokinesis.">An Arabidopsis mitogen-activated protein kinase kinase kinase gene family encodes essential positive regulators of cytokinesis.</a> Plant Cell. 14, 1109-1120 (2002).</li><li>Bush, S. M., Krysan, P. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=iTILLING:+a+personalized+approach+to+the+identification+of+induced+mutations+in+Arabidopsis.">iTILLING: a personalized approach to the identification of induced mutations in Arabidopsis.</a> Plant Physiol. 154, 25-35 (2010).</li><li>Comai, L., Henikoff, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=TILLING:+practical+single-nucleotide+mutation+discovery.">TILLING: practical single-nucleotide mutation discovery.</a> Plant J. 45, 684-694 (2006).</li><li>Henikoff, S., Till, B. J., Comai, L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=TILLING.+Traditional+mutagenesis+meets+functional+genomics.">TILLING. Traditional mutagenesis meets functional genomics.</a> Plant Physiol. 135, 630-636 (2004).</li><li>McCallum, C. M., Comai, L., Greene, E. A., Henikoff, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Targeting+induced+local+lesions+IN+genomes+(TILLING)+for+plant+functional+genomics.">Targeting induced local lesions IN genomes (TILLING) for plant functional genomics.</a> Plant Physiol. 123, 439-442 (2000).</li></ol>

No conflicts of interest declared.

The Ice-Cap method presented here enables one scientist to collect tissue samples from hundreds, or even thousands, of individual plants in a single day and efficiently extract genomic DNA from those samples for use in genotyping reactions. By giving an individual scientist the ability to genotype thousands of seedlings in a short period of time, the Ice-Cap method has the potential to facilitate a number of genetic experiments that would not otherwise be practical to perform. Several examples are provided below.
<ol>
	<li>Genetic Mapping. Fine-scale genetic mapping can be expedited if the researcher is able to identify recombination events within a specific interval along the chromosome 3. If this interval involves a very short genetic distance, then the recombination events will be relatively rare in the segregating mapping population. For this reason, it may be necessary to screen thousands of individual plants to find the desired recombinant individuals. This process could be greatly expedited through the use of Ice-Cap. Even in the era of genome-wide re-sequencing, it is still necessary to directly demonstrate that a given mutation is directly responsible for a phenotype of interest. In these cases, it will be necessary to segregate the mutation of interest away from other closely linked mutations in order to prove a candidate mutation is actually causative. In these situations, Ice-Cap would provide an efficient method for breaking linkage between a pair of tightly linked mutations.</li>
	<li>Multi-mutants. It has become common for researchers studying Arabidopsis to combine mutant alleles from several distinct loci into a single individual in order to overcome functional redundancy 4-6. As an example, consider a case where one wishes to combine mutant alleles from four different loci into a single plant through genetic crossing. For this project, it will be necessary to generate an individual that is heterozygous at these four loci as part of the crossing scheme. When this quadruple-heterozygote sets seed, the quadruple homozygote is expected to be present at a rate of one out of 256 in the resulting population of progeny. Screening for this rare individual by traditional methods would be quite labor intensive. By comparison, using Ice-Cap for this project would provide the scientist with an efficient strategy for identifying the rare quadruple homozygote in a single generation.</li>
	<li>iTILLING. Our laboratory recently described a novel approach to screening for the presence of induced mutations in genes of interest in Arabidopsis 7. This method is a variation on an established technique called TILLING that is used to find mutations in ordered populations of individuals treated with a chemical mutagen 8-10. We have named our method iTILLING because it is an individualized version of TILLING that allows an individual scientist to accomplish something that has traditionally required a large research team to complete. Ice-Cap forms an integral part of the iTILLING method 7, as described below.</li>
</ol>
The idea behind iTILLING is to produce an ephemeral mutant population, which stands in contrast to the durable mutant populations created for traditional TILLING projects. For iTILLING, seeds from a bulked M2 population are sown into 50 to 100 Ice Cap blocks, and DNA is extracted using the Ice-Cap method. Arabidopsis seedlings are then placed at 4&deg;C while mutation screening is performed using the Ice-Cap DNA preps. Tomato seedlings are stored at 12&deg;C.. Once seedlings carrying desired mutations have been identified, they are recovered from the Ice-Cap plates and transferred to soil. iTILLING is not intended to provide a long-lasting mutant population for an entire research community to screen. Instead, iTILLING provides a strategy by which one scientist can screen a custom mutant population for mutations in a handful of genes quickly, efficiently, and at a relatively low cost.
We have found Ice-Cap to be an effective method for growing and genotyping Arabidopsis, tomato, and rice. We expect that other species of plants should also be amenable to Ice-Cap. One limitation on the variety of species that can be accommodated by Ice-Cap is the size of the seeds. Only plants with seeds small enough to fit into the wells of a 96-well plate will be compatible with Ice-Cap in its present configuration.

<table border="1">
	<tbody>
		<tr>
			<td>Name of the reagent</td>
			<td>Company</td>
			<td>Catalogue number</td>
			<td>Comments (optional)</td>
		</tr>
		<tr>
			<td>GenoGrinder</td>
			<td>Spex/CertiPrep, Metuchen, NJ</td>
			<td>2000 Geno/Grinder</td>
			<td>Machine for shaking Root Plates for DNA extraction</td>
		</tr>
		<tr>
			<td>ABgene Thermo-Sealer</td>
			<td>ABgene USA</td>
			<td>AB-0384</td>
			<td>Manual heat sealing machine used to Root Plates prior to tissue disruption</td>
		</tr>
		<tr>
			<td>Centrifuge equipped with swinging microplate carriers</td>
			<td>Beckman Coulter</td>
			<td>Allegra 25R</td>
			<td>Any centrifuge with swinging microplate carriers would be suitable</td>
		</tr>
		<tr>
			<td>MicroFill Microplate Dispenser</td>
			<td>BioTek 
			www.biotek.com</td>
			<td>AF1000A</td>
			<td>Automated liquid dispenser for filling microplates</td>
		</tr>
		<tr>
			<td>Bialetti brand 17x11 inch Commercial Large Cookie Sheet</td>
			<td>Target Department Store</td>
			<td>www.bialetti.com</td>
			<td>This specific cookie sheet has the ideal depth for Ice-Cap</td>
		</tr>
		<tr>
			<td>Custom Made Metal Rack</td>
			<td>Hardware Store</td>
			<td>&nbsp;</td>
			<td>See text for full description</td>
		</tr>
		<tr>
			<td>33 Liter plastic storage box</td>
			<td>Target Department Store</td>
			<td>Sterilite Brand</td>
			<td>For Ice-Cap Fountain. Plastic storage box large enough to hold the 17x11 inch cookie sheet</td>
		</tr>
		<tr>
			<td>30 gallon per hour Fountain Pump</td>
			<td>Sunterra</td>
			<td>104506</td>
			<td>Small submersible fountain pump available at garden supply stores</td>
		</tr>
		<tr>
			<td>Hose for fountain pump</td>
			<td>Any lab supply company</td>
			<td>&nbsp;</td>
			<td>Hose compatible with fountain pump</td>
		</tr>
		<tr>
			<td>Plastic Clamp</td>
			<td>Hardware Store</td>
			<td>&nbsp;</td>
			<td>Clamp to hold hose to cookie sheet</td>
		</tr>
		<tr>
			<td>Clear plastic lids from Falcon Microtest flat bottom 96-well polystyrene plates</td>
			<td>BD Falcon 
			www.bdbiosciences.com</td>
			<td>351172</td>
			<td>Clear plastic lids for covering Ice-Cap Seedling Plates</td>
		</tr>
		<tr>
			<td>3M Micropore surgical tape</td>
			<td>Fisher Scientific</td>
			<td>19-027-761</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>3/32-inch diameter stainless steel balls</td>
			<td>Hartford Technologies, Rocky Hill, CT</td>
			<td>034-006-1K</td>
			<td>Used to disrupt root tissue after harvest</td>
		</tr>
		<tr>
			<td>3 inch Elastic hair bands</td>
			<td>Local grocery store</td>
			<td>&nbsp;</td>
			<td>Used to secure Root Plate to Seedling Plate</td>
		</tr>
		<tr>
			<td>4 mm diameter wooden skewers</td>
			<td>Local grocery store</td>
			<td>&nbsp;</td>
			<td>These skewers are typically used to prepare kabobs</td>
		</tr>
		<tr>
			<td>Fisher Scientific Nunc brand, 1-mL filter plates without frit</td>
			<td>Fisher Scientific</td>
			<td>278012</td>
			<td>96-well Seedling Plates with holes in bottom.</td>
		</tr>
		<tr>
			<td>Fisherbrand 96-Well Tall-Chimney PCR Plate</td>
			<td>Fisher Scientific</td>
			<td>14-230-242</td>
			<td>96-well Root Plates</td>
		</tr>
		<tr>
			<td>Agar - cell culture tested</td>
			<td>Sigma-Aldrich</td>
			<td>A1296</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>4-Morpholinoethanesulfonic acid (MES)</td>
			<td>Sigma-Aldrich</td>
			<td>M2933</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>Murashige and Skoog (MS) basal salt mixture</td>
			<td>Sigma-Aldrich</td>
			<td>M-5524</td>
			<td>&nbsp;</td>
		</tr>
		<tr>
			<td>Easy Peel heat sealing foil</td>
			<td>ABgene USA</td>
			<td>AB-0745</td>
			<td>Heat sealing film for sealing Root Plates prior to tissue disruption</td>
		</tr>
		<tr>
			<td>Duck Brand Extra Wide Packaging Tape, 3.00" x 54.6 yd</td>
			<td>OfficeMax 
			www.officemax.com</td>
			<td>Item no. 21242139</td>
			<td>Adhesive tape for sealing microplates containing DNA extracts for storage</td>
		</tr>
		<tr>
			<td>Sealing Roller</td>
			<td>Bio-Rad</td>
			<td>MSR-0001</td>
			<td>Hand held rolling tool for pressing adhesive sealing tape onto microplates</td>
		</tr>
		<tr>
			<td>96-well metal thermal block</td>
			<td>Cole-Parmer</td>
			<td>36400-66</td>
			<td>Used to freeze the Root Plates for tissue harvest</td>
		</tr>
		<tr>
			<td>Whatman Filter paper</td>
			<td>Whatman International</td>
			<td>1002 090</td>
			<td>Used for surface sterilizing seeds</td>
		</tr>
		<tr>
			<td>Disposable Pasteur Pipette</td>
			<td>Fisher Scientific</td>
			<td>13-678-6A</td>
			<td>5 &frac34;"disposable Pasteur pipette used for transferring seeds to Seedling Plate</td>
		</tr>
		<tr>
			<td>Pyrex baking dish (20 cm x 30 cm)</td>
			<td>Target Department Store</td>
			<td>&nbsp;</td>
			<td>Used to construct a dry ice/ethanol bath.</td>
		</tr>
	</tbody>
</table>

ice-cap: a method for growing arabidopsis and tomato plants in 96-well plates for high-throughput genotyping

It is becoming common for plant scientists to develop projects that require the genotyping of large numbers of plants. The first step in any genotyping project is to collect a tissue sample from each individual plant. The traditional approach to this task is to sample plants one-at-a-time. If one wishes to genotype hundreds or thousands of individuals, however, using this strategy results in a significant bottleneck in the genotyping pipeline. The Ice-Cap method that we describe here provides a high-throughput solution to this challenge by allowing one scientist to collect tissue from several thousand seedlings in a single day 1,2. This level of throughput is made possible by the fact that tissue is harvested from plants 96-at-a-time, rather than one-at-a-time.
The Ice-Cap method provides an integrated platform for performing seedling growth, tissue harvest, and DNA extraction. The basis for Ice-Cap is the growth of seedlings in a stacked pair of 96-well plates. The wells of the upper plate contain plugs of agar growth media on which individual seedlings germinate. The roots grow down through the agar media, exit the upper plate through a hole, and pass into a lower plate containing water. To harvest tissue for DNA extraction, the water in the lower plate containing root tissue is rapidly frozen while the seedlings in the upper plate remain at room temperature. The upper plate is then peeled away from the lower plate, yielding one plate with 96 root tissue samples frozen in ice and one plate with 96 viable seedlings. The technique is named "Ice-Cap" because it uses ice to capture the root tissue. The 96-well plate containing the seedlings can then wrapped in foil and transferred to low temperature. This process suspends further growth of the seedlings, but does not affect their viability. Once genotype analysis has been completed, seedlings with the desired genotype can be transferred from the 96-well plate to soil for further propagation. We have demonstrated the utility of the Ice-Cap method using Arabidopsis thaliana, tomato, and rice seedlings. We expect that the method should also be applicable to other species of plants with seeds small enough to fit into the wells of 96-well plates.

Watch this Scientific Journal Video about Ice-Cap: A Method for Growing Arabidopsis and Tomato Plants in 96-well Plates for High-Throughput Genotyping at JoVE.com

Ice-Cap: A Method for Growing Arabidopsis and Tomato Plants in 96-well Plates for High-Throughput Genotyping

The Ice-Cap method allows one to grow plants in 96-well plates and non-destructively harvest root tissue from each seedling. DNA extracted from this root tissue can be used for genotyping reactions. We have found that Ice-Cap works well for Arabidopsis thaliana, tomato, and rice seedlings.

Ice-Cap: A Method for Growing Arabidopsis and Tomato Plants in 96-well Plates for High-Throughput Genotyping

It is becoming common for plant scientists to develop projects that require the genotyping of large numbers of plants. The first step in any genotyping ...

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22.7K Views.  University of Wisconsin-Madison. The Ice-Cap method allows one to grow plants in 96-well plates and non-destructively harvest root tissue from each seedling. DNA extracted from this root tissue can be used for genotyping reactions. We have found that Ice-Cap works well for Arabidopsis thaliana, tomato, and rice seedlings.

Video: Ice-Cap: A Method for Growing Arabidopsis and Tomato Plants in 96-well Plates for High-Throughput Genotyping

Pyrosequencing: A Simple Method for Accurate Genotyping

Pharmacogenetic research benefits first-hand from the abundance of information provided by the completion of the Human Genome Project. With such a tremendous amount of data available comes an explosion of genotyping methods. Pyrosequencing(R) is one of the most thorough yet simple methods to date used to analyze polymorphisms. It also has the ability to identify tri-allelic, indels, short-repeat polymorphisms, along with determining allele percentages for methylation or pooled sample assessment. In addition, there is a standardized control sequence that provides internal quality control. This method has led to rapid and efficient single-nucleotide polymorphism evaluation including many clinically relevant polymorphisms. The technique and methodology of Pyrosequencing is explained.


Pyrosequencing(R) is one of the most thorough yet simple methods to date used to analyze polymorphisms. This method has led to rapid and efficient single-nucleotide polymorphism evaluation including many clinically relevant polymorphisms. The technique and methodology of Pyrosequencing is explained.

Pharmacogenetic research benefits first-hand from the abundance of information provided by the completion of the Human Genome Project. With such a ...

A High-Throughput Method For Zebrafish Sperm Cryopreservation and In Vitro Fertilization

This is a method for zebrafish sperm cryopreservation that is an adaptation of the Harvey method (Harvey et al., 1982).  We have introduced two changes to the original protocol that both streamline the procedure and increase sample uniformity.  First, we normalize all sperm volumes using freezing media that does not contain the cryoprotectant. Second, cryopreserved sperm are stored in cryovials instead of capillary tubes.  The rates of sperm freezing and thawing (&delta;&deg;C/time) are probably the two most critical variables to control in this procedure.  For this reason, do not substitute different tubes for those specified.  Working in teams of 2 it is possible to freeze the sperm of 100 males per team in ~2 hrs.  Sperm cryopreserved using this protocol has an average of 25% fertility (measured as the number of viable embryos generated in an in vitro fertilization divided by the total number of eggs fertilized) and this percent fertility is stable over many years.

A High-Throughput Method For Zebrafish Sperm Cryopreservation and In Vitro Fertilization

This is a high-throughput sperm cryopreservation protocol for zebrafish. Sperm cryopreserved using this protocol has an average of 25% fertility in subsequent vitro fertilization and is stable over many years.

This is a method for zebrafish sperm cryopreservation that is an adaptation of the Harvey method (Harvey et al., 1982).  We have introduced two changes to ...

A Rapid High-throughput Method for Mapping Ribonucleoproteins (RNPs) on Human pre-mRNA

Sequencing RNAs that co-immunoprecipitate (co-IP) with RNA binding proteins has increased our understanding of splicing by demonstrating that binding location often influences function of a splicing factor.  However, as with any sampling strategy the chance of identifying an RNA bound to a splicing factor is proportional to its cellular abundance.  We have developed a novel in vitro approach for surveying binding specificity on otherwise transient pre-mRNA. This approach utilizes a specifically designed oligonucleotide pool that tiles across introns, exons, splice junctions, or other pre-mRNA.  The pool is subjected to some kind of molecular selection. Here, we demonstrate the method by separating the oligonucleotide into a bound and unbound fraction and utilize a two color array strategy to record the enrichment of each oligonucleotide in the bound fraction. The array data generates high-resolution maps with the ability to identify sequence-specific and structural determinates of ribonucleoprotein (RNP) binding on pre-mRNA.  A unique advantage to this method is its ability to avoid the sampling bias towards mRNA associated with current IP and SELEX techniques, as the pool is specifically designed and synthesized from pre-mRNA sequence. The flexibility of the oligonucleotide pool is another advantage since the experimenter chooses which regions to study and tile across, tailoring the pool to their individual needs.  Using this technique, one can assay the effects of polymorphisms or mutations on binding on a large scale or clone the library into a functional splicing reporter and identify oligonucleotides that are enriched in the included fraction.  This novel in vitro high-resolution mapping scheme provides a unique way to study RNP interactions with transient pre-mRNA species, whose low abundance makes them difficult to study with current in vivo techniques.  



A Rapid High-throughput Method for Mapping Ribonucleoproteins RNPs on Human pre-mRNA

Due to the transient nature of pre-mRNA, it can be difficult to isolate and study in vivo. Here, we present a novel in vitro approach to investigate RNA-protein interactions using a synthetic oligo pool that tiles across selected regions of pre-mRNA.

Sequencing RNAs that co-immunoprecipitate (co-IP) with RNA binding proteins has increased our understanding of splicing by demonstrating that binding ...

Measuring Caenorhabditis elegans Life Span in 96 Well Microtiter Plates

Lifespan is a biological process regulated by several genetic pathways. One strategy to investigate the biology of aging is to study animals that harbor mutations in components of age-regulatory pathways. If these mutations perturb the function of the age-regulatory pathway and therefore alter the lifespan of the entire organism, they provide important mechanistic insights1-3.
Another strategy to investigate the regulation of lifespan is to use small molecules to perturb age-regulatory pathways. To date, a number of molecules are known to extend lifespan in various model organisms and are used as tools to study the biology of aging4-16. The number of molecules identified thus far is small compared to the genetic "toolset" that is available to study the biology of aging.
Caenorhabditis elegans is one of the principle models used to study aging because of its excellent genetics and short lifespan of three weeks. More recently, C.elegans has emerged as a model organism for phenotype based drug screens5,7,16-20 because of its small size and its ability to grow in microtiter plates.
Here we present an assay to measure C.elegans lifespan in 96 well microtiter plates. The assay was developed and successfully used to screen large libraries for molecules that extend C.elegans lifespan7. The reliability of the assay was evaluated in multiple tests: first, by measuring the lifespan of wild type animals grown at different temperatures; second, by measuring the lifespan of mutants with altered lifespans; third, by measuring changes in lifespan in response to different concentrations of the antidepressant Mirtazepine. Mirtazepine has previously been shown to extend lifespan in C.elegans7. The results of these tests show that the assay is able to replicate previous findings from other assays and is quantitative. The microtiter format also makes this lifespan assay compatible with automated liquid handling systems and allows integration into automated platforms.

Measuring Caenorhabditis elegans Life Span in 96 Well Microtiter Plates

In this protocol we present a method to measure Caenorhabditis elegans lifespan in 96 well microtiter plates.

Lifespan is a biological process regulated by several genetic pathways. One strategy to investigate the biology of aging is to study animals that harbor ...

A High-throughput Method for Measurement of Glomerular Filtration Rate in Conscious Mice

The measurement of glomerular filtration rate (GFR) is the gold standard in kidney function assessment. Currently, investigators determine GFR by measuring the level of the endogenous biomarker creatinine or exogenously applied radioactive labeled inulin (3H or 14C). Creatinine has the substantial drawback that proximal tubular secretion accounts for ~50% of total renal creatinine excretion and therefore creatinine is not a reliable GFR marker. Depending on the experiment performed, inulin clearance can be determined by an intravenous single bolus injection or continuous infusion (intravenous or osmotic minipump). Both approaches require the collection of plasma or plasma and urine, respectively. Other drawbacks of radioactive labeled inulin include usage of isotopes, time consuming surgical preparation of the animals, and the requirement of a terminal experiment. Here we describe a method which uses a single bolus injection of fluorescein isothiocyanate-(FITC) labeled inulin and the measurement of its fluorescence in 1-2 &mu;l of diluted plasma. By applying a two-compartment model, with 8 blood collections per mouse, it is possible to measure GFR in up to 24 mice per day using a special work-flow protocol. This method only requires brief isoflurane anesthesia with all the blood samples being collected in a non-restrained and awake mouse. Another advantage is that it is possible to follow mice over a period of several months and treatments (i.e. doing paired experiments with dietary changes or drug applications). We hope that this technique of measuring GFR is useful to other investigators studying mouse kidney function and will replace less accurate methods of estimating kidney function, such as plasma creatinine and blood urea nitrogen.

Measurement of glomerular filtration rate (GFR) is the gold standard for kidney function assessment. Here we describe a high-throughput method which allows the determination of GFR in conscious mice by using a single bolus injection, determination of fluorescein isothiocyanate (FITC)-inulin in plasma and calculation of GFR by a two-phase exponential decay model.

The measurement of  glomerular filtration rate (GFR) is the gold standard in kidney function  assessment. Currently, investigators determine GFR by ...

Measuring Spatial and Temporal Ca2+ Signals in Arabidopsis Plants

Developmental and environmental cues induce Ca2+ fluctuations in plant cells. Stimulus-specific spatial-temporal Ca2+ patterns are sensed by cellular Ca2+ binding proteins that initiate Ca2+ signaling cascades. However, we still know little about how stimulus specific Ca2+ signals are generated. The specificity of a Ca2+ signal may be attributed to the sophisticated regulation of the activities of Ca2+ channels and/or transporters in response to a given stimulus. To identify these cellular components and understand their functions, it is crucial to use systems that allow a sensitive and robust recording of Ca2+ signals at both the tissue and cellular levels. Genetically encoded Ca2+ indicators that are targeted to different cellular compartments have provided a platform for live cell confocal imaging of cellular Ca2+ signals. Here we describe instructions for the use of two Ca2+ detection systems: aequorin based FAS (film adhesive seedlings) luminescence Ca2+ imaging and case12 based live cell confocal fluorescence Ca2+ imaging. Luminescence imaging using the FAS system provides a simple, robust and sensitive detection of spatial and temporal Ca2+ signals at the tissue level, while live cell confocal imaging using Case12 provides simultaneous detection of cytosolic and nuclear Ca2+ signals at a high resolution.

Measuring Spatial and Temporal Ca2+ Signals in Arabidopsis Plants

Ca2+ signaling regulates diverse biological processes in plants. Here we present approaches for monitoring abiotic stress induced spatial and temporal Ca2+ signals in Arabidopsis cells and tissues using the genetically encoded Ca2+ indicators Aequorin or Case12.

Developmental and environmental cues induce Ca2+ fluctuations in plant cells. Stimulus-specific spatial-temporal Ca2+ patterns are sensed by cellular Ca2+ ...

High-throughput Screening for Chemical Modulators of Post-transcriptionally Regulated Genes

Both transcriptional and post-transcriptional regulation have a profound impact on genes expression. However, commonly adopted cell-based screening assays focus on transcriptional regulation, being essentially aimed at the identification of promoter-targeting molecules. As a result, post-transcriptional mechanisms are largely uncovered by gene expression targeted drug development. Here we describe a cell-based assay aimed at investigating the role of the 3&#39; untranslated region (3&#8217; UTR) in the modulation of the fate of its mRNA, and at identifying compounds able to modify it. The assay is based on the use of a luciferase reporter construct containing the 3&#8217; UTR of a gene of interest stably integrated into a disease-relevant cell line. The protocol is divided into two parts, with the initial focus on the primary screening aimed at the identification of molecules affecting luciferase activity after 24 hr of treatment. The second part of the protocol describes the counter-screening necessary to discriminate compounds modulating luciferase activity specifically through the 3&#8217; UTR. In addition to the detailed protocol and representative results, we provide important considerations about the assay development and the validation of the hit(s) on the endogenous target. The described cell-based reporter gene assay will allow scientists to identify molecules modulating protein levels via post-transcriptional mechanisms dependent on a 3&#8217; UTR.

Here we describe a cell-based reporter gene assay as a valuable tool to screen chemical libraries for compounds modulating post-transcriptional control mechanisms exerted through 3&#8217; UTR.

Both transcriptional and post-transcriptional regulation have a profound impact on genes expression. However, commonly adopted cell-based screening assays ...

Measuring Oxidative Stress Resistance of Caenorhabditis elegans in 96-well Microtiter Plates

Oxidative stress, which is the result of an imbalance between production and detoxification of reactive oxygen species, is a major contributor to chronic human disorders, including cardiovascular and neurodegenerative diseases, diabetes, aging, and cancer. Therefore, it is important to study oxidative stress not only in cell systems but also using whole organisms. C. elegans is an attractive model organism to study the genetics of oxidative stress signal transduction pathways, which are highly evolutionarily conserved.
Here, we provide a protocol to measure oxidative stress resistance in C. elegans in liquid. Briefly, ROS-inducing reagents such as paraquat (PQ) and H2O2 are dissolved in M9 buffer, and solutions are aliquoted in the wells of a 96 well microtiter plate. Synchronized L4/young adult C. elegans animals are transferred to the wells (5-8 animals/well) and survival is measured every hour until most worms are dead. When performing an oxidative stress resistance assay using a low concentration of stressors in plates, aging might influence the behavior of animals upon oxidative stress, which could lead to an incorrect interpretation of the data. However, in the assay described herein, this problem is unlikely to occur since only L4/young adult animals are being used. Moreover, this protocol is inexpensive and results are obtained in one day, which renders this technique attractive for genetic screens. Overall, this will help to understand oxidative stress signal transduction pathways, which could be translated into better characterization of oxidative stress-associated human disorders.

Measuring Oxidative Stress Resistance of Caenorhabditis elegans in 96-well Microtiter Plates

C. elegans is an attractive model organism to study signal transduction pathways involved in oxidative stress resistance. Here we provide a protocol to measure oxidative stress resistance of C. elegans animals in liquid phase, using several oxidizing agents in 96 well plates.

Oxidative stress, which is the result of an imbalance between production and detoxification of reactive oxygen species, is a major contributor to chronic ...

qPCRTag Analysis - A High Throughput, Real Time PCR Assay for Sc2.0 Genotyping

The Synthetic Yeast Genome Project (Sc2.0) aims to build 16 designer yeast chromosomes and combine them into a single yeast cell. To date one synthetic chromosome, synIII1, and one synthetic chromosome arm, synIXR2, have been constructed and their in vivo function validated in the absence of the corresponding wild type chromosomes. An important design feature of Sc2.0 chromosomes is the introduction of PCRTags, which are short, re-coded sequences within open reading frames (ORFs) that enable differentiation of synthetic chromosomes from their wild type counterparts. PCRTag primers anneal selectively to either synthetic or wild type chromosomes and the presence/absence of each type of DNA can be tested using a simple PCR assay. The standard readout of the PCRTag assay is to assess presence/absence of amplicons by agarose gel electrophoresis. However, with an average PCRTag amplicon density of one per 1.5 kb and a genome size of ~12 Mb, the completed Sc2.0 genome will encode roughly 8,000 PCRTags. To improve throughput, we have developed a real time PCR-based detection assay for PCRTag genotyping that we call qPCRTag analysis. The workflow specifies 500 nl reactions in a 1,536 multiwell plate, allowing us to test up to 768 PCRTags with both synthetic and wild type primer pairs in a single experiment.

Designer chromosomes of the Synthetic Yeast Genome project, Sc2.0, can be distinguished from their native counterparts using a PCR-based genotyping assay called PCRTagging, which has a presence/absence endpoint. Here we describe a high-throughput real time PCR detection method for PCRTag genotyping.

The Synthetic Yeast Genome Project (Sc2.0) aims to build 16 designer yeast chromosomes and combine them into a single yeast cell. To date one synthetic ...

High-throughput CRISPR Vector Construction and Characterization of DNA Modifications by Generation of Tomato Hairy Roots

Targeted DNA mutations generated by vectors with clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9 technology have proven useful for functional genomics studies. While most cloning strategies are simple to perform, they generally use multiple steps and can require several days to generate the ultimate constructs. The method presented here is based on DNA assembly and can produce fully functional CRISPR vectors in a single cloning reaction. Vector construction can also be pooled, further increasing the efficiency and utility of the process. A modification of the method is used to create CRISPR vectors with multiple gene targets. CRISPR vectors are then transformed into tomato hairy roots to generate transgenic materials with targeted DNA modifications. Hairy roots are a useful system for testing vector functionality as they are technically simple to generate and amenable to large-scale production. The methods presented here will have wide application as they can be used to generate a variety of CRISPR vectors and be used in a wide range of plant species.

Using DNA assembly, multiple CRISPR vectors can be constructed in parallel in a single cloning reaction, making the construction of large numbers of CRISPR vectors a simple task. Tomato hairy roots are an excellent model system to validate CRISPR vectors and generate mutant materials.

Targeted DNA mutations generated by vectors with clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9 technology have proven useful for ...