This work was supported by the Department of Neurosurgery, Memorial Hermann Foundation Staman Ogilvie Fund, the Bentsen Stroke Center at the University of Texas Health Science Center at Houston, and Mission Connect TIRR Foundation.

1. Design and Vector Construction for Targeting Vectors
<ol>
	<li>Once the lineage specific marker is determined, locate the genomic sequence of the gene and design the homology arms accordingly. The length of 5&#8217; homology arm is ~1 kb and of 3&#8217; homology arm is ~1.5 kb (Figure 1).</li>
	<li>Tag the reporter cassette sequentially downstream of the genomic sequence right before the stop codon, by subcloning, so that the endogenous expression is not altered or disrupted. Link the reporter, or dual reporter cassette(s), with self-cleaving 2A peptide sequences (F2A, E2A or T2A) 20,21, or internal ribosome entry site (IRES). 
	Note: Reporters may include fluorescent proteins such as GFP, tdTomato, tagRFP, YFP, luciferase, or antibiotic resistance cassette, a combination of fluorescent protein and antibiotic resistance cassette. An example is shown in Figure 1 for constructing targeting vector for human ALDH1L1 gene, tagged by EGFP and neomycin resistance cassette.</li>
	<li>Add a positive selection cassette downstream of the reporter. The positive selection is a floxed antibiotic resistant cassette which will be excised from the targeted iPSCs after the positive clones are selected and isolated.</li>
	<li>Include a negative selection cassette outside of the 3&#8217; homology arm. Common negative selection cassettes are thymidine kinase, TK, and diphtheria toxin A (DTA) 22.</li>
	<li>Obtain a human BAC clone containing the sequence of the lineage marker and verify the clone by PCR amplification. Construct the targeting vector in pKD46 containing-DH5&#945; using recombineering to pull down the targeting site 23. Apply multisite gateway, Golden gate strategies23,24 when necessary.</li>
</ol>
2. Design and Vector Construction of sgRNAs for CRISPR/Cas9 System.
<ol>
	<li>Determine the lineage specific marker that will be targeted to make the reporter. Copy the cDNA sequence from NCBI database. Go to the human BLAT search to obtain genomic DNA alignment.</li>
	<li>Click the tab &#8220;browser&#8221; to view the assembly of the gene. Under &#8220;View&#8221; tab, click &#8220;DNA&#8221; to obtain the full genomic DNA sequence in FASTA format.</li>
	<li>Locate the stop codon within the DNA sequence, where the 2A sequence and the reporter cassette will be tagged.</li>
	<li>Search for the protospacer adjacent motif (PAM, i.e., NGG) within the vinicity (~100 bp flanking area) of the stop codon. Scan both strands to locate the appropriate NGG sequence. Consider the specificity of the upstream sequences to avoid potential off-target events. Use open source tools such as BLAST and CasOT (see Step 5 for details).</li>
	<li>Copy the sequence of 20 bases immediately upstream of NGG and paste it into the web designing tool ZiFit to design oligos with overhangs compatible with human-gRNA-expression vector (with U6 promoter) MLM3636.</li>
	<li>Synthesize both forward and reverse oligos 7.</li>
	<li>To make double-stranded sgRNA, denature both oligos at 70 &#176;C for 15 min, and gradually cool down to RT. For a 50 &#181;l reaction, add 22.5 &#181;l of forward and reverse oligos (stock concentration is 0.1 mM) respectively, and 5 &#181;l of annealing buffer (100 mM Tris-HCl, 10 mM EDTA, 1.5 M NaCl, pH 8.0).</li>
	<li>Mix and ligate the oligos obtained from step 2.7 with BsmBI-digested human-gRNA-expression vector (with U6 promoter) MLM3636. For a 20 &#181;l reaction, add 1 &#181;l of oligos from Step 2.7, 100 ng of MLM3636, and 1 &#181;l (400 U) of T4 ligase. Incubate at RT O/N.</li>
	<li>Transform DH5&#945; competent cells with the ligation product by heat shock at 42&#176;C for 30 sec. Grow the bacteria in LB agar Ampicillin (100 &#956;g/ml) plate at 37&#176;C O/N. Pick 3~5 colonies for plasmid miniprep according to manufacturer&#8217;s protocol. Sequence the plasmid DNA to confirm using commercial vendors. Maxiprep the correct plasmid according to manufacturer&#8217;s protocol.</li>
	<li>Evaluate sgRNA by T7 endonuclease 1 (T7E1) assay (see Step 4 for details). Transfect hiPSC with the plasmid and sgRNA will be expressed under the built-in U6 promoter in the MLM3636 backbone (See step 6 for details).</li>
</ol>
3. Design and Construction of Cas9n Double Nickase sgRNA
<ol>
	<li>Obtain double nickase Cas9n D10A vector pX335-U6-Chimeric_BB-CBh-hSpCas9n (D10A).</li>
	<li>Design a pair of forward and reverse oligos for each targeting locus. Copy the sequence of 20 bases immediately upstream of NGG as described in Step 2 and paste it into web designing tool ZiFit</li>
	<li>To obtain oligos with overhangs compatible with pX335-U6-Chimeric_BB-CBh-hSpCas9n (D10A), remove the first and last base of both forward and reverse oligos that are shown by the ZiFit designing tool.</li>
	<li>Synthesize forward and reverse oligos7. Name these oligos as f(n)-F, f(n)-R for PAMs on one side of the target site, r(n)-F, r(n)-R for PAMs on the other side of the target site. Of these, n is the number to designate different PAMs, lowercase f and r represent the location of the PAMs either at sense (f) or antisense (r) strand,, F and R represent forward and reverse oligos.
	<ol>
		<li>Test multiple pairs (e.g., r5 and f2) using the T7E1 assay (detailed in Step 4) to identify the optimized pair of sgRNAs to be used for Cas9n.</li>
	</ol>
	</li>
	<li>To make double-stranded sgRNA, denature both oligos at 70 &#176;C for 15 min, and gradually cool down to RT. For a 50 &#181;l reaction, add 22.5 &#181;l of forward and of reverse oligos (stock concentration is 0.1 mM) respectively, and 5 &#181;l of annealing buffer (100 mM Tris-HCl, 10 mM EDTA, 1.5 M NaCl, pH 8.0).</li>
	<li>Mix and ligate the oligos obtained from step 3.5 with BbsI-digested pX335-U6-Chimeric_BB-CBh-hSpCas9n (D10A). For a 20 &#181;l reaction, add 1 &#181;l of sgRNA from Step 3.5, 100 ng of Cas9n (D10A), 1 &#181;l (400 U) of T4 ligase. Incubate at RT O/N.</li>
	<li>Transform DH5&#945; competent cells with the ligation product by heat shock at 42 &#176;C for 30 sec. Grow the bacteria in LB agar Ampicillin (100 &#956;g/ml) plate at 37 &#176;C O/N. Pick 3~5 colonies for plasmid miniprep according to manufacturer&#8217;s protocol. Sequence the plasmid DNA to confirm using commercial vendors. Maxiprep the correct plasmid according to manufacturer&#8217;s protocol.</li>
	<li>Evaluate sgRNA by T7E1 assay (see Step 4 for details). Transfect hiPSC with the plasmid and sgRNA will be expressed under the built-in U6 promoter in the Cas9n (D10A) backbone (See step 6 for details).</li>
</ol>
4. Evaluation of sgRNAs by T7 Endonuclease1 (T7E1) Assay
<ol>
	<li>For one 24-well plate, plate 2 x 105 293FT cells per well one day prior (day -1).</li>
	<li>On the day of transfection (day 0), co-transfect 293FT cells with sgRNA plasmid and Cas9 expression vector. Add 0.5 &#181;g of sgRNA vector, 0.5 &#181;g of Cas9 expression vector JDS246 (Cas9-003), and 1.5 &#181;l of Lipofectamine 2000.
	<ol>
		<li>For negative control, add 0.5 &#181;g of GFP expression vector (e.g., CMV promoter driven GFP in a pcDNA3 backbone) instead of sgRNA vectors.</li>
	</ol>
	</li>
	<li>After 72 hr (day 3), harvest cells by adding 100 &#181;l of DNA quick extraction buffer and triturating vigorously.</li>
	<li>Incubate the mixture at 68 &#176;C for 15 min, then 95 &#176;C for 8 min. This is the template for the subsequent PCR experiments.</li>
	<li>Design both forward and reverse PCR primers to amplify the sequence flanking PAM. Usually the targeting PCR product is around 400-500 bp in length. Synthesize the oligos7.</li>
	<li>For a 50 &#181;l PCR reaction, add 1 &#181;l of template from Step 4.5, 0.5 &#181;l of Herculase II, 0.5 &#181;l of DMSO, 10 &#181;l of 5x buffer, 0.5 &#181;l of dNTP mix, and 1 &#181;l of forward and reverse primer mix.</li>
	<li>Use the following PCR parameters: 98 &#176;C for 2 min, 35 cycles of 98 &#176;C for 20 sec, 59 &#176;C for 20 sec, 72 &#176;C for 1 min, with a final extension at 72 &#176;C for 5 min. 
	Note: The PCR parameters described here yield specific products for several genes tested. However, these conditions are dependent upon user-chosen genes of interest. PCRs using genomic DNA as template often require optimization to ensure that no extra bands appear. These extra bands can be confused with cleavage products after the T7E1 assay.</li>
	<li>Measure DNA concentration of the PCR products using a spectrometer at A260.</li>
	<li>Add 400 ng of PCR products to 2 &#181;l of Digestion buffer 2. Add ddH2O to a final reaction volume of 19 &#181;l. Incubate in boiling water for 5 min. Let the reaction sit on the bench and naturally cool down to RT (45-60 min).</li>
	<li>Add 1 &#181;l (10 units/&#181;l) of T7E1, incubate at 37 &#176;C for 15 min. Stop the reaction by adding 2 &#181;l of 0.25 M EDTA mixed with 6x DNA Loading Dye.</li>
	<li>Dissolve 2.5 g of agarose powder to 100 ml of 1xTAE. Microwave the mixture and pour gel onto a gel box. When gel is formed, load the whole 20 &#181;l reaction to the 2.5% agarose gel. Run the gel at 100-150 V for 30 min.</li>
	<li>Inspect the gel under UV light (Figure 3). T7E1 cuts at the mismatched sites. For sgRNAs that have caused non-homologous end joining, the PCR products will show additional fast migrating bands (smaller in size) compared to negative control (described in step 4.3).</li>
	<li>Estimate and rank sgRNA cutting efficiency and insertion and deletion percentage (indel%) by comparing the band density using Image J software.
	<ol>
		<li>For each sample that run on the gel, designate the gel bands as uncut band, cut band 1 and cut band 2.</li>
		<li>Measure the density of each band using ImageJ according to the software handbook.</li>
		<li>Calculate fcut using the following formula: fcut = (cut band 1 + cut band 2) / (uncut band + cut band 1 + cut band 2)</li>
		<li>Calculate Indel% using the following formula: Indel=1- &#8730;(1-fcut).</li>
	</ol>
	</li>
</ol>
5. In Silico Prediction of Potential Off-target Sites
Note: Potential off target sites can be predicted using an online open source tool called CasOT17, which is a Perl based program.
<ol>
	<li>For a Windows system, download the CasOT program and the human genome database files to local hard drive.</li>
	<li>Prepare the target file of the designed sgRNA in the FASTA format.</li>
	<li>Open the file named &#8220;casot&#8221;. A command window appears. Leave it as is for now.</li>
	<li>Open the file named &#8220;opt-generator&#8221; to generate option string. Paste the path and name of the target file into the dialog of &#8220;-t&#8221; or &#8220;-target&#8221; option.</li>
	<li>Paste the path of the genome sequence file into the dialog of &#8220;-g&#8221; or &#8220;-genome&#8221; option.</li>
	<li>Input values of &#8211;s or &#8211;seed (default value is 2) and &#8211;n or -nonseed (default value is 255). The option string is generated and will appear in the box at the top of the page.</li>
	<li>Copy the option string and paste it into the CasOT command window described in Step 5.3. 
	Note: It might take 30-90 min to run the CasOT program depending on the options and the computer used. Once completed, a folder named &#8216;&#60;input_target_file&#62;-&#60;genome_file&#62;-&#60;off-target_related_options&#62;&#8217; will be generated. Two files will be included in the folder, a &#8220;.stat&#8221; file describing the statistics and a .csv (comma-separated values) file containing the detailed search results.&#60;/off-target_related_options&#62;&#60;/genome_file&#62;&#60;/input_target_file&#62;</li>
	<li>Open the .csv file with a spreadsheet program. The following information is provided in the file for every off target site: chromosomal and genomic location, sequence of the site, mismatch (Mm) type, total number of mismatched bases, and exon information relating to the off target site.</li>
	<li>Design PCR primers for the sites that have &#60;2 Mm in either the seed or the non-seed sequence.</li>
	<li>Perform PCR for selected positive hiPSC clone using the following conditions: 98 &#176;C for 2 min, 35 cycles of 98 &#176;C for 20 sec, 59 &#176;C for 20 sec, 72 &#176;C for 1 min, with a final extension at 72 &#176;C for 5 min. 
	Note: The PCR parameters described here yield specific products for several genes tested in our lab. However, these conditions are dependent upon user-chosen genes of interest. PCRs using genomic DNA as template often require optimization to ensure that no extra bands appear.</li>
	<li>Sequence the PCR products, align sequencing results with predicted sequences and search for mutations. If mutations exist, then off-target events are identified.</li>
</ol>
6. Electroporation of hiPSCs to Make Neural Lineage Reporters
<ol>
	<li>Culture hiPSCs in TeSR-E8 medium on Geltrex coated dishes. Change medium to MEF-CM (Mouse embryonic fibroblasts conditioned medium) medium two days before electroporation. Incubate in 2 ml of Accutase for 5 min and collect cells.</li>
	<li>Electroporate hiPSCs with linearized targeting vector, Cas9-003 expression vector, and sgRNA vector using the following conditions: 1 x 107 hiPSCs, co-transfect 2.5 &#181;g of sgRNA, 2.5 &#181;g of Cas9 and 50 &#181;g of targeting vector. For double nickase strategy, add 50 &#181;g of targeting vector, 2.5 &#181;g of each sgRNA (with Cas9n co-expressed by the vector).</li>
	<li>Select clones by positive and negative selections as described24,25.</li>
	<li>Identify positive clones by Southern blot analysis or long range genomic PCR24,25.</li>
</ol>

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The authors have nothing to disclose.

Gene targeting is an essential tool in characterizing gene functions. However, the relatively low efficiency demands labor-intensive and time-consuming work. Recently development on genome editing tools such as the CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats)/Cas (CRISPR-associated) system has greatly improved the targeting efficiency. This manuscript describes a protocol for generating lineage specific human induced pluripotent stem cell (hiPSC) reporter using CRISPR/Cas system assisted homologous recombination. Steps ...

CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats)/Cas (CRISPR-associated) system, together with other genome editing tools, has revolutionized the human genome manipulation in recent years1-7. Major components in the CRISPR/Cas9 system are single guide RNA (sgRNA) and Cas9. Cas9 is an RNA-guided type II DNA endonuclease. It has two nuclease domains, HNH and RuvC, which are responsible for making DNA double-stranded breaks (DSBs) at a specific genomic region next to a protospacer adjacent motif (PAM)7-10.An sgRNA has a combined function of that of crRNA and tracrRNA, two adaptive immunity RNA molecules identified in bacteria (such as Streptococcus pyogenes) and archaea to fight against DNA invasion of exogenous sources9-11. When appropriately designed and co-introduced to mammalian cells, the sgRNA recognizes the PAM sequence, base-pairs with the complementary strand of target DNA, and guides and transactivates Cas9 to cleave at both DNA strands immediately upstream of PAM7. Subsequently, homologous directed recombination (HDR, in the presence of a targeting vector) or non-homologous end joining (NHEJ) will occur to repair the DSBs. Transgenes such as cDNAs, reporter cassettes, or antibiotic resistant fragments can be integrated, and transgenic or knockin lines made.
Although the CRISPR/Cas9 system is highly efficient and relatively specific, undesired off-target activities have been reported12-15. To minimize off-target events, Cas9 nickases (Cas9n) have also been engineered9,10,14,16,17. Cas9n (Cas9 D10A or Cas9 H840A) is Cas9 enzyme with mutations at one of the two nuclease domains, which only elicits a nick at one strand of DNA. To achieve cleavage at both strands, two sgRNAs are designed to guide a pair of nickases, which cuts separately at nearby loci of the two different DNA strands. The &#8220;double nicking&#8221; strategy requires a more stringent design than the conventional Cas9 platform, and offers both high efficiency and high specificity for gene editing experiments.
This manuscript describes a protocol for generating lineage specific human induced pluripotent stem cell (hiPSC) reporter using CRISPR/Cas system assisted homologous recombination. Steps for obtaining the necessary components for making neural lineage reporter lines using the CRISPR/Cas system mediated genome editing are described, with a focus on construction of targeting vectors and sgRNAs. This protocol has been successfully repeated in multiple hiPSC lines including those derived from healthy individuals and from patients with CNS diseases. Genes targeted in our laboratory include OLIG2, HB9 (MNX1), NEUROG2, SOX1, ALDH1L1 and SOD1. Targeting efficiency from CRISPR/Cas system mediated homologous recombination in hiPSCs ranges from 20-40%, which is consistent with previous reports1,18,19. Compared to a typical efficiency of 1-2% in conventional gene targeting experiments, the targeting efficiency is significantly improved.

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			<td height="20" style="height:20px;width:259px;">Name of Material/Equipment</td>
			<td style="width:265px;">Vendor</td>
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efficient generation of hipsc neural lineage specific knockin reporters using the crispr/cas9 and cas9 double nickase system

유전자 타겟팅은 현대 생물 의학 연구에서 유전자 기능을 특성화하기위한 중요한 방법입니다. 그러나, 인간의 세포에서 표적 유전자의 효율은 원하는 속도로 인간 세포주의 생성을 방지, 저왔다. 지난 2 년은 CRISPR (Interspaced 짧은 회문 반복 정기적으로 클러스터) / CAS (CRISPR 관련) 시스템으로 게놈 편집 도구에 의해 유전자 조작의 효율성을 향상에 신속한 진행을 목격했다. 이 원고는 상동 재조합 지원 CRISPR / CAS 시스템을 사용하여 혈통 특정 인간 유도 만능 줄기 세포 (hiPSC) 기자를 생성하기위한 프로토콜을 설명합니다. , CRISPR / CAS 시스템을 사용하여 신경 계통 리포터 라인을 만들기 위해 필요한 구성 요소를 획득 타겟팅 벡터 및 RNA는 단일 가이드의 구조에 초점을위한 절차가 설명된다. 이 프로토콜은 hiPSCs에서 플랫폼 구축 돌연변이 보정을 확장 할 수있다.

Targeting vectors with all necessary components including homology arms, reporter cassette, positive and negative selection cassettes are constructed (Figure 1). Based on the endogenous genomic locus, multiple (2 to 3) sgRNAs (if using the Cas9 system) or sgRNA pairs (if using the Cas9n double nickase strategy) are designed and constructed into human-gRNA-expression vector MLM3636 or pX335-U6-Chimeric_BB-CBh-hSpCas9n (D10A) backbones (Figure 2). Before transfecting hiPSCs, the sgRNAs are...

Watch this Scientific Journal Video about Efficient Generation of hiPSC Neural Lineage Specific Knockin Reporters Using the CRISPR/Cas9 and Cas9 Double Nickase System at JoVE.com

Efficient Generation of hiPSC Neural Lineage Specific Knockin Reporters Using the CRISPR/Cas9 and Cas9 Double Nickase System

Genome editing tools such as the CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats)/Cas (CRISPR-associated) system have greatly improved gene targeting efficiency in human induced pluripotent stem cells (hiPSCs). This manuscript describes a protocol for generating lineage specific hiPSC reporter using CRISPR/Cas system assisted homologous recombination.

hiPSC 신경 리니지 특정 올림피아 기자의 효율적인 생성 사용 CRISPR / Cas9 및 Cas9 더블 Nickase 시스템

Gene targeting is a critical approach for characterizing gene functions in modern biomedical research. However, the efficiency of gene targeting in human ...

efficient-generation-hipsc-neural-lineage-specific-knockin-reporters

Research

JoVE Journal

Developmental Biology

11.0K 조회수.  The University of Texas Health Science Center at Houston. Genome editing tools such as the CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats)/Cas (CRISPR-associated) system have greatly improved gene targeting efficiency in human induced pluripotent stem cells (hiPSCs). This manuscript describes a protocol for generating lineage specific hiPSC reporter using CRISPR/Cas system assisted homologous recombination.