Efficient and precise genome editing is essential for clinical applications and generating animal models, which requires engineered nucleases with high editing ability while low off-target activity. Here we present a high-throughput sequencing method, primer-extension-mediated sequencing (PEM-seq), to comprehensively assess both editing ability and specificity of engineered nucleases. We showed CRISPR/Cas9-generated breaks could lead to chromosomal translocations and large deletions by PEM-seq. We also found that Cas9 nickase possessed lower off-target activity while with some loss of target cleavage ability. However, high-fidelity Cas9 variants, including both eCas9 and the new FeCas9, could significantly reduce the Cas9 off-target activity with no obvious editing retardation. Moreover, we found AcrIIA4 inhibitor could greatly reduce the activities of Cas9, but off-target loci were not so effectively suppressed as the on-target sites. Therefore, PEM-seq fully evaluating engineered nucleases could help choose better genome editing strategy at given loci than other methods detecting only off-target activity.
The bacterial defense system CRISPR-Cas (clustered regularly interspaced short palindromic repeats and CRISPR-associated proteins) has been engineered to be a versatile genome editing tool1,2,3,4,5,6. CRISPR/Cas9 consists of a guide RNA (gRNA) complementary to target genomic sequence and a Cas9 nuclease to generate a double-stranded DNA break (DSB). Besides 20-bp gRNA-complementary sequence, CRISPR/Cas9 requires extra universal nucleotides NGG adjacent to the target site, termed as protospacer adjacent motif (PAM), to initiate DNA editing, which limits the choice of targeting site but helps to improve the specificity7.
CRISPR/Cas9 shows great potential in genome editing, however, its off-target activity usually causes damage at imperfectly matched genomic loci or leads to chromosomal rearrangements8,9,10,11,12, limiting its application for therapeutic purpose13. Many efforts have been made to reduce off-target activity of CRISPR/Cas9 and high-fidelity Cas9 variants have been generated for this purpose. Cas9 D10A nickase exhibits less detectable off-target activity, but it requires two neighbor gRNA-targeting sites to initiate genome editing9,14. Enhanced Cas9 (eCas9) has showed lower off-target activity due to less nonspecific contacts between Cas9 and target DNA15. Tunable system that controls the duration time of activated Cas9 may also help to lessen undesirable damages to the genome, such as the AcrIIA4 inhibitor that blocks Cas9 activity after cleavage16.
Couple high-throughput sequencing methods designed for detecting DSBs were adapted to identify CRISPR/Cas9 off-target hotspots17. Linear amplification-mediated high-throughput genome-wide translocation sequencing (LAM-HTGTS) employs a “bait” DSB site to capture genome-wide DSBs that form translocation with it9. GUIDE-seq10 and IDLV18 introduce a designed DNA fragment to randomly integrate into DSB sites as cloning primer anchoring site. Digenome-seq19, CIRCLE-seq20, and SITE-seq21 utilize in vitro Cas9 digestion and then capture the broken ends of Cas9-induced DSBs either by deep sequencing or end-tagging strategy. Compared to in vivo DSB-mapping methods, in vitro methods show higher sensitivity but higher background, and require further in vivo verification. In this context, BLISS22 employs ex vivo end-tagging in crosslinked cells that may help to reduce the background with a trade-off of lower end-tagging efficiency. However, neither of the above-mentioned methods is capable of determining in vivo editing efficiency of CRISPR/Cas enzymes. In this regard, targeted sequencing is an alternative high-throughput sequencing way to roughly determine the editing efficiency of CRISPR/Cas9 through counting minor mutations generated at the Cas9 cleavage sites2, but PCR amplification bias leads to quantification inaccuracy. Different with targeted deep sequencing, tracking of indels by decomposition (TIDE)23 utilizes Sanger sequencing and a specific algorithm to evaluate insertions/deletions (indels) amplified by PCR. Both T7 endonuclease I (T7EI) assay3 and restriction fragment length polymorphism (RFLP)24 amplify indels via PCR to omit deep sequencing, but T7EI tends to miss tiny indels and RFLP relies on an appropriate restriction enzyme cutting site spanning the Cas9 target site.
To simultaneously determine editing efficiency and specificity of CRISPR/Cas9, we developed the primer-extension-mediated sequencing (PEM-seq). PEM-seq combined LAM-HTGTS with targeted sequencing and thus could sensitively detect CRISPR/Cas9 off-target sites through translocation capture and assessed their editing efficiency by quantifying imperfect Cas9-induced DSB repair products. We characterized off-target sites as well as other abnormal chromosomal structures including small indels, large deletions, and genome-wide translocations of Cas9 by PEM-seq. We also employed PEM-seq to test several widely used methods developed to reduce Cas9 off-target activity and found that the ability of PEM-seq to comprehensively assess both editing efficiency and specificity of designed CRISPR/Cas9 could greatly help choose appropriate genome editing strategy at given loci. Notably, we generated a new high-fidelity variant named further eCas9 (FeCas9) that has extremely low off-target activity with no obvious loss of editing ability compared with wild-type (WT) Cas9.
PEM-seq sensitively identifies off-target hotspots of CRISPR/Cas9
Translocation requires the joining of two separate DSBs, so placing a locus-specific primer at induced DSBs helps to identify other unknown DSBs, as showed by LAM-HTGTS17. LAM-HTGTS identifies CRISPR/Cas9 off-target sites via mapping genome-wide translocation with target cleavage site9. It initiates with an 80-cycle linear amplification to generate multiple copies of the original DNA fragments, which makes it difficult to distinguish PCR duplicates from the original templates. To overcome this problem and thus to fully assess CRISPR/Cas9, we developed PEM-seq. PEM-seq captures Cas9-induced-DSB outcomes including insertions, deletions, and genomic rearrangements via translocation capture as LAM-HTGTS does. To enable PEM-seq to quantify these outcomes, we conduct primer extension to generate only one copy of the original templates and then isolate these surrogate fragments to join to adapters containing a 14-bp random molecular barcode (RMB) to label each fragment (Fig. 1a). A new bioinformatic pipeline was also prepared to effectively distinguish different DSB outcomes for PEM-seq (Supplementary Fig. S1a).
In order to compare with LAM-HTGTS, we used Cas9 to target the RAG1A site with 33 off-target sites identified by LAM-HTGTS in the HEK293T cells9. About 20 µg CRISPR/Cas9-treated genomic DNA was used for each PEM-seq library and the bait primer was placed within 200 bp from the cleavage site (Supplementary Table S1). We generated three biological replicates for each treatment and combined them for translocation junctional hotspots analysis (Fig. 1b, c; see Materials and methods for details). Via PEM-seq, we identified total 53 off-target sites containing 24 new sites and losing 4 weak sites identified by LAM-HTGTS (Fig. 1b–d and Supplementary Table S2). To verify these off-target sites, we amplified 8 of them, including 4 new sites and 4 overlapped ones, together with RAG1A on-target sites and applied them for in vitro CRISPR/Cas9 digestion. After 20-h incubation, the uncleaved bands of RAG1A on-target site were almost gone, while the “cold” DNA fragment containing no RAG1A target sites showed undetectable cleavage (Supplementary Fig. S1b). Cas9-induced specific cleavage on the 8 selected sites varied from 18 to 60%, much lower than that of RAG1A on-target site (Supplementary Fig. S1b). In addition, we performed PEM-seq analysis on two weakest off-target sites (OT6 and OT8 as indicated in Supplementary Fig. S1b) from the same Cas9:RAG1A-targeted DNA and found a few translocation junctions between these OT6/8 with several other off-target sites (Supplementary Fig. S1c). The miss of RAG1A on-target-involved translocation in libraries from OT6/8 target baits may due to delayed cleavage timing for off-target sites compared to on-target sites25,26,27. Taken together, detected off-target sites were indeed cleaved in vivo and these data suggested a higher sensitivity of PEM-seq to detect off-target sites than LAM-HTGTS did.
To test the compatibility of PEM-seq, we applied PEM-seq to study Cas9:RAG1A off-target hotspots in other cell types including HCT116, K562, and U2OS. To test whether PEM-seq works consistently in these cell lines, we checked the general patterns of genome-wide translocation junctions of these libraries. About half of the translocation junctions located in genic region in all the cell lines, in line with previous reports28,29, and the distribution profiles of translocation junctions at each chromosome were similar among different cell lines (Supplementary Fig. S1d–f). Moreover, PEM-seq detected 13–16 off-target sites (Supplementary Table S2) in the three tested cell lines, all of which had occurred in the HEK293T libraries (Fig. 1d, e). These results indicated that PEM-seq can be easily adapted to detect off-target loci in any editable cell line.
PEM-seq assesses editing ability of CRISPR/Cas9
We next used PEM-seq to quantify editing events including translocation and indels in addition to germline of RAG1A libraries. Germline could be either uncleaved or perfectly repaired target fragments, while indels indicated insertions or deletions resulting from rejoining of the Cas9-generated broken ends (Fig. 2a). As DSB repair products, the levels of translocation and indels are proportional to the cleavage ability of nucleases30, so we can estimate the editing efficiency of CRISPR/Cas9 through the numbers of translocation and indels generated during gene editing. In HEK293T cells treated with Cas9:RAG1A, the levels of translocation and indels were 2.7% and 35.7%, respectively, which added up to an editing efficiency at about 38.4% (Fig. 2a and Supplementary Table S1). Even though we took titrated amounts of sequenced raw reads to perform PEM-seq analysis for RAG1A site, the percentage of indels remained consistent (Supplementary Fig. S2a). Moreover, we mixed different ratios of untreated DNA and Cas9:RAG1A-treated DNA to prepare libraries and found the percentage of indels was proportional to the input ratio (Supplementary Fig. S2b). We also employed RFLP, T7EI, and single-cell RFLP to analyze CRISPR/Cas9 at RAG1A site, and the indels were 27–40% (Fig. 2c and Supplementary Fig. S2c–e), in the same range as PEM-seq. In addition, we employed TIDE to analyze indels of Cas9:RAG1A-treated samples and found a similar level of indel percentages as PEM-seq (Supplementary Fig. S2f). These data suggested that PEM-seq could reliably quantify massive junctions accumulated at on-target sites and thus help to assess editing efficiency of CRISPR/Cas9.
PEM-seq detects large deletions and translocation induced by CRISPR/Cas9
Translocation and indels might threaten genome stability of CRISPR/Cas9-treated cells, therefore we further analyzed the composition of identified translocation and indels after CRISPR/Cas9 treatment. About 1.1% identified translocation events occurred between target sites and off-target sites, while the other 1.6% happened between target sites and genome-wide low-level DSBs (Fig. 2d). With regards to indels, vast majority of them occurred within 20 bp around the target site, with 11.3% small insertions and 24.0% tiny deletions (Fig. 2e). Larger deletions frequently occurred within approximately 3 kb downstream of the primer with a moderate extension to 5 kb; inverted joinings also distributed in the upstream 5 kb region as previously reported9. In the Cas9:RAG1A-treated cells, about 2.5% of total editing events led to deletion or inversion within ±5 kb around the target site (Fig. 2f). Notably, there were low level of enriched junctions expanded as long as 50 kb from the target site downstream of the primer distributing in a biased orientation, which was a typical end resection-induced pattern. The levels of resection in the 5–50 kb region were about 0.05% of total editing events (Fig. 2g). These results indicated that CRISPR/Cas9 editing accumulates abnormal DSB repair products around the target site and PEM-seq could detect them accurately.
Cas9 nickase shows lower off-target activity with loss of target editing efficiency
Designing several Cas9-targeting sites for a certain locus is usually used to screen for a CRISPR/Cas9 balanced for target editing ability and off-target activity. With this regard, we tested Cas9 at alternative sites RAG1B and RAG1C within a 196-bp region around RAG1A9. Both Cas9:RAG1B and Cas9:RAG1C showed lower editing efficiencies (20.0 and 28.0%, Supplementary Table S1) but also less off-target sites (2 and 0, Supplementary Table S3) and lower levels of genome-wide translocations (0.4% for both) (Fig. 3). Compared to Cas9:RAG1A, Cas9:RAG1C is more balanced considering the off-target activity and could be a good choice for RAG1 gene targeting in this region, while Cas9:RAG1B is not a good choice.
Alternatively, employing Cas9 nickase to generating two neighbor DNA nicks can also be used for genome editing, and which was reported to induce less off-target damage14. We designed a new target site RAG1G with a 29-bp spacer between RAG1A cleavage site, and conducted RAG1 gene targeting with RAG1A/G nickases9. We found RAG1A/G nickases showed an editing efficiency at 19.3% (Fig. 3 and Supplementary Table S1), only about half of that of Cas9:RAG1A (38.4%). In addition, we captured five off-target sites by PEM-seq (Fig. 3), none of which was reported by LAM-HTGTS9. All the five identified off-target hotspots ranked top in the RAG1A off-target list and none related to RAG1G site (Supplementary Table S3). Therefore, Cas9 nickase reduces off-target damage during genome editing with a sacrifice of editing efficiency.
High-fidelity Cas9 variant FeCas9 showed very low off-target activity
Various variants were developed to improve the editing specificity of Cas9 (Fig. 4a). In this context, eCas915 showed high specificity due to mutations reducing nonspecific Cas9 and DNA contacts. We put eCas9 under the same promoter as WT Cas9 and directed it to target RAG1A locus in HEK293T cells. As anticipated, we detected only seven off-target sites for eCas9 with no obvious loss of editing efficiency (Fig. 4b–d, Supplementary Table S4). All the detected off-target hotspots for eCas9 ranked top on the list of RAG1A off-target hotspots (Fig. 4d).
Next, we sought to test whether reducing the PAM binding of eCas9 could destabilize Cas9-off-target contacts and thus to further improve its specificity. For this purpose, we generated a new variant FeCas9 by introducing D1135E31 mutation to eCas9 (Fig. 4a). Even though D1135E mutation retained most RAG1A off-target sites, FeCas9 showed higher specificity than eCas9 with only 3 detected off-target hotspots (Fig. 4c). In addition, FeCas9 exhibited comparable editing efficiency at RAG1A site as both WT Cas9 and eCas9 (Fig. 4b). We next tested the specificity of FeCas9 at other loci including one at EMX1 and another one close to c-MYC gene. We detected 18 off-targets for EMX1 site by WT Cas9 via PEM-seq, with a loss of 3 weak ones and a gain of 5 new sites compared to GUIDE-seq analysis in U2OS cells10 (Supplementary Fig. S3A and Supplementary Table S5). FeCas9 consistently showed very low off-target activity with no obvious change of editing efficiency at tested loci; with regards to editing specificity, FeCas9 was better than eCas9 at all tested sites (Fig. 4e–g, Supplementary Fig. S3b–3d and Supplementary Tables S5-S6).
AcrIIA4 inhibitor suppresses Cas9 off-target activity less effectively
We next used PEM-seq to demonstrate the ability of a widely used Cas9 inhibitor AcrIIA4 to block Cas9:RAG1A in HEK293T cells. We titrated the mass ratio of co-transfected Cas9:AcrIIA4 plasmids from 3:1 to 1:1 and finally 1:3. The editing efficiency of Cas9 decreased dramatically when AcrIIA4 was co-transfected. We found a 11-fold decrease of Cas9 editing efficiency at 3:1 and raising the ratio of AcrIIA4 to 1:1 and 1:3 further suppressed Cas9 activity (Fig. 5a). Correspondingly, AcrIIA4-treated Cas9 generated less off-target translocation junctions (Fig. 5b). However, the off-target activity decreased only 1.7–4.6 folds, not so dramatically as the loss of editing efficiency (Fig. 5c, Supplementary Fig. S4a, and Supplementary Table S7), suggesting that AcrIIA4 blocked Cas9 on-target activity more effectively than off-target activity. We also employed SaCas9 targeting MYC locus1 to unbiasedly capture both on- and off-target events of Cas9:RAG1A. The inhibitor had no impact to SaCas9 but caused a 22.8-fold decrease of Cas9 on-target activity while only 7-fold decrease for the off-target activity (Supplementary Fig. S4b–c and Supplementary Table S8), consistent with above finding.
We further tested five distinct loci with AcrIIA4 at 1:1 and detected significant suppression of Cas9 activity at all sites (Fig. 5d, e and Supplementary Table S9). Except for the RAG1B site containing too few off-target hotspots, the other four sites showed more robust suppression to on-target than off-target activity (Fig. 5f), in line with the finding for RAG1A site.
Here we developed PEM-seq to evaluate both editing efficiency and specificity of CRISPR/Cas9 in merely one Hiseq sequencing with 2–10 million reads. PEM-seq has two more advantages than currently used assays to assess CRISPR/Cas9 editing efficiency. First, primer extension and RMB in PEM-seq eliminate the amplification bias during PCR amplification used in other methods such as T7EI, RFLP, TIDE, and targeted sequencing. Second, PEM-seq detects small indels, large deletions, and genome-wide translocation, all of which are CRISPR/Cas9 editing events, while the above-mentioned three methods only detect small indels. PEM-seq also showed higher sensitivity to detect CRISPR/Cas9 off-target hotspots than LAM-HTGTS (Fig. 1), but improved HTGTS could also be very sensitive to detect off-target hotspots32. Compared to other methods designed only for off-target detecting, PEM-seq provides comprehensive information of CRISPR/Cas9 editing events, which definitely helps to choose appropriate target site or nucleases for genome editing. In this context, we showed that Cas9 nickases and AcrIIA4 inhibitor could be a better choice than Cas9 in consideration of only off-target activities, but it’s not true when taking both editing ability and off-target activities into account.
With regards to off-target damage, many factors can affect the final genome editing effect, such as target sequences, Cas9 variants, cell types, and Cas9 activation timing. In this context, FeCas9 could be a good candidate for genome editing (Fig. 4). In addition, control of activation timing could be an efficient way to rapidly revoke Cas9 activity, but co-transfection of Cas9 and AcrIIA4 inhibitor suppresses on-target activity severely than off-target damage, which may be due to that the NGG binding of Cas9 is not so crucial for cleavage at off-target sites but is key for efficient cleavage at on-target sites. In this context, delayed inhibitor delivery may be better since it retains high editing efficiency but nonetheless suppresses off-target activity33.
Besides off-target sites, other abnormal chromosomal structures derived from CRISPR/Cas9-induced DSBs also threaten genome stability. Here we showed that translocation could form when other DSBs including off-target DSBs and genome-wide low-level DSBs occur simultaneously with on-target DSBs, which could be tumor-driven when targeting oncogenes or tumor suppressors. In addition, inversions and deletions could also happen in the surrounding region of target sites9. Most of the deletions are very focal, but a detectable level of deletions can expand to 50 kb or an even larger region, which could lead to disruption of neighbor genes and thus cause unanticipated change to the edited cells. Since these abnormal structures are hallmarks of genome instability, PEM-seq can be easily adapted to study the function of various DNA repair factors in the DSB repair process, including the choice of repair pathway, the level of resection, formation of translocation, and so on.
Limitation of PEM-seq
PEM-seq relies heavily on bait DSBs to capture genome-wide translocation. For the base editors34,35 that directly generate mutations in the genome, the current version of PEM-seq is not suitable for assessing their editing specificity. However, PEM-seq can be adapted to capture occasional DSB intermediates generated during base editing, similar to the DSBs formed in the process of class switch recombination induced by activation-induced cytidine deaminase36. Moreover, PEM-seq can identify off-target sites of CRISPR/Cas9 but cannot quantify the frequencies of identified off-target sites for two reasons: first, spatially proximity impacts formation of translocation and different off-targets show varied spatially proximity to the on-target sites9,37; second, PEM-seq detects indels only for the bait sites and thus cannot capture indels on the off-target sites if using on-target sites as bait, but extra PEM-seq analysis with off-target sites as bait can provide the indel information for off-target sites. Lastly, translocation is a rare event, therefore PEM-seq requires at least tens of thousands of cells to identify the off-target sites of given CRISPR/Cas9.
Materials and methods
All the biotinylated primers are placed within 200-bp from the cleavage site. For primer extension, repeated annealing and denaturation for biotin primer (by Sangon, Shanghai) and 20 μg sonicated genomic DNA (0.3–2 kb) was performed as following: 95 °C 3 min; 95 °C 2 min, Ta (annealing temperature) 3 min, 5 cycles; Ta 3 min. Then Bst polymerase 3.0 (NEB) was added to perform primer extension: 65 °C 10 min, 80 °C 5 min. Excessive biotinylated primers were depleted by 1.2× AxyPrep Mag PCR Clean-Up beads (Axygen, US). Purified products were heated to 95 °C for 5 min and then quickly chilled on ice for 5 min for DNA denaturation. Biotinylated PCR products were enriched by Dynabeads™ MyOne™ Streptavidin C1 (Thermo Fisher).
|Biotin primer||Ta (°C)|
Bridge adapter (with RMB) ligation
PCR products on Streptavidin C1 beads were washed with 400 μl 1× B&W buffer twice (1 M NaCl, 5 mM Tris-HCl (pH 7.4), and 1 mM EDTA (pH 8.0)) followed by 400 μl dH2O washing. Then DNA-beads complex was resuspended with 42.4 μl dH2O. In the bridge adapter ligation step, ligation reaction was performed in 15% PEG8000 (Sigma) with T4 DNA ligase (Thermo Fisher Scientific) at room temperature overnight as following:
|10× T4 buffer||8 μl|
|Bridge adapter (50 μM)||1.6 μl|
|T4 DNA ligase (5 U/μl)||4 μl|
|50% (weight/volume) PEG8000||24 μl|
PCR amplification for Illumina sequencing
Ligation products were washed with 400 μl 1× B&W buffer twice, 400 μl dH2O, and then resuspended with 80 μl dH2O. The beads-DNA complex underwent on-beads nested PCR (Taq, Transgen Biotech, China) with I5 and I7 sequence primers for 16 cycles. Then PCR products were recovered by size-selection beads (Axygen, US) followed by PCR (Fastpfu, Transgen Biotech, China) tagged with Illumina P5 and P7 sequence. All the PEM-seq libraries were subjected to sequencing by 2 × 150 bp Hiseq.
All the gRNA sequences were listed (Supplementary Table S10). Cas9 targeting gRNAs used the pX330 backbone (Addgene 42230) and the Cas9 nickase using pX335 (Addgene 42335). Cas9 variants, SaCas9 were inserted into pX330 backbone as follows: Cas9 variants cDNAs (D1135E, eCas9(1.1), and FeCas9) were generated by mutation-overlap PCR and then inserted into pX330 plasmid through AgeI/EcoRI. SaCas9 cDNA was purified with AgeI/EcoRI from pX601 (Addgene 61591) and then directly ligated to AgeI/EcoRI-digested pX330 plasmid, and the U6 promoter-SaCas9 gRNA scaffold DNA from pX601 was inserted into pX330-SaCas9 between AflIII and XbaI. AcrIIA4 plasmid PJH376 was obtained from Addgene (Addgene 86842).
Cell line and cell transfection
293T, U2OS, and HCT116 cells were cultured in Dulbecco’s modified Eagle’s medium (Corning) with glutamine (Corning), 10% fetal bovine serum (FBS), and penicillin/streptomycin (Corning) at 37 °C with 5% CO2. K562 cells were cultured in RPMI 1640 (Corning) with glutamine, 15% FBS, and penicillin/streptomycin (Corning) at 37 °C with 5% CO2. Libraries for HEK293T cells were prepared by Ca-PO4 co-transfection with 7.2 μg nuclease plasmid and 1.8 μg pMAX-GFP in 6-cm dishes. Libraries for U2OS were co-transfected with 20 μg Cas9 plasmid and 5 μg green fluorescent protein (GFP) plasmid by PEI (Sigma) in 10 cm dishes. HCT116 were transfected with 20 μg Cas9 plasmid and 5 μg GFP plasmid by Lipofectamine 2000 (Invitrogen) in 10 cm dishes. Twenty micrograms of pX330 and 5 μg GFP were co-introduced into K562 cells by nucleofector 4D with FF120 program in SF buffer (Lonza). Cas9 inhibitor AcrIIA4 titration libraries were prepared from cells co-transfected with 2 μg Cas9:RAG1A plasmid, 6 μg AcrIIA4 plus blank plasmids in indicated ratios, and 1 μg GFP plasmid by Ca-PO4 in six-well dishes. For SaCas9:MYC1 libraries, 2 μg SaCas9:MYC locus1 plasmid, 2 μg Cas9:RAG1A plasmid, 2 μg AcrIIA4 or blank plasmid, and 1 μg GFP plasmid were co-transfected into cells cultured in six-well dishes. For other 1:1 libraries, HEK293T cells were co-transfected with 2 μg pX330 plasmid, 2 μg AcrIIA4 or blank plasmid, and 1 μg GFP plasmid. All the libraries were analyzed for GFP co-transfection efficiency by fluorescence-activated cell sorting 48 h after plasmid delivery.
“SuperQ” pipeline for PEM-seq analysis
Hiseq reads were processed as following. For initial reads preprocessing, both Illumina adapter sequences and ending low-quality sequences (QC < 30) were trimmed by cutadapt (http://cutadapt.readthedocs.io/en/stable/); remaining reads shorter than 25 bp were discarded. Then reads were de-multiplexed using fastq-multx (https://github.com/brwnj/fastq-multx) to distinguish index. For reads alignment and clustering, we adapted corresponding pipeline used in LAM-HTGTS9 to perform reads mapping and translocation break point detection. Note that we used the hg38 genome as reference. Uniquely mapped reads were filtered program as LAM-HTGTS did but all the duplicates were kept for following precession. A molecular barcode clustering algorithm38 was adapted to remove PCR duplicates at an editing distance of 2. Break-site and neighbor ±5 bp region was analyzed for indels; reads containing large deletions resulting from resection and rejoining in the break-site ±250 kb region were also categorized as indels (I). Reads without any detected mutations around break point were identified as germline (G). Genome-wide translocation (T) was identified as before. Taking uncut control and transfection efficiency (TE) into account, the editing efficiency was calculated as bellow:
where S represents the nuclease-treated library and C represents the control library.
Off-target hotspot identification
We excluded reads proximal to break-site (±250 kb) and used MACS2 callpeak mode to identify translocation enriched region: --extsize 50 -q 0.05 --llocal 10000000. MACS2 results were further filtered to remove sites with no target site-similar sequence or <3 junctions. A hotspot with highly similar sequence as target site and/or definite PAM and occurring in at least two library replicates was considered as an off-target site9. Briefly, the off-target hotspots are recurrent in a focal region containing cryptic target sequences and have a balanced directional distribution with a center right at the presumable cutting site. Yet, the off-target-independent translocations are usually low frequent and have biased directional distribution with no neighbor target-similar sequences. Total number of junctions within ±500 bp of off-target presumable cutting site was counted to calculate the off-target intensity after normalization to uncut control library:
In vitro digestion for DNA fragments by Cas9
Cas9 was purified as described previously39. gRNA and scaffold RNA were transcribed by T7 High Efficiency Transcription Kit (Transgen Biotech, China) in vitro. A unit of 100 nM Cas9 and 300 nM RNA were used for each reaction. DNA fragments were digested in the condition: 20 mM HEPES (pH 7.5), 5% glycerol, 100 mM KCl, 1 mM dithiothreitol, 10 mM MgCl2, and 0.5 mM EDTA at 37 °C for 20 h.
RFLP cleavage assay
RAG1A locus was PCR amplified by Fastpfu (Transgen Biotech, China) using listed primers (Supplementary Table S11). Amplicons recovered by 1.2× AxyPrep Mag PCR Clean-Up beads (Axygen, US) were cleaved by StyI (NEB) for an hour followed by agarose gel electrophoresis. Band intensity was quantified by Image J (version 1.51J8) and the indels was measured by the following formula:
IC is sum of the intensity of two cleaved bands, and IU is the intensity of the uncleaved bands.
T7EI cleavage assay
Fraction cleaved (FC) ratio was calculated using the method described before9. Final indels was measured by the following formula (assuming the annealing prior to T7EI cutting is completely random):
Single-cell RFLP cleavage assay
Single clone of Cas9:RAG1A transfected cells was picked into 96-well dish. Genomic DNA was extracted after 7-day incubation. And RFLP cleavage assay was performed as described in RFLP section. Cleavage products were classified into three categories: fully digested (II), partially digested (IH), and non-digested (IG). Since the HEK293T cell we used is triploid, we scored fully digested as 3 and non-digested as 0. With regards to partially digested, either one or two alleles can be edited by Cas9 with equal chance in theory, and thus we scored them as 1.5. Therefore, the indels percentage was measured by the following formula:
General process was referred to the method described before23. Primers were designed for RAG1A on-target site. Genomic DNA was extracted from Cas9:RAG1A transfected cells and 50 ng genomic DNA was used as template with routine PCR program for 30 cycles. Gel-purified PCR products were prepared for Sanger sequencing. The result file (.ab1) was analyzed by the website tool provided at https://tide.deskgen.com/.
Data were presented as mean ± SD and p < 0.05 was considered significant.
The “SuperQ” pipeline was deposited at github site: https://github.com/liumz93/superQ; and the PEM-seq data were deposited into GEO (GSE116231).
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We thank Dr. Hui Yang for gifts of plasmids and Dr. Zhou Du for his help on SuperQ pipeline. This work is supported by the National Key R&D Program of China (2017YFA0506700), the NSFC grant (31771485), the SLS-Qidong Innovation Fund, and the Thousand Talents Plan Youth Program to J.H. J.H. is a Bayer investigator and an investigator of PKU-TSU Center for Life Sciences.
J.Y., Y. Liu, and J.H. developed PEM-seq; M.L. wrote the SuperQ pipeline; J.Y., M.L., Y. Liu, and J.H. designed the experiments; J.Y., Y. Liu, T.G., W.Z., Y. Li, and Y.Z. performed the experiments; J.Y., M.L., Y. Liu, and J.H. analyzed the data; J.Y., M.L., Y. Liu, and J. H. wrote the paper.
Conflict of interest
The authors are applying for a patent for PEM-seq and FeCas9.
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Yin, J., Liu, M., Liu, Y. et al. Optimizing genome editing strategy by primer-extension-mediated sequencing. Cell Discov 5, 18 (2019). https://doi.org/10.1038/s41421-019-0088-8
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