CRISPR/Cas9 holds immense potential to treat a range of genetic disorders. Allele-specific gene disruption induced by non-homologous end-joining (NHEJ) DNA repair offers a potential treatment option for autosomal dominant disease. Here, we successfully delivered a plasmid encoding S. pyogenes Cas9 and sgRNA to the corneal epithelium by intrastromal injection and acheived long-term knockdown of a corneal epithelial reporter gene, demonstrating gene disruption via NHEJ in vivo. In addition, we used TGFBI corneal dystrophies as a model of autosomal dominant disease to assess the use of CRISPR/Cas9 in two allele-specific systems, comparing cleavage using a SNP-derived PAM to a guide specific approach. In vitro, cleavage via a SNP-derived PAM was found to confer stringent allele-specific cleavage, while a guide-specific approach lacked the ability to distinguish between the wild-type and mutant alleles. The failings of the guide-specific approach highlights the necessity for meticulous guide design and assessment, as various degrees of allele-specificity are achieved depending on the guide sequence employed. A major concern for the use of CRISPR/Cas9 is its tendency to cleave DNA non-specifically at “off-target” sites. Confirmation that S. pyogenes Cas9 lacks the specificity to discriminate between alleles differing by a single base-pair regardless of the position in the guide is demonstrated.
The promise of personalised gene therapy has been brought nearer fruition with the recent advances in the field of genome engineering, particularly the development of Clustered Regularly Interspaced Palindromic Repeats (CRISPR)/CRISPR associated protein (Cas) systems. CRISPR/Cas9 is an RNA guided endonuclease, that has been manipulated for use in mammalian cells to act as a two component system, requiring only a Cas9 nuclease and a single guide RNA (sgRNA)1,2,3. Cas9 can be directed to cut a desired sequence in the genome, provided it is directly upstream of a protospacer adjacent motif (PAM), by simply altering the guide RNA sequence (Fig. 1a). The site-specific sgRNA will direct the Cas9 nuclease to make a double strand break (DSB). The cell will then attempt to repair this damage, by either error-prone non-homologous end joining (NHEJ) or precise homology directed repair (HDR)4, and it is by these different cellular responses that different forms of gene editing can be achieved.
NHEJ can be utilised to generate gene knockouts, due to the high frequency of frameshifting mutations generated4,5. Allele-specific gene disruption via NHEJ is a potential approach to treat dominant negative disorders, in which the causative gene is haplosufficient; this involves targeting the mutant allele alone for disruption, leaving the wild-type allele intact and restoring the phenotype6,7,8,9. This approach relies on the ability of the targeting system to unequivocally discriminate between wild-type and mutant sequence.
Although CRISPR/Cas9 holds immense promise, one caveat to the use of the system is that Cas9 nuclease has been shown to tolerate mismatches between the guide sequence and the target10,11. This can lead to off-targeting elsewhere in the genome or, indeed in this case, cleavage of the wild-type allele. Efforts have been made to increase the specificity of Cas9 and eliminate off-target cutting, including; use of truncated guides12, Cas9 variants from other bacterial species to exploit more intricate PAMs13, rationally engineering the Cas9 nuclease14, and using the mutant sequence to induce specificity such as utilising a novel SNP-derived PAM15,16.
In particular utilising a novel PAM is an attractive option for allele-specific editing. Previous work has demonstrated that when mutations result in a novel PAM, guide RNAs can be designed, utilising this new PAM, allowing only the mutant allele to be targeted, producing an allele-specific knockout14.
The cornea offers an ideal platform for testing personalised gene therapy, due to its immediate accessibility, small surface area and immune-privileged status. Collectively the corneal dystrophies represent a group of inheritable blinding diseases that alter the shape or transparency of the cornea. Currently mutations in 14 genes are associated with corneal dystrophies, 9 of them presenting with an autosomal dominant inheritance pattern17. Corneal dystrophies linked to these 9 genes predominantly result from missense mutations or small in-frame insertions or deletions that cause disease by a dominant negative effect of the mutant protein17.
Transforming growth factor beta induced protein (TGFBIp) has been linked to a range of stromal or stromal-epithelial corneal dystrophies18,19,20. TGFBI is predominantly produced in the corneal epithelium and is transported to the stromal layer, where the mutant protein accumulates21. To-date a total of 60 missense mutations in TGFBI have been linked to various corneal dystrophies22,23. These mutations span the entire TGFBI gene but are clustered in hotspots found in exon 4, 11, 12 and 14.
Despite the wide spectrum of mutations, the vast majority of cases are due to 5 prevalent mutations found in either codon 124 (exon 4) or codon 555 (exon 12)24,25 (Fig. 1b). These 5 mutations include; R124C, R124H, R124L, R555Q and R555W and as described account for the bulk of reported cases of TGFBI corneal dystrophies26,27,28. Remarkably, each of these mutations, differing by only a single amino acid, result in strikingly different protein aggregates with a very strong genotype-phenotype correlation.
To achieve complete allele-specificity for a particular TGFBI mutation, stringent fidelity is required as an almost perfect off-target site exists in the form of the wild-type allele, which, for the majority of TGFBI mutations, differs by only one base pair from the mutant. This report uses TGFBI corneal dystrophies as a model of autosomal dominant disease to assess the specificity of the CRISPR/Cas9 system for autosomal dominant disorders. An allele-specific approach to target the five most prevalent TGFBI corneal dystrophy mutations is investigated, which highlights the promiscuity of Cas9 and the need for a validated, highly specific approach, that will encompass all possible TGFBI mutations.
In vivo corneal gene disruption induced by CRISPR/Cas9 gene editing and NHEJ-mediated DNA repair
We utilised a previously reported reporter knock-in mouse (Krt12+/luc2), that exclusively expresses firefly luciferase (luc2) in the corneal epithelium under control of the keratin K12 promoter, to study corneal delivery and activity of CRISPR/Cas9-mediated gene editing in living animals. To target the luciferase gene, an sgRNA utilising a PAM site 61 nucleotides downstream of the luc2 start codon was designed (Fig. 2a) and validated using a dual-luciferase assay (Fig. 2b). Therapeutic efficacy of this CRISPR/Cas9 system in living cornea was assessed following a single intrastromal injection in Krt12+/luc2 mice. Luciferase activity was evaluated with daily measurements up to 1 week following injection and weekly thereafter, for an additional 5 weeks (Fig. 2c). Luciferase activity was significantly reduced from post-injection day 1, with maximal silencing of >99% achieved at day 3 in one animal, and a maximal mean reduction of 82% ± 13% observed in 4 mice on day 4. Sustained silencing of luciferase expression was observed in 3 out of 4 mice over the entire monitoring period of the experiment (7 weeks), while in the remaining animal, luciferase inhibition persisted for 2 weeks (Fig. 2c).
Mutational analysis of TGFBI corneal dystrophy mutations
Currently the best characterised CRISPR/Cas9 system is that of Streptococcus pyogenes (SpCas9), which recognises a 5′-NGG-3′ PAM. An analysis of the 60 known TGFBI missense mutations (See Supplementary Table 1) was performed to determine if i) they generate a novel S. pyogenes PAM or ii) they have a S. pyogenes PAM nearby, placing the mutation within the seed region, defined here as the first 8 nucleotides immediately adjacent to the PAM29,30,31.
19/60 mutations generate a novel S. pyogenes PAM, while 44/60 have a naturally occurring adjacent PAM site that places the mutation within an eight nucleotide seed region. When these figures are considered together, 20% of the TGFBI missense mutations are not targetable by S. pyogenes (Fig. 3a).
Analysis of the most prevalent TGFBI mutations in codon 124 and codon 555 revealed that none generated a novel S. pyogenes PAM, however all mutations had a S. pyogenes PAM within the first eight nucleotides of the target sequence (Fig. 3b).
Further to this, an analysis was conducted to determine if any of the prevalent TGFBI mutations generated a novel PAM with a CRISPR system from a different bacterial species. It was found that the R555W mutation generated a novel PAM with Staphylococcus aureus Cas9 (SaCas9), which recognises a 5′-NNGRRT-3′ PAM. In addition to this the R124L mutation generated a novel PAM with a mutant Acidaminococcus Cpf1 (AsCpf1) system32, which is capable of recognising a 5′-VYCV-3′ PAM (Fig. 3c).
Validation of an S. pyogenes Cas9 PAM-specific approach
A PAM-specific approach has previously been shown to be an ideal way to achieve allele-specific editing14. To validate this approach a lattice corneal dystrophy-associated TGFBI mutation (L527R), was assessed33. The L527R mutation (c.1580 T > G) generates a novel PAM with S. pyogenes, (CTG > CGG) (Fig. 4a, top). A 20 nt sgRNA utilising the novel PAM was designed and an additional 20 nt sgRNA targeted to a naturally occurring PAM was designed as a positive control (Fig. 4a, bottom). Specificity was first assessed using a previously described in vitro dual-luciferase assay7,9,34 in which the two sgRNAs were co-expressed with either S. pyogenes Cas9, S.aureus Cas9 or AsCpf1 and a luciferase reporter containing a 50 bp region of either wild -type or mutant TGFBI sequence, which has been cloned into the multiple-cloning-site within the 3′UTR of Luc2. Cleavage of the TGFBI sequence within the reporter construct prevents transcription and processing of luciferase mRNA and results in an proportionate reduction of luciferase expression and therefore luciferase activity was measured as an indicator of sgRNA activity. The sgRNA utilising the novel PAM was shown to be highly specific, directing cutting of only the mutant TGFBI sequence, while both reporters were cleaved by the common sgRNA (Fig. 4b). In addition, an in vitro digestion using mutant 18 and 20 nt sgRNAs with a reporter containing either wild-type or mutant TGFBI sequence was carried out which confirmed the specificity observed in the dual-luciferase assay (Fig. 4c). Co-transfection with the mutant 18 and 20 nt sgRNAs only resulted in cleavage of the mutant reporter, the wild-type reporter template remained intact. Truncation of the guide did not appear to improve specificity.
Investigation of Cas9 orthologues S.aureus and AsCpf1
As none of the prevalent TGFBI mutations generated a novel PAM with S. pyogenes Cas9, alternative Cas9 orthologues were investigated. Although S.aureus Cas9 prefers a 5′-NNGRRT-3′ PAM, generated by the TGFBI R555W mutation (5′-GAGAAT-3′) (Fig. 3b). It has also been shown to recognise a 5′-NNGRRV-3′ PAM with comparable efficiencies35, and this is present in the wild-type TGFBI sequence. Since S.aureus Cas9 prefers a guide length of either 21 nucleotides or 22 nucleotides13. both 21 nt and 22 nt guides utilising the novel S.aureus PAM were designed and targeted to both wild-type and mutant R555W TGFBI sequences. No significant knockdown was observed with either guide length and the mutant R555W guide was unable to distinguish between wild-type and mutant TGFBI sequence (Fig. 5a).
A mutant AsCpf1 was generated that has the capability of recognising a 5′-VYVC-3′ PAM, as generated by the TGFBI R124L mutation (5′-CTCA-3′) (Fig. 3b). A 20 nt guide was designed utilising the novel mutant AsCpf1 PAM and targeted to both the wild-type and mutant R124L TGFBI sequences. Although the mutant guide can distinguish between wild-type and mutant TGFBI sequence the knockdown efficiency is very low with a maximal knockdown of 20% (Fig. 5b).
Investigation of a guide-specific approach using S. pyogenes Cas9
As none of the most prevalent TGFBI mutations generated a novel PAM with S. pyogenes Cas9 and adequate specificity or efficiency could not be achieved with Cas9 orthologues from other bacterial species, a guide-specific approach was explored; whereby the mutant guide differs from the wild-type sequence only by a single base pair. A dual-luciferase assay was employed to assess the specificity of a 20 nt guide for the 5 most prevalent TGFBI mutations; R124C, R124H, R124L, R555Q and R555W. Each guide was targeted to the wild-type and respective mutant sequence and the firefly luciferase activity was measured as an indicator of specificity (Fig. 6).
Cas9 directed by R124C sgRNA was able distinguish between wild-type and mutant sequence, although it cut with a low efficiency of 26%. R124H cut with an improved specificity and efficiency, although wild-type sequence was significantly cleaved (17%). R124L offered the most promising specificity profile, 60% cleavage of mutant sequence was observed in comparison to 23% of the wild-type sequence, however the wild-type sequence was still significantly cleaved when compared to the non-specific control. Although the R555Q guide directed efficient cleavage of the mutant reporter, the wild-type sequence was also substantially cut by 50%. Finally R555W preferentially cleaved mutant sequence, however the wild-type sequence was still cleaved by 10%.
Investigation of the effect of guide length on the specificity of S. pyogenes Cas9
Reports have indicated that truncating the length of the matching sequence within the guide to 18 nucleotides can reduce off-target cutting, while maintaining on-target efficiencies12. As none of the 20 nt guides provided adequate specificity an assessment of the effect of guide-length upon specificity using a dual-luciferase assay was conducted for the 5 most prevalent TGFBI mutations. Reports have shown that guide lengths <16 nt abolish cleavage activity36,37. For each mutation a range of guide lengths from 16–22 nucleotides were tested, each guide was targeted to the wild-type and respective mutant sequence and the firefly luciferase activity was measured as an indicator of specificity (Fig. 7).
For all mutations investigated the truncated guides did not provide a marked improvement of specificity, for most cases maximal discrimination occurred with guides 20 or 19 nucleotides in length. For R124C, a 20 nt guide seemed to confer allele-specificity, however no other guide length offered any adequate discrimination (Fig. 7a). In the case of the R555Q mutation guides in the 18–20 nt range did not offer sufficient discrimination, although, interestingly, the 21 nt guide provided convincing allele-specificity (Fig. 7d). R555W did not offer any considerable allele-specificity for any length tested (Fig. 7e). R124H and R124L displayed clear allele-specific cleavage, especially in the 18–20 nt sgRNA range, with minimal cutting of the wild-type sequence (Fig. 7b,c). Interestingly for the R124 mutations guide lengths of 21 nt seemed to impair cleavage activity in all cases.
Addition of 5′-GG to the 20 nt guide sequence
Standard design of sgRNA guides includes the addition of a guanine to the 5′ end of the guide sequence (5′-GX20-3′) to help facilitate efficient transcription4. An alternative guide design of 5′-GGX20-3′ has been reported to minimise off-target activity in certain cases, offering an improved specificity of Cas938. This parameter was tested using the 5 most prevalent TGFBI mutations (Fig. 8). The additional guanine at the 5′ end of the guide sequence did not provide an improved specificity in any case. In some instances a reduction in on-target activity was observed, confirming that specificity is guide dependent.
In vitro digestion to confirm specificity of S. pyogenes Cas9
In vitro digestion of either wild-type or mutant TGFBI sequence with Cas9 protein complexed with sgRNA was carried out to further assess the specificity profile of S. pyogenes Cas9 (Fig. 9). Guide lengths of 18 and 20 nucleotides were tested to evaluate the impact of truncating the guide sequence. For R124C the mutant 20 nt guide appeared to cut the mutant sequence more than the wild-type sequence. However, when truncated to 18 nt the mutant guide appeared to loose ability to distinguish between wild-type and mutant sequence, reflecting results from the dual luciferase assay. For R124H and R124L both mutant 20 nt and 18 nt guides appeared to clearly cut the mutant sequence preferentially over the wild-type sequence, again reflecting the dual-luciferase results. Interestingly, in both cases the wild-type guide appeared to result in more cleavage of the mutant sequence in comparison to the mutant sequence, although as the wild-type guide would not be implicated in a clinical setting it can be ignored. For R555Q and R555W the 20 nt or 18 nt guides did not confer allele-specificity under any conditions, cutting both wild-type and mutant sequence equally, demonstrating mismatches in the distal region of the guide are less critical in determining specificity of Cas9.
Dominant negative disorders that are the result of an accumulation of mutant protein can be targeted by allele-specific CRISPR mediated gene disruption via NHEJ. We have shown in vivo that gene disruption via NHEJ offers a viable approach to achieve gene silencing. Sustained knockdown of luciferase was observed in the corneal epithelium of reporter mice over several weeks in 3 out of 4 mice, following a single intrastromal injection of CRISPR/Cas9 components (Fig. 2c). Since the corneal epithelium is completely turned over every 1–2 weeks39, our data suggests permanent editing took place within the corneal stem cell compartment following in vivo delivery of CRISPR/Cas9. By extension, CRISPR/Cas9 gene editing using an sgRNA specific to pathologic mutant alleles delivered by intrastromal injection has great potential for editing resident corneal stem cells as a permanent cure for dominant-negative corneal disorders. However, in order to translate this strategy to the clinic as a therapy the issue of specificity must be addressed.
The prevalent TGFBI mutations offer an interesting real-life scenario in which to test different approaches to allele-specific CRISPR/Cas9 gene therapy as the different causative mutations with different phenotypes associated with the same codon create different specificity profiles.
Published reports illustrate that the region immediately adjacent to the PAM is critical to specificity25,26,27. The documented importance of this region has led to it being coined as the ‘seed’ region. The Cas9:sgRNA complex will initially identify the correct PAM, and only once the PAM has been identified will the Cas9:sgRNA complex then test the complementarity between the guide and target DNA. The PAM proximal region, or seed region, is critical in this step and mismatches in this region will prevent the ternary complex forming and therefore cleavage will not occur40. The exact length of the seed region is unclear, with reports ranging from 5–12 nucleotides29,30,31.
The TGFBI mutations investigated here gave the opportunity to investigate the extent of this seed region further. The mutations in codon 124 lie at guide positions 3 or 4, so are within the seed region of whichever definition, whereas, codon 555 mutations lie in guide positions 7 or 8, so can be considered either inside or outside the seed region. Accordingly, it was demonstrated that allele-specificity was achieved by guides targeting R124H and R124L mutations both found at position 3 of the guide. However, neither R124C, R555Q or R555W mutations found at positions 4, 7 and 8 respectively, were capable of adequate allele-specific cleavage. This confirms that the sequence immediately adjacent to the PAM is most critical in determining specificity of the guide, and mismatches are not well tolerated here. In contrast mismatches in positions 4, 7 or 8 of the guide are better tolerated and do not have as strong an influence on the fidelity of the guide41.
In addition, it has been demonstrated that U-rich seeds are linked with a low knockdown efficiency, due to RNA polymerase III being terminated by U-rich sequences. Interestingly, the R555W mutation in which minimal knockdown was observed has a very U-rich seed with 4 U’s within the first 6 bp: 3′-UCUCUU-5′30. Jiang et al. reported that mutations in positions ranging from position 1 in the guide to position 6 of the guide sequence abolish cleavage activity, except mutations at position 341. These TGFBI results directly contradict this, as the R124H and R124L mutations exhibit clear allele-specific cleavage and both mutations are present at position 3 of the guide. Therefore, it is evident that restrictions most likely vary from one guide sequence to another and in each case should be individually assessed.
That single mismatches in guide sequences can be tolerated regardless of their position in the guide has been confirmed in other reports11,42,38. Contrary to initial reports using other genes, manipulation of the guide sequence, in the form of truncation or addition of extra guanine bases, did not provide improved specificity in any case. This is consistent with follow up reports that demonstrate truncated guides or additional guanines do not offer improved specificity in most cases42,43. An intriguing observation was that for all R124 mutations the guide length of 21 nt seemed to impair cleavage activity, it is unclear why this happens but we hypothesise it may alter structure of stability of the sgRNA.
To confirm whether the results observed in vitro could be directly translated to a real-life scenario, it would be compelling to test these guides ex vivo in patient derived primary cells or in vivo in a mutation-specific animal model. This would demonstrate the effectiveness of a combined in vitro dual-luciferase and cleavage assay as a preliminary screening stage to ensure guides with adequate specificity are utilised downstream in a clinical setting.
The use of CRISPR therefore has clear limitations in targeting specific disease-causing mutations. In circumstances when one is not tied to targeting a specific disease-causing mutation, the criteria for selecting an appropriate sgRNA can be outlined as; avoid selecting guides that have predicted off-targets directly followed by a PAM, high global sequence similarity, mismatches only in the PAM distal region and those that do not have maximal consecutive mismatches10. However, when designing an sgRNA to targeting a particular disease-causing mutation there is no flexibility (other than guide length) to meet these criteria. Consequently, a guide-specific treatment strategy is not suitable for targeting the mutant alleles which cause TGFBI corneal dystrophies, as an almost perfect off-target site exists in the form of the wild-type allele.
Although here, and in previous reports, a SNP-derived PAM approach has been shown to provide highly specific cleavage15, this can only be applied to PAM-generating mutations. In the case of TGFBI corneal dystrophies, of the 60 causative mutations less than a third generate a novel S. pyogenes PAM. Therefore, even if the problems associated with Cas9/sgRNA delivery at present were overcome, the majority of patients with TGFBI would not have mutations that could be directly targeted.
Cas9 S. pyogenes orthologues are not as well characterised, therefore their off-target profiles are not as well understood as the that of S. pyogenes. In addition to this, they have much more intricate PAMs that occur much less frequently in the genome, reducing the fraction of TGFBI mutations that will result in a novel PAM. Furthermore, our results highlight another concern; even though the mutant SNP generated a novel PAM a non-canonical PAM existed in the wild-type sequence (Fig. 5b), meaning allele-specific cleavage could not be achieved. If non-canonical PAMs are considered within the analysis the number of targetable mutations would be even further reduced.
It is clear that individual guides perform with different cleavage efficiencies and specificity profiles. It is unrealistic to suggest a 60 allele-specific guide system as an effective treatment for TGFBI corneal dystrophies. A need for a highly-specific catch-all approach is apparent.
Materials and Methods
All oligonucleotides used in this study were purchased from Integrated DNA Technologies. Sequences are listed in Supplementary Table 2.
The S. pyogenes Cas9 vector plasmid used was pSpCas9(BB)-2A-Puro (PX459) V2.0, a gift from Feng Zhang (Addgene plasmid # 62988).The S.aureus Cas9 vector plasmid used was pX601-AAV-CMV::NLS-SaCas9-NLS-3xHA-bGHpA;U6::BsaI-sgRNA, a gift from Feng Zhang (Addgene plasmid # 61591). The mutant AsCpf1 used was kindly provided from Professor Feng Zhang, Broad Institute MIT. Wild-type TGFBI or mutant TGFBI guides were cloned into the various plasmids by standard molecular biology techniques. A detailed protocol is outlined by Ran et al.4. In brief, S. pyogenes Cas9 and mutant AsCpf1 were digested with BbsI (NEB Cat # R0539S) while S.aureus Cas9 was digested with BsaI (NEB Cat # R0535S). Guide sequences (shown in Supplementary Table 2) were annealed and cloned into the corresponding digested plasmid.
A firefly luciferase reporter plasmid was used to assess knockdown. The vector plasmid used was psiTEST-LUC-Target (York Bioscience Ltd, York, UK). 50 nucleotides of wild type TGFBI or mutant TGFBI sequence was cloned into the MCS by standard molecular biology techniques.
An expression construct for Renilla luciferase (pRL-CMV, Promega, Southampton, UK) was used for the dual-luciferase assay to normalize transfection efficiency. In brief, psiTEST-LUC-Target was digested with NheI and KpnI (NEB Cat # R0131S and # R0142S). Human wild-type or mutant TGFBI sequences (shown in Supplementary Table 2) were annealed and cloned into the digested plasmid.
Off-target and on-target scores were calculated using the ‘Optimised CRISPR Design Tool’, available online by the Zhang lab, MIT 2013 and ‘Benchling’s CRISPR Tool’ available online by Benchling.
A dual luciferase assay was used to determine the potency and allele specificity of the different guides previously described. HEK AD293 cells (Life Technologies) were co-transfected using Lipofectamine 2000 (Life Technologies) with a CRISPR plasmid, a firefly luciferase reporter plasmid and Renilla Luciferase expression plasmid. Cells were incubated for 72 hours, before being lysed and the activities of both Firefly luciferase and Renilla luciferase quantified.
Animals were used for the following experiments in accordance with the UK Animal Welfare Act; the experiments were approved by the Home Office (Scotland) and the DHSSPS (Northern Ireland). Prior to intrastromal injection of CRISPR components, mice were anaesthetised by intraperitoneal injection with a mix of Hypnorm (25 mg/kg; VetaPharma Ltd, Leeds, UK) and Hypnovel (25 mg/kg; Roche, Hertfordshire, UK). In addition, topical anaesthetic (0.5%w/v Tetracaine Hydrochloride; Bausch & Lomb, Aubenas, France) was applied to the eye. Following injection, mice were allowed to recover in a heated cabinet and monitored for adverse effects until the anesthesia had worn off fully. Cas9/sgRNA constructs were delivered to the mouse cornea by intrastromal injection, as previously described (Courtney et al.8). Both a guide targeted to Luc2 (sgLuc2 - right eye) and a non-specific control guide (sgNSC - left eye) were injected intrastromally in a total volume of 4 µl of PBS at a concentration of 500ng/µl.
Live animal imaging
All mice used for live imaging were aged between 12 and 25 weeks old. For imaging, mice were anaesthetised using 1.5–2% isoflurane (Abbott Laboratories Ltd., Berkshire, UK) in ~1.5 l/min flow of oxygen. A mix of luciferin substrate (30 mg/ml D-luciferin potassium salt; Gold Biotechnology, St. Louis, USA) mixed 1:1 w/v with Viscotears gel (Novartis, Camberley, UK) was dropped onto the eye of heterozygous Krt12 +/luc2 transgenic mice immediately prior to imaging. A Xenogen IVIS Lumina (Perkin Elmer, Cambridge, UK) was used to quantify luminescence. Live images of mice (n = 4) were taken every 24 hours for 7 days, then once every week thereafter for six weeks (42 days) in total. Quantification of luciferase inhibition was determined by calculating the right/left ratio, with values normalised to those at day 0 (as 100%).
In vitro digestion of circular plasmid and DNA template with purified S. pyogenes Cas9
A double-stranded DNA template was prepared by amplifying a region of the luciferase reporter plasmid containing the desired sequence using the following primers: 5′-ACCCCAACATCTTCGACGCGGGC-3′ and 3′-TGCTGTCCTGCCCCACCCCA-5′. A cleavage reaction was set up by incubating 30 nM S. pyogenes Cas9 nuclease (NEB UK) with 30 nM synthetic sgRNA (Synthego) for 10 minutes at 25 °C. The Cas9:sgRNA complex was then incubated with 3 nM of DNA template at 37 °C for 1 hour. Fragment analysis was then carried out on a 1% agarose gel.
All error bars represent the S.E.M. unless stated otherwise. Significance was calculated using a Mann-Whitney test. Statistical significance wasset at p < 0.05. Variance was calculated among groups and deemed to be similar.
No datasets were generated or analysed during the current study.
Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
We are grateful to Prof Feng Zhang, Broad Institute MIT, USA for kindly providing a novel AsCpf1 mutant nuclease pre-publication. This work has been supported by Avellino Laboratories.
Electronic supplementary material
About this article
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.