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results
n5:contains
_:vb74855038 _:vb74855039 _:vb74855056 _:vb74855057 _:vb74855058 _:vb74855059 _:vb74855060 _:vb74855061 _:vb74855062 _:vb74855063 _:vb74855064 _:vb74855065 _:vb74855066 _:vb74855067 _:vb74855068 _:vb74855069 _:vb74855070 _:vb74855071 _:vb74855040 _:vb74855041 _:vb74855042 _:vb74855043 _:vb74855044 _:vb74855045 _:vb74855046 _:vb74855047 _:vb74855048 _:vb74855049 _:vb74855050 _:vb74855051 _:vb74855052 _:vb74855053 _:vb74855054 _:vb74855055 _:vb74855072 _:vb74855073 _:vb74855074 _:vb74855075 _:vb74855076
Subject Item
_:vb74855038
rdf:type
n2:Context
rdf:value
To link Cas9 DNA recognition to phage propagation during PACE, we developed a bacterial one-hybrid selection>>20<<,23,24 in which the SP encodes a catalytically dead SpCas9 (dCas9) fused to the ω subunit of bacterial RNA polymerase.
n2:mentions
n3:26258293
Subject Item
_:vb74855039
rdf:type
n2:Context
rdf:value
To link Cas9 DNA recognition to phage propagation during PACE, we developed a bacterial one-hybrid selection20,>>23<<,24 in which the SP encodes a catalytically dead SpCas9 (dCas9) fused to the ω subunit of bacterial RNA polymerase.
n2:mentions
n3:17406209
Subject Item
_:vb74855040
rdf:type
n2:Context
rdf:value
To link Cas9 DNA recognition to phage propagation during PACE, we developed a bacterial one-hybrid selection20,23,>>24<< in which the SP encodes a catalytically dead SpCas9 (dCas9) fused to the ω subunit of bacterial RNA polymerase.
n2:mentions
n3:9121589
Subject Item
_:vb74855041
rdf:type
n2:Context
rdf:value
All three AP libraries were introduced into host E. coli cells harboring the mutagenesis plasmid MP>>617<<. The resulting host cells were incubated overnight with SP containing ω(I12N)–dCas9. This phage-assisted non-continuous evolution (PANCE) system19,21 preferentially replicates Cas9 variants that bind a greater variety of PAM sequences,
n2:mentions
n3:26443021
Subject Item
_:vb74855042
rdf:type
n2:Context
rdf:value
This phage-assisted non-continuous evolution (PANCE) system>>19<<,21 preferentially replicates Cas9 variants that bind a greater variety of PAM sequences, similar to PACE, but with lower stringency since there is no outflow of phage.
n2:mentions
n3:27120167
Subject Item
_:vb74855043
rdf:type
n2:Context
rdf:value
1c), two residues known to play a critical role in PAM recognition>>25<<. The mixture of phage from the final PANCE pool were further evolved for 72 h in PACE on host cells containing the same AP libraries harboring NNN PAM sequences.
n2:mentions
n3:25079318
Subject Item
_:vb74855044
rdf:type
n2:Context
rdf:value
1d) and could play a role in mediating DNA sequence recognition and the switching of Cas9 from the open to the closed conformation upon target recognition>>26<<,27. Since the entire Cas9 gene was subject to mutagenesis during PACE, the mechanism of xCas9 may differ from that of engineered Cas9 variants that primarily mutated DNA-contacting residues15,16,28.
n2:mentions
n3:28931002
Subject Item
_:vb74855045
rdf:type
n2:Context
rdf:value
1d) and could play a role in mediating DNA sequence recognition and the switching of Cas9 from the open to the closed conformation upon target recognition26,>>27<<. Since the entire Cas9 gene was subject to mutagenesis during PACE, the mechanism of xCas9 may differ from that of engineered Cas9 variants that primarily mutated DNA-contacting residues15,16,28.
n2:mentions
n3:26524520
Subject Item
_:vb74855046
rdf:type
n2:Context
rdf:value
Since the entire Cas9 gene was subject to mutagenesis during PACE, the mechanism of xCas9 may differ from that of engineered Cas9 variants that primarily mutated DNA-contacting residues>>15<<,16,28.
n2:mentions
n3:26524662
Subject Item
_:vb74855047
rdf:type
n2:Context
rdf:value
Since the entire Cas9 gene was subject to mutagenesis during PACE, the mechanism of xCas9 may differ from that of engineered Cas9 variants that primarily mutated DNA-contacting residues15,>>16<<,28.
n2:mentions
n3:26098369
Subject Item
_:vb74855048
rdf:type
n2:Context
rdf:value
Since the entire Cas9 gene was subject to mutagenesis during PACE, the mechanism of xCas9 may differ from that of engineered Cas9 variants that primarily mutated DNA-contacting residues15,16,>>28<<.
n2:mentions
n3:28581492
Subject Item
_:vb74855049
rdf:type
n2:Context
rdf:value
The xCas9 3.0–3.13 clones were tested in a PAM depletion assay>>15<<,16 in which they were given the opportunity to cleave a library of plasmids containing a protospacer and all possible NNN PAM sequences in an antibiotic resistance gene in bacterial cells.
n2:mentions
n3:26524662
Subject Item
_:vb74855050
rdf:type
n2:Context
rdf:value
The xCas9 3.0–3.13 clones were tested in a PAM depletion assay15,>>16<< in which they were given the opportunity to cleave a library of plasmids containing a protospacer and all possible NNN PAM sequences in an antibiotic resistance gene in bacterial cells.
n2:mentions
n3:26098369
Subject Item
_:vb74855051
rdf:type
n2:Context
rdf:value
To test for transcriptional activation, catalytically dead versions of xCas9 were fused to the transcriptional activator VP64–p65–Rta (dxCas9–VPR)>>29<<. Plasmids encoding dxCas9–VPR, a GFP reporter downstream of a target protospacer, and a corresponding sgRNA were co-transfected into HEK293T cells29. Target gene transcriptional activation was measured by cellular GFP fluorescence after
n2:mentions
n3:25730490
Subject Item
_:vb74855052
rdf:type
n2:Context
rdf:value
Plasmids encoding dxCas9–VPR, a GFP reporter downstream of a target protospacer, and a corresponding sgRNA were co-transfected into HEK293T cells>>29<<. Target gene transcriptional activation was measured by cellular GFP fluorescence after three days. Three different target site PAM sets were tested: a single reporter with an NGG PAM, a reporter library containing a NNN PAM library, and
n2:mentions
n3:25730490
Subject Item
_:vb74855053
rdf:type
n2:Context
rdf:value
Target site dependence is also well-known for SpCas>>930<<.
n2:mentions
n3:25184501
Subject Item
_:vb74855054
rdf:type
n2:Context
rdf:value
The four NGA PAM sites averaged 32±2.4% indels for xCas9 and 20±2.7% for SpCas9, a 1.6-fold increase, consistent with previous reports that NGA can serve as a secondary PAM for SpCas>>931<<. While indel frequencies at the endogenous NGC PAM sites were more variable, ranging from 4.8–31%, xCas9 3.7 averaged 13±0.90% indels compared to 6.3±0.77% for SpCas9, a 2.1-fold increase. Among the three GAA and GAT sites tested, SpCas9
n2:mentions
n3:24956376
Subject Item
_:vb74855055
rdf:type
n2:Context
rdf:value
2 and Extended Data Figs 5–7) may reflect more extensive requirements for DNA cleavage than DNA binding>>27<<,32, or differences in the chromatin state of plasmid (Fig.
n2:mentions
n3:26524520
Subject Item
_:vb74855056
rdf:type
n2:Context
rdf:value
2 and Extended Data Figs 5–7) may reflect more extensive requirements for DNA cleavage than DNA binding27,>>32<<, or differences in the chromatin state of plasmid (Fig.
n2:mentions
n3:25513782
Subject Item
_:vb74855057
rdf:type
n2:Context
rdf:value
nucleobase deaminase enzyme and, in some cases, a DNA glycosylase inhibitor to directly convert a target C•G to T•A, or a target A•T to G•C, without introducing double-stranded DNA breaks or requiring homology-directed repair>>4<<,5,33. The suitability of a target site for base editing is highly dependent on the presence of a suitably positioned PAM, which must exist within a narrow window downstream of the target base pair (typically 15±2 nucleotides).
n2:mentions
n3:27096365
Subject Item
_:vb74855058
rdf:type
n2:Context
rdf:value
nucleobase deaminase enzyme and, in some cases, a DNA glycosylase inhibitor to directly convert a target C•G to T•A, or a target A•T to G•C, without introducing double-stranded DNA breaks or requiring homology-directed repair4,>>5<<,33. The suitability of a target site for base editing is highly dependent on the presence of a suitably positioned PAM, which must exist within a narrow window downstream of the target base pair (typically 15±2 nucleotides).
n2:mentions
n3:29160308
Subject Item
_:vb74855059
rdf:type
n2:Context
rdf:value
nucleobase deaminase enzyme and, in some cases, a DNA glycosylase inhibitor to directly convert a target C•G to T•A, or a target A•T to G•C, without introducing double-stranded DNA breaks or requiring homology-directed repair4,5,>>33<<. The suitability of a target site for base editing is highly dependent on the presence of a suitably positioned PAM, which must exist within a narrow window downstream of the target base pair (typically 15±2 nucleotides).
n2:mentions
n3:28191901
Subject Item
_:vb74855060
rdf:type
n2:Context
rdf:value
To evaluate C•G-to-T•A base editing activity of xCas9 variants, we substituted SpCas9 with xCas9 3.7 and 3.6 in the third-generation (BE3) base editor architecture>>4<<. Both xCas9–BE3s and SpCas9–BE3 were separately transfected into mammalian cells to compare editing efficiency on all 20 sites tested above for endogenous genomic DNA cleavage (Fig.
n2:mentions
n3:27096365
Subject Item
_:vb74855061
rdf:type
n2:Context
rdf:value
Overall, these results indicate that xCas9 variants are compatible with the BE3 architecture, and enable cytidine base editing of target sites that cannot be accessed by SpCas9–BE3 or, with the exception of NGA PAM sites>>33<<, by any other previously reported base editors.
n2:mentions
n3:28191901
Subject Item
_:vb74855062
rdf:type
n2:Context
rdf:value
We also tested xCas9 3.7 in the BE4 architecture designed to reduce undesired byproducts>>34<<, and observed fewer indels and higher product purities, although with slightly lower editing efficiencies (Extended Data Fig.
n2:mentions
n3:28875174
Subject Item
_:vb74855063
rdf:type
n2:Context
rdf:value
The recent development of an adenine base editor (ABE) enables programmable installation of A•T to G•C mutations>>5<<. No ABEs have been reported yet that can target non-NGG PAM sites, limiting its targeting scope.
n2:mentions
n3:29160308
Subject Item
_:vb74855064
rdf:type
n2:Context
rdf:value
Because PAM recognition is a crucial component of Cas9 DNA specificity>>27<<, the substantially broadened PAM compatibility of xCas9s would be expected to increase their off-target activity32,35.
n2:mentions
n3:26524520
Subject Item
_:vb74855065
rdf:type
n2:Context
rdf:value
Because PAM recognition is a crucial component of Cas9 DNA specificity27, the substantially broadened PAM compatibility of xCas9s would be expected to increase their off-target activity>>32<<,35. Indeed, the engineered S. aureus KKH-SaCas9, which accepts an NNNRRT PAM instead of the native NNGRRT SaCas9 PAM, exhibits comparable or higher off-target editing than SaCas915.
n2:mentions
n3:25513782
Subject Item
_:vb74855066
rdf:type
n2:Context
rdf:value
Because PAM recognition is a crucial component of Cas9 DNA specificity27, the substantially broadened PAM compatibility of xCas9s would be expected to increase their off-target activity32,>>35<<. Indeed, the engineered S. aureus KKH-SaCas9, which accepts an NNNRRT PAM instead of the native NNGRRT SaCas9 PAM, exhibits comparable or higher off-target editing than SaCas915.
n2:mentions
n3:21822273
Subject Item
_:vb74855067
rdf:type
n2:Context
rdf:value
Indeed, the engineered S. aureus KKH-SaCas9, which accepts an NNNRRT PAM instead of the native NNGRRT SaCas9 PAM, exhibits comparable or higher off-target editing than SaCas>>915<<. Most of the xCas9 mutations are close to the PAM or to the DNA:sgRNA interface (Fig. 1), raising the possibility that these mutations might alter the degree to which mismatches between the spacer and protospacer impede productive DNA
n2:mentions
n3:26524662
Subject Item
_:vb74855068
rdf:type
n2:Context
rdf:value
Previous studies have demonstrated that some mutations near the Cas9:DNA interface can reduce off-target activity, in some cases without sacrificing on-target modification efficiency>>26<<,36,37.
n2:mentions
n3:28931002
Subject Item
_:vb74855069
rdf:type
n2:Context
rdf:value
Previous studies have demonstrated that some mutations near the Cas9:DNA interface can reduce off-target activity, in some cases without sacrificing on-target modification efficiency26,>>36<<,37.
n2:mentions
n3:26628643
Subject Item
_:vb74855070
rdf:type
n2:Context
rdf:value
Previous studies have demonstrated that some mutations near the Cas9:DNA interface can reduce off-target activity, in some cases without sacrificing on-target modification efficiency26,36,>>37<<.
n2:mentions
n3:26735016
Subject Item
_:vb74855071
rdf:type
n2:Context
rdf:value
In order to test the off-target activity of xCas9 variants, we performed GUIDE-seq, an unbiased genome-wide off-target analysis>>32<<, on xCas9 3.7, xCas9 3.6, and SpCas9 in HEK293T and U2OS cells.
n2:mentions
n3:25513782
Subject Item
_:vb74855072
rdf:type
n2:Context
rdf:value
For the known highly promiscuous target sites HEK site 4 and VEGFA>>32<<, the off-target:
n2:mentions
n3:25513782
Subject Item
_:vb74855073
rdf:type
n2:Context
rdf:value
These results, together with the success of multiple independent efforts to create high-fidelity Cas9 variants>>26<<,36,37, suggest that the DNA promiscuity of wild-type Cas9, which likely evolved to impede viral evasion, can readily be overcome by protein engineering or evolution.
n2:mentions
n3:28931002
Subject Item
_:vb74855074
rdf:type
n2:Context
rdf:value
These results, together with the success of multiple independent efforts to create high-fidelity Cas9 variants26,>>36<<,37, suggest that the DNA promiscuity of wild-type Cas9, which likely evolved to impede viral evasion, can readily be overcome by protein engineering or evolution.
n2:mentions
n3:26628643
Subject Item
_:vb74855075
rdf:type
n2:Context
rdf:value
These results, together with the success of multiple independent efforts to create high-fidelity Cas9 variants26,36,>>37<<, suggest that the DNA promiscuity of wild-type Cas9, which likely evolved to impede viral evasion, can readily be overcome by protein engineering or evolution.
n2:mentions
n3:26735016
Subject Item
_:vb74855076
rdf:type
n2:Context
rdf:value
Indeed, compared to SpCas9–BE3, xCas9(3.7)–BE3 increases the percentage of 4,422 pathogenic SNPs in the ClinVar database>>38<< that in principle could be targeted by C•G to T•A base editing from 26% to 73% (Fig.
n2:mentions
n3:24234437
Subject Item
_:vb74855077
rdf:type
n5:Section
dc:title
methods
n5:contains
_:vb74855088 _:vb74855078 _:vb74855079 _:vb74855080 _:vb74855081 _:vb74855082 _:vb74855083 _:vb74855084 _:vb74855085 _:vb74855086 _:vb74855087
Subject Item
_:vb74855078
rdf:type
n2:Context
rdf:value
Cas9 genes and plasmid backbones for PACE were obtained from previously reported plasmids>>19<<,20 available from Addgene.
n2:mentions
n3:27120167
Subject Item
_:vb74855079
rdf:type
n2:Context
rdf:value
Cas9 genes and plasmid backbones for PACE were obtained from previously reported plasmids19,>>20<< available from Addgene.
n2:mentions
n3:26258293
Subject Item
_:vb74855080
rdf:type
n2:Context
rdf:value
Plasmids encoding dxCas9–VPR>>29<<, xCas9 nucleases, xCas9–BE34, xCas9-BE434, and xCas9-ABE5 were constructed by replacing SpCas9 using Gibson cloning.
n2:mentions
n3:25730490
Subject Item
_:vb74855081
rdf:type
n2:Context
rdf:value
Plasmids encoding dxCas9–VPR29, xCas9 nucleases, xCas9–BE>>34<<, xCas9-BE434, and xCas9-ABE5 were constructed by replacing SpCas9 using Gibson cloning.
n2:mentions
n3:27096365
Subject Item
_:vb74855082
rdf:type
n2:Context
rdf:value
Plasmids encoding dxCas9–VPR29, xCas9 nucleases, xCas9–BE34, xCas9-BE>>434<<, and xCas9-ABE5 were constructed by replacing SpCas9 using Gibson cloning.
n2:mentions
n3:28875174
Subject Item
_:vb74855083
rdf:type
n2:Context
rdf:value
Plasmids encoding dxCas9–VPR29, xCas9 nucleases, xCas9–BE34, xCas9-BE434, and xCas9-ABE>>5<< were constructed by replacing SpCas9 using Gibson cloning.
n2:mentions
n3:29160308
Subject Item
_:vb74855084
rdf:type
n2:Context
rdf:value
Analysis was carried out using previously published Matlab code>>5<<, provided in Supplementary Notes 1 and 2.
n2:mentions
n3:29160308
Subject Item
_:vb74855085
rdf:type
n2:Context
rdf:value
Bioinformatic analysis of the ClinVar database was carried out in a manner similar to previously described analysis>>33<<. The code is provided in Supplementary Note 3.
n2:mentions
n3:28191901
Subject Item
_:vb74855086
rdf:type
n2:Context
rdf:value
The DNA was sheared to an average of 500 bp using a Covaris S220 focused ultrasonicator as previously described>>32<<. End repair, dA-tailing, adapter ligation, tag-specific PCR1, and tag-specific PCR2 were carried out using the primers and methods previously described32. DNA concentration was quantified with the KAPA Library Quantification Kit-Illumina
n2:mentions
n3:25513782
Subject Item
_:vb74855087
rdf:type
n2:Context
rdf:value
End repair, dA-tailing, adapter ligation, tag-specific PCR1, and tag-specific PCR2 were carried out using the primers and methods previously described>>32<<. DNA concentration was quantified with the KAPA Library Quantification Kit-Illumina (KAPA Biosystems) and sequenced on an Illumina MiSeq instrument according to the manufacturer’s protocols. Analysis was carried out using the previously
n2:mentions
n3:25513782
Subject Item
_:vb74855088
rdf:type
n2:Context
rdf:value
Analysis was carried out using the previously published Python code>>32<<.
n2:mentions
n3:25513782
Subject Item
_:vb74855089
rdf:type
n5:Section
dc:title
extended data
n5:contains
_:vb74855090 _:vb74855091 _:vb74855092 _:vb74855093
Subject Item
_:vb74855090
rdf:type
n2:Context
rdf:value
HTS of the library before versus after selection enables quantification of the change in library composition, resulting in a sequence logo>>39<< for the PAM preference of SpCas9 (left) and xCas9 3.7 (right).
n2:mentions
n3:15173120
Subject Item
_:vb74855091
rdf:type
n2:Context
rdf:value
b, c, PAM depletion scores of Cas9 variants from spectinomycin selection in E. coli, calculated as described previously>>35<<, with 1.0 representing complete cleavage of that PAM sequence.
n2:mentions
n3:21822273
Subject Item
_:vb74855092
rdf:type
n2:Context
rdf:value
d, Of the 20 sites in (c), seven contained an A in the canonical window for ABE editing>>5<< and were tested for A•T to G•C base editing by SpCas9–ABE and xCas9(3.6)–ABE.
n2:mentions
n3:29160308
Subject Item
_:vb74855093
rdf:type
n2:Context
rdf:value
b, Test of xCas9 3.7 in the BE4 architecture>>34<< on the same sites tested in Fig. 3.
n2:mentions
n3:28875174
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_:vb644632977
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144
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137
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132
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107
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105
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96
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89
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88
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84
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83
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72
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72
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68
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63
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55
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54
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53
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53
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52
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46
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45
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45
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44
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43
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42
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42
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41
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41
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41
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40
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39
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38
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35
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35
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