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Insertion sequence transposition inactivates CRISPR-Cas immunity

delete2023-07-20
delete6
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OA
AI
Y
Yong Sheng
H
Hengyu Wang
Y
Yixin Ou
Y
Ying‐Ying Wu
W
Wei Ding
陶美凤 (Meifeng Tao)
S
Shuangjun Lin
Z
Zixin Deng
L
Linquan Bai
康前进 (Qianjin Kang) *
DOI:10.1038/s41467-023-39964-7delete
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Abstract

Abstract

En 中文
CRISPR-Cas immunity systems safeguard prokaryotic genomes by inhibiting the invasion of mobile genetic elements. Here, we screened prokaryotic genomic sequences and identified multiple natural transpositions of insertion sequences (ISs) into cas genes, thus inactivating CRISPR-Cas defenses. We then generated an IS-trapping system, using Escherichia coli strains with various ISs and an inducible cas nuclease, to monitor IS insertions into cas genes following the induction of double-strand DNA breakage as a physiological host stress. We identified multiple events mediated by different ISs, especially IS1 and IS10, displaying substantial relaxed target specificity. IS transposition into cas was maintained in the presence of DNA repair machinery, and transposition into other host defense systems was also detected. Our findings highlight the potential of ISs to counter CRISPR activity, thus increasing bacterial susceptibility to foreign DNA invasion. CRISPR-Cas immunity systems safeguard prokaryotic genomes by inhibiting the invasion of mobile genetic elements. Here, the authors show that insertion sequences can efficiently insert into cas genes, thus inactivating CRISPR defenses and increasing bacterial susceptibility to foreign DNA invasion.
Keywords:
HORIZONTAL GENE-TRANSFER
GENOME PLASTICITY
ELEMENTS
DNA
PATTERNS
IMPACT
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Journal

Nature Communications cover
Nature Communications
IF:
15.7
Papers:
9.3W
Citations:
91.2W

Organization

S
shanghai jiao tong university
Scholars:
15.6W
Papers: 11.6W
Citations: 159