Insertion sequence transposition inactivates CRISPR-Cas immunity

Abstract 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....

Full description

Bibliographic Details
Main Authors: Yong Sheng, Hengyu Wang, Yixin Ou, Yingying Wu, Wei Ding, Meifeng Tao, Shuangjun Lin, Zixin Deng, Linquan Bai, Qianjin Kang
Format: Article
Language:English
Published: Nature Portfolio 2023-07-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-023-39964-7
_version_ 1797774075573043200
author Yong Sheng
Hengyu Wang
Yixin Ou
Yingying Wu
Wei Ding
Meifeng Tao
Shuangjun Lin
Zixin Deng
Linquan Bai
Qianjin Kang
author_facet Yong Sheng
Hengyu Wang
Yixin Ou
Yingying Wu
Wei Ding
Meifeng Tao
Shuangjun Lin
Zixin Deng
Linquan Bai
Qianjin Kang
author_sort Yong Sheng
collection DOAJ
description Abstract 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.
first_indexed 2024-03-12T22:15:45Z
format Article
id doaj.art-3ba99588949d43d9b6f109ea27b45e01
institution Directory Open Access Journal
issn 2041-1723
language English
last_indexed 2024-03-12T22:15:45Z
publishDate 2023-07-01
publisher Nature Portfolio
record_format Article
series Nature Communications
spelling doaj.art-3ba99588949d43d9b6f109ea27b45e012023-07-23T11:18:56ZengNature PortfolioNature Communications2041-17232023-07-0114111910.1038/s41467-023-39964-7Insertion sequence transposition inactivates CRISPR-Cas immunityYong Sheng0Hengyu Wang1Yixin Ou2Yingying Wu3Wei Ding4Meifeng Tao5Shuangjun Lin6Zixin Deng7Linquan Bai8Qianjin Kang9State Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic & Developmental Sciences, and School of Life Sciences & Biotechnology, Shanghai Jiao Tong UniversityState Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic & Developmental Sciences, and School of Life Sciences & Biotechnology, Shanghai Jiao Tong UniversityState Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic & Developmental Sciences, and School of Life Sciences & Biotechnology, Shanghai Jiao Tong UniversityState Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic & Developmental Sciences, and School of Life Sciences & Biotechnology, Shanghai Jiao Tong UniversityState Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic & Developmental Sciences, and School of Life Sciences & Biotechnology, Shanghai Jiao Tong UniversityState Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic & Developmental Sciences, and School of Life Sciences & Biotechnology, Shanghai Jiao Tong UniversityState Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic & Developmental Sciences, and School of Life Sciences & Biotechnology, Shanghai Jiao Tong UniversityState Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic & Developmental Sciences, and School of Life Sciences & Biotechnology, Shanghai Jiao Tong UniversityState Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic & Developmental Sciences, and School of Life Sciences & Biotechnology, Shanghai Jiao Tong UniversityState Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic & Developmental Sciences, and School of Life Sciences & Biotechnology, Shanghai Jiao Tong UniversityAbstract 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.https://doi.org/10.1038/s41467-023-39964-7
spellingShingle Yong Sheng
Hengyu Wang
Yixin Ou
Yingying Wu
Wei Ding
Meifeng Tao
Shuangjun Lin
Zixin Deng
Linquan Bai
Qianjin Kang
Insertion sequence transposition inactivates CRISPR-Cas immunity
Nature Communications
title Insertion sequence transposition inactivates CRISPR-Cas immunity
title_full Insertion sequence transposition inactivates CRISPR-Cas immunity
title_fullStr Insertion sequence transposition inactivates CRISPR-Cas immunity
title_full_unstemmed Insertion sequence transposition inactivates CRISPR-Cas immunity
title_short Insertion sequence transposition inactivates CRISPR-Cas immunity
title_sort insertion sequence transposition inactivates crispr cas immunity
url https://doi.org/10.1038/s41467-023-39964-7
work_keys_str_mv AT yongsheng insertionsequencetranspositioninactivatescrisprcasimmunity
AT hengyuwang insertionsequencetranspositioninactivatescrisprcasimmunity
AT yixinou insertionsequencetranspositioninactivatescrisprcasimmunity
AT yingyingwu insertionsequencetranspositioninactivatescrisprcasimmunity
AT weiding insertionsequencetranspositioninactivatescrisprcasimmunity
AT meifengtao insertionsequencetranspositioninactivatescrisprcasimmunity
AT shuangjunlin insertionsequencetranspositioninactivatescrisprcasimmunity
AT zixindeng insertionsequencetranspositioninactivatescrisprcasimmunity
AT linquanbai insertionsequencetranspositioninactivatescrisprcasimmunity
AT qianjinkang insertionsequencetranspositioninactivatescrisprcasimmunity