生物
原噬菌体
基因
免疫系统
水平基因转移
转座因子
激活剂(遗传学)
抑制因子lexA
细胞生物学
发起人
DNA
抑制因子
细菌
突变
基因表达调控
细胞
遗传学
外源DNA
细菌接合
微生物学
基因表达
质粒
溶解
基因产物
转录调控
分子生物学
调节基因
作者
Emma J. Banks,Pavol Bárdy,Ngat T. Tran,Phuong M. Nguyen,Boris Stojilković,Kevin Gozzi,Abbas Maqbool,Tung B. K. Le
标识
DOI:10.1038/s41564-026-02316-4
摘要
Bacteria use immune systems to detect and defend against mobile genetic elements including phages. Gene transfer agents (GTAs) are domesticated prophages with phage-like characteristics including the ability to induce host cell lysis for gene transfer. Whether GTAs elicit or avoid bacterial immune systems is poorly understood. Here, a transposon mutagenesis with deep sequencing screen in Caulobacter crescentus identified a tripartite system, LypABC, essential for GTA-mediated cell lysis and gene transfer. LypABC resembles a caspase recruitment domain-nucleotide-binding leucine-rich repeat (CARD-NLR) anti-phage defence system. LypABC is dispensable for DNA packaging into GTA particles but required for host cell lysis, involving the peptidase domains of LypA and LypC, and the ATPase domain of LypB. As LypABC overproduction is toxic, strict regulation through the transcriptional repressor CdxB is required. CdxB binds the promoters of lypABC and of essential GTA activator genes, coupling GTA activation to host cell lysis. Our findings suggest that bacterial immune systems can be co-opted to support horizontal gene transfer by GTAs.
科研通智能强力驱动
Strongly Powered by AbleSci AI