生物
转座酶
遗传学
转座因子
谱系(遗传)
基因组
清脆的
核糖核酸
基因
流动遗传元素
计算生物学
细菌基因组大小
核酸内切酶
作者
Peter H. Yoon,Petr Skopintsev,Honglue Shi,Lin-Xing Chen,Benjamin A. Adler,Muntathar Al-Shimary,Rory J. Craig,Kenneth Loi,Evan C DeTurk,Zheng Li,Jasmine Amerasekera,Marena Trinidad,Hunter Nisonoff,Kai Chen,Arushi Lahiri,Ron Boger,Steve Jacobsen,Jillian F. Banfield,Jennifer A. Doudna
摘要
RNA-guided endonucleases form the crux of diverse biological processes and technologies, including adaptive immunity, transposition, and genome editing. Some of these enzymes are components of insertion sequences (IS) in the IS200/IS605 and IS607 transposon families. Both IS families encode a TnpA transposase and a TnpB nuclease, an RNA-guided enzyme ancestral to CRISPR-Cas12s. In eukaryotes, TnpB homologs occur as two distinct types, Fanzor1s and Fanzor2s. We analyzed the evolutionary relationships between prokaryotic TnpBs and eukaryotic Fanzors, which revealed that both Fanzor1s and Fanzor2s stem from a single lineage of IS607 TnpBs with unusual active site arrangement. The widespread nature of Fanzors implies that the properties of this particular lineage of IS607 TnpBs were particularly suited to adaptation in eukaryotes. Biochemical analysis of an IS607 TnpB and Fanzor1s revealed common strategies employed by TnpBs and Fanzors to co-evolve with their cognate transposases. Collectively, our results provide a new model of sequential evolution from IS607 TnpBs to Fanzor2s, and Fanzor2s to Fanzor1s that details how genes of prokaryotic origin evolve to give rise to new protein families in eukaryotes.
科研通智能强力驱动
Strongly Powered by AbleSci AI