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座子相关的TnpB是一种可编程的RNA引导的DNA核酸内切酶
2021-10-10 22:45

立陶宛维尔纽斯大学Virginijus Siksnys、Tautvydas Karvelis等研究人员合作发现,转座子相关的TnpB是一种可编程的RNA引导的DNA核酸内切酶 。相关论文于2021年10月7日在线发表在《自然》杂志上。

据研究人员介绍,转位在重塑所有生物体的基因组中起着关键作用。IS200/IS605和IS607家族的插入序列(IS)是最简单的移动遗传元件之一,只包含其转座及其调节所需的基因。这些元件编码的tnpA转座酶对转座是必不可少的,并且经常携带一个附属的tnpB基因,该基因对转座是不需要的。尽管TnpA在IS200/IS605转座子动员中的作用有据可查,但TnpB的功能在很大程度上仍是未知的。有人认为TnpB在转座调控中发挥了作用,但没有确定其机制。有趣的是,一项生物信息学分析表明,TnpB可能是CRISPR-Cas9/Cas12核酸酶的前身。然而,TnpB没有被赋予任何生化活性。
 
研究人员表明,放射菌ISDra2的TnpB是一种RNA引导的核酸酶,在RE-衍生的RNA(reRNA)的引导下,切割5′TTGAT转座子相关模体(TAM)旁边的DNA。研究人员还表明,TnpB可以被重新编程,在人类细胞中切割DNA靶点。总之,这项研究通过强调TnpB在转座中的作用,扩大了人们对转座机制的理解,在实验中证实了TnpB是CRISPR-Cas核酸的功能性祖先,并将TnpB确立为基因组编辑的新系统原型。
 
附:英文原文

Title: Transposon-associated TnpB is a programmable RNA-guided DNA endonuclease

Author: Karvelis, Tautvydas, Druteika, Gytis, Bigelyte, Greta, Budre, Karolina, Zedaveinyte, Rimante, Silanskas, Arunas, Kazlauskas, Darius, Venclovas, eslovas, Siksnys, Virginijus

Issue&Volume: 2021-10-07

Abstract: Transposition plays a key role in reshaping genomes of all living organisms1. Insertion sequences (ISs) of IS200/IS605 and IS607 families2 are among the simplest mobile genetic elements and contain only the genes required for their transposition and its regulation. These elements encode tnpA transposase that is essential for mobilization and often carry an accessory tnpB gene which is dispensable for transposition. Although the role of TnpA in IS200/IS605 transposon mobilization is well documented, the function of TnpB had remained largely unknown. It had been suggested that TnpB plays a role in transposition regulation though no mechanism for this was established3–5. Intriguingly, a bioinformatic analysis indicated that TnpB might be a predecessor of the CRISPR–Cas9/Cas12 nucleases6–8. However, no biochemical activities had been ascribed to TnpB. Here we show that TnpB of Deinococcus radiodurans ISDra2 is an RNA-directed nuclease that is guided by RE-derived RNA (reRNA) to cleave DNA next to the 5′ TTGAT transposon associated motif (TAM). We also show that TnpB could be reprogrammed to cleave DNA target sites in human cells. Together, this study expands our understanding of transposition mechanisms by highlighting the role of TnpB in transposition, experimentally confirms that TnpB is a functional progenitor of CRISPR-Cas nucleases and establishes TnpB as a prototype of a new system for genome editing.

DOI: 10.1038/s41586-021-04058-1

Source: https://www.nature.com/articles/s41586-021-04058-1

 

Nature:《自然》,创刊于1869年。隶属于施普林格·自然出版集团,最新IF:69.504
官方网址:http://www.nature.com/
投稿链接:http://www.nature.com/authors/submit_manuscript.html


本期文章:《自然》:Online/在线发表

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