首页> 美国卫生研究院文献>Cell Regulation >A Highlights from MBoC Selection: A Domesticated piggyBac Transposase Plays Key Roles in Heterochromatin Dynamics and DNA Cleavage during Programmed DNA Deletion in Tetrahymena thermophila
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A Highlights from MBoC Selection: A Domesticated piggyBac Transposase Plays Key Roles in Heterochromatin Dynamics and DNA Cleavage during Programmed DNA Deletion in Tetrahymena thermophila

机译:MBoC选择的亮点:在嗜热四膜膜虫的程控DNA删除过程中驯化的piggyBac转座酶在异染色质动力学和DNA切割中起关键作用。

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摘要

Transposons comprise large fractions of eukaryotic genomes and provide genetic reservoirs for the evolution of new cellular functions. We identified TPB2, a homolog of the piggyBac transposase gene that is required for programmed DNA deletion in Tetrahymena. TPB2 was expressed exclusively during the time of DNA excision, and its encoded protein Tpb2p was localized in DNA elimination heterochromatin structures. Notably, silencing of TPB2 by RNAi disrupts the final assembly of these heterochromatin structures and prevents DNA deletion to occur. In vitro studies revealed that Tpb2p is an endonuclease that produces double-strand breaks with four-base 5′ protruding ends, similar to the ends generated during DNA deletion. These findings suggest that Tpb2p plays a key role in the assembly of specialized DNA elimination chromatin architectures and is likely responsible for the DNA cleavage step of programmed DNA deletion.
机译:转座子包含大部分真核生物基因组,并为新细胞功能的进化提供了遗传贮藏库。我们确定了TPB2,piggyBac转座酶基因的同源物,在四膜虫中编程的DNA缺失是必需的。 TPB2仅在DNA切除时表达,其编码的蛋白Tpb2p位于DNA消除异染色质结构中。值得注意的是,RNAi使TPB2沉默会破坏这些异染色质结构的最终装配,并防止DNA缺失的发生。体外研究表明,Tpb2p是一种核酸内切酶,可产生具有4个碱基的5'突出末端的双链断裂,类似于DNA缺失过程中产生的末端。这些发现表明,Tpb2p在专门的DNA消除染色质体系结构的组装中起关键作用,并且可能负责程序化DNA缺失的DNA裂解步骤。

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