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RNA解旋酶MVH和TDRD9在PIWI切割引发的哺乳动物piRNA生物发生及功能中的不同作用

Distinct Roles of RNA Helicases MVH and TDRD9 in PIWI Slicing-Triggered Mammalian piRNA Biogenesis and Function.

作者信息

Wenda Joanna M, Homolka David, Yang Zhaolin, Spinelli Pietro, Sachidanandam Ravi, Pandey Radha Raman, Pillai Ramesh S

机构信息

Department of Molecular Biology, University of Geneva, 30 Quai Ernest-Ansermet, 1211 Geneva, Switzerland.

European Molecular Biology Laboratory, Grenoble Outstation, 71 Avenue des Martyrs, 38042 Grenoble, France.

出版信息

Dev Cell. 2017 Jun 19;41(6):623-637.e9. doi: 10.1016/j.devcel.2017.05.021.

Abstract

Small RNAs called PIWI-interacting RNAs (piRNAs) act as an immune system to suppress transposable elements in the animal gonads. A poorly understood adaptive pathway links cytoplasmic slicing of target RNA by the PIWI protein MILI to loading of target-derived piRNAs into nuclear MIWI2. Here we demonstrate that MILI slicing generates a 16-nt by-product that is discarded and a pre-piRNA intermediate that is used for phased piRNA production. The ATPase activity of Mouse Vasa Homolog (MVH) is essential for processing the intermediate into piRNAs, ensuring transposon silencing and male fertility. The ATPase activity controls dissociation of an MVH complex containing PIWI proteins, piRNAs, and slicer products, allowing safe handover of the intermediate. In contrast, ATPase activity of TDRD9 is dispensable for piRNA biogenesis but is essential for transposon silencing and male fertility. Our work implicates distinct RNA helicases in specific steps along the nuclear piRNA pathway.

摘要

被称为PIWI相互作用RNA(piRNA)的小RNA,在动物性腺中作为一种免疫系统来抑制转座元件。一条理解不足的适应性途径将PIWI蛋白MILI对靶RNA的细胞质切割与靶标来源的piRNA加载到核MIWI2中联系起来。在这里,我们证明MILI切割产生一个被丢弃的16个核苷酸的副产物和一个用于阶段性piRNA产生的前体piRNA中间体。小鼠Vasa同源物(MVH)的ATP酶活性对于将中间体加工成piRNA至关重要,可确保转座子沉默和雄性生育力。ATP酶活性控制包含PIWI蛋白、piRNA和切割产物的MVH复合物的解离,允许中间体的安全交接。相比之下,TDRD9的ATP酶活性对于piRNA生物发生是可有可无的,但对于转座子沉默和雄性生育力至关重要。我们的工作表明不同的RNA解旋酶在核piRNA途径的特定步骤中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1136/5481186/3fadc9a6fcf1/fx1.jpg

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