Spracklin George, Fields Brandon, Wan Gang, Becker Diveena, Wallig Ashley, Shukla Aditi, Kennedy Scott
Laboratory of Genetics, University of Wisconsin-Madison, Madison, Wisconsin 53706.
Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115.
Genetics. 2017 Jul;206(3):1403-1416. doi: 10.1534/genetics.116.198812. Epub 2017 May 22.
Gene silencing mediated by dsRNA (RNAi) can persist for multiple generations in (termed RNAi inheritance). Here we describe the results of a forward genetic screen in that has identified six factors required for RNAi inheritance: GLH-1/VASA, PUP-1/CDE-1, MORC-1, SET-32, and two novel nematode-specific factors that we term here (heritable RNAi defective) HRDE-2 and HRDE-4 The new RNAi inheritance factors exhibit mortal germline (Mrt) phenotypes, which we show is likely caused by epigenetic deregulation in germ cells. We also show that HRDE-2 contributes to RNAi inheritance by facilitating the binding of small RNAs to the inheritance Argonaute (Ago) HRDE-1 Together, our results identify additional components of the RNAi inheritance machinery whose conservation provides insights into the molecular mechanism of RNAi inheritance, further our understanding of how the RNAi inheritance machinery promotes germline immortality, and show that HRDE-2 couples the inheritance Ago HRDE-1 with the small RNAs it needs to direct RNAi inheritance and germline immortality.
由双链RNA介导的基因沉默(RNA干扰)可在多代中持续存在(称为RNA干扰遗传)。在此,我们描述了在秀丽隐杆线虫中进行的一项正向遗传学筛选的结果,该筛选鉴定出了RNA干扰遗传所需的六个因子:GLH-1/VASA、PUP-1/CDE-1、MORC-1、SET-32,以及两个新的线虫特异性因子,我们在此将其称为(遗传性RNA干扰缺陷)HRDE-2和HRDE-4。这些新的RNA干扰遗传因子表现出种系死亡(Mrt)表型,我们表明这可能是由生殖细胞中的表观遗传失调引起的。我们还表明,HRDE-2通过促进小RNA与遗传AGO(Ago)HRDE-1的结合来促进RNA干扰遗传。总之,我们的结果鉴定出了RNA干扰遗传机制的其他组成部分,其保守性为RNA干扰遗传的分子机制提供了见解,进一步加深了我们对RNA干扰遗传机制如何促进种系永生的理解,并表明HRDE-2将遗传AGO HRDE-1与其指导RNA干扰遗传和种系永生所需的小RNA联系起来。