Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI 48109.
Department of Life Sciences, Graduate School of Arts and Sciences, The University of Tokyo, 153-8902 Tokyo, Japan.
Proc Natl Acad Sci U S A. 2020 Dec 1;117(48):30799-30804. doi: 10.1073/pnas.2014419117. Epub 2020 Nov 16.
Eukaryotic genomes are pervasively transcribed, yet most transcribed sequences lack conservation or known biological functions. In , RNA polymerase V (Pol V) produces noncoding transcripts, which base pair with small interfering RNA (siRNA) and allow specific establishment of RNA-directed DNA methylation (RdDM) on transposable elements. Here, we show that Pol V transcribes much more broadly than previously expected, including subsets of both heterochromatic and euchromatic regions. At already established RdDM targets, Pol V and siRNA work together to maintain silencing. In contrast, some euchromatic sequences do not give rise to siRNA but are covered by low levels of Pol V transcription, which is needed to establish RdDM de novo if a transposon is reactivated. We propose a model where Pol V surveils the genome to make it competent to silence newly activated or integrated transposons. This indicates that pervasive transcription of nonconserved sequences may serve an essential role in maintenance of genome integrity.
真核基因组广泛转录,但大多数转录序列缺乏保守性或已知的生物学功能。在这里,RNA 聚合酶 V(Pol V)产生非编码转录本,这些转录本与小干扰 RNA(siRNA)配对,并允许在转座元件上特异性建立 RNA 指导的 DNA 甲基化(RdDM)。我们发现,Pol V 的转录范围比以前预期的要广泛得多,包括异染色质和常染色质区域的子集。在已经建立的 RdDM 靶标上,Pol V 和 siRNA 共同作用以维持沉默。相比之下,一些常染色质序列不会产生 siRNA,但会被低水平的 Pol V 转录覆盖,如果转座子被重新激活,则需要 Pol V 转录来建立新的 RdDM。我们提出了一个模型,其中 Pol V 监测基因组,使其能够沉默新激活或整合的转座子。这表明非保守序列的广泛转录可能在维持基因组完整性方面发挥着重要作用。