Institute of Biological Chemistry, Academia Sinica, Taipei, Taiwan.
PLoS Genet. 2021 Feb 1;17(2):e1009349. doi: 10.1371/journal.pgen.1009349. eCollection 2021 Feb.
The piRNA pathway is a highly conserved mechanism to repress transposon activation in the germline in Drosophila and mammals. This pathway starts from transcribing piRNA clusters to generate long piRNA precursors. The majority of piRNA clusters lack conventional promoters, and utilize heterochromatin- and HP1D/Rhino-dependent noncanonical mechanisms for transcription. However, information regarding the transcriptional regulation of piRNA clusters is limited. Here, we report that the Drosophila acetyltransferase Enok, which can activate transcription by acetylating H3K23, is critical for piRNA production from 54% of piRNA clusters including 42AB, the major piRNA source. Surprisingly, we found that Enok not only promotes rhino expression by acetylating H3K23, but also directly enhances transcription of piRNA clusters by facilitating Rhino recruitment. Taken together, our study provides novel insights into the regulation of noncanonical transcription at piRNA clusters and transposon silencing.
piRNA 通路是一种高度保守的机制,可抑制果蝇和哺乳动物生殖细胞中转座子的激活。该通路从转录 piRNA 簇开始,生成长的 piRNA 前体。大多数 piRNA 簇缺乏传统的启动子,利用异染色质和 HP1D/Rhino 依赖的非典型机制进行转录。然而,关于 piRNA 簇转录调控的信息有限。在这里,我们报告果蝇乙酰转移酶 Enok 可以通过乙酰化 H3K23 激活转录,对于包括 42AB 在内的 54%的 piRNA 簇的 piRNA 产生至关重要,42AB 是主要的 piRNA 来源。令人惊讶的是,我们发现 Enok 通过乙酰化 H3K23 不仅促进 rhino 的表达,还通过促进 Rhino 募集直接增强 piRNA 簇的转录。总之,我们的研究为 piRNA 簇和转座子沉默的非典型转录调控提供了新的见解。