| Literature DB >> 31835033 |
Peng Dai1, Xin Wang1, Lan-Tao Gou2, Zhi-Tong Li1, Ze Wen1, Zong-Gui Chen3, Min-Min Hua4, Ai Zhong1, Lingbo Wang5, Haiyang Su6, Huida Wan7, Kun Qian6, Lujian Liao7, Jinsong Li8, Bin Tian9, Dangsheng Li1, Xiang-Dong Fu10, Hui-Juan Shi11, Yu Zhou12, Mo-Fang Liu13.
Abstract
Spermiogenesis is a highly orchestrated developmental process during which chromatin condensation decouples transcription from translation. Spermiogenic mRNAs are transcribed earlier and stored in a translationally inert state until needed for translation; however, it remains largely unclear how such repressed mRNAs become activated during spermiogenesis. We previously reported that the MIWI/piRNA machinery is responsible for mRNA elimination during late spermiogenesis in preparation for spermatozoa production. Here we unexpectedly discover that the same machinery is also responsible for activating translation of a subset of spermiogenic mRNAs to coordinate with morphological transformation into spermatozoa. Such action requires specific base-pairing interactions of piRNAs with target mRNAs in their 3' UTRs, which activates translation through coupling with cis-acting AU-rich elements to nucleate the formation of a MIWI/piRNA/eIF3f/HuR super-complex in a developmental stage-specific manner. These findings reveal a critical role of the piRNA system in translation activation, which we show is functionally required for spermatid development.Entities:
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Year: 2019 PMID: 31835033 PMCID: PMC8139323 DOI: 10.1016/j.cell.2019.11.022
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582