A Translation-Activating Function of MIWI/piRNA during Mouse Spermiogenesis
Author(s) -
Peng Dai,
Xin Wang,
LanTao Gou,
Zhitong Li,
Ze Wen,
Zonggui Chen,
Min-Min Hua,
Ai Zhong,
Lingbo Wang,
Haiyang Su,
Huida Wan,
Kun Qian,
Lujian Liao,
Jinsong Li,
Bin Tian,
Dangsheng Li,
XiangDong Fu,
Huijuan Shi,
Yu Zhou,
MoFang Liu
Publication year - 2019
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2019.11.022
Subject(s) - spermiogenesis , biology , spermatid , microbiology and biotechnology , piwi interacting rna , translation (biology) , transcription (linguistics) , genetics , messenger rna , gene , transposable element , mutant , linguistics , philosophy , nucleus , sperm
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.
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