4.8 Article

A Translation-Activating Function of MIWI/piRNA during Mouse Spermiogenesis

期刊

CELL
卷 179, 期 7, 页码 1566-+

出版社

CELL PRESS
DOI: 10.1016/j.cell.2019.11.022

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资金

  1. National Key R&D Program of China [2017YFA0504400]
  2. Chinese Academy of Sciences [XDB19010203]
  3. National Natural Science Foundation of China [31830109, 31821004, 91940305, 91640201]
  4. Shanghai Municipal Science and Technology Major Project [17JC1420100, 19JC1410200, 2017SHZDZX01]
  5. Foundation of Key Laboratory of Gene Engineering of the Ministry of Education
  6. SA-SIBS Scholarship Program
  7. China Postdoctoral Science Foundation [2016M600335]
  8. NIH [GM052872, HG004659]

向作者/读者索取更多资源

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 30 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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