CNOT6L couples the selective degradation of maternal transcripts to meiotic cell cycle progression in mouse oocyte

EMBO J. 2018 Dec 14;37(24):e99333. doi: 10.15252/embj.201899333. Epub 2018 Nov 26.

Abstract

Meiotic resumption-coupled degradation of maternal transcripts occurs during oocyte maturation in the absence of mRNA transcription. The CCR4-NOT complex has been identified as the main eukaryotic mRNA deadenylase. In vivo functional and mechanistic information regarding its multiple subunits remains insufficient. Cnot6l, one of four genes encoding CCR4-NOT catalytic subunits, is preferentially expressed in mouse oocytes. Genetic deletion of Cnot6l impaired deadenylation and degradation of a subset of maternal mRNAs during oocyte maturation. Overtranslation of these undegraded mRNAs caused microtubule-chromosome organization defects, which led to activation of spindle assembly checkpoint and meiotic cell cycle arrest at prometaphase. Consequently, Cnot6l-/- female mice were severely subfertile. The function of CNOT6L in maturing oocytes is mediated by RNA-binding protein ZFP36L2, not maternal-to-zygotic transition licensing factor BTG4, which interacts with catalytic subunits CNOT7 and CNOT8 of CCR4-NOT Thus, recruitment of different adaptors by different catalytic subunits ensures stage-specific degradation of maternal mRNAs by CCR4-NOT This study provides the first direct genetic evidence that CCR4-NOT-dependent and particularly CNOT6L-dependent decay of selective maternal mRNAs is a prerequisite for meiotic maturation of oocytes.

Keywords: CCR4–NOT; maternal mRNA decay; maternal‐to‐zygotic transition; meiotic maturation; oocyte.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Exoribonucleases
  • Female
  • Gene Deletion
  • Meiosis*
  • Mice
  • Mice, Knockout
  • Oocytes / cytology
  • Oocytes / metabolism*
  • Proteins / genetics
  • Proteins / metabolism
  • RNA Stability*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism*
  • Repressor Proteins
  • Ribonucleases / genetics
  • Ribonucleases / metabolism*
  • Tristetraprolin / genetics
  • Tristetraprolin / metabolism

Substances

  • Proteins
  • RNA, Messenger
  • Repressor Proteins
  • Tristetraprolin
  • Zfp36 protein, mouse
  • Cnot6l protein, mouse
  • Cnot7 protein, mouse
  • Exoribonucleases
  • Ribonucleases