DND1 maintains germline stem cells via recruitment of the CCR4-NOT complex to target mRNAs

Nature. 2017 Mar 23;543(7646):568-572. doi: 10.1038/nature21690. Epub 2017 Mar 15.

Abstract

The vertebrate-conserved RNA-binding protein DND1 is required for the survival of primordial germ cells (PGCs), as well as the suppression of germ cell tumours in mice. Here we show that in mice DND1 binds a UU(A/U) trinucleotide motif predominantly in the 3' untranslated regions of mRNA, and destabilizes target mRNAs through direct recruitment of the CCR4-NOT deadenylase complex. Transcriptomic analysis reveals that the extent of suppression is dependent on the number of DND1-binding sites. This DND1-dependent mRNA destabilization is required for the survival of mouse PGCs and spermatogonial stem cells by suppressing apoptosis. The spectrum of target RNAs includes positive regulators of apoptosis and inflammation, and modulators of signalling pathways that regulate stem-cell pluripotency, including the TGFβ superfamily, all of which are aberrantly elevated in DND1-deficient PGCs. We propose that the induction of the post-transcriptional suppressor DND1 synergizes with concurrent transcriptional changes to ensure precise developmental transitions during cellular differentiation and maintenance of the germ line.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions / genetics
  • Animals
  • Apoptosis / genetics
  • Base Sequence
  • Binding Sites
  • Cell Differentiation / genetics
  • Gene Expression Profiling
  • Gene Silencing
  • Humans
  • Inflammation / genetics
  • Male
  • Mice
  • Multiprotein Complexes / chemistry
  • Multiprotein Complexes / metabolism*
  • Neoplasm Proteins / deficiency
  • Neoplasm Proteins / metabolism*
  • Nucleotide Motifs
  • Pluripotent Stem Cells / cytology
  • Protein Binding
  • RNA Stability*
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism*
  • Ribonucleases / chemistry
  • Ribonucleases / metabolism*
  • Signal Transduction / genetics
  • Spermatogonia / cytology*
  • Spermatogonia / metabolism
  • Stem Cells / cytology*
  • Stem Cells / metabolism
  • Transcription Factors / metabolism*
  • Transcription, Genetic / genetics
  • Transforming Growth Factor beta / genetics

Substances

  • 3' Untranslated Regions
  • Dnd1 protein, mouse
  • Multiprotein Complexes
  • Neoplasm Proteins
  • RNA, Messenger
  • Transcription Factors
  • Transforming Growth Factor beta
  • Ribonucleases
  • mRNA deadenylase