A novel evolutionary conserved mechanism of RNA stability regulates synexpression of primordial germ cell-specific genes prior to the sex-determination stage in medaka

PLoS Biol. 2019 Apr 4;17(4):e3000185. doi: 10.1371/journal.pbio.3000185. eCollection 2019 Apr.

Abstract

Dmrt1 is a highly conserved transcription factor, which is critically involved in regulation of gonad development of vertebrates. In medaka, a duplicate of dmrt1-acting as master sex-determining gene-has a tightly timely and spatially controlled gonadal expression pattern. In addition to transcriptional regulation, a sequence motif in the 3' UTR (D3U-box) mediates transcript stability of dmrt1 mRNAs from medaka and other vertebrates. We show here that in medaka, two RNA-binding proteins with antagonizing properties target this D3U-box, promoting either RNA stabilization in germ cells or degradation in the soma. The D3U-box is also conserved in other germ-cell transcripts, making them responsive to the same RNA binding proteins. The evolutionary conservation of the D3U-box motif within dmrt1 genes of metazoans-together with preserved expression patterns of the targeting RNA binding proteins in subsets of germ cells-suggest that this new mechanism for controlling RNA stability is not restricted to fishes but might also apply to other vertebrates.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions / genetics
  • Animals
  • Biological Evolution
  • Female
  • Fish Proteins / genetics
  • Gene Expression Regulation, Developmental / genetics*
  • Germ Cells / metabolism
  • Male
  • Oryzias / genetics*
  • RNA Recognition Motif Proteins / metabolism
  • RNA Stability / genetics
  • RNA, Messenger / metabolism
  • Sex Determination Processes / genetics*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Vertebrates / metabolism

Substances

  • 3' Untranslated Regions
  • DMRT1 protein
  • Fish Proteins
  • RNA Recognition Motif Proteins
  • RNA, Messenger
  • Transcription Factors

Grants and funding

This work was supported by the Deutsche Forschungsgemeinschaft by a grant (SCHA 408/12-1; HE 7135/2-1) to AH and MS as well as Crédits Incitatifs Phase 2015/Emergence to AH. AH was additionally funded by the project AquaCRISPR (ANR-16-COFA-0004-01). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.