Stem cells. m6A mRNA methylation facilitates resolution of naïve pluripotency toward differentiation

Science. 2015 Feb 27;347(6225):1002-6. doi: 10.1126/science.1261417. Epub 2015 Jan 1.

Abstract

Naïve and primed pluripotent states retain distinct molecular properties, yet limited knowledge exists on how their state transitions are regulated. Here, we identify Mettl3, an N(6)-methyladenosine (m(6)A) transferase, as a regulator for terminating murine naïve pluripotency. Mettl3 knockout preimplantation epiblasts and naïve embryonic stem cells are depleted for m(6)A in mRNAs, yet are viable. However, they fail to adequately terminate their naïve state and, subsequently, undergo aberrant and restricted lineage priming at the postimplantation stage, which leads to early embryonic lethality. m(6)A predominantly and directly reduces mRNA stability, including that of key naïve pluripotency-promoting transcripts. This study highlights a critical role for an mRNA epigenetic modification in vivo and identifies regulatory modules that functionally influence naïve and primed pluripotency in an opposing manner.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine / analogs & derivatives*
  • Adenosine / metabolism
  • Animals
  • Blastocyst / enzymology
  • Cell Differentiation / genetics
  • Cell Differentiation / physiology*
  • Cell Line
  • Embryo Loss / genetics
  • Epigenesis, Genetic
  • Female
  • Gene Knockout Techniques
  • Male
  • Methylation
  • Methyltransferases / genetics
  • Methyltransferases / physiology*
  • Mice
  • Mice, Knockout
  • Pluripotent Stem Cells / cytology*
  • Pluripotent Stem Cells / enzymology
  • RNA, Messenger / metabolism*

Substances

  • RNA, Messenger
  • N-methyladenosine
  • Methyltransferases
  • Mettl3 protein, mouse
  • Adenosine

Associated data

  • GEO/GSE61998