Asymmetric Expression of LincGET Biases Cell Fate in Two-Cell Mouse Embryos

Cell. 2018 Dec 13;175(7):1887-1901.e18. doi: 10.1016/j.cell.2018.11.039.

Abstract

In early mammalian embryos, it remains unclear how the first cell fate bias is initially triggered and amplified toward cell fate segregation. Here, we report that a long noncoding RNA, LincGET, is transiently and asymmetrically expressed in the nucleus of two- to four-cell mouse embryos. Overexpression of LincGET in one of the two-cell blastomeres biases its progeny predominantly toward the inner cell mass (ICM) fate. Mechanistically, LincGET physically binds to CARM1 and promotes the nuclear localization of CARM1, which can further increase the level of H3 methylation at Arginine 26 (H3R26me), activate ICM-specific gene expression, upregulate transposons, and increase global chromatin accessibility. Simultaneous overexpression of LincGET and depletion of Carm1 no longer biased embryonic fate, indicating that the effect of LincGET in directing ICM lineage depends on CARM1. Thus, our data identify LincGET as one of the earliest known lineage regulators to bias cell fate in mammalian 2-cell embryos.

Keywords: CARM1; cell fate determination; chromatin accessibility; early embryos; long noncoding RNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blastocyst / cytology
  • Blastocyst / metabolism*
  • Blastomeres / cytology
  • Blastomeres / metabolism*
  • Cell Lineage / physiology*
  • Female
  • Gene Expression Regulation, Developmental / physiology*
  • Histones / metabolism
  • Methylation
  • Mice
  • Mice, Inbred ICR
  • Protein-Arginine N-Methyltransferases / biosynthesis
  • Protein-Arginine N-Methyltransferases / genetics
  • RNA, Long Noncoding / biosynthesis*
  • RNA, Long Noncoding / genetics

Substances

  • Histones
  • RNA, Long Noncoding
  • Protein-Arginine N-Methyltransferases
  • coactivator-associated arginine methyltransferase 1