Chromatin-associated YTHDC1 coordinates heat-induced reprogramming of gene expression

Cell Rep. 2022 Dec 13;41(11):111784. doi: 10.1016/j.celrep.2022.111784.

Abstract

Heat stress (HS) induces a cellular response leading to profound changes in gene expression. Here, we show that human YTHDC1, a reader of N6-methyladenosine (m6A) RNA modification, mostly associates to the chromatin fraction and that HS induces a redistribution of YTHDC1 across the genome, including to heat-induced heat shock protein (HSP) genes. YTHDC1 binding to m6A-modified HSP transcripts co-transcriptionally promotes expression of HSPs. In parallel, hundreds of the genes enriched in YTHDC1 during HS have their transcripts undergoing YTHDC1- and m6A-dependent intron retention. Later, YTHDC1 concentrates within nuclear stress bodies (nSBs) where it binds to m6A-modified SATIII non-coding RNAs, produced in an HSF1-dependent manner upon HS. These findings reveal that YTHDC1 plays a central role in a chromatin-associated m6A-based reprogramming of gene expression during HS. Furthermore, they support the model where the subsequent and temporary sequestration of YTHDC1 within nSBs calibrates the timing of this YTHDC1-dependent gene expression reprogramming.

Keywords: CP: Molecular biology; HSF1; HSP; HSPs; N(6)-methyladenosine; RNA; YTH; chromatin; heat shock proteins; heat stress; intron retention; m(6)A; m6A; nSBs; ncRNA; ncRNAs; non-coding RNAs; nuclear stress bodies; nuclear stress body; satellite RNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromatin*
  • Gene Expression
  • Heat-Shock Proteins / metabolism
  • Heat-Shock Response* / genetics
  • Humans
  • Nerve Tissue Proteins / metabolism
  • RNA Splicing Factors / metabolism

Substances

  • Chromatin
  • Heat-Shock Proteins
  • YTHDC1 protein, human
  • RNA Splicing Factors
  • Nerve Tissue Proteins