The CRTC-1 transcriptional domain is required for COMPASS complex-mediated longevity in C. elegans

Nat Aging. 2023 Nov;3(11):1358-1371. doi: 10.1038/s43587-023-00517-8. Epub 2023 Nov 9.

Abstract

Loss of function during aging is accompanied by transcriptional drift, altering gene expression and contributing to a variety of age-related diseases. CREB-regulated transcriptional coactivators (CRTCs) have emerged as key regulators of gene expression that might be targeted to promote longevity. Here we define the role of the Caenorhabditis elegans CRTC-1 in the epigenetic regulation of longevity. Endogenous CRTC-1 binds chromatin factors, including components of the COMPASS complex, which trimethylates lysine 4 on histone H3 (H3K4me3). CRISPR editing of endogenous CRTC-1 reveals that the CREB-binding domain in neurons is specifically required for H3K4me3-dependent longevity. However, this effect is independent of CREB but instead acts via the transcription factor AP-1. Strikingly, CRTC-1 also mediates global histone acetylation levels, and this acetylation is essential for H3K4me3-dependent longevity. Indeed, overexpression of an acetyltransferase enzyme is sufficient to promote longevity in wild-type worms. CRTCs, therefore, link energetics to longevity by critically fine-tuning histone acetylation and methylation to promote healthy aging.

MeSH terms

  • Animals
  • Caenorhabditis elegans* / genetics
  • Epigenesis, Genetic
  • Histones / chemistry
  • Longevity* / genetics
  • Transcription Factors / genetics

Substances

  • Histones
  • Transcription Factors
  • CRTC-1 protein, C elegans