The dark proteome: translation from noncanonical open reading frames

Trends Cell Biol. 2022 Mar;32(3):243-258. doi: 10.1016/j.tcb.2021.10.010. Epub 2021 Nov 26.

Abstract

Omics-based technologies have revolutionized our understanding of the coding potential of the genome. In particular, these studies revealed widespread unannotated open reading frames (ORFs) throughout genomes and that these regions have the potential to encode novel functional (micro-)proteins and/or hold regulatory roles. However, despite their genomic prevalence, relatively few of these noncanonical ORFs have been functionally characterized, likely in part due to their under-recognition by the broader scientific community. The few that have been investigated in detail have demonstrated their essentiality in critical and divergent biological processes. As such, here we aim to discuss recent advances in understanding the diversity of noncanonical ORFs and their roles, as well as detail biologically important examples within the context of the mammalian genome.

Keywords: CRISPR; microproteins; noncanonical ORFs; ribosome profiling; short ORFs; translation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Genome*
  • Genomics
  • Humans
  • Mammals
  • Open Reading Frames / genetics
  • Proteome* / genetics

Substances

  • Proteome