Reduce, retain, recycle: Mechanisms for promoting histone protein degradation versus stability and retention

Ann K. Hogan, Daniel R. Foltz*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

13 Scopus citations

Abstract

The eukaryotic genome is packaged into chromatin. The nucleosome, the basic unit of chromatin, is composed of DNA coiled around a histone octamer. Histones are among the longest-lived protein species in mammalian cells due to their thermodynamic stability and their associations with DNA and histone chaperones. Histone metabolism plays an integral role in homeostasis. While histones are largely stable, the degradation of histone proteins is necessary under specific conditions. Here, we review the physiological and cellular contexts that promote histone degradation. We describe specific known mechanisms that drive histone proteolysis. Finally, we discuss the importance of histone degradation and regulation of histone supply for organismal and cellular fitness.

Original languageEnglish (US)
Article numbere00007-21
JournalMolecular and cellular biology
Volume41
Issue number6
DOIs
StatePublished - May 2021

Funding

D.R.F. is supported by a Zell Scholarship from the Robert H. Lurie Comprehensive Cancer Center, Northwestern University, and by the NIGMS (R01GM111907) and NCI (U01CA260699).

Keywords

  • Chaperone
  • Chromatin
  • DNA replication
  • Histone
  • Nucleosome
  • Nucleus
  • Posttranslational modification
  • Transcription

ASJC Scopus subject areas

  • Molecular Biology
  • Cell Biology

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