4.6 Review

The Role of MacroH2A Histone Variants in Cancer

Journal

CANCERS
Volume 13, Issue 12, Pages -

Publisher

MDPI
DOI: 10.3390/cancers13123003

Keywords

macroH2A; histone variants; epigenetics; chromatin; cancer; macrodomain; tumor suppressor; oncohistone; malignant transformation

Categories

Funding

  1. Fundacio La Marato de TV3 [257/C/2019]
  2. MCIU [PRE2019-088529]
  3. MINECO [RTI2018094005-B-I00]
  4. Marie Sklodowska Curie Training network 'INTER-CEPT-MDS' [H2020-MSCAITN-2015-953407]
  5. AGAUR [2017-SGR-305]
  6. MINECO-ISCIII [PIE16/00011]
  7. Deutsche Jose Carreras Leukamie Stiftung [DJCLS 14R/2018]
  8. 'La Caixa' Foundation
  9. Fundacio Internacional Josep Carreras, Celgene Spain
  10. CERCA Programme/Generalitat de Catalunya

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This paper provides a concise review on a group of histone variants called macroH2A, discussing their additional domains that contribute to molecular functions in normal cells and their roles in gene expression and cancer. The importance of epigenetic regulation in physiological tissue homeostasis and malignant transformation is highlighted, with a focus on the least understood mechanism of histone variants. The study focuses on the tripartite structure of macroH2A histone variants and how they mediate molecular functions related to chromatin architecture, transcription, and DNA repair, emphasizing their dysregulated expression in different cancer subtypes and their variable prognostic impact.
Simple Summary The structural unit of chromatin is the nucleosome that is composed of DNA wrapped around a core of eight histone proteins. Histone variants can replace 'standard' histones at specific sites of the genome. Thus, histone variants modulate all functions in the context of chromatin, such as gene expression. Here, we provide a concise review on a group of histone variants termed macroH2A. They contain two additional domains that contribute to their increased size. We discuss how these domains mediate molecular functions in normal cells and the role of macroH2As in gene expression and cancer. The epigenome regulates gene expression and provides a molecular memory of cellular events. A growing body of evidence has highlighted the importance of epigenetic regulation in physiological tissue homeostasis and malignant transformation. Among epigenetic mechanisms, the replacement of replication-coupled histones with histone variants is the least understood. Due to differences in protein sequence and genomic distribution, histone variants contribute to the plasticity of the epigenome. Here, we focus on the family of macroH2A histone variants that are particular in having a tripartite structure consisting of a histone fold, an intrinsically disordered linker and a globular macrodomain. We discuss how these domains mediate different molecular functions related to chromatin architecture, transcription and DNA repair. Dysregulated expression of macroH2A histone variants has been observed in different subtypes of cancer and has variable prognostic impact, depending on cellular context and molecular background. We aim to provide a concise review regarding the context- and isoform-dependent contributions of macroH2A histone variants to cancer development and progression.

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