4.4 Article

Epigenetics in the heart: the role of histone modifications in cardiac remodelling

Journal

BIOCHEMICAL SOCIETY TRANSACTIONS
Volume 41, Issue -, Pages 789-796

Publisher

PORTLAND PRESS LTD
DOI: 10.1042/BST20130012

Keywords

cardiac hypertrophy; chromatin; epigenetics; histone; histone methylation

Funding

  1. Babraham Institute
  2. Biotechnology and Biological Sciences Research Council [Epigenetics ISPG (Institute Strategic Programme Grant)]
  3. British Heart Foundation
  4. Marie Curie Fellowship [253644]
  5. Cambridge Commonwealth Trust (Jawaharlal Nehru Memorial Trust)
  6. BBSRC [BBS/E/B/0000S256, BBS/E/B/0000H326, BBS/E/B/0000C237, BBS/E/B/0000H114] Funding Source: UKRI
  7. Biotechnology and Biological Sciences Research Council [BBS/E/B/0000C116, BBS/E/B/0000S256, BBS/E/B/0000C237, BBS/E/B/0000H114, BBS/E/B/0000H326] Funding Source: researchfish
  8. British Heart Foundation [PG/11/12/28717] Funding Source: researchfish

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Understanding the molecular mechanisms underlying cardiac development and growth has been a longstanding goal for developing therapies for cardiovascular disorders. The heart adapts to a rise in its required output by an increase in muscle mass and alteration in the expression of a large number of genes. However, persistent stress diminishes the plasticity of the heart, consequently resulting in its maladaptive growth, termed pathological hypertrophy. Recent developments suggest that the concomitant genome-wide remodelling of the gene expression programme is largely driven through epigenetic mechanisms such as post-translational histone modifications and DNA methylation. In the last few years, the distinct functions of histone modifications and of the enzymes catalysing their formation have begun to be elucidated in processes important for cardiac development, disease and cardiomyocyte proliferation. The present review explores how repressive histone modifications, in particular methylation of H3K9 (histone H3 Lys(9)), govern aspects of cardiac biology.

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