4.5 Review

Chromatin remodeling regulation by small molecules and metabolites

Journal

BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS
Volume 1799, Issue 10-12, Pages 671-680

Publisher

ELSEVIER
DOI: 10.1016/j.bbagrm.2010.05.007

Keywords

Chromatin remodeling; ATP; AcCoA; SAM; NAD; Poly-ADP-ribosylation; Phosphatidylinositide; Inositol polyphosphates

Funding

  1. FIRC
  2. Telethon
  3. Fondazione Telethon
  4. Giovanni Armenise Harvard Foundation
  5. FIRB-MIUR
  6. AIRC
  7. Compagnia San Paolo

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The eukaryotic genome is a highly organized nucleoprotein structure comprising of DNA, histones, nonhistone proteins, and RNAs, referred to as chromatin. The chromatin exists as a dynamic entity, shuttling between the open and closed forms at specific nuclear regions and loci based on the requirement of the cell. This dynamicity is essential for the various DNA-templated phenomena like transcription, replication, and repair and is achieved through the activity of ATP-dependent chromatin remodeling complexes and covalent modifiers of chromatin. A growing body of data indicates that chromatin enzymatic activities are finely and specifically regulated by a variety of small molecules derived from the intermediary metabolism. This review tries to summarize the work conducted in many laboratories and on different model organisms showing how ATP-dependent chromatin remodeling complexes are regulated by small molecules and metabolites such as adenosine triphosphate (ATP), acetyl coenzyme A (AcCoA), S-adenosyl methionine (SAM), nicotinamide adenine dinucleotide (NAD), and inositol polyphosphates (IPs). (C) 2010 Elsevier B.V. All rights reserved.

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