Literature DB >> 21596309

Acetyl-CoA induces cell growth and proliferation by promoting the acetylation of histones at growth genes.

Ling Cai1, Benjamin M Sutter, Bing Li, Benjamin P Tu.   

Abstract

The decision by a cell to enter a round of growth and division must be intimately coordinated with nutrient availability and its metabolic state. These metabolic and nutritional requirements, and the mechanisms by which they induce cell growth and proliferation, remain poorly understood. Herein, we report that acetyl-CoA is the downstream metabolite of carbon sources that represents a critical metabolic signal for growth and proliferation. Upon entry into growth, intracellular acetyl-CoA levels increase substantially and consequently induce the Gcn5p/SAGA-catalyzed acetylation of histones at genes important for growth, thereby enabling their rapid transcription and commitment to growth. Thus, acetyl-CoA functions as a carbon-source rheostat that signals the initiation of the cellular growth program by promoting the acetylation of histones specifically at growth genes.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21596309      PMCID: PMC3109073          DOI: 10.1016/j.molcel.2011.05.004

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


  52 in total

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  302 in total

Review 1.  Cellular metabolism and disease: what do metabolic outliers teach us?

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3.  Signaling in control of cell growth and metabolism.

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Review 4.  MYC: connecting selective transcriptional control to global RNA production.

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Review 5.  Protein acetylation in metabolism - metabolites and cofactors.

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Journal:  Nat Rev Endocrinol       Date:  2015-10-27       Impact factor: 43.330

Review 6.  Immunometabolism: Cellular Metabolism Turns Immune Regulator.

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7.  Histone methylation has dynamics distinct from those of histone acetylation in cell cycle reentry from quiescence.

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8.  A high-confidence interaction map identifies SIRT1 as a mediator of acetylation of USP22 and the SAGA coactivator complex.

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9.  Downregulation of the acetyl-CoA metabolic network in adipose tissue of obese diabetic individuals and recovery after weight loss.

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Journal:  Diabetologia       Date:  2014-08-07       Impact factor: 10.122

10.  Acetyl-CoA induces transcription of the key G1 cyclin CLN3 to promote entry into the cell division cycle in Saccharomyces cerevisiae.

Authors:  Lei Shi; Benjamin P Tu
Journal:  Proc Natl Acad Sci U S A       Date:  2013-04-15       Impact factor: 11.205

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