Carbohydrates induce mono-ubiquitination of H2B in yeast Journal Article


Authors: Dong, L.; Xu, C. W.
Article Title: Carbohydrates induce mono-ubiquitination of H2B in yeast
Abstract: Histone modifications have emerged to be a major regulatory mechanism for gene expression (1-4). However, it is not clear how histone modifications are physiologically regulated. Here, we show that mono-ubiquitinated H2B at lysine 123 (uH2B) in the yeast (Saccharomyces cerevisiae) is present in exponential phase and absent in stationary phase. A wide array of carbohydrates or sugars, including glucose, fructose, mannose, and sucrose, are capable of inducing uH2B in stationary phase yeast. In contrast, non-metabolic glucose analogs are defective in inducing uH2B. Furthermore, uH2B induction is inhibited by iodoacetate, an inhibitor of glyceraldehyde-3-phosphate dehydrogenase in glycolysis. Moreover, uH2B induction is markedly impaired in yeast mutants, in which glycolytic genes are deleted. These data indicate that glycolysis is required for the carbohydrate-induced mono-ubiquitination of H2B at lysine 123. Therefore, our study reveals a novel paradigm of metabolic regulation of histone modifications.
Keywords: gene deletion; nonhuman; ubiquitin; metabolism; enzyme inhibition; physiology; gene expression regulation; regulatory mechanism; ubiquitination; genetic engineering; saccharomyces cerevisiae; glucose; glyceraldehyde 3 phosphate dehydrogenase; gene induction; yeast; saccharomyces cerevisiae proteins; histone h2b; histones; glycolysis; mutagenesis; lysine; carbohydrate; chemical modification; histone modifications; saccharomyces; mannose; fructose; priority journal; article; iodoacetic acid
Journal Title: Journal of Biological Chemistry
Volume: 279
Issue: 3
ISSN: 0021-9258
Publisher: American Society for Biochemistry and Molecular Biology  
Date Published: 2004-01-16
Start Page: 1577
End Page: 1580
Language: English
DOI: 10.1074/jbc.C300505200
PROVIDER: scopus
PUBMED: 14660635
DOI/URL:
Notes: J. Biol. Chem. -- Cited By (since 1996):14 -- Export Date: 16 June 2014 -- CODEN: JBCHA -- Source: Scopus
Altmetric
Citation Impact
BMJ Impact Analytics
MSK Authors
  1. Chanxing Wilson Xu
    8 Xu
  2. Lin Dong
    6 Dong