The role of holocarboxylase synthetase in genome stability is mediated partly by epigenomic synergies between methylation and biotinylation events

Epigenetics

Volumn 6, Issue 7, 2011, Pages 892-894

  Zempleni, Janos ^a   Li, Yong ^a   Xue, Jing ^a   Cordonier, Elizabeth L ^a  

^a UNIVERSITY OF NEBRASKA LINCOLN   (United States)

Author keywords

Biotin; DNMT1; EHMT 1; Genome stability; Histone; Holocarboxylase synthetase; MeCP2; Methylation

Indexed keywords

BIOTIN; BIOTIN DERIVATIVE; CARBOXYLASE; CYTOSINE; DNA METHYLTRANSFERASE 1; HISTONE H2B; HISTONE H3; HISTONE H4; HOLOCARBOXYLASE SYNTHETASE; UNCLASSIFIED DRUG;

ARTICLE; ATOMIC FORCE MICROSCOPY; BINDING SITE; CANDIDA ALBICANS; CELLULAR DISTRIBUTION; CHROMATIN; CHROMATIN IMMUNOPRECIPITATION; DIETARY INTAKE; DISORDERS OF CARBOHYDRATE METABOLISM; DROSOPHILA MELANOGASTER; EPIGENETICS; GENE CONTROL; GENE MUTATION; GENE REPRESSION; GENOMIC INSTABILITY; HEAT TOLERANCE; HISTONE BIOTINYLATION; HISTONE METHYLATION; HISTONE MODIFICATION; HISTONE PHOSPHORYLATION; HUMAN; LONG TERMINAL REPEAT; MASS SPECTROMETRY; METABOLISM; NONHUMAN; NUCLEAR LAMINA; PHENOTYPE; RETROPOSON; TELOMERE;

EID: 79960123143     PISSN: 15592294     EISSN: 15592308     Source Type: Journal    
DOI: 10.4161/epi.6.7.15544     Document Type: Article

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