Relationship between DNA methylation, histone H4 acetylation and gene expression in the mouse imprinted Igf2‐H19 domain

FEBS Letters

Sado, Takashi¹  Ferguson-Smith, Anne¹  Turner, Bryan²  O'Neill, Laura²  Grandjean, Valerie¹ 

[1] Department of Anatomy, University of Cambridge, Downing Street, Cambridge CB2 3DY, UK;Department of Anatomy, University of Birmingham Medical School, Birmingham B15 2TT, UK

关键词: Imprinting;    Histone acetylation;    DNA methylation;    Chromatin;    Igf2/H19;   

DOI  :  10.1016/S0014-5793(00)02349-8

学科分类：生物化学/生物物理

来源: John Wiley & Sons Ltd.

【 摘 要 】

DNA methylation and histone H4 acetylation play a role in gene regulation by modulating the structure of the chromatin. Recently, these two epigenetic modifications have dynamically and physically been linked. Evidence suggests that both modifications are involved in regulating imprinted genes – a subset of genes whose expression depends on their parental origin. Using immunoprecipitation assays, we investigate the relationship between DNA methylation, histone H4 acetylation and gene expression in the well-characterised imprinted Igf2-H19 domain on mouse chromosome 7. A systematic regional analysis of the acetylation status of the domain shows that parental-specific differences in acetylation of the core histone H4 are present in the promoter regions of both Igf2 and H19 genes, with the expressed alleles being more acetylated than the silent alleles. A correlation between DNA methylation, histone hypoacetylation and gene repression is evident only at the promoter region of the H19 gene. Treatment with trichostatin A, a specific inhibitor of histone deacetylase, reduces the expression of the active maternal H19 allele and this can be correlated with regional changes in acetylation within the upstream regulatory domain. The data suggest that histone H4 acetylation and DNA methylation have distinct functions on the maternal and paternal Igf2-H19 domains.

【 授权许可】

Unknown