Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 1998 Sep 1;17(17):4905-8.
doi: 10.1093/emboj/17.17.4905.

CpG methylation, chromatin structure and gene silencing-a three-way connection

Affiliations
Review

CpG methylation, chromatin structure and gene silencing-a three-way connection

A Razin. EMBO J. .

Abstract

The three-way connection between DNA methylation, gene activity and chromatin structure has been known for almost two decades. Nevertheless, the molecular link between methyl groups on the DNA and the positioning of nucleosomes to form an inactive chromatin configuration was missing. This review discusses recent experimental data that may, for the first time, shed light on this molecular link. MeCP2, which is a known methylcytosine-binding protein, has been shown to possess a transcriptional repressor domain (TRD) that binds the corepressor mSin3A. This corepressor protein constitutes the core of a multiprotein complex that includes histone deacetylases (HDAC1 and HDAC2). Transfection and injection experiments with methylated constructs have revealed that the silenced state of a methylated gene, which is associated with a deacetylated nucleosomal structure, could be relieved by the deacetylase inhibitor, trichostatin A. Thus, methylation plays a pivotal role in establishing and maintaining an inactive state of a gene by rendering the chromatin structure inaccessible to the transcription machinery.

PubMed Disclaimer

References

    1. Proc Natl Acad Sci U S A. 1980 Nov;77(11):6463-7 - PubMed
    1. J Cell Biol. 1979 Nov;83(2 Pt 1):403-27 - PubMed
    1. Proc Natl Acad Sci U S A. 1983 Aug;80(16):4919-21 - PubMed
    1. Proc Natl Acad Sci U S A. 1983 Sep;80(18):5490-4 - PubMed
    1. Cell. 1986 Feb 28;44(4):535-43 - PubMed

Publication types