The Methyl-CpG-Binding Protein MBD7 Facilitates Active DNA Demethylation to Limit DNA Hyper-Methylation and Transcriptional Gene Silencing

  • Zhaobo Lang
  • , Mingguang Lei
  • , Xingang Wang
  • , Kai Tang
  • , Daisuke Miki
  • , Huiming Zhang
  • , Satendra K. Mangrauthia
  • , Wenshan Liu
  • , Wenfeng Nie
  • , Guojie Ma
  • , Jun Yan
  • , Cheng Guo Duan
  • , Chuan Chih Hsu
  • , Chunlei Wang
  • , W. Andy Tao
  • , Zhizhong Gong
  • , Jian Kang Zhu*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

120 Scopus citations

Abstract

DNA methylation is a conserved epigenetic mark that plays important roles in plant and vertebrate development, genome stability, and gene regulation. Canonical Methyl-CpG-binding domain (MBD) proteins are important interpreters of DNA methylation that recognize methylated CG sites and recruit chromatin remodelers, histone deacetylases, and histone methyltransferases to repress transcription. Here, we show that Arabidopsis MBD7 and Increased DNA Methylation 3 (IDM3) are anti-silencing factors that prevent gene repression and DNA hypermethylation. MBD7 preferentially binds to highly methylated, CG-dense regions and physically associates with other anti-silencing factors, including the histone acetyltransferase IDM1 and the alpha-crystallin domain proteins IDM2 and IDM3. IDM1 and IDM2 were previously shown to facilitate active DNA demethylation by the 5-methylcytosine DNA glycosylase/lyase ROS1. Thus, MBD7 tethers the IDM proteins to methylated DNA, which enables the function of DNA demethylases that in turn limit DNA methylation and prevent transcriptional gene silencing.

Original languageEnglish
Pages (from-to)971-983
Number of pages13
JournalMolecular Cell
Volume57
Issue number6
DOIs
StatePublished - 19 Mar 2015
Externally publishedYes

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