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Regulation of DNMT1 stability through SET7-mediated lysine methylation in mammalian cells.
Estève, Pierre-Olivier; Chin, Hang Gyeong; Benner, Jack; Feehery, George R; Samaranayake, Mala; Horwitz, Gregory A; Jacobsen, Steven E; Pradhan, Sriharsa.
Affiliation
  • Estève PO; New England Biolabs Incorporated, 240 County Road, Ipswich, MA 01938, USA.
Proc Natl Acad Sci U S A ; 106(13): 5076-81, 2009 Mar 31.
Article in En | MEDLINE | ID: mdl-19282482
ABSTRACT
Inheritance of epigenetic information encoded by cytosine DNA methylation patterns is crucial for mammalian cell survival, in large part through the activity of the maintenance DNA methyltransferase (DNMT1). Here, we show that SET7, a known histone methyltransferase, is involved in the regulation of protein stability of DNMT1. SET7 colocalizes and directly interacts with DNMT1 and specifically monomethylates Lys-142 of DNMT1. Methylated DNMT1 peaks during the S and G(2) phases of the cell cycle and is prone to proteasome-mediated degradation. Overexpression of SET7 leads to decreased DNMT1 levels, and siRNA-mediated knockdown of SET7 stabilizes DNMT1. These results demonstrate that signaling through SET7 represents a means of DNMT1 enzyme turnover.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Histone-Lysine N-Methyltransferase / DNA (Cytosine-5-)-Methyltransferases / Lysine Limits: Animals / Humans Language: En Journal: Proc Natl Acad Sci U S A Year: 2009 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Histone-Lysine N-Methyltransferase / DNA (Cytosine-5-)-Methyltransferases / Lysine Limits: Animals / Humans Language: En Journal: Proc Natl Acad Sci U S A Year: 2009 Type: Article Affiliation country: United States