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Interactions within the mammalian DNA methyltransferase family
Authors:Jean?B?Margot  author-information"  >  author-information__contact u-icon-before"  >  mailto:margot@fvk-berlin.de"   title="  margot@fvk-berlin.de"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author,Ann?E?Ehrenhofer-Murray,Heinrich?Leonhardt  author-information"  >  author-information__contact u-icon-before"  >  mailto:Heinrich.Leonhardt@lrz.uni-muenchen.de"   title="  Heinrich.Leonhardt@lrz.uni-muenchen.de"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:(1) Department of Biology II, Ludwig Maximilians University, Goethestr. 31, D-80336 Munich, Germany;(2) Otto Warburg Laboratories, Max Planck Institute of Molecular Genetics, Ihnestr. 73, D-14195 Berlin, Germany;(3) Max Delbruck Center for Molecular Medicine, D-13125 Berlin, Germany
Abstract:

Background  

In mammals, epigenetic information is established and maintained via the postreplicative methylation of cytosine residues by the DNA methyltransferases Dnmt1, Dnmt3a and Dnmt3b. Dnmt1 is required for maintenance methylation whereas Dnmt3a and Dnmt3b are responsible for de novo methylation. Contrary to Dnmt3a or Dnmt3b, the isolated C-terminal region of Dnmt1 is catalytically inactive, despite the presence of the sequence motifs typical of active DNA methyltransferases. Deletion analysis has revealed that a large part of the N-terminal domain is required for enzymatic activity.
Keywords:
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