Literature DB >> 15509558

Processive methylation of hemimethylated CpG sites by mouse Dnmt1 DNA methyltransferase.

Giedrius Vilkaitis1, Isao Suetake, Saulius Klimasauskas, Shoji Tajima.   

Abstract

DNA methyltransferase Dnmt1 ensures clonal transmission of lineage-specific DNA methylation patterns in a mammalian genome during replication. Dnmt1 is targeted to replication foci, interacts with PCNA, and favors methylating the hemimethylated form of CpG sites. To understand the underlying mechanism of its maintenance function, we purified recombinant forms of full-length Dnmt1, a truncated form of Dnmt1-(291-1620) lacking the binding sites for PCNA and DNA and examined their processivity using a series of long unmethylated and hemimethylated DNA substrates. Direct analysis of methylation patterns using bisulfite-sequencing and hairpin-PCR techniques demonstrated that full-length Dnmt1 methylates hemimethylated DNA with high processivity and a fidelity of over 95%, but unmethylated DNA with much less processivity. The truncated form of Dnmt1 showed identical properties to full-length Dnmt1 indicating that the N-terminal 290-amino acid residue region of Dnmt1 is not required for preferential activity toward hemimethylated sites or for processivity of the enzyme. Remarkably, our analyses also revealed that Dnmt1 methylates hemimethylated CpG sites on one strand of double-stranded DNA during a single processive run. Our findings suggest that these inherent enzymatic properties of Dnmt1 play an essential role in the faithful and efficient maintenance of methylation patterns in the mammalian genome.

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Year:  2004        PMID: 15509558     DOI: 10.1074/jbc.M411126200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  72 in total

1.  Structural insight into maintenance methylation by mouse DNA methyltransferase 1 (Dnmt1).

Authors:  Kohei Takeshita; Isao Suetake; Eiki Yamashita; Michihiro Suga; Hirotaka Narita; Atsushi Nakagawa; Shoji Tajima
Journal:  Proc Natl Acad Sci U S A       Date:  2011-04-25       Impact factor: 11.205

Review 2.  Male germline control of transposable elements.

Authors:  Jianqiang Bao; Wei Yan
Journal:  Biol Reprod       Date:  2012-05-31       Impact factor: 4.285

3.  Mutations in DNA methyltransferase (DNMT3A) observed in acute myeloid leukemia patients disrupt processive methylation.

Authors:  Celeste Holz-Schietinger; Doug M Matje; Norbert O Reich
Journal:  J Biol Chem       Date:  2012-06-21       Impact factor: 5.157

4.  Laccaic acid A is a direct, DNA-competitive inhibitor of DNA methyltransferase 1.

Authors:  Rebecca L Fagan; Diane E Cryderman; Levy Kopelovich; Lori L Wallrath; Charles Brenner
Journal:  J Biol Chem       Date:  2013-07-09       Impact factor: 5.157

5.  The DNA methyltransferase Dnmt1 directly interacts with the SET and RING finger-associated (SRA) domain of the multifunctional protein Uhrf1 to facilitate accession of the catalytic center to hemi-methylated DNA.

Authors:  Ahmet Can Berkyurek; Isao Suetake; Kyohei Arita; Kohei Takeshita; Atsushi Nakagawa; Masahiro Shirakawa; Shoji Tajima
Journal:  J Biol Chem       Date:  2013-11-19       Impact factor: 5.157

6.  Topoisomerase II regulates the maintenance of DNA methylation.

Authors:  Lin-Yu Lu; Henry Kuang; Gautam Korakavi; Xiaochun Yu
Journal:  J Biol Chem       Date:  2014-12-01       Impact factor: 5.157

7.  Kinetics and mechanisms of mitotic inheritance of DNA methylation and their roles in aging-associated methylome deterioration.

Authors:  Xuan Ming; Zhuqiang Zhang; Zhuoning Zou; Cong Lv; Qiang Dong; Qixiang He; Yangyang Yi; Yingfeng Li; Hailin Wang; Bing Zhu
Journal:  Cell Res       Date:  2020-06-24       Impact factor: 25.617

8.  Suppression of intestinal neoplasia by deletion of Dnmt3b.

Authors:  Haijiang Lin; Yasuhiro Yamada; Suzanne Nguyen; Heinz Linhart; Laurie Jackson-Grusby; Alexander Meissner; Konstantinos Meletis; Grace Lo; Rudolf Jaenisch
Journal:  Mol Cell Biol       Date:  2006-04       Impact factor: 4.272

9.  DNMT3L modulates significant and distinct flanking sequence preference for DNA methylation by DNMT3A and DNMT3B in vivo.

Authors:  Bethany L Wienholz; Michael S Kareta; Amir H Moarefi; Catherine A Gordon; Paul A Ginno; Frédéric Chédin
Journal:  PLoS Genet       Date:  2010-09-09       Impact factor: 5.917

10.  A directed evolution design of a GCG-specific DNA hemimethylase.

Authors:  Ruta Gerasimaite; Giedrius Vilkaitis; Saulius Klimasauskas
Journal:  Nucleic Acids Res       Date:  2009-11       Impact factor: 16.971

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