Literature DB >> 12483518

Gene silencing in phenomena related to DNA repair.

Tsunehiro Mukai1, Mutsuo Sekiguchi.   

Abstract

DNA methylation is essential for embryonic development and important for transcriptional repression, as observed in several biological phenomena. These include genomic imprinting, X-inactivation and carcinogenesis. The basic mechanism by which DNA methylation silences transcription is generally understood, but there is still much to be learned about how DNA methyltransferase is targeted to a specific region of the gene. Silencing by DNA methylation occurs at an early stage of carcinogenesis, when the DNA repair genes, MGMT and hMLH1, are frequently inactivated, resulting in mutations in key cancer-related genes in cells. Mice defective in Mgmt and/or Mlh1 gave clear evidence of the significant roles of these proteins in carcinogenesis. Recently, it has been demonstrated that DNA methylation is linked to histone methylation in fungi and plants, although it remains unknown whether this mechanism occurs in mammalian systems.

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Year:  2002        PMID: 12483518     DOI: 10.1038/sj.onc.1206095

Source DB:  PubMed          Journal:  Oncogene        ISSN: 0950-9232            Impact factor:   9.867


  4 in total

1.  Mutually exclusive promoter hypermethylation patterns of hMLH1 and O6-methylguanine DNA methyltransferase in colorectal cancer.

Authors:  Edward J Fox; Dermot T Leahy; Robert Geraghty; Hugh E Mulcahy; David Fennelly; John M Hyland; Diarmuid P O'Donoghue; Kieran Sheahan
Journal:  J Mol Diagn       Date:  2006-02       Impact factor: 5.568

2.  Promoter methylation status of MGMT, hMSH2, and hMLH1 and its relationship to corresponding protein expression and TP53 mutations in human esophageal squamous cell carcinoma.

Authors:  Yaoyao Su; Lihong Yin; Ran Liu; Jingyi Sheng; Miao Yang; Yi Wang; Enchun Pan; Wei Guo; Yuepu Pu; Juan Zhang; Geyu Liang
Journal:  Med Oncol       Date:  2013-12-24       Impact factor: 3.064

3.  The mouse Murr1 gene is imprinted in the adult brain, presumably due to transcriptional interference by the antisense-oriented U2af1-rs1 gene.

Authors:  Youdong Wang; Keiichiro Joh; Sadahiko Masuko; Hitomi Yatsuki; Hidenobu Soejima; Akira Nabetani; Colin V Beechey; Satoshi Okinami; Tsunehiro Mukai
Journal:  Mol Cell Biol       Date:  2004-01       Impact factor: 4.272

4.  Sequence Variants and the Risk of Head and Neck Cancer: Pooled Analysis in the INHANCE Consortium.

Authors:  Shu-Chun Chuang; Antonio Agudo; Wolfgang Ahrens; Devasena Anantharaman; Simone Benhamou; Stefania Boccia; Chu Chen; David I Conway; Eleonora Fabianova; Richard B Hayes; Claire M Healy; Ivana Holcatova; Kristina Kjaerheim; Pagona Lagiou; Philip Lazarus; Tatiana V Macfarlane; Manoj B Mahimkar; Dana Mates; Keitaro Matsuo; Franco Merletti; Andres Metspalu; Hal Morgenstern; Joshua Muscat; Gabriella Cadoni; Andrew F Olshan; Mark Purdue; Heribert Ramroth; Peter Rudnai; Stephen M Schwartz; Lorenzo Simonato; Elaine M Smith; Erich M Sturgis; Neonilia Szeszenia-Dabrowska; Renato Talamini; Peter Thomson; Qingyi Wei; David Zaridze; Zuo-Feng Zhang; Ariana Znaor; Paul Brennan; Paolo Boffetta; Mia Hashibe
Journal:  Front Oncol       Date:  2011-07-12       Impact factor: 6.244

  4 in total

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