Literature DB >> 24389641

Regulation of protein stability of DNA methyltransferase 1 by post-translational modifications.

Anthony Scott1, Jing Song, Rob Ewing, Zhenghe Wang.   

Abstract

DNA methylation is an important epigenetic mechanism that ensures correct gene expression and maintains genetic stability. DNA methyltransferase 1 (DNMT1) is the primary enzyme that maintains DNA methylation during replication. Dysregulation of DNMT1 is implicated in a variety of diseases. DNMT1 protein stability is regulated via various post-translational modifications, such as acetylation and ubiquitination, but also through protein-protein interactions. These mechanisms ensure DNMT1 is properly activated during the correct time of the cell cycle and at correct genomic loci, as well as in response to appropriate extracellular cues. Further understanding of these regulatory mechanisms may help to design novel therapeutic approaches for human diseases.

Entities:  

Keywords:  DNA (cytosine-5-)-methyltransferase; epi-genetics; neoplasms; post-translational modification; protein stability

Mesh:

Substances:

Year:  2014        PMID: 24389641      PMCID: PMC3932833          DOI: 10.1093/abbs/gmt146

Source DB:  PubMed          Journal:  Acta Biochim Biophys Sin (Shanghai)        ISSN: 1672-9145            Impact factor:   3.848


  72 in total

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6.  DNA methylation of multiple tumor-related genes in association with overexpression of DNA methyltransferase 1 (DNMT1) during multistage carcinogenesis of the pancreas.

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7.  Role of DNA 5-methylcytosine transferase in cell transformation by fos.

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  12 in total

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4.  NOS2 and S-nitrosothiol signaling induces DNA hypomethylation and LINE-1 retrotransposon expression.

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5.  β-elemene inhibited expression of DNA methyltransferase 1 through activation of ERK1/2 and AMPKα signalling pathways in human lung cancer cells: the role of Sp1.

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6.  LSD1 dual function in mediating epigenetic corruption of the vitamin D signaling in prostate cancer.

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7.  miR-377 induces senescence in human skin fibroblasts by targeting DNA methyltransferase 1.

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8.  Activation of SAPK/JNK mediated the inhibition and reciprocal interaction of DNA methyltransferase 1 and EZH2 by ursolic acid in human lung cancer cells.

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Review 10.  Epigenetic Effects Induced by Methamphetamine and Methamphetamine-Dependent Oxidative Stress.

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