학술논문

Epigenetic regulation of RNA polymerase III transcription in early breast tumorigenesis
Document Type
article
Source
Oncogene. 36(49)
Subject
Biological Sciences
Genetics
Women's Health
Cancer
Human Genome
Breast Cancer
Generic health relevance
Breast
Cell Transformation
Neoplastic
Cells
Cultured
Chromatin
DNA
DNA Methylation
Epigenesis
Genetic
Epithelial Cells
Humans
Protein Binding
Proto-Oncogene Proteins c-myc
RNA Polymerase III
RNA
Untranslated
Transcription
Genetic
Clinical Sciences
Oncology and Carcinogenesis
Oncology & Carcinogenesis
Biochemistry and cell biology
Oncology and carcinogenesis
Language
Abstract
RNA polymerase III (Pol III) transcribes medium-sized non-coding RNAs (collectively termed Pol III genes). Emerging diverse roles of Pol III genes suggest that individual Pol III genes are exquisitely regulated by transcription and epigenetic factors. Here we report global Pol III expression/methylation profiles and molecular mechanisms of Pol III regulation that have not been as extensively studied, using nc886 as a representative Pol III gene. In a human mammary epithelial cell system that recapitulates early breast tumorigenesis, the fraction of actively transcribed Pol III genes increases reaching a plateau during immortalization. Hyper-methylation of Pol III genes inhibits Pol III binding to DNA via inducing repressed chromatin and is a determinant for the Pol III repertoire. When Pol III genes are hypo-methylated, MYC amplifies their transcription, regardless of its recognition DNA motif. Thus, Pol III expression during tumorigenesis is delineated by methylation and magnified by MYC.