| Literature DB >> 29861157 |
Quan Zhu1, Nien Hoong1, Aaron Aslanian2, Toshiro Hara1, Christopher Benner3, Sven Heinz3, Karen H Miga4, Eugene Ke1, Sachin Verma1, Jan Soroczynski5, John R Yates6, Tony Hunter7, Inder M Verma8.
Abstract
Heterochromatic repetitive satellite RNAs are extensively transcribed in a variety of human cancers, including BRCA1 mutant breast cancer. Aberrant expression of satellite RNAs in cultured cells induces the DNA damage response, activates cell cycle checkpoints, and causes defects in chromosome segregation. However, the mechanism by which satellite RNA expression leads to genomic instability is not well understood. Here we provide evidence that increased levels of satellite RNAs in mammary glands induce tumor formation in mice. Using mass spectrometry, we further show that genomic instability induced by satellite RNAs occurs through interactions with BRCA1-associated protein networks required for the stabilization of DNA replication forks. Additionally, de-stabilized replication forks likely promote the formation of RNA-DNA hybrids in cells expressing satellite RNAs. These studies lay the foundation for developing novel therapeutic strategies that block the effects of non-coding satellite RNAs in cancer cells.Entities:
Keywords: BRCA1-associated proteins; DNA damage response; breast tumor formation; heterochromatic RNAs; satellite RNAs
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Year: 2018 PMID: 29861157 PMCID: PMC6545586 DOI: 10.1016/j.molcel.2018.04.023
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970