| Literature DB >> 26724866 |
Sungyul Lee1, Florian Kopp2, Tsung-Cheng Chang2, Anupama Sataluri2, Beibei Chen3, Sushama Sivakumar4, Hongtao Yu5, Yang Xie6, Joshua T Mendell7.
Abstract
Long noncoding RNAs (lncRNAs) have emerged as regulators of diverse biological processes. Here, we describe the initial functional analysis of a poorly characterized human lncRNA (LINC00657) that is induced after DNA damage, which we termed "noncoding RNA activated by DNA damage", or NORAD. NORAD is highly conserved and abundant, with expression levels of approximately 500-1,000 copies per cell. Remarkably, inactivation of NORAD triggers dramatic aneuploidy in previously karyotypically stable cell lines. NORAD maintains genomic stability by sequestering PUMILIO proteins, which repress the stability and translation of mRNAs to which they bind. In the absence of NORAD, PUMILIO proteins drive chromosomal instability by hyperactively repressing mitotic, DNA repair, and DNA replication factors. These findings introduce a mechanism that regulates the activity of a deeply conserved and highly dosage-sensitive family of RNA binding proteins and reveal unanticipated roles for a lncRNA and PUMILIO proteins in the maintenance of genomic stability.Entities:
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Year: 2015 PMID: 26724866 PMCID: PMC4715682 DOI: 10.1016/j.cell.2015.12.017
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582