| Literature DB >> 25971364 |
C J Blume1, A Hotz-Wagenblatt2, J Hüllein1, L Sellner1,3, A Jethwa1, T Stolz1, M Slabicki1, K Lee1, A Sharathchandra4, A Benner5, S Dietrich1,3, C C Oakes6, P Dreger3, D te Raa7,8, A P Kater7,8, A Jauch9, O Merkel1,10, M Oren4, T Hielscher5, T Zenz1,3.
Abstract
Mutations of the tumor suppressor p53 lead to chemotherapy resistance and a dismal prognosis in chronic lymphocytic leukemia (CLL). Whereas p53 targets are used to identify patient subgroups with impaired p53 function, a comprehensive assessment of non-coding RNA targets of p53 in CLL is missing. We exploited the impaired transcriptional activity of mutant p53 to map out p53 targets in CLL by small RNA sequencing. We describe the landscape of p53-dependent microRNA/non-coding RNA induced in response to DNA damage in CLL. Besides the key p53 target miR-34a, we identify a set of p53-dependent microRNAs (miRNAs; miR-182-5p, miR-7-5p and miR-320c/d). In addition to miRNAs, the long non-coding RNAs (lncRNAs) nuclear enriched abundant transcript 1 (NEAT1) and long intergenic non-coding RNA p21 (lincRNA-p21) are induced in response to DNA damage in the presence of functional p53 but not in CLL with p53 mutation. Induction of NEAT1 and lincRNA-p21 are closely correlated to the induction of cell death after DNA damage. We used isogenic lymphoma cell line models to prove p53 dependence of NEAT1 and lincRNA-p21. The current work describes the p53-dependent miRNome and identifies lncRNAs NEAT1 and lincRNA-p21 as novel elements of the p53-dependent DNA damage response machinery in CLL and lymphoma.Entities:
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Year: 2015 PMID： 25971364 DOI： 10.1038/leu.2015.119
Source DB: PubMed Journal: Leukemia ISSN： 0887-6924 Impact factor: 11.528