| Literature DB >> 28833069 |
Aparna Anantharaman1, Omid Gholamalamdari1, Abid Khan1, Je-Hyun Yoon2, Michael F Jantsch3, Jochen C Hartner4, Myriam Gorospe2, Supriya G Prasanth1, Kannanganattu V Prasanth1.
Abstract
Adenosine deaminases acting on RNA (ADARs) are proteins that catalyse widespread A-to-I editing within RNA sequences. We recently reported that ADAR2 edits and stabilizes nuclear-retained Cat2 transcribed nuclear RNA (Ctn RNA). Here, we report that ADAR1 coordinates with ADAR2 to regulate editing and stability of Ctn RNA. We observe an RNA-dependent interaction between ADAR1 and ADAR2. Furthermore, ADAR1 negatively regulates interaction of Ctn RNA with RNA-destabilizing proteins. We also show that breast cancer (BC) cells display elevated ADAR1 but not ADAR2 levels, compared to nontumourigenic cells. Additionally, BC patients with elevated levels of ADAR1 show low survival. Our findings provide insights into overlapping substrate preferences of ADARs and potential involvement of ADAR1 in BC.Entities:
Keywords: zzm321990ADARzzm321990; zzm321990Ctn RNAzzm321990; HuR; RNA editing; breast cancer; mRNA stability
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Year: 2017 PMID: 28833069 PMCID: PMC5612911 DOI: 10.1002/1873-3468.12795
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124