USTIANENKO, Dmytro, Josef PASULKA, Zuzana FEKETOVÁ, Lukáš BEDNAŘÍK, Dagmar ZIGÁČKOVÁ, Andrea FOŘTOVÁ, Mihaela ZAVOLAN and Štěpánka VAŇÁČOVÁ. TUT-DIS3L2 is a mammalian surveillance pathway for aberrant structured non-coding RNAs. EMBO JOURNAL. Hoboken: Wiley-Blackwell, 2016, vol. 35, No 20, p. 2179-2191. ISSN 0261-4189. Available from: https://dx.doi.org/10.15252/embj.201694857.
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Basic information
Original name TUT-DIS3L2 is a mammalian surveillance pathway for aberrant structured non-coding RNAs
Authors USTIANENKO, Dmytro (804 Ukraine, belonging to the institution), Josef PASULKA (203 Czech Republic, belonging to the institution), Zuzana FEKETOVÁ (703 Slovakia, belonging to the institution), Lukáš BEDNAŘÍK (203 Czech Republic, belonging to the institution), Dagmar ZIGÁČKOVÁ (203 Czech Republic, belonging to the institution), Andrea FOŘTOVÁ (203 Czech Republic, belonging to the institution), Mihaela ZAVOLAN (756 Switzerland) and Štěpánka VAŇÁČOVÁ (203 Czech Republic, guarantor, belonging to the institution).
Edition EMBO JOURNAL, Hoboken, Wiley-Blackwell, 2016, 0261-4189.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10600 1.6 Biological sciences
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 9.792
RIV identification code RIV/00216224:14740/16:00088170
Organization unit Central European Institute of Technology
Doi http://dx.doi.org/10.15252/embj.201694857
UT WoS 000385708000003
Keywords in English DIS3L2; RNA surveillance; TSSa; ncRNAs; uridylation
Tags rivok
Changed by Changed by: Mgr. Eva Špillingová, učo 110713. Changed: 22/2/2017 13:52.
Abstract
Uridylation of various cellular RNA species at the 3' end has been generally linked to RNA degradation. In mammals, uridylated pre-let-7 miRNAs and mRNAs are targeted by the 3' to 5' exoribonuclease DIS3L2. Mutations in DIS3L2 have been associated with Perlman syndrome and with Wilms tumor susceptibility. Using in vivo cross-linking and immunoprecipitation (CLIP) method, we discovered the DIS3L2-dependent cytoplasmic uridylome of human cells. We found a broad spectrum of uridylated RNAs including rRNAs, snRNAs, snoRNAs, tRNAs, vault, 7SL, Y RNAs, mRNAs, lncRNAs, and transcripts from pseudogenes. The unifying features of most of these identified RNAs are aberrant processing and the presence of stable secondary structures. Most importantly, we demonstrate that uridylation mediates DIS3L2 degradation of short RNA polymerase II-derived RNAs. Our findings establish the role of DIS3L2 and oligouridylation as the cytoplasmic quality control for highly structured ncRNAs.
Links
GAP305/11/1095, research and development projectName: Funkční a biochemická charakterizace proteinu Dis3L2, třetího lidského homologu hlavní kvasinkové exosomové nukleázy Dis3p
Investor: Czech Science Foundation, Functional and biochemical characterization of Dis3L2, the third mammalian homolog of the key yeast exosome nuclease Dis3p
GA16-21341S, research and development projectName: Studium úlohy uridylace RNA v lidských buňkách
Investor: Czech Science Foundation
LQ1601, research and development projectName: CEITEC 2020 (Acronym: CEITEC2020)
Investor: Ministry of Education, Youth and Sports of the CR
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