Fatscher, Tobias and Gehring, Niels H. ORCID: 0000-0001-7792-1164 (2016). Harnessing short poly(A)-binding protein-interacting peptides for the suppression of nonsense-mediated mRNA decay. Sci Rep, 6. LONDON: NATURE PUBLISHING GROUP. ISSN 2045-2322

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Abstract

Nonsense-mediated mRNA decay (NMD) is a cellular process that eliminates messenger RNA (mRNA) substrates with premature translation termination codons (PTCs). In addition, NMD regulates the expression of a number of physiological mRNAs, for example transcripts containing long 3'UTRs. Current models implicate the interaction between cytoplasmic poly(A)-binding protein (PABPC1) and translation termination in NMD. Accordingly, PABPC1 present within close proximity of a termination codon antagonizes NMD. Here, we use reporter mRNAs with different NMD-inducing 3'UTRs to establish a general NMD-inhibiting property of PABPC1. NMD-inhibition is not limited to PABPC1, but can also be achieved by peptides consisting of the PABP-interacting motif 2 (PAM2) of different proteins when recruited to an NMD-inhibiting position of NMD reporter transcripts. The short PAM2 peptides efficiently suppress NMD activated by a long 3'UTR, an exon-junction complex (EJC) and individual EJC components, and stabilize a PTC-containing beta-globin mRNA. In conclusion, our results establish short PABPC1-recruiting peptides as potent but position-dependent inhibitors of mammalian NMD.

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Fatscher, TobiasUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Gehring, Niels H.UNSPECIFIEDorcid.org/0000-0001-7792-1164UNSPECIFIED
URN: urn:nbn:de:hbz:38-255534
DOI: 10.1038/srep37311
Journal or Publication Title: Sci Rep
Volume: 6
Date: 2016
Publisher: NATURE PUBLISHING GROUP
Place of Publication: LONDON
ISSN: 2045-2322
Language: English
Faculty: Faculty of Mathematics and Natural Sciences
Divisions: Faculty of Mathematics and Natural Sciences > Department of Biology > Institute for Genetics
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
EXON-JUNCTION COMPLEX; C-TERMINAL DOMAIN; EUKARYOTIC TRANSLATION; INITIATION-FACTOR; BINDING-PROTEIN; UPF1 GENE; SURVEILLANCE; PABC; IDENTIFICATION; RECOGNITIONMultiple languages
Multidisciplinary SciencesMultiple languages
Refereed: Yes
URI: http://kups.ub.uni-koeln.de/id/eprint/25553

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