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Identification of lncRNA MEG3 Binding Protein Using MS2-Tagged RNA Affinity Purification and Mass Spectrometry.

Authors :
Liu S
Zhu J
Jiang T
Zhong Y
Tie Y
Wu Y
Zheng X
Jin Y
Fu H
Source :
Applied biochemistry and biotechnology [Appl Biochem Biotechnol] 2015 Aug; Vol. 176 (7), pp. 1834-45. Date of Electronic Publication: 2015 Jul 09.
Publication Year :
2015

Abstract

Long noncoding RNAs (lncRNAs) are nonprotein coding transcripts longer than 200 nucleotides. Recently in mammals, thousands of long noncoding RNAs have been identified and studied as key molecular players in different biological processes with protein complexes. As a long noncoding RNA, maternally expressed gene 3 (MEG3) plays an important role in many cellular processes. However, the mechanism underlying MEG3 regulatory effects remains enigmatic. By using the specific interaction between MS2 coat protein and MS2 RNA hairpin, we developed a method (MS2-tagged RNA affinity purification and mass spectrometry (MTRAP-MS)) to identify proteins that interact with MEG3. Mass spectrometry and gene ontology (GO) analysis showed that MEG3 binding proteins possess nucleotide binding properties and take part in transport, translation, and other biological processes. In addition, interleukin enhancer binding factor 3 (ILF3) and poly(A) binding protein, cytoplasmic 3 (PABPC3) were validated for their interaction with MEG3. These findings indicate that the newly developed method can effectively enrich lncRNA binding proteins and provides a strong basis for studying MEG3 functions.

Details

Language :
English
ISSN :
1559-0291
Volume :
176
Issue :
7
Database :
MEDLINE
Journal :
Applied biochemistry and biotechnology
Publication Type :
Academic Journal
Accession number :
26155902
Full Text :
https://doi.org/10.1007/s12010-015-1680-5