Cargando…

Human oncoprotein Musashi-2 N-terminal RNA recognition motif backbone assignment and identification of RNA-binding pocket

RNA-binding protein Musashi-2 (MSI2) is a key regulator in stem cells, it is over-expressed in a variety of cancers and its higher expression is associated with poor prognosis. Like Musashi-1, it contains two N-terminal RRMs (RNA-recognition Motifs, also called RBDs (RNA-binding Domains)), RRM1 and...

Descripción completa

Detalles Bibliográficos
Autores principales: Lan, Lan, Xing, Minli, Douglas, Justin T., Gao, Philip, Hanzlik, Robert P., Xu, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5739758/
https://www.ncbi.nlm.nih.gov/pubmed/29290973
http://dx.doi.org/10.18632/oncotarget.22540
_version_ 1783287933130768384
author Lan, Lan
Xing, Minli
Douglas, Justin T.
Gao, Philip
Hanzlik, Robert P.
Xu, Liang
author_facet Lan, Lan
Xing, Minli
Douglas, Justin T.
Gao, Philip
Hanzlik, Robert P.
Xu, Liang
author_sort Lan, Lan
collection PubMed
description RNA-binding protein Musashi-2 (MSI2) is a key regulator in stem cells, it is over-expressed in a variety of cancers and its higher expression is associated with poor prognosis. Like Musashi-1, it contains two N-terminal RRMs (RNA-recognition Motifs, also called RBDs (RNA-binding Domains)), RRM1 and RRM2, which mediate the binding to their target mRNAs. Previous studies have obtained the three-dimensional structures of the RBDs of Musashi-1 and the RBD1:RNA complex. Here we show the binding of MSI2-RRM1 to a 15nt Numb RNA in Fluorescence Polarization assay and time resolved Fluorescence Resonance Energy Transfer assay. Using nuclear magnetic resonance (NMR) spectroscopy we assigned the backbone resonances of MSI2-RRM1, and characterized the direct interaction of RRM1 to Numb RNA r(GUAGU). Our NMR titration and structure modeling studies showed that MSI2-RRM1 and MSI1-RBD1 have similar RNA binding events and binding pockets. This work adds significant information to MSI2-RRM1 structure and RNA binding pocket, and contributes to the development of MSI2 specific and MSI1/MSI2 dual inhibitors.
format Online
Article
Text
id pubmed-5739758
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Impact Journals LLC
record_format MEDLINE/PubMed
spelling pubmed-57397582017-12-29 Human oncoprotein Musashi-2 N-terminal RNA recognition motif backbone assignment and identification of RNA-binding pocket Lan, Lan Xing, Minli Douglas, Justin T. Gao, Philip Hanzlik, Robert P. Xu, Liang Oncotarget Research Paper RNA-binding protein Musashi-2 (MSI2) is a key regulator in stem cells, it is over-expressed in a variety of cancers and its higher expression is associated with poor prognosis. Like Musashi-1, it contains two N-terminal RRMs (RNA-recognition Motifs, also called RBDs (RNA-binding Domains)), RRM1 and RRM2, which mediate the binding to their target mRNAs. Previous studies have obtained the three-dimensional structures of the RBDs of Musashi-1 and the RBD1:RNA complex. Here we show the binding of MSI2-RRM1 to a 15nt Numb RNA in Fluorescence Polarization assay and time resolved Fluorescence Resonance Energy Transfer assay. Using nuclear magnetic resonance (NMR) spectroscopy we assigned the backbone resonances of MSI2-RRM1, and characterized the direct interaction of RRM1 to Numb RNA r(GUAGU). Our NMR titration and structure modeling studies showed that MSI2-RRM1 and MSI1-RBD1 have similar RNA binding events and binding pockets. This work adds significant information to MSI2-RRM1 structure and RNA binding pocket, and contributes to the development of MSI2 specific and MSI1/MSI2 dual inhibitors. Impact Journals LLC 2017-11-20 /pmc/articles/PMC5739758/ /pubmed/29290973 http://dx.doi.org/10.18632/oncotarget.22540 Text en Copyright: © 2017 Lan et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Lan, Lan
Xing, Minli
Douglas, Justin T.
Gao, Philip
Hanzlik, Robert P.
Xu, Liang
Human oncoprotein Musashi-2 N-terminal RNA recognition motif backbone assignment and identification of RNA-binding pocket
title Human oncoprotein Musashi-2 N-terminal RNA recognition motif backbone assignment and identification of RNA-binding pocket
title_full Human oncoprotein Musashi-2 N-terminal RNA recognition motif backbone assignment and identification of RNA-binding pocket
title_fullStr Human oncoprotein Musashi-2 N-terminal RNA recognition motif backbone assignment and identification of RNA-binding pocket
title_full_unstemmed Human oncoprotein Musashi-2 N-terminal RNA recognition motif backbone assignment and identification of RNA-binding pocket
title_short Human oncoprotein Musashi-2 N-terminal RNA recognition motif backbone assignment and identification of RNA-binding pocket
title_sort human oncoprotein musashi-2 n-terminal rna recognition motif backbone assignment and identification of rna-binding pocket
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5739758/
https://www.ncbi.nlm.nih.gov/pubmed/29290973
http://dx.doi.org/10.18632/oncotarget.22540
work_keys_str_mv AT lanlan humanoncoproteinmusashi2nterminalrnarecognitionmotifbackboneassignmentandidentificationofrnabindingpocket
AT xingminli humanoncoproteinmusashi2nterminalrnarecognitionmotifbackboneassignmentandidentificationofrnabindingpocket
AT douglasjustint humanoncoproteinmusashi2nterminalrnarecognitionmotifbackboneassignmentandidentificationofrnabindingpocket
AT gaophilip humanoncoproteinmusashi2nterminalrnarecognitionmotifbackboneassignmentandidentificationofrnabindingpocket
AT hanzlikrobertp humanoncoproteinmusashi2nterminalrnarecognitionmotifbackboneassignmentandidentificationofrnabindingpocket
AT xuliang humanoncoproteinmusashi2nterminalrnarecognitionmotifbackboneassignmentandidentificationofrnabindingpocket