Mechanism of β-actin mRNA Recognition by ZBP1

Zipcode binding protein 1 (ZBP1) is an oncofetal RNA-binding protein that mediates the transport and local translation of β-actin mRNA by the KH3-KH4 di-domain, which is essential for neuronal development. The high-resolution structures of KH3-KH4 with their respective target sequences show that KH4...

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Main Authors: Giuseppe Nicastro, Adela M. Candel, Michael Uhl, Alain Oregioni, David Hollingworth, Rolf Backofen, Stephen R. Martin, Andres Ramos
Format: Article
Language:English
Published: Elsevier 2017-01-01
Series:Cell Reports
Subjects:
NMR
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124717300013
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spelling doaj-fc9af46783534be98494a16d4cdcbc902020-11-24T21:35:59ZengElsevierCell Reports2211-12472017-01-011851187119910.1016/j.celrep.2016.12.091Mechanism of β-actin mRNA Recognition by ZBP1Giuseppe Nicastro0Adela M. Candel1Michael Uhl2Alain Oregioni3David Hollingworth4Rolf Backofen5Stephen R. Martin6Andres Ramos7Macromolecular Structure Laboratory, The Francis Crick Institute, London NW1 1AT, UKAt the former MRC National Institute for Medical Research, Mill Hill, LondonBioinformatics Group, Department of Computer Science, University of Freiburg, 79110 Freiburg, GermanyMRC Biomedical NMR Centre, The Francis Crick Institute, London NW1 1AT, UKMycobacterial Systems Biology Laboratory, The Francis Crick Institute, London NW1 1AT, UKBioinformatics Group, Department of Computer Science, University of Freiburg, 79110 Freiburg, GermanyStructural Biology Science Technology Platform, The Francis Crick Institute, London NW1 1AT, UKInstitute of Structural and Molecular Biology, University College London, London WC1E 6XA, UKZipcode binding protein 1 (ZBP1) is an oncofetal RNA-binding protein that mediates the transport and local translation of β-actin mRNA by the KH3-KH4 di-domain, which is essential for neuronal development. The high-resolution structures of KH3-KH4 with their respective target sequences show that KH4 recognizes a non-canonical GGA sequence via an enlarged and dynamic hydrophobic groove, whereas KH3 binding to a core CA sequence occurs with low specificity. A data-informed kinetic simulation of the two-step binding reaction reveals that the overall reaction is driven by the second binding event and that the moderate affinities of the individual interactions favor RNA looping. Furthermore, the concentration of ZBP1, but not of the target RNA, modulates the interaction, which explains the functional significance of enhanced ZBP1 expression during embryonic development.http://www.sciencedirect.com/science/article/pii/S2211124717300013protein-RNA interactionsNMRbinding mechanismneuronal mRNA granulesneuronal developmentmRNA local translationZBP1IMP1
collection DOAJ
language English
format Article
sources DOAJ
author Giuseppe Nicastro
Adela M. Candel
Michael Uhl
Alain Oregioni
David Hollingworth
Rolf Backofen
Stephen R. Martin
Andres Ramos
spellingShingle Giuseppe Nicastro
Adela M. Candel
Michael Uhl
Alain Oregioni
David Hollingworth
Rolf Backofen
Stephen R. Martin
Andres Ramos
Mechanism of β-actin mRNA Recognition by ZBP1
Cell Reports
protein-RNA interactions
NMR
binding mechanism
neuronal mRNA granules
neuronal development
mRNA local translation
ZBP1
IMP1
author_facet Giuseppe Nicastro
Adela M. Candel
Michael Uhl
Alain Oregioni
David Hollingworth
Rolf Backofen
Stephen R. Martin
Andres Ramos
author_sort Giuseppe Nicastro
title Mechanism of β-actin mRNA Recognition by ZBP1
title_short Mechanism of β-actin mRNA Recognition by ZBP1
title_full Mechanism of β-actin mRNA Recognition by ZBP1
title_fullStr Mechanism of β-actin mRNA Recognition by ZBP1
title_full_unstemmed Mechanism of β-actin mRNA Recognition by ZBP1
title_sort mechanism of β-actin mrna recognition by zbp1
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2017-01-01
description Zipcode binding protein 1 (ZBP1) is an oncofetal RNA-binding protein that mediates the transport and local translation of β-actin mRNA by the KH3-KH4 di-domain, which is essential for neuronal development. The high-resolution structures of KH3-KH4 with their respective target sequences show that KH4 recognizes a non-canonical GGA sequence via an enlarged and dynamic hydrophobic groove, whereas KH3 binding to a core CA sequence occurs with low specificity. A data-informed kinetic simulation of the two-step binding reaction reveals that the overall reaction is driven by the second binding event and that the moderate affinities of the individual interactions favor RNA looping. Furthermore, the concentration of ZBP1, but not of the target RNA, modulates the interaction, which explains the functional significance of enhanced ZBP1 expression during embryonic development.
topic protein-RNA interactions
NMR
binding mechanism
neuronal mRNA granules
neuronal development
mRNA local translation
ZBP1
IMP1
url http://www.sciencedirect.com/science/article/pii/S2211124717300013
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AT michaeluhl mechanismofbactinmrnarecognitionbyzbp1
AT alainoregioni mechanismofbactinmrnarecognitionbyzbp1
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