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...
Main Authors: | , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2017-01-01
|
Series: | Cell Reports |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2211124717300013 |
id |
doaj-fc9af46783534be98494a16d4cdcbc90 |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT giuseppenicastro mechanismofbactinmrnarecognitionbyzbp1 AT adelamcandel mechanismofbactinmrnarecognitionbyzbp1 AT michaeluhl mechanismofbactinmrnarecognitionbyzbp1 AT alainoregioni mechanismofbactinmrnarecognitionbyzbp1 AT davidhollingworth mechanismofbactinmrnarecognitionbyzbp1 AT rolfbackofen mechanismofbactinmrnarecognitionbyzbp1 AT stephenrmartin mechanismofbactinmrnarecognitionbyzbp1 AT andresramos mechanismofbactinmrnarecognitionbyzbp1 |
_version_ |
1725942906206814208 |