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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5300891/ https://www.ncbi.nlm.nih.gov/pubmed/28147274 http://dx.doi.org/10.1016/j.celrep.2016.12.091 |
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author | Nicastro, Giuseppe Candel, Adela M. Uhl, Michael Oregioni, Alain Hollingworth, David Backofen, Rolf Martin, Stephen R. Ramos, Andres |
author_facet | Nicastro, Giuseppe Candel, Adela M. Uhl, Michael Oregioni, Alain Hollingworth, David Backofen, Rolf Martin, Stephen R. Ramos, Andres |
author_sort | Nicastro, Giuseppe |
collection | PubMed |
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. |
format | Online Article Text |
id | pubmed-5300891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-53008912017-02-17 Mechanism of β-actin mRNA Recognition by ZBP1 Nicastro, Giuseppe Candel, Adela M. Uhl, Michael Oregioni, Alain Hollingworth, David Backofen, Rolf Martin, Stephen R. Ramos, Andres Cell Rep Article 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. Cell Press 2017-01-31 /pmc/articles/PMC5300891/ /pubmed/28147274 http://dx.doi.org/10.1016/j.celrep.2016.12.091 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Nicastro, Giuseppe Candel, Adela M. Uhl, Michael Oregioni, Alain Hollingworth, David Backofen, Rolf Martin, Stephen R. Ramos, Andres Mechanism of β-actin mRNA Recognition by ZBP1 |
title | 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_short | Mechanism of β-actin mRNA Recognition by ZBP1 |
title_sort | mechanism of β-actin mrna recognition by zbp1 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5300891/ https://www.ncbi.nlm.nih.gov/pubmed/28147274 http://dx.doi.org/10.1016/j.celrep.2016.12.091 |
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