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Engineering a conserved RNA regulatory protein repurposes its biological function in vivo
PUF (PUmilio/FBF) RNA-binding proteins recognize distinct elements. In C. elegans, PUF-8 binds to an 8-nt motif and restricts proliferation in the germline. Conversely, FBF-2 recognizes a 9-nt element and promotes mitosis. To understand how motif divergence relates to biological function, we first d...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6351103/ https://www.ncbi.nlm.nih.gov/pubmed/30652968 http://dx.doi.org/10.7554/eLife.43788 |
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author | Bhat, Vandita D McCann, Kathleen L Wang, Yeming Fonseca, Dallas R Shukla, Tarjani Alexander, Jacqueline C Qiu, Chen Wickens, Marv Lo, Te-Wen Tanaka Hall, Traci M Campbell, Zachary T |
author_facet | Bhat, Vandita D McCann, Kathleen L Wang, Yeming Fonseca, Dallas R Shukla, Tarjani Alexander, Jacqueline C Qiu, Chen Wickens, Marv Lo, Te-Wen Tanaka Hall, Traci M Campbell, Zachary T |
author_sort | Bhat, Vandita D |
collection | PubMed |
description | PUF (PUmilio/FBF) RNA-binding proteins recognize distinct elements. In C. elegans, PUF-8 binds to an 8-nt motif and restricts proliferation in the germline. Conversely, FBF-2 recognizes a 9-nt element and promotes mitosis. To understand how motif divergence relates to biological function, we first determined a crystal structure of PUF-8. Comparison of this structure to that of FBF-2 revealed a major difference in a central repeat. We devised a modified yeast 3-hybrid screen to identify mutations that confer recognition of an 8-nt element to FBF-2. We identified several such mutants and validated structurally and biochemically their binding to 8-nt RNA elements. Using genome engineering, we generated a mutant animal with a substitution in FBF-2 that confers preferential binding to the PUF-8 element. The mutant largely rescued overproliferation in animals that spontaneously generate tumors in the absence of puf-8. This work highlights the critical role of motif length in the specification of biological function. |
format | Online Article Text |
id | pubmed-6351103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-63511032019-01-30 Engineering a conserved RNA regulatory protein repurposes its biological function in vivo Bhat, Vandita D McCann, Kathleen L Wang, Yeming Fonseca, Dallas R Shukla, Tarjani Alexander, Jacqueline C Qiu, Chen Wickens, Marv Lo, Te-Wen Tanaka Hall, Traci M Campbell, Zachary T eLife Developmental Biology PUF (PUmilio/FBF) RNA-binding proteins recognize distinct elements. In C. elegans, PUF-8 binds to an 8-nt motif and restricts proliferation in the germline. Conversely, FBF-2 recognizes a 9-nt element and promotes mitosis. To understand how motif divergence relates to biological function, we first determined a crystal structure of PUF-8. Comparison of this structure to that of FBF-2 revealed a major difference in a central repeat. We devised a modified yeast 3-hybrid screen to identify mutations that confer recognition of an 8-nt element to FBF-2. We identified several such mutants and validated structurally and biochemically their binding to 8-nt RNA elements. Using genome engineering, we generated a mutant animal with a substitution in FBF-2 that confers preferential binding to the PUF-8 element. The mutant largely rescued overproliferation in animals that spontaneously generate tumors in the absence of puf-8. This work highlights the critical role of motif length in the specification of biological function. eLife Sciences Publications, Ltd 2019-01-17 /pmc/articles/PMC6351103/ /pubmed/30652968 http://dx.doi.org/10.7554/eLife.43788 Text en http://creativecommons.org/publicdomain/zero/1.0/ http://creativecommons.org/publicdomain/zero/1.0/This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication (http://creativecommons.org/publicdomain/zero/1.0/) . |
spellingShingle | Developmental Biology Bhat, Vandita D McCann, Kathleen L Wang, Yeming Fonseca, Dallas R Shukla, Tarjani Alexander, Jacqueline C Qiu, Chen Wickens, Marv Lo, Te-Wen Tanaka Hall, Traci M Campbell, Zachary T Engineering a conserved RNA regulatory protein repurposes its biological function in vivo |
title | Engineering a conserved RNA regulatory protein repurposes its biological function in vivo |
title_full | Engineering a conserved RNA regulatory protein repurposes its biological function in vivo |
title_fullStr | Engineering a conserved RNA regulatory protein repurposes its biological function in vivo |
title_full_unstemmed | Engineering a conserved RNA regulatory protein repurposes its biological function in vivo |
title_short | Engineering a conserved RNA regulatory protein repurposes its biological function in vivo |
title_sort | engineering a conserved rna regulatory protein repurposes its biological function in vivo |
topic | Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6351103/ https://www.ncbi.nlm.nih.gov/pubmed/30652968 http://dx.doi.org/10.7554/eLife.43788 |
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