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Regulation of zebrafish dorsoventral patterning by phase separation of RNA-binding protein Rbm14

RNA-binding proteins with intrinsically disordered regions (IDRs) such as Rbm14 can phase separate in vitro. To what extent the phase separation contributes to their physiological functions is however unclear. Here we show that zebrafish Rbm14 regulates embryonic dorsoventral patterning through phas...

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Autores principales: Xiao, Yue, Chen, Jiehui, Wan, Yihan, Gao, Qi, Jing, Naihe, Zheng, Yixian, Zhu, Xueliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6796953/
https://www.ncbi.nlm.nih.gov/pubmed/31636951
http://dx.doi.org/10.1038/s41421-019-0106-x
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author Xiao, Yue
Chen, Jiehui
Wan, Yihan
Gao, Qi
Jing, Naihe
Zheng, Yixian
Zhu, Xueliang
author_facet Xiao, Yue
Chen, Jiehui
Wan, Yihan
Gao, Qi
Jing, Naihe
Zheng, Yixian
Zhu, Xueliang
author_sort Xiao, Yue
collection PubMed
description RNA-binding proteins with intrinsically disordered regions (IDRs) such as Rbm14 can phase separate in vitro. To what extent the phase separation contributes to their physiological functions is however unclear. Here we show that zebrafish Rbm14 regulates embryonic dorsoventral patterning through phase separation. Zebrafish rbm14 morphants displayed dorsalized phenotypes associated with attenuated BMP signaling. Consistently, depletion of mammalian Rbm14 downregulated BMP regulators and effectors Nanog, Smad4/5, and Id1/2, whereas overexpression of the BMP-related proteins in the morphants significantly restored the developmental defects. Importantly, the IDR of zebrafish Rbm14 demixed into liquid droplets in vitro despite poor sequence conservation with its mammalian counterpart. While its phase separation mutants or IDR failed to rescue the morphants, its chimeric proteins containing an IDR from divergent phase separation proteins were effective. Rbm14 complexed with proteins involved in RNA metabolism and phase separated into cellular ribonucleoprotein compartments. Consistently, RNA deep sequencing analysis on the morphant embryos revealed increased alternative splicing events as well as large-scale transcriptomic downregulations. Our results suggest that Rbm14 functions in ribonucleoprotein compartments through phase separation to modulate multiple aspects of RNA metabolism. Furthermore, IDRs conserve in phase separation ability but not primary sequence and can be functionally interchangeable.
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spelling pubmed-67969532019-10-21 Regulation of zebrafish dorsoventral patterning by phase separation of RNA-binding protein Rbm14 Xiao, Yue Chen, Jiehui Wan, Yihan Gao, Qi Jing, Naihe Zheng, Yixian Zhu, Xueliang Cell Discov Article RNA-binding proteins with intrinsically disordered regions (IDRs) such as Rbm14 can phase separate in vitro. To what extent the phase separation contributes to their physiological functions is however unclear. Here we show that zebrafish Rbm14 regulates embryonic dorsoventral patterning through phase separation. Zebrafish rbm14 morphants displayed dorsalized phenotypes associated with attenuated BMP signaling. Consistently, depletion of mammalian Rbm14 downregulated BMP regulators and effectors Nanog, Smad4/5, and Id1/2, whereas overexpression of the BMP-related proteins in the morphants significantly restored the developmental defects. Importantly, the IDR of zebrafish Rbm14 demixed into liquid droplets in vitro despite poor sequence conservation with its mammalian counterpart. While its phase separation mutants or IDR failed to rescue the morphants, its chimeric proteins containing an IDR from divergent phase separation proteins were effective. Rbm14 complexed with proteins involved in RNA metabolism and phase separated into cellular ribonucleoprotein compartments. Consistently, RNA deep sequencing analysis on the morphant embryos revealed increased alternative splicing events as well as large-scale transcriptomic downregulations. Our results suggest that Rbm14 functions in ribonucleoprotein compartments through phase separation to modulate multiple aspects of RNA metabolism. Furthermore, IDRs conserve in phase separation ability but not primary sequence and can be functionally interchangeable. Nature Publishing Group UK 2019-07-23 /pmc/articles/PMC6796953/ /pubmed/31636951 http://dx.doi.org/10.1038/s41421-019-0106-x Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Xiao, Yue
Chen, Jiehui
Wan, Yihan
Gao, Qi
Jing, Naihe
Zheng, Yixian
Zhu, Xueliang
Regulation of zebrafish dorsoventral patterning by phase separation of RNA-binding protein Rbm14
title Regulation of zebrafish dorsoventral patterning by phase separation of RNA-binding protein Rbm14
title_full Regulation of zebrafish dorsoventral patterning by phase separation of RNA-binding protein Rbm14
title_fullStr Regulation of zebrafish dorsoventral patterning by phase separation of RNA-binding protein Rbm14
title_full_unstemmed Regulation of zebrafish dorsoventral patterning by phase separation of RNA-binding protein Rbm14
title_short Regulation of zebrafish dorsoventral patterning by phase separation of RNA-binding protein Rbm14
title_sort regulation of zebrafish dorsoventral patterning by phase separation of rna-binding protein rbm14
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6796953/
https://www.ncbi.nlm.nih.gov/pubmed/31636951
http://dx.doi.org/10.1038/s41421-019-0106-x
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