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Spatial organization and function of RNA molecules within phase-separated condensates are controlled by Dnd1
Germ granules, condensates of phase-separated RNA and protein, are organelles essential for germline development in different organisms The patterning of the granules and its relevance for germ cell fate are not fully understood. Combining three-dimensional in vivo structural and functional analyses...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10350045/ https://www.ncbi.nlm.nih.gov/pubmed/37461638 http://dx.doi.org/10.1101/2023.07.09.548244 |
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author | Westerich, Kim Joana Tarbashevich, Katsiaryna Schick, Jan Gupta, Antra Zhu, Mingzhao Hull, Kenneth Romo, Daniel Zeuschner, Dagmar Goudarzi, Mohammad Gross-Thebing, Theresa Raz, Erez |
author_facet | Westerich, Kim Joana Tarbashevich, Katsiaryna Schick, Jan Gupta, Antra Zhu, Mingzhao Hull, Kenneth Romo, Daniel Zeuschner, Dagmar Goudarzi, Mohammad Gross-Thebing, Theresa Raz, Erez |
author_sort | Westerich, Kim Joana |
collection | PubMed |
description | Germ granules, condensates of phase-separated RNA and protein, are organelles essential for germline development in different organisms The patterning of the granules and its relevance for germ cell fate are not fully understood. Combining three-dimensional in vivo structural and functional analyses, we study the dynamic spatial organization of molecules within zebrafish germ granules. We find that localization of RNA molecules to the periphery of the granules, where ribosomes are localized depends on translational activity at this location. In addition, we find that the vertebrate-specific Dead end (Dnd1) protein is essential for nanos3 RNA localization at the condensates’ periphery. Accordingly, in the absence of Dnd1, or when translation is inhibited, nanos3 RNA translocates into the granule interior, away from the ribosomes, a process that is correlated with loss of germ cell fate. These findings highlight the relevance of sub-granule compartmentalization for posttranscriptional control, and its importance for preserving germ cell totipotency. |
format | Online Article Text |
id | pubmed-10350045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-103500452023-07-17 Spatial organization and function of RNA molecules within phase-separated condensates are controlled by Dnd1 Westerich, Kim Joana Tarbashevich, Katsiaryna Schick, Jan Gupta, Antra Zhu, Mingzhao Hull, Kenneth Romo, Daniel Zeuschner, Dagmar Goudarzi, Mohammad Gross-Thebing, Theresa Raz, Erez bioRxiv Article Germ granules, condensates of phase-separated RNA and protein, are organelles essential for germline development in different organisms The patterning of the granules and its relevance for germ cell fate are not fully understood. Combining three-dimensional in vivo structural and functional analyses, we study the dynamic spatial organization of molecules within zebrafish germ granules. We find that localization of RNA molecules to the periphery of the granules, where ribosomes are localized depends on translational activity at this location. In addition, we find that the vertebrate-specific Dead end (Dnd1) protein is essential for nanos3 RNA localization at the condensates’ periphery. Accordingly, in the absence of Dnd1, or when translation is inhibited, nanos3 RNA translocates into the granule interior, away from the ribosomes, a process that is correlated with loss of germ cell fate. These findings highlight the relevance of sub-granule compartmentalization for posttranscriptional control, and its importance for preserving germ cell totipotency. Cold Spring Harbor Laboratory 2023-07-09 /pmc/articles/PMC10350045/ /pubmed/37461638 http://dx.doi.org/10.1101/2023.07.09.548244 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Westerich, Kim Joana Tarbashevich, Katsiaryna Schick, Jan Gupta, Antra Zhu, Mingzhao Hull, Kenneth Romo, Daniel Zeuschner, Dagmar Goudarzi, Mohammad Gross-Thebing, Theresa Raz, Erez Spatial organization and function of RNA molecules within phase-separated condensates are controlled by Dnd1 |
title | Spatial organization and function of RNA molecules within phase-separated condensates are controlled by Dnd1 |
title_full | Spatial organization and function of RNA molecules within phase-separated condensates are controlled by Dnd1 |
title_fullStr | Spatial organization and function of RNA molecules within phase-separated condensates are controlled by Dnd1 |
title_full_unstemmed | Spatial organization and function of RNA molecules within phase-separated condensates are controlled by Dnd1 |
title_short | Spatial organization and function of RNA molecules within phase-separated condensates are controlled by Dnd1 |
title_sort | spatial organization and function of rna molecules within phase-separated condensates are controlled by dnd1 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10350045/ https://www.ncbi.nlm.nih.gov/pubmed/37461638 http://dx.doi.org/10.1101/2023.07.09.548244 |
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