Cargando…

Vasa nucleates asymmetric translation along the mitotic spindle during unequal cell divisions

mRNA translation on the spindle is hypothesized to be an essential strategy for the localized production of cell regulators. This mechanism may be important particularly in early embryonic cells, which have a large diffusion volume and that undergo rapid cell divisions. Evidence to test such a hypot...

Descripción completa

Detalles Bibliográficos
Autores principales: Fernandez-Nicolas, Ana, Uchida, Alicia, Poon, Jessica, Yajima, Mamiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9021227/
https://www.ncbi.nlm.nih.gov/pubmed/35444184
http://dx.doi.org/10.1038/s41467-022-29855-8
_version_ 1784689760665600000
author Fernandez-Nicolas, Ana
Uchida, Alicia
Poon, Jessica
Yajima, Mamiko
author_facet Fernandez-Nicolas, Ana
Uchida, Alicia
Poon, Jessica
Yajima, Mamiko
author_sort Fernandez-Nicolas, Ana
collection PubMed
description mRNA translation on the spindle is hypothesized to be an essential strategy for the localized production of cell regulators. This mechanism may be important particularly in early embryonic cells, which have a large diffusion volume and that undergo rapid cell divisions. Evidence to test such a hypothesis has been, however, limited. Here, we use an embryo with both symmetric and asymmetric cell divisions and manipulate Vasa protein, an RNA-helicase, on the spindle in live sea urchin embryos. We learned that the spindle serves as a major site of translation and that protein synthesis within a single spindle can be unequal and help drive asymmetric cell divisions during embryogenesis. Recruiting Vasa to the ectopic sub-cellular region induced a new site of translation, disturbed asymmetric translation on the spindle, and changed the cell fate. Based on these observations, we conclude that Vasa functions in localized translation, which provides a spatiotemporal control in protein synthesis and is essential for rapidly developing embryonic cells.
format Online
Article
Text
id pubmed-9021227
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-90212272022-04-28 Vasa nucleates asymmetric translation along the mitotic spindle during unequal cell divisions Fernandez-Nicolas, Ana Uchida, Alicia Poon, Jessica Yajima, Mamiko Nat Commun Article mRNA translation on the spindle is hypothesized to be an essential strategy for the localized production of cell regulators. This mechanism may be important particularly in early embryonic cells, which have a large diffusion volume and that undergo rapid cell divisions. Evidence to test such a hypothesis has been, however, limited. Here, we use an embryo with both symmetric and asymmetric cell divisions and manipulate Vasa protein, an RNA-helicase, on the spindle in live sea urchin embryos. We learned that the spindle serves as a major site of translation and that protein synthesis within a single spindle can be unequal and help drive asymmetric cell divisions during embryogenesis. Recruiting Vasa to the ectopic sub-cellular region induced a new site of translation, disturbed asymmetric translation on the spindle, and changed the cell fate. Based on these observations, we conclude that Vasa functions in localized translation, which provides a spatiotemporal control in protein synthesis and is essential for rapidly developing embryonic cells. Nature Publishing Group UK 2022-04-20 /pmc/articles/PMC9021227/ /pubmed/35444184 http://dx.doi.org/10.1038/s41467-022-29855-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Fernandez-Nicolas, Ana
Uchida, Alicia
Poon, Jessica
Yajima, Mamiko
Vasa nucleates asymmetric translation along the mitotic spindle during unequal cell divisions
title Vasa nucleates asymmetric translation along the mitotic spindle during unequal cell divisions
title_full Vasa nucleates asymmetric translation along the mitotic spindle during unequal cell divisions
title_fullStr Vasa nucleates asymmetric translation along the mitotic spindle during unequal cell divisions
title_full_unstemmed Vasa nucleates asymmetric translation along the mitotic spindle during unequal cell divisions
title_short Vasa nucleates asymmetric translation along the mitotic spindle during unequal cell divisions
title_sort vasa nucleates asymmetric translation along the mitotic spindle during unequal cell divisions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9021227/
https://www.ncbi.nlm.nih.gov/pubmed/35444184
http://dx.doi.org/10.1038/s41467-022-29855-8
work_keys_str_mv AT fernandeznicolasana vasanucleatesasymmetrictranslationalongthemitoticspindleduringunequalcelldivisions
AT uchidaalicia vasanucleatesasymmetrictranslationalongthemitoticspindleduringunequalcelldivisions
AT poonjessica vasanucleatesasymmetrictranslationalongthemitoticspindleduringunequalcelldivisions
AT yajimamamiko vasanucleatesasymmetrictranslationalongthemitoticspindleduringunequalcelldivisions