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Furry is required for cell movements during gastrulation and functionally interacts with NDR1

Gastrulation is a key event in animal embryogenesis during which germ layer precursors are rearranged and the embryonic axes are established. Cell polarization is essential during gastrulation, driving asymmetric cell division, cell movements, and cell shape changes. The furry (fry) gene encodes an...

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Autores principales: Cervino, Ailen S., Moretti, Bruno, Stuckenholz, Carsten, Grecco, Hernán E., Davidson, Lance A., Cirio, M. Cecilia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7987989/
https://www.ncbi.nlm.nih.gov/pubmed/33758327
http://dx.doi.org/10.1038/s41598-021-86153-x
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author Cervino, Ailen S.
Moretti, Bruno
Stuckenholz, Carsten
Grecco, Hernán E.
Davidson, Lance A.
Cirio, M. Cecilia
author_facet Cervino, Ailen S.
Moretti, Bruno
Stuckenholz, Carsten
Grecco, Hernán E.
Davidson, Lance A.
Cirio, M. Cecilia
author_sort Cervino, Ailen S.
collection PubMed
description Gastrulation is a key event in animal embryogenesis during which germ layer precursors are rearranged and the embryonic axes are established. Cell polarization is essential during gastrulation, driving asymmetric cell division, cell movements, and cell shape changes. The furry (fry) gene encodes an evolutionarily conserved protein with a wide variety of cellular functions, including cell polarization and morphogenesis in invertebrates. However, little is known about its function in vertebrate development. Here, we show that in Xenopus, Fry plays a role in morphogenetic processes during gastrulation, in addition to its previously described function in the regulation of dorsal mesoderm gene expression. Using morpholino knock-down, we demonstrate a distinct role for Fry in blastopore closure and dorsal axis elongation. Loss of Fry function drastically affects the movement and morphological polarization of cells during gastrulation and disrupts dorsal mesoderm convergent extension, responsible for head-to-tail elongation. Finally, we evaluate a functional interaction between Fry and NDR1 kinase, providing evidence of an evolutionarily conserved complex required for morphogenesis.
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spelling pubmed-79879892021-03-25 Furry is required for cell movements during gastrulation and functionally interacts with NDR1 Cervino, Ailen S. Moretti, Bruno Stuckenholz, Carsten Grecco, Hernán E. Davidson, Lance A. Cirio, M. Cecilia Sci Rep Article Gastrulation is a key event in animal embryogenesis during which germ layer precursors are rearranged and the embryonic axes are established. Cell polarization is essential during gastrulation, driving asymmetric cell division, cell movements, and cell shape changes. The furry (fry) gene encodes an evolutionarily conserved protein with a wide variety of cellular functions, including cell polarization and morphogenesis in invertebrates. However, little is known about its function in vertebrate development. Here, we show that in Xenopus, Fry plays a role in morphogenetic processes during gastrulation, in addition to its previously described function in the regulation of dorsal mesoderm gene expression. Using morpholino knock-down, we demonstrate a distinct role for Fry in blastopore closure and dorsal axis elongation. Loss of Fry function drastically affects the movement and morphological polarization of cells during gastrulation and disrupts dorsal mesoderm convergent extension, responsible for head-to-tail elongation. Finally, we evaluate a functional interaction between Fry and NDR1 kinase, providing evidence of an evolutionarily conserved complex required for morphogenesis. Nature Publishing Group UK 2021-03-23 /pmc/articles/PMC7987989/ /pubmed/33758327 http://dx.doi.org/10.1038/s41598-021-86153-x Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Cervino, Ailen S.
Moretti, Bruno
Stuckenholz, Carsten
Grecco, Hernán E.
Davidson, Lance A.
Cirio, M. Cecilia
Furry is required for cell movements during gastrulation and functionally interacts with NDR1
title Furry is required for cell movements during gastrulation and functionally interacts with NDR1
title_full Furry is required for cell movements during gastrulation and functionally interacts with NDR1
title_fullStr Furry is required for cell movements during gastrulation and functionally interacts with NDR1
title_full_unstemmed Furry is required for cell movements during gastrulation and functionally interacts with NDR1
title_short Furry is required for cell movements during gastrulation and functionally interacts with NDR1
title_sort furry is required for cell movements during gastrulation and functionally interacts with ndr1
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7987989/
https://www.ncbi.nlm.nih.gov/pubmed/33758327
http://dx.doi.org/10.1038/s41598-021-86153-x
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