Cargando…

RSU-1 Maintains Integrity of Caenorhabditis elegans Vulval Muscles by Regulating α-Actinin

Egg-laying behavior in Caenorhabditis elegans is a well-known model for investigating fundamental cellular processes. In egg-laying, muscle contraction is the relaxation of the vulval muscle to extrude eggs from the vulva. Unlike skeletal muscle, vulval muscle lacks visible striations of the sarcome...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Xinyan, Huang, Shuai, Zheng, Cunni, Ge, Wei, Wu, Chuanyue, Tse, Yu Chung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7341117/
https://www.ncbi.nlm.nih.gov/pubmed/32461202
http://dx.doi.org/10.1534/g3.120.401185
_version_ 1783555166412210176
author Wang, Xinyan
Huang, Shuai
Zheng, Cunni
Ge, Wei
Wu, Chuanyue
Tse, Yu Chung
author_facet Wang, Xinyan
Huang, Shuai
Zheng, Cunni
Ge, Wei
Wu, Chuanyue
Tse, Yu Chung
author_sort Wang, Xinyan
collection PubMed
description Egg-laying behavior in Caenorhabditis elegans is a well-known model for investigating fundamental cellular processes. In egg-laying, muscle contraction is the relaxation of the vulval muscle to extrude eggs from the vulva. Unlike skeletal muscle, vulval muscle lacks visible striations of the sarcomere. Therefore, vulval muscle must counteract the mechanical stress, caused by egg extrusion and body movement, from inducing cell-shape distortion by maintaining its cytoskeletal integrity. However, the underlying mechanisms that regulate the cellular integrity in vulval muscles remain unclear. Here, we demonstrate that C. elegans egg-laying requires proper vulval muscle 1 (vm1), in which the actin bundle organization of vm1 muscles is regulated by Ras suppressor protein 1 (RSU-1). In the loss of RSU-1, as well as Ras(LET-60) overactivation, blister-like membrane protrusions and disorganized actin bundles were observed in the vm1 muscles. Moreover, Ras(LET-60) depletion diminished the defected actin-bundles in rsu-1 mutant. These results reveal the genetic interaction of RSU-1 and Ras(LET-60) in vivo. In addition, our results further demonstrated that the fifth to seventh leucine-rich region of RSU-1 is required to promote actin-bundling protein, α-actinin, for actin bundle stabilization in the vm1 muscles. This expands our understanding of the molecular mechanisms of actin bundle organization in a specialized smooth muscle.
format Online
Article
Text
id pubmed-7341117
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Genetics Society of America
record_format MEDLINE/PubMed
spelling pubmed-73411172020-07-21 RSU-1 Maintains Integrity of Caenorhabditis elegans Vulval Muscles by Regulating α-Actinin Wang, Xinyan Huang, Shuai Zheng, Cunni Ge, Wei Wu, Chuanyue Tse, Yu Chung G3 (Bethesda) Investigations Egg-laying behavior in Caenorhabditis elegans is a well-known model for investigating fundamental cellular processes. In egg-laying, muscle contraction is the relaxation of the vulval muscle to extrude eggs from the vulva. Unlike skeletal muscle, vulval muscle lacks visible striations of the sarcomere. Therefore, vulval muscle must counteract the mechanical stress, caused by egg extrusion and body movement, from inducing cell-shape distortion by maintaining its cytoskeletal integrity. However, the underlying mechanisms that regulate the cellular integrity in vulval muscles remain unclear. Here, we demonstrate that C. elegans egg-laying requires proper vulval muscle 1 (vm1), in which the actin bundle organization of vm1 muscles is regulated by Ras suppressor protein 1 (RSU-1). In the loss of RSU-1, as well as Ras(LET-60) overactivation, blister-like membrane protrusions and disorganized actin bundles were observed in the vm1 muscles. Moreover, Ras(LET-60) depletion diminished the defected actin-bundles in rsu-1 mutant. These results reveal the genetic interaction of RSU-1 and Ras(LET-60) in vivo. In addition, our results further demonstrated that the fifth to seventh leucine-rich region of RSU-1 is required to promote actin-bundling protein, α-actinin, for actin bundle stabilization in the vm1 muscles. This expands our understanding of the molecular mechanisms of actin bundle organization in a specialized smooth muscle. Genetics Society of America 2020-05-27 /pmc/articles/PMC7341117/ /pubmed/32461202 http://dx.doi.org/10.1534/g3.120.401185 Text en Copyright © 2020 Wang et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Wang, Xinyan
Huang, Shuai
Zheng, Cunni
Ge, Wei
Wu, Chuanyue
Tse, Yu Chung
RSU-1 Maintains Integrity of Caenorhabditis elegans Vulval Muscles by Regulating α-Actinin
title RSU-1 Maintains Integrity of Caenorhabditis elegans Vulval Muscles by Regulating α-Actinin
title_full RSU-1 Maintains Integrity of Caenorhabditis elegans Vulval Muscles by Regulating α-Actinin
title_fullStr RSU-1 Maintains Integrity of Caenorhabditis elegans Vulval Muscles by Regulating α-Actinin
title_full_unstemmed RSU-1 Maintains Integrity of Caenorhabditis elegans Vulval Muscles by Regulating α-Actinin
title_short RSU-1 Maintains Integrity of Caenorhabditis elegans Vulval Muscles by Regulating α-Actinin
title_sort rsu-1 maintains integrity of caenorhabditis elegans vulval muscles by regulating α-actinin
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7341117/
https://www.ncbi.nlm.nih.gov/pubmed/32461202
http://dx.doi.org/10.1534/g3.120.401185
work_keys_str_mv AT wangxinyan rsu1maintainsintegrityofcaenorhabditiselegansvulvalmusclesbyregulatingaactinin
AT huangshuai rsu1maintainsintegrityofcaenorhabditiselegansvulvalmusclesbyregulatingaactinin
AT zhengcunni rsu1maintainsintegrityofcaenorhabditiselegansvulvalmusclesbyregulatingaactinin
AT gewei rsu1maintainsintegrityofcaenorhabditiselegansvulvalmusclesbyregulatingaactinin
AT wuchuanyue rsu1maintainsintegrityofcaenorhabditiselegansvulvalmusclesbyregulatingaactinin
AT tseyuchung rsu1maintainsintegrityofcaenorhabditiselegansvulvalmusclesbyregulatingaactinin