Cargando…

Diverse roles of actin in C. elegans early embryogenesis

BACKGROUND: The actin cytoskeleton plays critical roles in early development in Caenorhabditis elegans. To further understand the complex roles of actin in early embryogenesis we use RNAi and in vivo imaging of filamentous actin (F-actin) dynamics. RESULTS: Using RNAi, we found processes that are di...

Descripción completa

Detalles Bibliográficos
Autores principales: Velarde, Nathalie, Gunsalus, Kristin C, Piano, Fabio
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2323969/
https://www.ncbi.nlm.nih.gov/pubmed/18157918
http://dx.doi.org/10.1186/1471-213X-7-142
_version_ 1782152697326075904
author Velarde, Nathalie
Gunsalus, Kristin C
Piano, Fabio
author_facet Velarde, Nathalie
Gunsalus, Kristin C
Piano, Fabio
author_sort Velarde, Nathalie
collection PubMed
description BACKGROUND: The actin cytoskeleton plays critical roles in early development in Caenorhabditis elegans. To further understand the complex roles of actin in early embryogenesis we use RNAi and in vivo imaging of filamentous actin (F-actin) dynamics. RESULTS: Using RNAi, we found processes that are differentially sensitive to levels of actin during early embryogenesis. Mild actin depletion shows defects in cortical ruffling, pseudocleavage, and establishment of polarity, while more severe depletion shows defects in polar body extrusion, cytokinesis, chromosome segregation, and eventually, egg production. These defects indicate that actin is required for proper oocyte development, fertilization, and a wide range of important events during early embryogenesis, including proper chromosome segregation. In vivo visualization of the cortical actin cytoskeleton shows dynamics that parallel but are distinct from the previously described myosin dynamics. Two distinct types of actin organization are observed at the cortex. During asymmetric polarization to the anterior, or the establishment phase (Phase I), actin forms a meshwork of microfilaments and focal accumulations throughout the cortex, while during the anterior maintenance phase (Phase II) it undergoes a morphological transition to asymmetrically localized puncta. The proper asymmetric redistribution is dependent on the PAR proteins, while both asymmetric redistribution and morphological transitions are dependent upon PFN-1 and NMY-2. Just before cytokinesis, actin disappears from most of the cortex and is only found around the presumptive cytokinetic furrow. Finally, we describe dynamic actin-enriched comets in the early embryo. CONCLUSION: During early C. elegans embryogenesis actin plays more roles and its organization is more dynamic than previously described. Morphological transitions of F-actin, from meshwork to puncta, as well as asymmetric redistribution, are regulated by the PAR proteins. Results from this study indicate new insights into the cellular and developmental roles of the actin cytoskeleton.
format Text
id pubmed-2323969
institution National Center for Biotechnology Information
language English
publishDate 2007
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-23239692008-04-22 Diverse roles of actin in C. elegans early embryogenesis Velarde, Nathalie Gunsalus, Kristin C Piano, Fabio BMC Dev Biol Research Article BACKGROUND: The actin cytoskeleton plays critical roles in early development in Caenorhabditis elegans. To further understand the complex roles of actin in early embryogenesis we use RNAi and in vivo imaging of filamentous actin (F-actin) dynamics. RESULTS: Using RNAi, we found processes that are differentially sensitive to levels of actin during early embryogenesis. Mild actin depletion shows defects in cortical ruffling, pseudocleavage, and establishment of polarity, while more severe depletion shows defects in polar body extrusion, cytokinesis, chromosome segregation, and eventually, egg production. These defects indicate that actin is required for proper oocyte development, fertilization, and a wide range of important events during early embryogenesis, including proper chromosome segregation. In vivo visualization of the cortical actin cytoskeleton shows dynamics that parallel but are distinct from the previously described myosin dynamics. Two distinct types of actin organization are observed at the cortex. During asymmetric polarization to the anterior, or the establishment phase (Phase I), actin forms a meshwork of microfilaments and focal accumulations throughout the cortex, while during the anterior maintenance phase (Phase II) it undergoes a morphological transition to asymmetrically localized puncta. The proper asymmetric redistribution is dependent on the PAR proteins, while both asymmetric redistribution and morphological transitions are dependent upon PFN-1 and NMY-2. Just before cytokinesis, actin disappears from most of the cortex and is only found around the presumptive cytokinetic furrow. Finally, we describe dynamic actin-enriched comets in the early embryo. CONCLUSION: During early C. elegans embryogenesis actin plays more roles and its organization is more dynamic than previously described. Morphological transitions of F-actin, from meshwork to puncta, as well as asymmetric redistribution, are regulated by the PAR proteins. Results from this study indicate new insights into the cellular and developmental roles of the actin cytoskeleton. BioMed Central 2007-12-24 /pmc/articles/PMC2323969/ /pubmed/18157918 http://dx.doi.org/10.1186/1471-213X-7-142 Text en Copyright © 2007 Velarde et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Velarde, Nathalie
Gunsalus, Kristin C
Piano, Fabio
Diverse roles of actin in C. elegans early embryogenesis
title Diverse roles of actin in C. elegans early embryogenesis
title_full Diverse roles of actin in C. elegans early embryogenesis
title_fullStr Diverse roles of actin in C. elegans early embryogenesis
title_full_unstemmed Diverse roles of actin in C. elegans early embryogenesis
title_short Diverse roles of actin in C. elegans early embryogenesis
title_sort diverse roles of actin in c. elegans early embryogenesis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2323969/
https://www.ncbi.nlm.nih.gov/pubmed/18157918
http://dx.doi.org/10.1186/1471-213X-7-142
work_keys_str_mv AT velardenathalie diverserolesofactinincelegansearlyembryogenesis
AT gunsaluskristinc diverserolesofactinincelegansearlyembryogenesis
AT pianofabio diverserolesofactinincelegansearlyembryogenesis