The Caenorhabditis elegans ect-2 RhoGEF gene regulates cytokinesis and migration of epidermal P cells

A reduction‐of‐function mutation in ect‐2 was isolated as a suppressor of the Multivulva phenotype of a lin‐31 mutation. Analysis using markers indicates that this mutation causes defects in both the cytokinesis and migration of epidermal P cells, phenotypes similar to those caused by expressing a r...

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Published inEMBO reports Vol. 6; no. 12; pp. 1163 - 1168
Main Authors Morita, Kiyokazu, Hirono, Keiko, Han, Min
Format Journal Article
LanguageEnglish
Published Chichester, UK John Wiley & Sons, Ltd 01.12.2005
Blackwell Publishing Ltd
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Summary:A reduction‐of‐function mutation in ect‐2 was isolated as a suppressor of the Multivulva phenotype of a lin‐31 mutation. Analysis using markers indicates that this mutation causes defects in both the cytokinesis and migration of epidermal P cells, phenotypes similar to those caused by expressing a rho‐1 dominant‐negative construct. ect‐2 encodes the Caenorhabditis elegans orthologue of the mouse Ect2 and Drosophila Pebble that function as guanine nucleotide exchange factors (GEFs) for Rho GTPases. The ect‐2∷GFP reporter is expressed in embryonic cells and P cells. RNA interference of ect‐2 causes sterility and embryonic lethality, in addition to the P‐cell defects. We have determined the lesions of two ect‐2 alleles, and described their differences in phenotypes in specific tissues. We propose a model in which ECT‐2GEF not only activates RHO‐1 for P‐cell cytokinesis, but also collaborates with UNC‐73GEF and at least two Rac proteins to regulate P‐cell migration.
Bibliography:ark:/67375/WNG-FVH07VQC-M
ArticleID:EMBR7400533
istex:EE8F99405A8F44186AAF071A5624E9F4B8138FB7
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ISSN:1469-221X
1469-3178
1469-221X
DOI:10.1038/sj.embor.7400533