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GxcDD, a putative RacGEF, is involved in Dictyostelium development

BACKGROUND: Rho subfamily GTPases are implicated in a large number of actin-related processes. They shuttle from an inactive GDP-bound form to an active GTP-bound form. This reaction is catalysed by Guanine nucleotide exchange factor (GEFs). GTPase activating proteins (GAPs) help the GTPase return t...

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Autores principales: Mondal, Subhanjan, Neelamegan, Dhamodharan, Rivero, Francisco, Noegel, Angelika A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1914345/
https://www.ncbi.nlm.nih.gov/pubmed/17584488
http://dx.doi.org/10.1186/1471-2121-8-23
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author Mondal, Subhanjan
Neelamegan, Dhamodharan
Rivero, Francisco
Noegel, Angelika A
author_facet Mondal, Subhanjan
Neelamegan, Dhamodharan
Rivero, Francisco
Noegel, Angelika A
author_sort Mondal, Subhanjan
collection PubMed
description BACKGROUND: Rho subfamily GTPases are implicated in a large number of actin-related processes. They shuttle from an inactive GDP-bound form to an active GTP-bound form. This reaction is catalysed by Guanine nucleotide exchange factor (GEFs). GTPase activating proteins (GAPs) help the GTPase return to the inactive GDP-bound form. The social amoeba Dictyostelium discoideum lacks a Rho or Cdc42 ortholog but has several Rac related GTPases. Compared to our understanding of the downstream effects of Racs our understanding of upstream mechanisms that activate Rac GTPases is relatively poor. RESULTS: We report on GxcDD (Guanine exchange factor for Rac GTPases), a Dictyostelium RacGEF. GxcDD is a 180-kDa multidomain protein containing a type 3 CH domain, two IQ motifs, three PH domains, a RhoGEF domain and an ArfGAP domain. Inactivation of the gene results in defective streaming during development under different conditions and a delay in developmental timing. The characterization of single domains revealed that the CH domain of GxcDD functions as a membrane association domain, the RhoGEF domain can physically interact with a subset of Rac GTPases, and the ArfGAP-PH tandem accumulates in cortical regions of the cell and on phagosomes. Our results also suggest that a conformational change may be required for activation of GxcDD, which would be important for its downstream signaling. CONCLUSION: The data indicate that GxcDD is involved in proper streaming and development. We propose that GxcDD is not only a component of the Rac signaling pathway in Dictyostelium, but is also involved in integrating different signals. We provide evidence for a Calponin Homology domain acting as a membrane association domain. GxcDD can bind to several Rac GTPases, but its function as a nucleotide exchange factor needs to be studied further.
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spelling pubmed-19143452007-07-13 GxcDD, a putative RacGEF, is involved in Dictyostelium development Mondal, Subhanjan Neelamegan, Dhamodharan Rivero, Francisco Noegel, Angelika A BMC Cell Biol Research Article BACKGROUND: Rho subfamily GTPases are implicated in a large number of actin-related processes. They shuttle from an inactive GDP-bound form to an active GTP-bound form. This reaction is catalysed by Guanine nucleotide exchange factor (GEFs). GTPase activating proteins (GAPs) help the GTPase return to the inactive GDP-bound form. The social amoeba Dictyostelium discoideum lacks a Rho or Cdc42 ortholog but has several Rac related GTPases. Compared to our understanding of the downstream effects of Racs our understanding of upstream mechanisms that activate Rac GTPases is relatively poor. RESULTS: We report on GxcDD (Guanine exchange factor for Rac GTPases), a Dictyostelium RacGEF. GxcDD is a 180-kDa multidomain protein containing a type 3 CH domain, two IQ motifs, three PH domains, a RhoGEF domain and an ArfGAP domain. Inactivation of the gene results in defective streaming during development under different conditions and a delay in developmental timing. The characterization of single domains revealed that the CH domain of GxcDD functions as a membrane association domain, the RhoGEF domain can physically interact with a subset of Rac GTPases, and the ArfGAP-PH tandem accumulates in cortical regions of the cell and on phagosomes. Our results also suggest that a conformational change may be required for activation of GxcDD, which would be important for its downstream signaling. CONCLUSION: The data indicate that GxcDD is involved in proper streaming and development. We propose that GxcDD is not only a component of the Rac signaling pathway in Dictyostelium, but is also involved in integrating different signals. We provide evidence for a Calponin Homology domain acting as a membrane association domain. GxcDD can bind to several Rac GTPases, but its function as a nucleotide exchange factor needs to be studied further. BioMed Central 2007-06-20 /pmc/articles/PMC1914345/ /pubmed/17584488 http://dx.doi.org/10.1186/1471-2121-8-23 Text en Copyright © 2007 Mondal 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
Mondal, Subhanjan
Neelamegan, Dhamodharan
Rivero, Francisco
Noegel, Angelika A
GxcDD, a putative RacGEF, is involved in Dictyostelium development
title GxcDD, a putative RacGEF, is involved in Dictyostelium development
title_full GxcDD, a putative RacGEF, is involved in Dictyostelium development
title_fullStr GxcDD, a putative RacGEF, is involved in Dictyostelium development
title_full_unstemmed GxcDD, a putative RacGEF, is involved in Dictyostelium development
title_short GxcDD, a putative RacGEF, is involved in Dictyostelium development
title_sort gxcdd, a putative racgef, is involved in dictyostelium development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1914345/
https://www.ncbi.nlm.nih.gov/pubmed/17584488
http://dx.doi.org/10.1186/1471-2121-8-23
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