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SrfB, a member of the Serum Response Factor family of transcription factors, regulates starvation response and early development in Dictyostelium
The Serum Response Factor (SRF) is an important regulator of cell proliferation and differentiation. Dictyostelium discoideum srfB gene codes for an SRF homologue and is expressed in vegetative cells and during development under the control of three alternative promoters, which show different cell-t...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819988/ https://www.ncbi.nlm.nih.gov/pubmed/18339368 http://dx.doi.org/10.1016/j.ydbio.2008.01.026 |
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author | Galardi-Castilla, María Pergolizzi, Barbara Bloomfield, Gareth Skelton, Jason Ivens, Al Kay, Robert R. Bozzaro, Salvatore Sastre, Leandro |
author_facet | Galardi-Castilla, María Pergolizzi, Barbara Bloomfield, Gareth Skelton, Jason Ivens, Al Kay, Robert R. Bozzaro, Salvatore Sastre, Leandro |
author_sort | Galardi-Castilla, María |
collection | PubMed |
description | The Serum Response Factor (SRF) is an important regulator of cell proliferation and differentiation. Dictyostelium discoideum srfB gene codes for an SRF homologue and is expressed in vegetative cells and during development under the control of three alternative promoters, which show different cell-type specific patterns of expression. The two more proximal promoters directed gene transcription in prestalk AB, stalk and lower-cup cells. The generation of a strain where the srfB gene has been interrupted (srfB(−)) has shown that this gene is required for regulation of actin–cytoskeleton-related functions, such as cytokinesis and macropinocytosis. The mutant failed to develop well in suspension, but could be rescued by cAMP pulsing, suggesting a defect in cAMP signaling. srfB(−) cells showed impaired chemotaxis to cAMP and defective lateral pseudopodium inhibition. Nevertheless, srfB(−) cells aggregated on agar plates and nitrocellulose filters 2 h earlier than wild type cells, and completed development, showing an increased tendency to form slug structures. Analysis of wild type and srfB(−) strains detected significant differences in the regulation of gene expression upon starvation. Genes coding for lysosomal and ribosomal proteins, developmentally-regulated genes, and some genes coding for proteins involved in cytoskeleton regulation were deregulated during the first stages of development. |
format | Online Article Text |
id | pubmed-3819988 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-38199882013-11-07 SrfB, a member of the Serum Response Factor family of transcription factors, regulates starvation response and early development in Dictyostelium Galardi-Castilla, María Pergolizzi, Barbara Bloomfield, Gareth Skelton, Jason Ivens, Al Kay, Robert R. Bozzaro, Salvatore Sastre, Leandro Dev Biol Article The Serum Response Factor (SRF) is an important regulator of cell proliferation and differentiation. Dictyostelium discoideum srfB gene codes for an SRF homologue and is expressed in vegetative cells and during development under the control of three alternative promoters, which show different cell-type specific patterns of expression. The two more proximal promoters directed gene transcription in prestalk AB, stalk and lower-cup cells. The generation of a strain where the srfB gene has been interrupted (srfB(−)) has shown that this gene is required for regulation of actin–cytoskeleton-related functions, such as cytokinesis and macropinocytosis. The mutant failed to develop well in suspension, but could be rescued by cAMP pulsing, suggesting a defect in cAMP signaling. srfB(−) cells showed impaired chemotaxis to cAMP and defective lateral pseudopodium inhibition. Nevertheless, srfB(−) cells aggregated on agar plates and nitrocellulose filters 2 h earlier than wild type cells, and completed development, showing an increased tendency to form slug structures. Analysis of wild type and srfB(−) strains detected significant differences in the regulation of gene expression upon starvation. Genes coding for lysosomal and ribosomal proteins, developmentally-regulated genes, and some genes coding for proteins involved in cytoskeleton regulation were deregulated during the first stages of development. Elsevier 2008-04-15 /pmc/articles/PMC3819988/ /pubmed/18339368 http://dx.doi.org/10.1016/j.ydbio.2008.01.026 Text en © 2008 Elsevier Inc. https://creativecommons.org/licenses/by/4.0/ Open Access under CC BY 4.0 (https://creativecommons.org/licenses/by/4.0/) license |
spellingShingle | Article Galardi-Castilla, María Pergolizzi, Barbara Bloomfield, Gareth Skelton, Jason Ivens, Al Kay, Robert R. Bozzaro, Salvatore Sastre, Leandro SrfB, a member of the Serum Response Factor family of transcription factors, regulates starvation response and early development in Dictyostelium |
title | SrfB, a member of the Serum Response Factor family of transcription factors, regulates starvation response and early development in Dictyostelium |
title_full | SrfB, a member of the Serum Response Factor family of transcription factors, regulates starvation response and early development in Dictyostelium |
title_fullStr | SrfB, a member of the Serum Response Factor family of transcription factors, regulates starvation response and early development in Dictyostelium |
title_full_unstemmed | SrfB, a member of the Serum Response Factor family of transcription factors, regulates starvation response and early development in Dictyostelium |
title_short | SrfB, a member of the Serum Response Factor family of transcription factors, regulates starvation response and early development in Dictyostelium |
title_sort | srfb, a member of the serum response factor family of transcription factors, regulates starvation response and early development in dictyostelium |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819988/ https://www.ncbi.nlm.nih.gov/pubmed/18339368 http://dx.doi.org/10.1016/j.ydbio.2008.01.026 |
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