KeaA, a <it>Dictyostelium </it>kelch-domain protein that regulates the response to stress and development

<p>Abstract</p> <p>Background</p> <p>The protein kinase YakA is responsible for the growth arrest and induction of developmental processes that occur upon starvation of <it>Dictyostelium </it>cells. <it>yakA<sup>- </sup></it>cells are...

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Main Authors: Souza Glaucia M, Bagattini Raquel, Mantzouranis Luciana
Format: Article
Language:English
Published: BMC 2010-07-01
Series:BMC Developmental Biology
Online Access:http://www.biomedcentral.com/1471-213X/10/79
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spelling doaj-44c91238d3cd4ceeaa34c04f5ace8da62020-11-24T20:48:00ZengBMCBMC Developmental Biology1471-213X2010-07-011017910.1186/1471-213X-10-79KeaA, a <it>Dictyostelium </it>kelch-domain protein that regulates the response to stress and developmentSouza Glaucia MBagattini RaquelMantzouranis Luciana<p>Abstract</p> <p>Background</p> <p>The protein kinase YakA is responsible for the growth arrest and induction of developmental processes that occur upon starvation of <it>Dictyostelium </it>cells. <it>yakA<sup>- </sup></it>cells are aggregation deficient, have a faster cell cycle and are hypersensitive to oxidative and nitrosoative stress. With the aim of isolating members of the YakA pathway, suppressors of the death induced by nitrosoative stress in the <it>yakA<sup>- </sup></it>cells were identified. One of the suppressor mutations occurred in <it>keaA</it>, a gene identical to DG1106 and similar to Keap1 from mice and the Kelch protein from Drosophila, among others that contain Kelch domains.</p> <p>Results</p> <p>A mutation in <it>keaA </it>suppresses the hypersensitivity to oxidative and nitrosoative stresses but not the faster growth phenotype of <it>yakA<sup>- </sup></it>cells. The growth profile of <it>keaA </it>deficient cells indicates that this gene is necessary for growth. <it>keaA </it>deficient cells are more resistant to nitrosoative and oxidative stress and <it>keaA </it>is necessary for the production and detection of cAMP. A morphological analysis of <it>keaA </it>deficient cells during multicellular development indicated that, although the mutant is not absolutely deficient in aggregation, cells do not efficiently participate in the process. Gene expression analysis using cDNA microarrays of wild-type and <it>keaA </it>deficient cells indicated a role for KeaA in the regulation of the cell cycle and pre-starvation responses.</p> <p>Conclusions</p> <p>KeaA is required for cAMP signaling following stress. Our studies indicate a role for kelch proteins in the signaling that regulates the cell cycle and development in response to changes in the environmental conditions.</p> http://www.biomedcentral.com/1471-213X/10/79
collection DOAJ
language English
format Article
sources DOAJ
author Souza Glaucia M
Bagattini Raquel
Mantzouranis Luciana
spellingShingle Souza Glaucia M
Bagattini Raquel
Mantzouranis Luciana
KeaA, a <it>Dictyostelium </it>kelch-domain protein that regulates the response to stress and development
BMC Developmental Biology
author_facet Souza Glaucia M
Bagattini Raquel
Mantzouranis Luciana
author_sort Souza Glaucia M
title KeaA, a <it>Dictyostelium </it>kelch-domain protein that regulates the response to stress and development
title_short KeaA, a <it>Dictyostelium </it>kelch-domain protein that regulates the response to stress and development
title_full KeaA, a <it>Dictyostelium </it>kelch-domain protein that regulates the response to stress and development
title_fullStr KeaA, a <it>Dictyostelium </it>kelch-domain protein that regulates the response to stress and development
title_full_unstemmed KeaA, a <it>Dictyostelium </it>kelch-domain protein that regulates the response to stress and development
title_sort keaa, a <it>dictyostelium </it>kelch-domain protein that regulates the response to stress and development
publisher BMC
series BMC Developmental Biology
issn 1471-213X
publishDate 2010-07-01
description <p>Abstract</p> <p>Background</p> <p>The protein kinase YakA is responsible for the growth arrest and induction of developmental processes that occur upon starvation of <it>Dictyostelium </it>cells. <it>yakA<sup>- </sup></it>cells are aggregation deficient, have a faster cell cycle and are hypersensitive to oxidative and nitrosoative stress. With the aim of isolating members of the YakA pathway, suppressors of the death induced by nitrosoative stress in the <it>yakA<sup>- </sup></it>cells were identified. One of the suppressor mutations occurred in <it>keaA</it>, a gene identical to DG1106 and similar to Keap1 from mice and the Kelch protein from Drosophila, among others that contain Kelch domains.</p> <p>Results</p> <p>A mutation in <it>keaA </it>suppresses the hypersensitivity to oxidative and nitrosoative stresses but not the faster growth phenotype of <it>yakA<sup>- </sup></it>cells. The growth profile of <it>keaA </it>deficient cells indicates that this gene is necessary for growth. <it>keaA </it>deficient cells are more resistant to nitrosoative and oxidative stress and <it>keaA </it>is necessary for the production and detection of cAMP. A morphological analysis of <it>keaA </it>deficient cells during multicellular development indicated that, although the mutant is not absolutely deficient in aggregation, cells do not efficiently participate in the process. Gene expression analysis using cDNA microarrays of wild-type and <it>keaA </it>deficient cells indicated a role for KeaA in the regulation of the cell cycle and pre-starvation responses.</p> <p>Conclusions</p> <p>KeaA is required for cAMP signaling following stress. Our studies indicate a role for kelch proteins in the signaling that regulates the cell cycle and development in response to changes in the environmental conditions.</p>
url http://www.biomedcentral.com/1471-213X/10/79
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