cDNA cloning, biochemical and phylogenetic characterization of β- and β' -subunits of Candida albicans protein kinase CK2

Autores
Zelada, Alicia Mercedes; Silva Junqueira de Souza, Flavio; Walz, Katherina; Giasson, Luc; Di Bernardo, Maria Susana
Año de publicación
2003
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
We have previously reported that Candida albicans protein kinase CK2 is composed of two distinct catalytic (α- and α′-) and two distinct regulatory (β- and β′-) subunits. We report here the isolation of two cDNAs clones, CaCKB1 and CaCKB2, encoding C. albicans β- and β′-subunits, respectively. The predicted β- and β′- proteins have calculated molecular masses of 34 kDa and 31 kDa and show all major features conserved in β-subunits of other organisms, including the N-terminal autophosphorylation site, the internal acidic region and a potential metal-binding motif. The deduced amino acid sequence of C. albicans β-subunit displays 48% identity with that of Saccharomyces cerevisiae and has an unusually long C-terminal acidic region containing a putative autophosphorylation site. C. albicans β′ shows 54% sequence identity with its S. cerevisiae homologue. Semi-quantitative RT-PCR analyses indicate that the mRNAs corresponding to both subunits are present in similar amounts in the yeast and hyphal forms of the fungus. To evaluate the biochemical properties of C. albicans β- and β′-subunits, both proteins were expressed in Escherichia coli and purified. Experiments performed in vitro indicate that both recombinant subunits reconstitute a fully functional holoenzyme when incubated with stoichiometric amounts of human recombinant α-subunit, as judged by their ability to abolish basal phosphorylation of calmodulin by human recombinant α-subunit and the reversion of the inhibitory effect by polylysine. In addition, both regulatory subunits can be phosphorylated by human recombinant α subunit. Phylogenetic analysis of β- and β′-proteins of C. albicans and other organisms shows that the CKB gene duplication occurred before the split of the ascomycete and basidiomycete lineages. cDNA sequences of C. albicans CKB1 (Accession No. AF0599060) and CKB2 (Accession No. AY172319) have been deposited in the GenBank database.
Fil: Zelada, Alicia Mercedes. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Invetigaciones Bioquímicas y Fisiologicas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Silva Junqueira de Souza, Flavio. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Walz, Katherina. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Invetigaciones Bioquímicas y Fisiologicas; Argentina
Fil: Giasson, Luc. Laval University; Canadá
Fil: Di Bernardo, Maria Susana. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Invetigaciones Bioquímicas y Fisiologicas; Argentina
Materia
Candida Albicans
Ck2
Phylogeny
Protein Kinase
Regulatory Subunit
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/79765

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repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling cDNA cloning, biochemical and phylogenetic characterization of β- and β' -subunits of Candida albicans protein kinase CK2Zelada, Alicia MercedesSilva Junqueira de Souza, FlavioWalz, KatherinaGiasson, LucDi Bernardo, Maria SusanaCandida AlbicansCk2PhylogenyProtein KinaseRegulatory Subunithttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1We have previously reported that Candida albicans protein kinase CK2 is composed of two distinct catalytic (α- and α′-) and two distinct regulatory (β- and β′-) subunits. We report here the isolation of two cDNAs clones, CaCKB1 and CaCKB2, encoding C. albicans β- and β′-subunits, respectively. The predicted β- and β′- proteins have calculated molecular masses of 34 kDa and 31 kDa and show all major features conserved in β-subunits of other organisms, including the N-terminal autophosphorylation site, the internal acidic region and a potential metal-binding motif. The deduced amino acid sequence of C. albicans β-subunit displays 48% identity with that of Saccharomyces cerevisiae and has an unusually long C-terminal acidic region containing a putative autophosphorylation site. C. albicans β′ shows 54% sequence identity with its S. cerevisiae homologue. Semi-quantitative RT-PCR analyses indicate that the mRNAs corresponding to both subunits are present in similar amounts in the yeast and hyphal forms of the fungus. To evaluate the biochemical properties of C. albicans β- and β′-subunits, both proteins were expressed in Escherichia coli and purified. Experiments performed in vitro indicate that both recombinant subunits reconstitute a fully functional holoenzyme when incubated with stoichiometric amounts of human recombinant α-subunit, as judged by their ability to abolish basal phosphorylation of calmodulin by human recombinant α-subunit and the reversion of the inhibitory effect by polylysine. In addition, both regulatory subunits can be phosphorylated by human recombinant α subunit. Phylogenetic analysis of β- and β′-proteins of C. albicans and other organisms shows that the CKB gene duplication occurred before the split of the ascomycete and basidiomycete lineages. cDNA sequences of C. albicans CKB1 (Accession No. AF0599060) and CKB2 (Accession No. AY172319) have been deposited in the GenBank database.Fil: Zelada, Alicia Mercedes. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Invetigaciones Bioquímicas y Fisiologicas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaFil: Silva Junqueira de Souza, Flavio. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaFil: Walz, Katherina. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Invetigaciones Bioquímicas y Fisiologicas; ArgentinaFil: Giasson, Luc. Laval University; CanadáFil: Di Bernardo, Maria Susana. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Invetigaciones Bioquímicas y Fisiologicas; ArgentinaJohn Wiley & Sons Ltd2003-04info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/79765Zelada, Alicia Mercedes; Silva Junqueira de Souza, Flavio; Walz, Katherina; Giasson, Luc; Di Bernardo, Maria Susana; cDNA cloning, biochemical and phylogenetic characterization of β- and β' -subunits of Candida albicans protein kinase CK2; John Wiley & Sons Ltd; Yeast; 20; 6; 4-2003; 471-4780749-503XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1002/yea.977info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/yea.977info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:44:11Zoai:ri.conicet.gov.ar:11336/79765instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:44:12.408CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv cDNA cloning, biochemical and phylogenetic characterization of β- and β' -subunits of Candida albicans protein kinase CK2
title cDNA cloning, biochemical and phylogenetic characterization of β- and β' -subunits of Candida albicans protein kinase CK2
spellingShingle cDNA cloning, biochemical and phylogenetic characterization of β- and β' -subunits of Candida albicans protein kinase CK2
Zelada, Alicia Mercedes
Candida Albicans
Ck2
Phylogeny
Protein Kinase
Regulatory Subunit
title_short cDNA cloning, biochemical and phylogenetic characterization of β- and β' -subunits of Candida albicans protein kinase CK2
title_full cDNA cloning, biochemical and phylogenetic characterization of β- and β' -subunits of Candida albicans protein kinase CK2
title_fullStr cDNA cloning, biochemical and phylogenetic characterization of β- and β' -subunits of Candida albicans protein kinase CK2
title_full_unstemmed cDNA cloning, biochemical and phylogenetic characterization of β- and β' -subunits of Candida albicans protein kinase CK2
title_sort cDNA cloning, biochemical and phylogenetic characterization of β- and β' -subunits of Candida albicans protein kinase CK2
dc.creator.none.fl_str_mv Zelada, Alicia Mercedes
Silva Junqueira de Souza, Flavio
Walz, Katherina
Giasson, Luc
Di Bernardo, Maria Susana
author Zelada, Alicia Mercedes
author_facet Zelada, Alicia Mercedes
Silva Junqueira de Souza, Flavio
Walz, Katherina
Giasson, Luc
Di Bernardo, Maria Susana
author_role author
author2 Silva Junqueira de Souza, Flavio
Walz, Katherina
Giasson, Luc
Di Bernardo, Maria Susana
author2_role author
author
author
author
dc.subject.none.fl_str_mv Candida Albicans
Ck2
Phylogeny
Protein Kinase
Regulatory Subunit
topic Candida Albicans
Ck2
Phylogeny
Protein Kinase
Regulatory Subunit
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv We have previously reported that Candida albicans protein kinase CK2 is composed of two distinct catalytic (α- and α′-) and two distinct regulatory (β- and β′-) subunits. We report here the isolation of two cDNAs clones, CaCKB1 and CaCKB2, encoding C. albicans β- and β′-subunits, respectively. The predicted β- and β′- proteins have calculated molecular masses of 34 kDa and 31 kDa and show all major features conserved in β-subunits of other organisms, including the N-terminal autophosphorylation site, the internal acidic region and a potential metal-binding motif. The deduced amino acid sequence of C. albicans β-subunit displays 48% identity with that of Saccharomyces cerevisiae and has an unusually long C-terminal acidic region containing a putative autophosphorylation site. C. albicans β′ shows 54% sequence identity with its S. cerevisiae homologue. Semi-quantitative RT-PCR analyses indicate that the mRNAs corresponding to both subunits are present in similar amounts in the yeast and hyphal forms of the fungus. To evaluate the biochemical properties of C. albicans β- and β′-subunits, both proteins were expressed in Escherichia coli and purified. Experiments performed in vitro indicate that both recombinant subunits reconstitute a fully functional holoenzyme when incubated with stoichiometric amounts of human recombinant α-subunit, as judged by their ability to abolish basal phosphorylation of calmodulin by human recombinant α-subunit and the reversion of the inhibitory effect by polylysine. In addition, both regulatory subunits can be phosphorylated by human recombinant α subunit. Phylogenetic analysis of β- and β′-proteins of C. albicans and other organisms shows that the CKB gene duplication occurred before the split of the ascomycete and basidiomycete lineages. cDNA sequences of C. albicans CKB1 (Accession No. AF0599060) and CKB2 (Accession No. AY172319) have been deposited in the GenBank database.
Fil: Zelada, Alicia Mercedes. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Invetigaciones Bioquímicas y Fisiologicas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Silva Junqueira de Souza, Flavio. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Walz, Katherina. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Invetigaciones Bioquímicas y Fisiologicas; Argentina
Fil: Giasson, Luc. Laval University; Canadá
Fil: Di Bernardo, Maria Susana. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Invetigaciones Bioquímicas y Fisiologicas; Argentina
description We have previously reported that Candida albicans protein kinase CK2 is composed of two distinct catalytic (α- and α′-) and two distinct regulatory (β- and β′-) subunits. We report here the isolation of two cDNAs clones, CaCKB1 and CaCKB2, encoding C. albicans β- and β′-subunits, respectively. The predicted β- and β′- proteins have calculated molecular masses of 34 kDa and 31 kDa and show all major features conserved in β-subunits of other organisms, including the N-terminal autophosphorylation site, the internal acidic region and a potential metal-binding motif. The deduced amino acid sequence of C. albicans β-subunit displays 48% identity with that of Saccharomyces cerevisiae and has an unusually long C-terminal acidic region containing a putative autophosphorylation site. C. albicans β′ shows 54% sequence identity with its S. cerevisiae homologue. Semi-quantitative RT-PCR analyses indicate that the mRNAs corresponding to both subunits are present in similar amounts in the yeast and hyphal forms of the fungus. To evaluate the biochemical properties of C. albicans β- and β′-subunits, both proteins were expressed in Escherichia coli and purified. Experiments performed in vitro indicate that both recombinant subunits reconstitute a fully functional holoenzyme when incubated with stoichiometric amounts of human recombinant α-subunit, as judged by their ability to abolish basal phosphorylation of calmodulin by human recombinant α-subunit and the reversion of the inhibitory effect by polylysine. In addition, both regulatory subunits can be phosphorylated by human recombinant α subunit. Phylogenetic analysis of β- and β′-proteins of C. albicans and other organisms shows that the CKB gene duplication occurred before the split of the ascomycete and basidiomycete lineages. cDNA sequences of C. albicans CKB1 (Accession No. AF0599060) and CKB2 (Accession No. AY172319) have been deposited in the GenBank database.
publishDate 2003
dc.date.none.fl_str_mv 2003-04
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/79765
Zelada, Alicia Mercedes; Silva Junqueira de Souza, Flavio; Walz, Katherina; Giasson, Luc; Di Bernardo, Maria Susana; cDNA cloning, biochemical and phylogenetic characterization of β- and β' -subunits of Candida albicans protein kinase CK2; John Wiley & Sons Ltd; Yeast; 20; 6; 4-2003; 471-478
0749-503X
CONICET Digital
CONICET
url http://hdl.handle.net/11336/79765
identifier_str_mv Zelada, Alicia Mercedes; Silva Junqueira de Souza, Flavio; Walz, Katherina; Giasson, Luc; Di Bernardo, Maria Susana; cDNA cloning, biochemical and phylogenetic characterization of β- and β' -subunits of Candida albicans protein kinase CK2; John Wiley & Sons Ltd; Yeast; 20; 6; 4-2003; 471-478
0749-503X
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
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info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/yea.977
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv John Wiley & Sons Ltd
publisher.none.fl_str_mv John Wiley & Sons Ltd
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
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instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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