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

被引:2
作者
Zelada, A
De Souza, FSJ
Walz, K
Giasson, L
Passeron, S
机构
[1] Consejo Nacl Invest Cient & Tecn, INGEBI, Inst Genet & Biol Mol, RA-1428 Buenos Aires, DF, Argentina
[2] Univ Buenos Aires, CONICET, IBYF, Fac Agron,Catedra Microbiol, RA-1417 Buenos Aires, DF, Argentina
[3] Univ Laval, GREB, Sch Dent, St Foy, PQ G1K 7P4, Canada
关键词
Candida albicans; protein kinase CK2; regulatory subunit; phylogeny;
D O I
10.1002/yea.977
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have previously reported that Candida albicans protein kinase CK2 is composed of two distinct catalytic (alpha- and alpha'-) and two distinct regulatory (beta- and beta'-) subunits. We report here the isolation of two cDNAs clones, CaCKB1 and CaCKB2, encoding C albicans beta- and beta'-subunits, respectively. The predicted beta- and beta'-proteins have calculated molecular masses of 34 kDa and 31 kDa and show all major features conserved in beta-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 beta-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 beta' 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 beta- and beta'-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 a-subunit, as judged by their ability to abolish basal phosphorylation of calmodulin by human recombinant alpha-subunit and the reversion of the inhibitory effect by polylysine. In addition, both regulatory subunits can be phosphorylated by human recombinant alpha subunit. Phylogenetic analysis of beta- and beta'-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. Copyright (C) 2003 John Wiley Sons, Ltd.
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页码:471 / 478
页数:8
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