CLONING AND DISRUPTION OF CKB1, THE GENE ENCODING THE 38-KDA BETA-SUBUNIT OF SACCHAROMYCES-CEREVISIAE CASEIN KINASE-II (CKII) - DELETION OFCKII REGULATORY SUBUNITS ELICITS A SALT-SENSITIVE PHENOTYPE
Ap. Bidwai et al., CLONING AND DISRUPTION OF CKB1, THE GENE ENCODING THE 38-KDA BETA-SUBUNIT OF SACCHAROMYCES-CEREVISIAE CASEIN KINASE-II (CKII) - DELETION OFCKII REGULATORY SUBUNITS ELICITS A SALT-SENSITIVE PHENOTYPE, The Journal of biological chemistry, 270(18), 1995, pp. 10395-10404
Saccharomyces cerevisiae casein kinase II (CKII) contains two distinct
catalytic (alpha and alpha') and regulatory (beta and beta') subunits
, We report here the isolation and disruption of the gene, CKB1, encod
ing the 38-kDa beta subunit. The predicted Ckb1 sequence includes the
N-terminal autophosphorylation site, internal acidic domain, and poten
tial metal binding motif (CPX(3)C-X(22)-CPXC) present in other beta su
bunits but is unique in that it contains two additional autophosphoryl
ation sites as well as a 30-amino-acid acidic insert. CKB1 is located
on the left arm of chromosome VII, approximately 33 kilobases from the
centromere and does not correspond to any previously characterized ge
netic locus. Haploid and diploid strains lacking either or both beta s
ubunit genes are viable, demonstrating that the regulatory subunit of
CKII is dispensable in S. cerevisiae. Such strains exhibit wild type b
ehavior with regard to growth on both fermentable and nonfermentable c
arbon sources, mating, sporulation, spore germination, and resistance
to heatshock and nitrogen starvation, but are salt sensitive. Salt sen
sitivity is specific for NaCl and LiCl and is not observed with KCI or
agents which increase osmotic pressure alone, These data suggest a ro
le for CKII in ion homeostasis in S. cerevisiae.