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PMID: 7759525 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

Casein kinase I gamma subfamily. Molecular cloning, expression, and characterization of three mammalian isoforms and complementation of defects in the Saccharomyces cerevisiae YCK genes.

The Journal of biological chemistry ·Vol. 270 ·No. 21 ·1995-05-26 ·Pages 12717-24

Zhai L, Graves PR, Robinson LC, Italiano M, Culbertson MR, Rowles J, Cobb MH, DePaoli-Roach AA, Roach PJ

Abstract

Casein kinase I, one of the first protein kinases identified biochemically, is known to exist in multiple isoforms in mammals. Using a partial cDNA fragment corresponding to an isoform termed CK1 gamma, three full-length rat testis cDNAs were cloned that defined three separate members of this subfamily. The isoforms, designated CK1 gamma 1, CK1 gamma 2, and CK1 gamma 3, have predicted molecular masses of 43,000, 45,500, and 49,700. CK1 gamma 3 may also exist in an alternatively spliced form. The proteins are more than 90% identical to each other within the protein kinase domain but only 51-59% identical to other casein kinase I isoforms within this region. Messages for CK1 gamma 1 (2 kilobases (kb)), CK1 gamma 2 (1.5 and 2.4 kb), and CK1 gamma 3 (2.8 kb) were detected by Northern hybridization of testis RNA. Message for CK1 gamma 3 was also observed in brain, heart, kidney, lung, liver, and muscle whereas CK1 gamma 1 and CK1 gamma 2 messages were restricted to testis. All three CK1 gamma isoforms were expressed as active enzymes in Escherichia coli and partially purified. The enzymes phosphorylated typical in vitro casein kinase I substrates such as casein, phosvitin, and a synthetic peptide, D4. Phosphorylation of the D4 peptide was activated by heparin whereas phosphorylation of the protein substrates was inhibited. The known casein kinase I inhibitor CK1-7 also inhibited the CK1 gamma s although less effectively than the CK1 alpha or CK1 delta isoforms. All three CK1 gamma s underwent autophosphorylation when incubated with ATP and Mg2+. The YCK1 and YCK2 genes in Saccharomyces cerevisiae encode casein kinase I homologs, defects in which lead to aberrant morphology and growth arrest. Expression of mammalian CK1 gamma 1 or CK1 gamma 3 restored growth and normal morphology to a yeast mutant carrying a disruption of YCK1 and a temperature-sensitive allele of YCK2, suggesting overlap of function between the yeast Yck proteins and these CK1 isoforms.

MeSH Terms
Amino Acid Sequence Animals Base Sequence Casein Kinase I Casein Kinases Cloning, Molecular Genes, Fungal/genetics Genetic Complementation Test Heparin/pharmacology Isoenzymes/classification,genetics Male Molecular Sequence Data Multigene Family/genetics Phosphorylation Protein Kinases/classification,drug effects,genetics RNA, Messenger/analysis Rats Restriction Mapping Saccharomyces cerevisiae/enzymology,genetics Saccharomyces cerevisiae Proteins Sequence Homology, Amino Acid Testis/enzymology Tissue Distribution
Chemicals
Isoenzymes RNA, Messenger Saccharomyces cerevisiae Proteins Heparin Protein Kinases Casein Kinase I Casein Kinases YCK1 protein, S cerevisiae YCK2 protein, S cerevisiae
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Zhai L
Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis 46202-5122, USA.
Graves P R
Robinson L C
Italiano M
Culbertson M R
Rowles J
Cobb M H
DePaoli-Roach A A
Roach P J
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1995-05-26
Pages
12717-24
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIDDK NIH HHS · DK27221 · United States
NIGMS NIH HHS · GM26217 · United States
NIGMS NIH HHS · GM44140 · United States
Databases
GENBANK
U22296, U22297, U22321
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