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PMID:7480353
Citation |
Klimczak, LJ, Farini, D, Lin, C, Ponti, D, Cashmore, AR and Giuliano, G (1995) Multiple isoforms of Arabidopsis casein kinase I combine conserved catalytic domains with variable carboxyl-terminal extensions. Plant Physiol. 109:687-96 |
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Abstract |
Three cDNA clones encoding isoforms of casein kinase I (CKI) were isolated from Arabidopsis thaliana. One full-length clone, designated CKI1, contained an open reading frame of 1371 bp encoding a protein of 51,949 D with an isoelectric point of 9.7. In addition to the highly conserved catalytic domain (of about 300 amino acids), the Arabidopsis CKI isoforms contain 150 to 180 amino acid carboxyl-terminal extensions, which show among themselves a lower level of sequence conservation. These extensions do not show any sequence similarity to nonplant CKI isoforms, such as rat testis CKI delta, which is their closest isolated homolog, or to yeast CKI isoforms. Three additional isoforms of Arabidopsis CKI were found in the data bases of expressed sequence tags and/or were isolated serendipitously in nonspecific screening procedures by others. One of them also shows a carboxyl-terminal extension, but of only 80 amino acids. Casein kinase activity was detected in the soluble fraction of Escherichia coli strains expressing the CKI1 protein. This activity showed the crucial properties of CKI, including the ability to phosphorylate the D4 peptide, a specific substrate of CKI, and inhibition by N-(2-aminoethyl)-5-chloroisoquinoline-8-sulfonamide, a specific CKI inhibitor. Like several recombinant CKI isoforms from yeast, CKI1 was able to phosphorylate tyrosine-containing acidic polymers. |
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Keywords |
Amino Acid Sequence; Animals; Arabidopsis/enzymology; Arabidopsis/genetics; Base Sequence; Binding Sites; Casein Kinases; Cloning, Molecular; Conserved Sequence; Escherichia coli; Humans; Isoenzymes/biosynthesis; Isoenzymes/chemistry; Isoenzymes/genetics; Male; Molecular Sequence Data; Molecular Weight; Open Reading Frames; Phylogeny; Protein Kinases/biosynthesis; Protein Kinases/chemistry; Protein Kinases/genetics; RNA, Messenger/analysis; RNA, Messenger/biosynthesis; Rats; Recombinant Proteins/biosynthesis; Recombinant Proteins/chemistry; Restriction Mapping; Saccharomyces cerevisiae/enzymology; Sequence Homology, Amino Acid; Testis/enzymology |
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Annotations
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