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Molecular Cloning and Characterization of Protein Kinase C from the Sea Urchin Lytechinus pictus
Author(s) -
Rakow Terese L.,
Shen Sheldon S.
Publication year - 1994
Publication title -
development, growth and differentiation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.864
H-Index - 66
eISSN - 1440-169X
pISSN - 0012-1592
DOI - 10.1111/j.1440-169x.1994.00489.x
Subject(s) - sea urchin , biology , protein kinase c , protein kinase a , diacylglycerol kinase , microbiology and biotechnology , complementary dna , biochemistry , kinase , gene
Protein kinase C (PKC) has been shown to play a role in events involved in fertilization such as activation of the Na + /H + antiporter and an NADPH dependent oxidase. In addition, it is involved in cell fate programming later in development of the sea urchin embryo. In order to further address the role of PKC in sea urchin development, we have screened a Lytechinus pictus ovary tissue cDNA library and identified one clone for sea urchin protein kinase C (suPKC1). This clone encodes a deduced protein with a molecular mass of 72.4 kDa, which shows strong homology to invertebrate and mammalian protein kinase C (PKC) sequences. PKC has been partially purified from eggs of L. pictus. This kinase activity has been shown to be dependent upon phosphatidylserine, diacylglycerol and Ca 2+ . In agreement with this biochemical data, suPKC1 has a C2 or Ca 2+ ‐binding domain suggesting its activity would be Ca 2+ ‐dependent. Polyclonal antibodies raised against peptides of the suPKC1 sequence recognize an antigen of approximately 71 kDa in DE52 fractions that contain PKC activity; this reactivity is not observed in fractions that lack PKC activity. Using a ribonuclease protection assay, we have demonstrated the presence of suPKC1 message throughout developmental stages of the sea urchin embryo.