Abstract

During the sequencing of the long arm of chromosome 7 in the Human Genome Project, a predicted protein product of 40 kDa was identified, which contained two approximately 10-amino acid segments homologous to the ATP and lipase consensus sequences present in the founding members of a family of calcium-independent phospholipases A(2). Detailed inspection of the identified sequence (residues 79, 671-109,912 GenBank accession no. AC005058) demonstrated that it represented only a partial sequence of a larger undefined polypeptide product. Accordingly, we identified the complete genomic organization of this putative phospholipase A(2) through analyses of previously published expressed sequence tags, PCR of human heart cDNA, and 5'-rapid amplification of cDNA ends. Polymerase chain reaction and Northern blotting demonstrated a 3.4-kilobase message, which encoded a polypeptide with a maximum calculated molecular weight of 88476.9. This 3.4-kilobase message was present in multiple human parenchymal tissues including heart, skeletal muscle, placenta, brain, liver, and pancreas. Cloning and expression of the protein encoded by this message in Sf9 cells resulted in the production of two proteins of apparent molecular masses of 77 and 63 kDa as assessed by Western analyses utilizing immunoaffinity-purified antibody. Membranes from Sf9 cells expressing recombinant protein released fatty acid from sn-2-radiolabeled phosphatidylcholine and plasmenylcholine up to 10-fold more rapidly than controls. The initial rate of fatty acid release from the membrane fraction was 0. 3 nmol/mg.min. The recombinant protein was entirely calcium-independent, had a pH optimum of 8.0, was inhibited by (E)-6-(bromomethylene)-3-(1-naphthalenyl)-2H-tetrahydropyran-2-one (IC(50) = 3 microM), and was predominantly present in the membrane-associated fraction. Collectively, these results describe the genomic organization, complete mRNA sequence, and sn-2-lipase activity of a novel intracellular calcium-independent membrane-associated phospholipase A(2).

Highlights

  • Phospholipases A2 catalyze the esterolytic cleavage of fatty acids from the sn-2-position of phospholipids, thereby regulating the release of lipid second messengers, growth factors, and membrane physical properties [1,2,3,4,5]

  • Characterization of the Full-length Message Encoding iPLA2␥—Inspection of the sequence encoding the putative 40kDa phospholipase reported by the Human Genome Sequencing Project

  • We performed a TBLASTN data base search [36] of GenBankTM to find expressed sequence tags (ESTs) that could align with the 5Ј-end of the putative iPLA2␥ sequence

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Summary

Introduction

Phospholipases A2 catalyze the esterolytic cleavage of fatty acids from the sn-2-position of phospholipids, thereby regulating the release of lipid second messengers (e.g. eicosanoids and lysophospholipids), growth factors (lysophosphatidic acid), and membrane physical properties [1,2,3,4,5]. We report the entire genomic organization, complete mRNA sequence, cloning, expression, and initial activity analyses of the protein encoded by this gene, which we term iPLA2␥.

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