Human pancreatic islets express mRNA species encoding two distinct catalytically active isoforms of group VI phospholipase A(2) (iPLA(2)) that arise from an exon-skipping mechanism of alternative splicing of the transcript from the iPLA(2) gene on chromosome 22q13.1

Citation
Zm. Ma et al., Human pancreatic islets express mRNA species encoding two distinct catalytically active isoforms of group VI phospholipase A(2) (iPLA(2)) that arise from an exon-skipping mechanism of alternative splicing of the transcript from the iPLA(2) gene on chromosome 22q13.1, J BIOL CHEM, 274(14), 1999, pp. 9607-9616
Citations number
64
Categorie Soggetti
Biochemistry & Biophysics
Journal title
JOURNAL OF BIOLOGICAL CHEMISTRY
ISSN journal
00219258 → ACNP
Volume
274
Issue
14
Year of publication
1999
Pages
9607 - 9616
Database
ISI
SICI code
0021-9258(19990402)274:14<9607:HPIEMS>2.0.ZU;2-T
Abstract
An 85-kDa Group VI phospholipase A, enzyme (iPLA(2)) that does not require Ca2+ for catalysis has recently been cloned from three rodent species. A ho mologous 88-kDa enzyme has been cloned from human B-lymphocyte lines that c ontains a 54-amino acid insert not present in the rodent enzymes, but human cells have not previously been observed to express catalytically active iP LA(2) isoforms other than the 88-kDa protein. We have cloned cDNA species t hat encode two distinct iPLA(2) isoforms from human pancreatic islet RNA an d a human insulinoma cDNA library. One isoform is an 85-kDa protein (short isoform of human iPLA(2) (SH-iPLA(2))) and the other an 88-kDa protein (lon g isoform of human iPLA, (LH-iPLA(2))). Transcripts encoding both isoforms are also observed in human promonocytic U937 cells. Recombinant SH-iPLA(2) and LH-iPLA(2) are both catalytically active in the absence of Ca2+ and inh ibited by a bromoenol lactone suicide substrate, but LH-iPLA(2) is activate d by ATP, whereas SH-iPLA(2) is not. The human iPLA(2) gene has been found to reside on chromosome 22 in region q13.1 and to contain 16 exons represen ted in the LH-iPLA(2) transcript. Exon 8 is not represented in the SH-iPLA( 2) transcript, indicating that it arises by an exon-skipping mechanism of a lternative splicing. The amino acid sequence encoded by exon 8 of the human iPLA(2) gene is proline-rich and shares a consensus motif of PX(5)PX(8)HHP X(12)NX(4)Q with the proline-rich middle linker domains of the Smad protein s DAF-3 and Smad4, Expression of mRNA species encoding two active iPLA(2) i soforms with distinguishable catalytic properties in two different types of human cells demonstrated here may have regulatory or functional implicatio ns about the roles of products of the iPLA(2) gene in cell biologic process es.