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
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
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.