J Biol Chem, Vol. 274, Issue 26, 18693-18701, June 25, 1999
The Bovine Mimecan Gene
MOLECULAR CLONING AND CHARACTERIZATION OF TWO MAJOR RNA
TRANSCRIPTS GENERATED BY ALTERNATIVE USE OF TWO SPLICE ACCEPTOR SITES
IN THE THIRD EXON
Elena S.
Tasheva,
Martha L.
Funderburgh,
James
McReynolds,
James
L.
Funderburgh, and
Gary W.
Conrad
From the Division of Biology, Kansas State University,
Manhattan, Kansas 66506-4901
Mimecan is a proteoglycan expressed by many
connective tissues. It was originally isolated in a truncated form as a
bone-associated glycoprotein, osteoglycin, and was considered an
osteoinductive factor. Recently, we demonstrated that the full-length
translation product of the cDNA encoding mimecan is a corneal
keratan sulfate proteoglycan present in other tissues without keratan
sulfate chains. We also described multiple mimecan mRNA transcripts
generated by differential splicing and alternative polyadenylation. In
this study, we isolated genomic clones and determined the genomic
organization of the bovine mimecan gene. The gene is spread over >33
kilobases of continuous DNA sequence and contains eight exons. The
newly discovered first exon, identified by 5'-rapid amplification of cDNA ends, consists of a 5'-untranslated region and is enriched in
C+G nucleotides. Two transcription initiation sites starting at the
first and at the second exons were determined by primer extension.
Molecular characterization shows that alternatively spliced RNA
isoforms are generated by the use of two distinct splice acceptor sites
in the third exon situated 278 base pairs apart. We determined a
partial genomic structure of the human mimecan gene and demonstrated
two alternatively spliced RNA transcripts that are generated likewise.
Despite the diversity of mimecan transcripts, the primary structure of
the core protein is encoded from exons 3 to 8 and remains unchanged,
indicating its functional importance. Using ribonuclease protection
assay, we analyzed the patterns of spliced RNA expressed in cultured
bovine keratocytes. We demonstrated that their expression is
differentially modulated in a temporal manner by basic fibroblast
growth factor.
Copyright © 1999 by The American Society for Biochemistry and Molecular Biology, Inc.