THE MURINE DECORIN - COMPLETE CDNA CLONING, GENOMIC ORGANIZATION, CHROMOSOMAL ASSIGNMENT, AND EXPRESSION DURING ORGANOGENESIS AND TISSUE DIFFERENTIATION
T. Scholzen et al., THE MURINE DECORIN - COMPLETE CDNA CLONING, GENOMIC ORGANIZATION, CHROMOSOMAL ASSIGNMENT, AND EXPRESSION DURING ORGANOGENESIS AND TISSUE DIFFERENTIATION, The Journal of biological chemistry, 269(45), 1994, pp. 28270-28281
Decorin, a proteoglycan known to interact with collagen and growth fac
tors, may play key roles during ontogenesis, tissue remodeling, and ca
ncer. We have deciphered the complete protein sequence of the murine d
ecorin by cDNA cloning, elucidated its gene structure and chromosomal
location, and investigated its expression in the developing embryo. Th
e decorin protein and the gene were highly conserved vis a vis the hum
an counterpart; however, the murine gene lacked a leader exon, exon Ib
, which was found only in the human. Using interspecific backcrossing,
we assigned the gene to chromosome 10 just proximally to the Steel ge
ne locus. In situ hybridization studies of developing mouse embryos sh
owed a distinct pattern of expression with a progressive increase of d
ecorin mRNA during ontogenesis. At early stages (day 11 postconception
), decorin was detectable only in the floor plate region. Subsequently
(days 13-16 postconception), decorin expression was especially promin
ent in the meninges and mesothelial linings of pericardium, pleura, an
d coelomic cavity, as well as in the dermis and subepithelial layers o
f the intestine and urinary bladder. In contrast, the major parenchyma
l organs were only weakly positive for decorin mRNA. These findings su
ggest that decorin may play a role in epithelial/mesenchymal interacti
ons during organ development and shaping.