The murine decorin. Complete cDNA cloning, genomic organization, chromosomal assignment, and expression during organogenesis and tissue differentiation

• Published in: The Journal of biological chemistry 1994-11, Vol.269 (45), p.28270-28281
• Main Authors: Scholzen, T, Solursh, M, Suzuki, S, Reiter, R, Morgan, J L, Buchberg, A M, Siracusa, L D, Iozzo, R V
• Format: Article
• Language: English
• Subjects: 3T3 Cells; Amino Acid Sequence; Animals; Base Sequence; Cattle; Cell Differentiation; Chickens; Chromosome Mapping; Cloning, Molecular; Conserved Sequence; Crosses, Genetic; Decorin; Embryonic and Fetal Development; Exons; Extracellular Matrix Proteins; Fetus - metabolism; Fetus - physiology; Genetic Linkage; Humans; Introns; Kidney - metabolism; Mice - genetics; Mice, Inbred Strains; Molecular Sequence Data; Muridae; Myocardium - metabolism; Organ Specificity; Polymerase Chain Reaction; Protein Sorting Signals - genetics; Proteoglycans - biosynthesis; Proteoglycans - genetics; Rats; Repetitive Sequences, Nucleic Acid; Skin - metabolism; Spleen - metabolism
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/s0021-9258(18)46924-4

Decorin, a proteoglycan known to interact with collagen and growth factors, may play key roles during ontogenesis, tissue remodeling, and cancer. We have deciphered the complete protein sequence of the murine decorin by cDNA cloning, elucidated its gene structure and chromosomal location, and investigated its expression in the developing embryo. The decorin protein and the gene were highly conserved vis à vis the human 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 gene locus. In situ hybridization studies of developing mouse embryos showed a distinct pattern of expression with a progressive increase of decorin 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 prominent in the meninges and mesothelial linings of pericardium, pleura, and coelomic cavity, as well as in the dermis and subepithelial layers of the intestine and urinary bladder. In contrast, the major parenchymal organs were only weakly positive for decorin mRNA. These findings suggest that decorin may play a role in epithelial/mesenchymal interactions during organ development and shaping.