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Cloning of a fibrillar collagen gene expressed in the mesenchymal cells of the developing sea urchin embryo
We have cloned and characterized several overlapping cDNAs that specify a large portion of a Paracentrotus lividus fibrillar collagen molecule. Our conclusions are based on sequencing data, which showed that the clones code for a 786-amino acid collagenous domain composed of an uninterrupted series...
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Published in: | The Journal of biological chemistry 1990-04, Vol.265 (12), p.7050-7054 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | We have cloned and characterized several overlapping cDNAs that specify a large portion of a Paracentrotus lividus fibrillar
collagen molecule. Our conclusions are based on sequencing data, which showed that the clones code for a 786-amino acid collagenous
domain composed of an uninterrupted series of Gly-X-Y repeats and for a 265-amino acid carboxyl-terminal globular extension.
The latter domain exhibits features highly reminiscent of those of the vertebrate counterparts, notably a putative carboxyl-peptidase
cleavage site, a series of similarly arranged cysteinyl residues, and an N-linked glycosylation attachment site. In situ and
Northern blot hybridizations have established the size, time of appearance, and tissue localization of the collagen mRNA during
sea urchin development. The collagen transcript, 9 kilobases in length, is first detected in the primary and, more predominantly,
in the secondary mesenchyme cells of late gastrulae where it progressively accumulates thereafter. This and other work (D'Alessio,
M., Ramirez, F., Suzuki, H.R., Solursh, M., and Gambino, R. (1989) Proc. Natl. Acad. Sci. U. S. A. 86, 9303-9307) provide
evidence of a genetic heterogeneity of fibrillar collagens in the sea urchin embryo and suggest that the two genes are activated
in the same cell lineages at distinct developmental stages. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1016/s0021-9258(19)39257-9 |