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Originally published In Press as doi:10.1074/jbc.M005871200 on August 23, 2000
J. Biol. Chem., Vol. 275, Issue 50, 39589-39599, December 15, 2000
Characterization of Hydra Type IV Collagen
TYPE IV COLLAGEN IS ESSENTIAL FOR HEAD REGENERATION AND ITS
EXPRESSION IS UP-REGULATED UPON EXPOSURE TO GLUCOSE*
Susan J.
Fowler,
Sheba
Jose,
Xiaoming
Zhang§¶,
Rainer
Deutzmann ,
Michael P.
Sarras Jr.§, and
Raymond P.
Boot-Handford**
From the Wellcome Trust Centre for Cell-Matrix Research, School of
Biological Sciences, University of Manchester, Manchester M13 9PT,
United Kingdom, the § Department of Anatomy and Cell
Biology, University of Kansas Medical Centre, Kansas City, Kansas
66160, the Institut fur Biochemie I, University of Regensburg,
Regensburg, D-8400, Germany, and the ¶ Department of
Biomedical Sciences, Southwest Missouri State University,
Springfield, Missouri 65804-0094
Hydra vulgaris mesoglea is a
primitive basement membrane that also exhibits some features of an
interstitial matrix. We have characterized cDNAs that encode the
full-length hydra 1(IV) chain. The 5169-base pair transcript encodes
a protein of 1723 amino acids, including an interrupted 1455-residue
collagenous domain and a 228-residue C-terminal noncollagenous domain.
N-terminal sequence analyses of collagen IV peptides suggest the
molecule is homotrimeric. Denatured hydra type IV collagen protein
occurs as dimers and higher order aggregates held together by
nonreducible cross-links. Hydra collagen IV exhibits no functional
evidence for the presence of a 7 S domain. Type IV collagen is
expressed by the ectoderm along the entire longitudinal axis of the
animal but is most intense at the base of the tentacles at the site of battery cell transdifferentiation. Antisense studies show that inhibition of collagen IV translation causes a blockage in head regeneration, indicating its importance in normal hydra development. Exposure of adult hydra to 15 mM glucose resulted in
up-regulation of type IV collagen mRNA levels within 48 h and
significant thickening of the mesoglea within 14 days, suggesting that
basement membrane thickening seen in diabetes may be, in evolutionary
terms, an ancient glucose-mediated response.
*
This work was funded by grants from the Dr. Hadwen Trust for
Humane Research and the Royal Society (to R. B.-H.), National Institutes of Health Grant DK47840 (to M. P. S.), and Grant
SFB 521/A4 from the Deutsche Forschungsgemeinschaft (to R. D.).The costs of publication of this
article were defrayed in part by the
payment of page charges. The article
must therefore be hereby marked
"advertisement" in
accordance with 18 U.S.C. Section
1734 solely to indicate this fact.
The nucleotide sequence(s) reported in this paper has been submitted to the GenBankTM/EMBL Data Bank with accession number(s) AF282902.
**
To whom correspondence should be addressed: Wellcome Trust Centre
for Cell-Matrix Research, 2.205 Stopford, School of Biological Sciences, University of Manchester, Manchester M13 9PT, UK. Fax: 161-275-5082; E-mail" Ray.Boot-Handford@man.ac.uk.
Copyright © 2000 by The American Society for Biochemistry and Molecular Biology, Inc.

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