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Submitted on November 30, 2007
Accepted on March 5, 2008
INRA, UR1037 SCRIBE, IFR140, Ouest-Genopole, 35000 Rennes, France
* To whom correspondence should be addressed. E-mail: Julien.Bobe{at}rennes.inra.fr.
A cDNA encoding for a novel rainbow trout shbg was identified and characterized. Phylogenetic analysis showed that this novel shbg, named shbgb, was a highly divergent paralog of the classical shbg (shbga) form previously known in vertebrates including zebrafish, seabass and rainbow trout. Using all available sequences, no shbgb-like sequence could be identified in any fish species besides Atlantic salmon. Rainbow trout shbga and shbgb only share 26% sequence identity at the amino acid level and exhibit totally distinct tissue distribution thus demonstrating a functional shift of shbgb. Indeed, shbga mRNA was predominantly expressed in liver and spleen but could not be detected in the ovary while shbgb had a predominant ovarian expression but could not be detected in liver. Despite its high divergence, rainbow trout shbgb expressed in COS-7 cells could bind estradiol and testosterone with high affinity and specificity. Both rainbow trout shbgb mRNA and proteins were localized to the granulosa cells of vitellogenic ovarian follicles while shbgb immunoreactivity was also found in theca cells. Finally, shbgb ovarian mRNA expression exhibited a significant drop between late vitellogenesis and oocyte maturation at a time when ovarian aromatase (cyp19a) gene expression and E2 circulating levels exhibit a dramatic decrease. Together, these observations show that shbgb is a functional and highly divergent shbg paralog probably arising from a salmonid-specific duplication of the shbg gene.
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