Biol Reprod Track the topics, authors and articles important to you
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


BOR - Papers in Press, published online ahead of print December 1, 2004.
Biol Reprod 2004, 10.1095/biolreprod.104.033746
This Article
Right arrow Full Text (Rapid PDF)
Right arrow All Versions of this Article:
72/4/851    most recent
biolreprod.104.033746v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Seenundun, S.
Right arrow Articles by Robaire, B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Seenundun, S.
Right arrow Articles by Robaire, B.
Agricola
Right arrow Articles by Seenundun, S.
Right arrow Articles by Robaire, B.
Submitted June 29, 2004
Returned for revision July 20, 2004
Accepted November 9, 2004

Male Reproductive Tract


Cloning and Characterization of the 5{alpha}-Reductase Type 2 Promoter in the Rat Epididymis

Shayesta Seenundun and Bernard Robaire *

* To whom correspondence should be addressed. E-mail: bernard.robaire{at}mcgill.ca.

Abstract
Steroid 5{alpha}-reductase converts testosterone to the more potent androgen, dihydrotestosterone. The molecular mechanisms responsible for maintaining high concentrations of the 5{alpha}-reductase type 2 mRNA in the caput epididymidis and for regulating its region-specific expression are unknown. To gain insight into its transcriptional regulation, the cloning and characterization of the 5'upstream region of 5{alpha}-reductase type 2 were undertaken. Sequential deletion analysis was done to map the 2243-bp cloned 5'upstream region, and the constructs were transfected into epididymal PC1 cells and prostatic PC3 cells. In both cell lines, regulatory elements and the minimal promoter were mapped to the 485-bp region upstream of the start codon. Primer extension and 5'RACE identified one transcriptional start site at 33-bp upstream of the start codon. Using EMSA, a specific band was observed in the -68 to -32 bp region in the presence of nuclear extracts. Supershift and mutational studies confirmed the binding of Sp1, and to a lesser extent Sp3, to the two potential Sp1 binding sites and the preference of these proteins to one binding site over the other. Sp1 and Sp3 were both predominantly immunolocalized to the principal cells of the epididymis and follow distinct distribution patterns in this tissue. These results provide a framework crucial in the further investigation of the transcriptional regulation of 5{alpha}-reductase type 2 in the rat epididymis.

Key words: Male Reproductive Tract • Epididymis • Gene regulation • Steroid hormones • Testosterone


This article has been cited by other articles:


Home page
Biol. Reprod.Home page
J. Dufresne and D. G. Cyr
Activation of an SP Binding Site Is Crucial for the Expression of Claudin 1 in Rat Epididymal Principal Cells
Biol Reprod, May 1, 2007; 76(5): 825 - 832.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
S. Seenundun and B. Robaire
Time-Dependent Rescue of Gene Expression by Androgens in the Mouse Proximal Caput Epididymidis-1 Cell Line after Androgen Withdrawal
Endocrinology, January 1, 2007; 148(1): 173 - 188.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Copyright © 2004 by the Society for the Study of Reproduction.