Biol Reprod Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


BOR - Papers in Press, published online ahead of print November 13, 2002.
Biol Reprod 2002, 10.1095/biolreprod.102.008961
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
68/3/1015    most recent
biolreprod.102.008961v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
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 My Folders
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 Telgmann, R.
Right arrow Articles by Ivell, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Telgmann, R.
Right arrow Articles by Ivell, R.
Agricola
Right arrow Articles by Telgmann, R.
Right arrow Articles by Ivell, R.
BIOLOGY OF REPRODUCTION 68, 1015–1026 (2003)
DOI: 10.1095/biolreprod.102.008961
© 2003 by the Society for the Study of Reproduction, Inc.


Female Reproductive Tract

Transcriptional Regulation of the Bovine Oxytocin Receptor Gene1

Ralph Telgmann4,a, Ross A.D. Bathgate3,4,a, Stefanie Jaegera, Gina Tillmanna, and Richard Ivell2,a

a Institute for Hormone and Fertility Research University of Hamburg, 22529 Hamburg, Germany

The oxytocin receptor (OTR) is expressed in the cow uterus at high levels at estrus and at term of pregnancy. This expression appears to be controlled mostly at the transcriptional level and correlates with increasing estrogen concentration and progesterone withdrawal. Approximately 3200 base pairs of the upstream region of the bovine OTR gene were cloned and analyzed using a combination of bioinformatic, electrophoretic mobility shift (EMSA), and transfection analyses. Using nuclear proteins from high- and low-expressing tissues, EMSA indicated no significant quantitative or qualitative changes in specific DNA-protein binding, suggesting that transcription is probably controlled by signalling systems targeting constitutive factors. Using various cell types, including primary and immortalized ruminant endometrial epithelial cells, as hosts for transfection of promoter-reporter constructs showed that endogenous activity resided only in the longest, i.e., 3.2-kb, construct but not in those shorter than 1.0 kb. While estrogen appears to be important in vivo, no effect of estradiol was found on any construct directly; only when the longest 3.2-kb construct was used in combination with some cotransfected steroid receptor cofactors, e.g., SRC1e, was an estradiol-dependent effect observed. A putative interferon-responsive element (IRE) was found at approximately -2,400 from the transcription start site. This element was shown to bind mouse IRF1 and IRF2 as well as similar proteins from bovine endometrial and myometrial nuclear extracts. This element also responded to these factors when cotransfected into various cell types. The bovine equivalents to IRF1 and IRF2 were molecularly cloned from endometrial tissue and shown to be expressed in a temporal fashion, supporting the role of interferon-tau in maternal recognition of pregnancy. Of many factors tested or analyzed, these components of the IFN system are the only ones found to significantly influence the transcription of the bovine OTR gene.

1 This research was supported by a grant from the Deutsche Forschungsgemeinschaft (Iv7/8-3) to R.I. R.A.D.B. was a fellow of the Alexander-von-Humboldt Foundation, Bonn, Germany.

2 Correspondence: Richard Ivell, Institute for Hormone and Fertility Research, University of Hamburg, Grandweg 64, 22529 Hamburg, Germany. FAX: 49 40 56190864; e-mail: ivell{at}rrz.uni-hamburg.de

3 Current address: Howard Florey Institute, University of Melbourne, Australia

4 R.T. and R.A.D.B. are equal-ranking first authors




This article has been cited by other articles:


Home page
FASEB J.Home page
R. Telgmann, C. Dordelmann, E. Brand, V. Nicaud, C. Hagedorn, H. Pavenstadt, F. Cambien, L. Tiret, M. Paul, and S.-M. Brand-Herrmann
Molecular genetic analysis of a human insulin-like growth factor 1 promoter P1 variation
FASEB J, May 1, 2009; 23(5): 1303 - 1313.
[Abstract] [Full Text] [PDF]


Home page
J ANIM SCIHome page
F. Stormshak and C. V. Bishop
BOARD-INVITED REVIEW: Estrogen and progesterone signaling: Genomic and nongenomic actions in domestic ruminants
J Anim Sci, February 1, 2008; 86(2): 299 - 315.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
J. G. W. Fleming, T. E. Spencer, S. H. Safe, and F. W. Bazer
Estrogen Regulates Transcription of the Ovine Oxytocin Receptor Gene through GC-Rich SP1 Promoter Elements
Endocrinology, February 1, 2006; 147(2): 899 - 911.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2003 by the Society for the Study of Reproduction.