help button home button Endocrine Society Endocrinology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH

This version published online on February 7, 2008
Endocrinology, doi:10.1210/en.2007-1237
A more recent version of this article appeared on May 1, 2008
This Article
Right arrow Author Manuscript (PDF)
Right arrow All Versions of this Article:
149/5/2168    most recent
Author Manuscript (PDF)
Right arrow Purchase Article
Right arrow View Shopping Cart
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 Request Copyright Permission
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Mouillet, J.-F.
Right arrow Articles by Sadovsky, Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Mouillet, J.-F.
Right arrow Articles by Sadovsky, Y.

Submitted on September 7, 2007
Accepted on January 25, 2008

DP103 (Ddx20) is essential for early embryonic development and modulates ovarian morphology and function

Jean-François Mouillet, Xiaomei Yan, Qinglin Ou, Lingling Jin, Louis J. Muglia, Peter A. Crawford, and Yoel Sadovsky*

Department of Obstetrics and Gynecology, Department of Cell Biology and Physiology, Department of Pediatrics, Department of Molecular Biology and Pharmacology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA

* To whom correspondence should be addressed. E-mail: ysadovsky{at}mwri.magee.edu.

The DEAD-box helicase DP103 (Ddx20, Gemin3) is a multifunctional protein that interacts with Epstein-Barr virus nuclear proteins (EBNA2/EBNA3) and is a part of the spliceosomal small nuclear ribonucleoproteins complex. DP103 also aggregates with the microRNA machinery complex. We have previously shown that DP103 interacts with the nuclear receptor steroidogenic factor -1 (SF-1, NR5A1), a key regulator of reproductive development, and represses its transcriptional activity. To further explore the physiological function of DP103 we disrupted the corresponding gene in mice. Homozygous Dp103 null mice die early in embryonic development prior to a four-cell stage. Although heterozygous mice are healthy and fertile, analysis of steroidogenic tissues revealed minor abnormalities in mutant females, including larger ovaries, altered estrous cycle and reduced basal secretion of ACTH. Our data point to diverse functions of murine DP103, with an obligatory role during early embryonic development and also in modulation of steroidogenesis.


Key words: DP103 • Ddx20 • Gemin3 • SF-1 • embryo • ovary







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Endocrinology Endocrine Reviews J. Clin. End. & Metab.
Molecular Endocrinology Recent Prog. Horm. Res. All Endocrine Journals
Copyright © 2008 by The Endocrine Society