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 December 15, 2004.
Biol Reprod 2004, 10.1095/biolreprod.104.035964
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
72/4/780    most recent
biolreprod.104.035964v1
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 Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Oyhenart, J.
Right arrow Articles by Raich, N.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Oyhenart, J.
Right arrow Articles by Raich, N.
Agricola
Right arrow Articles by Oyhenart, J.
Right arrow Articles by Raich, N.
BIOLOGY OF REPRODUCTION 72, 780–787 (2005)
DOI: 10.1095/biolreprod.104.035964
© 2005 by the Society for the Study of Reproduction, Inc.

Putative Homeodomain Transcription Factor 1 Interacts with the Feminization Factor Homolog Fem1b in Male Germ Cells1

J. Oyhenart3,4, S. Benichou4, and N. Raich2,4

INSERM U.567 CNRS-UMR 8104, Département d'Hématologie, Maternité de Port-Royal4 Département de Maladies Infectieuses, Institut Cochin,5 Université René Descartes, 75014 Paris, France

The Phtf1 gene encodes a membrane protein abundantly expressed in male germinal cells. Using a two-hybrid screening procedure we have identified FEM1B, an ortholog of the C. elegans feminization factor 1 (FEM-1), as a binding partner for PHTF1. We studied FEM1B expression in the rodent testis and found that Fem1b mRNA is present at high levels during meiosis and after, during spermiogenesis, in a similar manner to Phtf1 mRNA. Accordingly, Western blot and immunofluorescence revealed the presence of PHTF1 and FEM1B in the same cell types, and by coimmunoprecipitation we demonstrated the association between these proteins. We characterized some aspects of this interaction and showed that the ANK domain of FEM1B is necessary for the interaction with the amino extremity of PHTF1. Next, we found that FEM1B can bind several intracellular organelles and demonstrated that PHTF1 would recruit FEM1B to the endoplasmic reticulum membrane. Previous in vitro experiments had suggested that the human FEM1B was involved in apoptosis. After comparing expression profiles of FEM1B and PHTF1 with apoptotic events occurring in the normal seminiferous tubules, we suggest that neither FEM1B nor PHTF1 are directly implicated in apoptosis in this tissue.

1 This work was supported by INSERM and CNRS, and by CONICET and FRM grants to J.O.

2 Correspondence: Natacha Raich, INSERM U 567-UMR 8104, 123 boulevard de Port-Royal, 75014 Paris, France. FAX: 33 01 4325 1167; raich{at}infobiogen.fr

3 Current address: UCSF Comprehensive Cancer Center, San Francisco, CA







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2005 by the Society for the Study of Reproduction.