Biol Reprod Lalor Postdoctoral Fellowships -- Application Deadline January 15, 2009
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


BOR - Papers in Press, published online ahead of print October 4, 2002.
Biol Reprod 2002, 10.1095/biolreprod.101.002550
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
67/6/1824    most recent
biolreprod.101.002550v1
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 Ohinata, Y.
Right arrow Articles by Mitsui, Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ohinata, Y.
Right arrow Articles by Mitsui, Y.
Agricola
Right arrow Articles by Ohinata, Y.
Right arrow Articles by Mitsui, Y.
Biology of Reproduction 67, 1824-1831 (2002)
DOI: 10.1095/biolreprod.101.002550 © 2002 Society for the Study of Reproduction, Inc.


Male Reproductive Tract

Male-Enhanced Antigen-1 Gene Flanked by Two Overlapping Genes Is Expressed in Late Spermatogenesis1

Yasuhide Ohinataa,b, Shizuyo Sutoua, Masaaki Kondoc, Tomoko Takahashia, and Youji Mitsui2,a,b

a Institute of Molecular & Cell Biology (IMCB), National Institute of Advanced Industrial Science & Technology (AIST), Tsukuba, Ibaraki 305-8566, Japan b Institute of Applied Biochemistry, University of Tsukuba, Tsukuba, Ibaraki 305-0006, Japan c Central Research Institute, Itoham Foods, Inc., Moriya, Ibaraki 302-0104, Japan

The male-enhanced antigen-1 gene (Mea1) was originally isolated from a murine testicular cDNA library using anti-H-Y antigen antisera and was assigned to chromosome 17. On analysis of its structure and expression, we found that the Mea1 genomic sequence is flanked by two other genes: Ppp2r5d present in its 3'-terminus in a tail-to-tail orientation and a novel gene called Peas in its 5'-terminus in a head-to-head orientation. The coding sequences of the two genes embedded in the Mea1 sequence are located on the opposite DNA strands of Mea1. Cap-site analysis of Mea1 revealed that it is transcribed from at least seven sites. Most splice variants of Mea1 were abundantly expressed in the testis; the d-type was weakly expressed in the other tissues. AP-2-binding motifs were detected in the transcription-initiation sites. In situ hybridization and immunohistochemical studies revealed Mea1 expression in pachytene spermatocytes. This expression was most prominent in spermatids and residual bodies. The Mea1 protein was also localized in the cytoplasm of elongated spermatids and residual bodies. Localization of the Mea1 suggests that it may function in the very late stages of spermiogenesis. The possibility that Mea1 is one of the serologically detectable male antigens is discussed.

1 Supported by special research grants to Y.M. from the National Institute of Advanced Industrial Science & Technology and from Tsukuba University.

2 Correspondence: Youji Mitsui, National Institute of Advanced Industrial Science & Technology, Institute of Molecular & Cell Biology, Central 6-5, Higashi 1-1-1, Tsukuba, Ibaraki 305-8566, Japan. FAX: 81 298 61 9498; y-mitsui{at}aist.go.jp







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2002 by the Society for the Study of Reproduction.