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MBC in Press, published online ahead of print January 12, 2004
Mol. Biol. Cell 10.1091/mbc.E03-10-0762

A more recent version of this article appeared on March 1, 2004
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Submitted on October 24, 2003
Revised on December 1, 2003
Accepted on December 1, 2003

Expression profiling of mammalian male meiosis and gametogenesis identifies novel candidate genes for roles in the regulation of fertility

Ulrich Schlecht1, Philippe Demougin2, Reinhold Koch2, Leandro Hermida3, Christa Wiederkehr3, Patrick Descombes4, Charles Pineau5, Bernard Jégou5, and Michael Primig3*

1 Biozentrum & Swiss Institute of Bioinformatics; Klingelbergstrasse 50-70; 4056 Basel; Switzerland,these authors contributed equally
2 Biozentrum & Swiss Institute of Bioinformatics; Klingelbergstrasse 50-70; 4056 Basel; Switzerland, these authors contributed equally
3 Biozentrum & Swiss Institute of Bioinformatics; Klingelbergstrasse 50-70; 4056 Basel; Switzerland
4 Genomics Platform, NCCR Frontiers in Genetics, Université de Genève/CMU, 1, rue Michel-Servet, 1211 Geneva, Switzerland
5 GERM-INSERM U. 435, Université de Rennes I, Campus de Beaulieu, 35042 Rennes cedex - Bretagne, France

* Corresponding author. E-mail address: michael.primig{at}unibas.ch.

We report a comprehensive large-scale expression profiling analysis of mammalian male germ cells undergoing mitotic growth, meiosis and gametogenesis using High Density Oligonucleotide Microarrays and highly enriched cell populations. Among 11955 rat loci investigated, 1268 were identified as differentially transcribed in germ cells at subsequent developmental stages as compared with total testis, somatic Sertoli cells as well as brain and skeletal muscle controls. The loci were organized into four expression clusters that correspond to somatic, mitotic, meiotic and postmeiotic cell types. This work provides information about expression patterns of ~200 genes known to be important during male germ cell development. Approximately 40 of those are included in a group of 121 transcripts for which we report germ cell expression and lack of transcription in three somatic control cell types. Moreover, we demonstrate the testicular expression and transcriptional induction in mitotic, meiotic and/or postmeiotic germ cells of 293 as yet uncharacterized transcripts some of which are likely to encode factors involved in spermatogenesis and fertility. This group also contains numerous potential germ cell specific targets for innovative contraceptives. A graphical display of the data is conveniently accessible through the GermOnline database at http://www.germonline.org.




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