Impaired male fertility and atrophy of seminiferous tubules caused by haploinsufficiency for Foxa3

• Published in: Developmental biology 2007-06, Vol.306 (2), p.636-645
• Main Authors: Behr, Rüdiger, Sackett, Sara D., Bochkis, Irina M., Le, Phillip Phuc, Kaestner, Klaus H.
• Format: Article
• Language: English
• Subjects: Animals; Antigens, Neoplasm - metabolism; Base Sequence; Fertility; Foxa3; Haploinsufficiency; Hepatocyte Nuclear Factor 3-gamma - genetics; Hepatocyte Nuclear Factor 3-gamma - metabolism; Hepatocyte Nuclear Factor 3-gamma - physiology; Infertility, Male - genetics; Kallikreins; Leydig cell; Leydig Cells - metabolism; Male; Mice; Mice, Inbred C57BL; Mice, Transgenic; Molecular Sequence Data; Nerve Tissue Proteins - metabolism; Paracrine signalling; RNA, Messenger - metabolism; Seminiferous Tubules - pathology; Sequence Homology, Nucleic Acid; Sertoli cell; Spermatids - metabolism; Spermatogenesis; Testis; Winged helix transcription factor
• ISSN: 0012-1606; 1095-564X
• DOI: 10.1016/j.ydbio.2007.03.525

Foxa1, 2 and 3 (formerly HNF-3α, -β and -γ) constitute a sub-family of winged helix transcription factors with multiple roles in mammalian organ development. While all three Foxa mRNAs are present in endoderm derivatives including liver and pancreas, only Foxa3 is expressed in the testis. Here we demonstrate by genetic lineage tracing that Foxa3 is expressed in postmeiotic germ and interstitial Leydig cells. The germinal epithelium of Foxa3-deficient testes is characterized by a loss of germ cells secondary to an increase in germ cell apoptosis that ultimately leads to a Sertoli cell-only syndrome. Remarkably, not only the Foxa3 −/− mice but also Foxa3 +/− mice exhibited loss of germ cells. This cellular phenotype caused significantly reduced fertility and testis weight of both Foxa3 −/− and Foxa3 +/− mice. Using microarray analysis, we found a dramatic downregulation of the zinc finger protein 93 and the testicular tumor-associated paraneoplastic Ma antigen (PNMA) and increased expression of a number of genes including zinc finger protein 94 and several kallikrein 1-related peptidases which could account for at least part of the observed phenotype. In summary, we have identified Foxa3 as a transcriptional regulator with a dominant phenotype in germ cell maintenance and suggest FOXA3 as a potential candidate gene for subfertility in man.