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Molecular and Cellular Biology, November 2006, p. 8099-8108, Vol. 26, No. 21
0270-7306/06/$08.00+0     doi:10.1128/MCB.01332-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Hspa4l-Deficient Mice Display Increased Incidence of Male Infertility and Hydronephrosis Development{triangledown}

Torsten Held,1 Ilona Paprotta,1 Janchiv Khulan,1 Bernhardt Hemmerlein,2 Lutz Binder,3 Stephan Wolf,1 Stephanie Schubert,4 Andreas Meinhardt,5 Wolfgang Engel,1 and Ibrahim M. Adham1*

Institute of Human Genetics,1 Department of Pathology,2 Department of Clinical Chemistry, University of Göttingen, Göttingen,3 Department of Human Genetics, Hannover Medical School, Hannover,4 Department of Anatomy and Cell Biology, University of Giessen, Giessen, Germany5

Received 20 July 2006/ Accepted 15 August 2006

The Hspa4l gene, also known as Apg1 or Osp94, belongs to the HSP110 heat shock gene family, which includes three genes encoding highly conserved proteins. This study shows that Hspa4l is expressed ubiquitously and predominantly in the testis. The protein is highly expressed in spermatogenic cells, from late pachytene spermatocytes to postmeiotic spermatids. In the kidney, the protein is restricted to cortical segments of distal tubules. To study the physiological role of this gene in vivo, we generated mice deficient in Hspa4l by gene targeting. Hspa4l-deficient mice were born at expected ratios and appeared healthy. However, approximately 42% of Hspa4l–/– male mice suffered from fertility defects. Whereas the seminiferous tubules of Hspa4l–/– testes contained all stages of germ cells, the number of mature sperm in the epididymis and sperm motility were drastically reduced. The reduction of the sperm count was due to the elimination of a significant number of developing germ cells via apoptosis. No defects in fertility were observed in female mutants. In addition, 12% of null mutant mice developed hydronephrosis. Concentrations of plasma and urine electrolytes in Hspa4l–/– mice were similar to wild-type values, suggesting that the renal function was not impaired. However, Hspa4l–/– animals were preferentially susceptible to osmotic stress. These results provide evidence that Hspa4l is required for normal spermatogenesis and suggest that Hspa4l plays a role in osmotolerance.


* Corresponding author. Mailing address: Institute of Human Genetics, Heinrich-Düker-Weg 12, D-37073 Göttingen, Germany. Phone: 49-551-397522. Fax: 49-551-399303. E-mail: iadham{at}gwdg.de.

{triangledown} Published ahead of print on 21 August 2006.


Molecular and Cellular Biology, November 2006, p. 8099-8108, Vol. 26, No. 21
0270-7306/06/$08.00+0     doi:10.1128/MCB.01332-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.




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