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Molecular Human Reproduction, Vol. 6, No. 3, 207-214, March 2000
© 2000 European Society of Human Reproduction and Embryology


Testis and spermatozoa

The size of the CAG repeat in exon 1 of the androgen receptor gene shows no significant relationship to impaired spermatogenesis in an infertile Caucasoid sample of German origin

S. Dadze1,6, C. Wieland1,2, S. Jakubiczka3, K. Funke4, E. Schröder2, B. Royer-Pokora2, R. Willers5 and P.F. Wieacker3

1 Centre for Reproductive Medicine, Graf-Salm Straße 8, D-50181 Bedburg, 2 Institute of Human Genetics and Anthropology, University of Düsseldorf, Universitätsstraße 1, D-40225 Düsseldorf, 3 Institute of Human Genetics, University of Magdeburg, Leipziger Straße 44, D-39120 Magdeburg, 4 Institute of Medical Statistics, Information Technology and Epidemiology, University of Cologne, Josef-Stelzmann Str. 9, D-50931 Cologne and 5 Computer Science Department, University of Düsseldorf, Universitätsstraße 1, D-40225 Düsseldorf, Germany

Abstract

The androgen receptor (AR) gene, located on the X-chromosome at Xq11-12, contains in exon 1 a polymorphic CAG repeat which codes for a polyglutamine tract. Contractions of the CAG repeat are said to be related to prostate cancer. In contrast, sizeable expansion of the CAG repeat can cause spinal and bulbar muscular atrophy (SBMA). In infertile patients of Chinese origin and in a Melbourne multinational population impaired sperm production has been postulated to be related to moderate expansions of the polyglutamine tract. In a study of a Swedish population of infertile patients these findings could not be corroborated. The aim of our investigation was to examine the correlation between the length of the CAG repeat and impaired sperm production in an infertile Caucasoid patient sample of German ethnic origin. We found no statistically significant relationship between the size of the CAG repeat or polyglutamine tract and idiopathic impaired sperm production in the population studied. The variability of the results by various investigators may be attributed to different ethnic origins and hence different genetic modifiers of the populations studied and/or to the high probability that these infertile males may represent a heterogeneous group with respect to the causes of defective spermatogenesis.

androgen receptor gene/CAG repeat/defective spermatogenesis/male infertility

Notes

6 To whom correspondence should be addressed


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