Abstract | OBJECTIVE: Defect of some genes related to spermatogenesis may result in male infertility with azoospermia. This study aimed to clone some of the genes. METHODS: Testis tissues from a patient with idiopathic azoospermia and from a normal fathered man were investigated with an improved mRNA differential display approach. RESULTS: Significant difference was observed between the two tissues in gene expression. Five differential expressed sequence-tags (ESTs) were cloned and sequenced. Homology analysis with software advanced BLAST 2.0 showed that one EST shared 100% homology with cosmid L27h9, which located in Huntington's disease region on 4p16.3; the other 4 showed very low homology with sequences in GenBank. CONCLUSION:
Azoospermia has complex genetic heterogeneity. A gene located in Huntington's disease region on 4p16.3 is expressed in human testis during the spermatogenesis, and a loss of its function may associate with azoospermia.
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Authors | J Yang, C Xiao, S Zhang, M Huang, T Fan, Q Xia |
Journal | Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
(Zhonghua Yi Xue Yi Chuan Xue Za Zhi)
Vol. 16
Issue 4
Pg. 220-3
(Aug 1999)
ISSN: 1003-9406 [Print] China |
PMID | 10431046
(Publication Type: English Abstract, Journal Article)
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Chemical References |
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Topics |
- Cloning, Organism
- Humans
- Huntington Disease
(genetics)
- Male
- Oligospermia
(genetics)
- RNA, Messenger
(analysis)
- Sequence Homology, Amino Acid
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