Source:http://linkedlifedata.com/resource/pubmed/id/10908277
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2000-9-19
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pubmed:abstractText |
Molecular deletions of the Y chromosome long arm are a frequent cause of male infertility. Because these deletions are thought to be inherited from fathers without Y chromosome deletions, the question arises as to whether their relatively high incidence in the male population could be due to the existence of a mosaicism in somatic and/or germinal paternal cells. This study included a total of 181 infertile men, among whom 18 were found to have an abnormal karyotype. In the other 163, polymerase chain reaction (PCR) analysis detected nine (5.5%) Y chromosome microdeletions. Blood, spermatozoa or testicular cells from 47 men (27 oligozoospermia, 20 azoospermia), including six Y-deleted patients, were screened for mosaicism using double target fluorescence in-situ hybridization (FISH) with Y centromeric and deleted in azoospermia (DAZ) gene-specific probes. Results indicated that: (i) percentages of double (intact Y chromosome) or single (deleted Y chromosome) fluorescent signals by FISH were in agreement with PCR data, thus demonstrating the reliability of the method; and (ii) a weak germ cell mosaicism was found in only two oligozoospermic patients, carrying 1.97 and 4.13% respectively of spermatozoa with a deleted Y chromosome. Further studies on larger populations are needed to evaluate precisely the incidence of Y deletion mosaicisms in infertile men.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1360-9947
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
6
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
688-93
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10908277-Chromosome Aberrations,
pubmed-meshheading:10908277-Chromosome Deletion,
pubmed-meshheading:10908277-Humans,
pubmed-meshheading:10908277-In Situ Hybridization, Fluorescence,
pubmed-meshheading:10908277-Infertility, Male,
pubmed-meshheading:10908277-Karyotyping,
pubmed-meshheading:10908277-Male,
pubmed-meshheading:10908277-Mosaicism,
pubmed-meshheading:10908277-Oligospermia,
pubmed-meshheading:10908277-Polymerase Chain Reaction,
pubmed-meshheading:10908277-RNA-Binding Proteins,
pubmed-meshheading:10908277-Spermatozoa,
pubmed-meshheading:10908277-Testis,
pubmed-meshheading:10908277-Y Chromosome
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pubmed:year |
2000
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pubmed:articleTitle |
Y chromosome microdeletions and germinal mosaicism in infertile males.
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pubmed:affiliation |
Service d'Histologie, Biologie de la Reproduction et Cytogénétique et CECOS, Hôpital Tenon, 4 Rue de la Chine, 75020 Paris, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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