Identification of meiotic anomalies with multiplex fluorescence in situ hybridization

To characterize meiotic anomalies in infertile men by multiplex fluorescence in situ hybridization (M-FISH) and to determine whether synaptic problems affect specific bivalents or whether anomalies are random. Analysis of meiotic preparations with standard techniques and M-FISH. Assisted reproductio...

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Detalhes bibliográficos
Autores: Sarrate Navas, Zaida|||0000-0001-9677-1376, Blanco, Joan|||0000-0003-0647-3856, Egozcue, Susana, Vidal, Francesca|||0000-0002-0985-7348, Egozcue, Josep
Formato: artículo
Fecha de publicación:2004
País:España
Recursos:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:288845
Acesso em linha:https://ddd.uab.cat/record/288845
https://dx.doi.org/urn:doi:10.1016/j.fertnstert.2004.02.122
Access Level:acceso abierto
Palavra-chave:Meiosis
Chromosome reorganizations
Multiplex FISH
Synaptic anomalies
Descrição
Resumo:To characterize meiotic anomalies in infertile men by multiplex fluorescence in situ hybridization (M-FISH) and to determine whether synaptic problems affect specific bivalents or whether anomalies are random. Analysis of meiotic preparations with standard techniques and M-FISH. Assisted reproduction centers and Universitat Autònoma de Barcelona. Three fertile men undergoing vasectomy, four sterile patients with oligoasthenoteratozoospermia, and one patient with a Robertsonian translocation t(13;14). Unilateral testicular biopsy in controls and patients with oligoasthenoteratozoospermia and collection of a semen sample from the translocation carrier. Identification of bivalents in metaphase I and chromosomes in metaphase II and characterization of chromosome abnormalities. All bivalents in metaphase I and all chromosomes in metaphase II could be identified. In controls and in one patient with oligoasthenoteratozoospermia, meiosis was normal. Other patients with oligoasthenoteratozoospermia showed different types of anomaly: desynapsis, breaks, precocious XY separation, or cryptic reorganizations. The Robertsonian translocation t(13;14) was easily identified. Results confirm the high incidence of synaptic errors in oligoasthenoteratozoospermia patients. Bivalents in metaphase I and chromosomes in metaphase II were individually identifiable. Nondisjunctional errors or small reorganizations overlooked in classic meiotic preparations were identified. Synaptic anomalies seem to affect meiotic bivalents at random. © 2004 by American Society for Reproductive Medicine.