Meiotic studies in an azoospermic human translocation (Y;1) carrier.

نویسندگان

  • F Sun
  • M Oliver-Bonet
  • P J Turek
  • E Ko
  • R H Martin
چکیده

A reciprocal translocation between the long arm of the Y chromosome and the long arm of chromosome 1 was observed in an infertile man with non-obstructive azoospermia. The study was performed using a combination of techniques: immunocytogenetic analysis, which allows the detection of synaptonemal complexes (SCs) and recombination sites (MLH1) simultaneously, and fluorescence in-situ hybridization analysis. Meiotic pairing analysis on 100 pachytene spreads showed the presence of a quadrivalent containing chromosomes 1 and Y. There were many abnormalities in chromosome pairing and recombination. These abnormalities included a great reduction of recombination events (as many as one fifth of the SCs had no MLH1 foci), and high proportions of unpaired regions and discontinuities in the SCs. We discuss the possibility that infertility in this patient may be due to transcriptional repression of part of chromosome 1 involved in the translocation, silencing some genes necessary for the progression of meiosis and causing defective meiotic pairing and recombination.

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Abnormal synapses and recombination in an azoospermic male carrier of a reciprocal translocation t(1;21).

OBJECTIVE To study the meiotic abnormalities during prophase I in an azoospermic man with t(1;21) reciprocal translocation. DESIGN Analysis of synapses, recombination, and transcription inactivation in a testicular biopsy sample. SETTING Research laboratory. PATIENT(S) One azoospermic patient with t(1;21) and five men with normal spermatogenesis. INTERVENTION(S) Immunostaining for SCP3,...

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Molecular Dissection Using Array Comparative Genomic Hybridization and Clinical Evaluation of An Infertile Male Carrier of An Unbalanced Y;21 Translocation: A Case Report and Review of The Literature

Chromosomal defects are relatively frequent in infertile men however, translocations between the Y chromosome and autosomes are rare and less than 40 cases of Y-autosome translocation have been reported. In particular, only three individuals has been described with a Y;21 translocation, up to now. We report on an additional case of an infertile man in whom a Y;21 translocation was associated wi...

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عنوان ژورنال:
  • Molecular human reproduction

دوره 11 5  شماره 

صفحات  -

تاریخ انتشار 2005