Literature DB >> 11098026

Sex chromosome mosaicism in males carrying Y chromosome long arm deletions.

J P Siffroi1, C Le Bourhis, C Krausz, S Barbaux, L Quintana-Murci, S Kanafani, H Rouba, L Bujan, G Bourrouillou, I Seifer, D Boucher, M Fellous, K McElreavey, J P Dadoune.   

Abstract

Microdeletions of the long arm of the Y chromosome (Yq) are a common cause of male infertility. Since large structural rearrangements of the Y chromosome are commonly associated with a 45,XO/46,XY chromosomal mosaicism, we studied whether submicroscopic Yq deletions could also be associated with the development of 45,XO cell lines. We studied blood samples from 14 infertile men carrying a Yq microdeletion as revealed by polymerase chain reaction (PCR). Patients were divided into two groups: group 1 (n = 6), in which karyotype analysis demonstrated a 45,X/46,XY mosaicism, and group 2 (n = 8) with apparently a normal 46,XY karyotype. 45,XO cells were identified by fluorescence in-situ hybridization (FISH) using X and Y centromeric probes. Lymphocytes from 11 fertile men were studied as controls. In addition, sperm cells were studied in three oligozoospermic patients in group 2. Our results showed that large and submicroscopic Yq deletions were associated with significantly increased percentages of 45,XO cells in lymphocytes and of sperm cells nullisomic for gonosomes, especially for the Y chromosome. Moreover, two isodicentric Y chromosomes, classified as normal by cytogenetic methods, were detected. Therefore, Yq microdeletions may be associated with Y chromosomal instability leading to the formation of 45,XO cell lines.

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Year:  2000        PMID: 11098026     DOI: 10.1093/humrep/15.12.2559

Source DB:  PubMed          Journal:  Hum Reprod        ISSN: 0268-1161            Impact factor:   6.918


  14 in total

Review 1.  Mosaic loss of human Y chromosome: what, how and why.

Authors:  Xihan Guo; Xueqin Dai; Tao Zhou; Han Wang; Juan Ni; Jinglun Xue; Xu Wang
Journal:  Hum Genet       Date:  2020-02-04       Impact factor: 4.132

2.  Evaluation of chromosomal abnormalities and Y-chromosome microdeletions in 1696 Turkish cases with primary male infertility: A single-center study.

Authors:  Taha Reşid Özdemir; Berk Özyılmaz; Özgür Çakmak; Özge Özer Kaya; Can Köse; Özgür Kırbıyık; Mehmet Zeynel Keskin; Altuğ Koç; Tuğba Zeyrek; Yaşar Bekir Kutbay; Kadri Murat Erdoğan; Merve Saka Güvenç
Journal:  Turk J Urol       Date:  2019-11-29

Review 3.  Spermatogenic failure and the Y chromosome.

Authors:  C Krausz; E Casamonti
Journal:  Hum Genet       Date:  2017-04-29       Impact factor: 4.132

Review 4.  Novel concepts in male factor infertility: clinical and laboratory perspectives.

Authors:  Sandro C Esteves
Journal:  J Assist Reprod Genet       Date:  2016-07-16       Impact factor: 3.412

Review 5.  Clinical management of infertile men with nonobstructive azoospermia.

Authors:  Sandro C Esteves
Journal:  Asian J Androl       Date:  2015 May-Jun       Impact factor: 3.285

Review 6.  EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions: state-of-the-art 2013.

Authors:  C Krausz; L Hoefsloot; M Simoni; F Tüttelmann
Journal:  Andrology       Date:  2014-01       Impact factor: 3.842

7.  Examination of Y-Chromosomal Microdeletions and Partial Microdeletions in Idiopathic Infertility in East Hungarian Patients.

Authors:  Attila Mokánszki; Anikó Ujfalusi; Éva Gombos; István Balogh
Journal:  J Hum Reprod Sci       Date:  2018 Oct-Dec

Review 8.  A comprehensive review of genetics and genetic testing in azoospermia.

Authors:  Alaa J Hamada; Sandro C Esteves; Ashok Agarwal
Journal:  Clinics (Sao Paulo)       Date:  2013       Impact factor: 2.365

9.  Screening of Y chromosome microdeletions in 46,XY partial gonadal dysgenesis and in patients with a 45,X/46,XY karyotype or its variants.

Authors:  Ana Paula dos Santos; Juliana Gabriel Ribeiro Andrade; Cristiane Santos Cruz Piveta; Juliana de Paulo; Gil Guerra; Maricilda Palandi de Mello; Andréa Trevas Maciel-Guerra
Journal:  BMC Med Genet       Date:  2013-11-05       Impact factor: 2.103

10.  Gonadoblastoma with Dysgerminoma in a Phenotypically Turner-Like Girl with 45,X/46,XY Karyotype.

Authors:  Özge Yüce; Esra Döğer; Nurullah Çelik; Hamdi Cihan Emeksiz; Mahmut Orhun Çamurdan; Aysun Bideci; Peyami Cinaz
Journal:  J Clin Res Pediatr Endocrinol       Date:  2015-12
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