Literature DB >> 12477514

Clinical relevance of partial AZFc deletions.

Jan W A de Vries1, Sjoerd Repping, Saskia K M van Daalen, Cindy M Korver, Nico J Leschot, Fulco van der Veen.   

Abstract

To determine the number of DAZ gene clusters in the Y-bearing spermatozoa of patients who underwent intracytoplasmic sperm injection (ICSI) and to compare the outcome with the number of clusters found in the spermatozoa of normospermic men. Prospective study. Academic hospital.Forty-seven patients with impaired spermatogenesis who were attending our clinic for ICSI and 56 semen donors. Peripheral blood was drawn to obtain somatic DNA for polymerase chain reaction (PCR) analysis and leukocytes for karyotyping and FISH analysis. Three-color FISH was performed on the spermatozoa remaining after ICSI and on the spermatozoa of semen donors to determine the presence of the X and Y chromosome as well as the number of DAZ gene clusters. Number of DAZ gene clusters in Y-bearing spermatozoa. Five patients had only one DAZ gene cluster, one patient had a complete AZFc deletion, and one patient had three clusters on average. One of the semen donors also showed three DAZ gene clusters in his Y-bearing spermatozoa. None of the semen donors had only one DAZ gene cluster. Besides complete AZFc deletions, partial deletions are also associated with impaired spermatogenesis. As a result, these partial deletions that are not recognized by routine PCR are reintroduced into the population by the ICSI technique.

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Year:  2002        PMID: 12477514     DOI: 10.1016/s0015-0282(02)04390-x

Source DB:  PubMed          Journal:  Fertil Steril        ISSN: 0015-0282            Impact factor:   7.329


  6 in total

1.  No partial DAZ deletions but frequent gene conversion events on the Y chromosome of fertile men.

Authors:  Anne Claire Lepretre; Catherine Patrat; Michael Mitchell; Pierre Jouannet; Thierry Bienvenu
Journal:  J Assist Reprod Genet       Date:  2005-04       Impact factor: 3.412

2.  Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility.

Authors:  N Machev; N Saut; G Longepied; P Terriou; A Navarro; N Levy; M Guichaoua; C Metzler-Guillemain; P Collignon; A-M Frances; J Belougne; E Clemente; J Chiaroni; C Chevillard; C Durand; A Ducourneau; N Pech; K McElreavey; M-G Mattei; M J Mitchell
Journal:  J Med Genet       Date:  2004-11       Impact factor: 6.318

3.  Association of partial AZFc region deletions with spermatogenic impairment and male infertility.

Authors:  A Ferlin; A Tessari; F Ganz; E Marchina; S Barlati; A Garolla; B Engl; C Foresta
Journal:  J Med Genet       Date:  2005-03       Impact factor: 6.318

4.  Quantitative PCR technique for the identification of microrearrangements of the AZFc region.

Authors:  Virginie Rozé; Jean Luc Bresson; Florence Fellmann
Journal:  J Assist Reprod Genet       Date:  2007-04-05       Impact factor: 3.412

5.  High frequencies of Non Allelic Homologous Recombination (NAHR) events at the AZF loci and male infertility risk in Indian men.

Authors:  Deepa Selvi Rani; Singh Rajender; Kadupu Pavani; Gyaneshwer Chaubey; Avinash A Rasalkar; Nalini J Gupta; Mamta Deendayal; Baidyanath Chakravarty; Kumarasamy Thangaraj
Journal:  Sci Rep       Date:  2019-04-18       Impact factor: 4.379

6.  Early detection of Y chromosome microdeletions in infertile men is helpful to guide clinical reproductive treatments in southwest of China.

Authors:  Ting Liu; Yu-Xin Song; Yong-Mei Jiang
Journal:  Medicine (Baltimore)       Date:  2019-02       Impact factor: 1.817

  6 in total

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