scholarly journals Y-chromosome haplogroups and susceptibility to azoospermia factor c microdeletion in an Italian population

2006 ◽  
Vol 44 (3) ◽  
pp. 205-208 ◽  
Author(s):  
B. Arredi ◽  
A. Ferlin ◽  
E. Speltra ◽  
C. Bedin ◽  
D. Zuccarello ◽  
...  
2014 ◽  
Vol 26 (2) ◽  
pp. 307 ◽  
Author(s):  
Byunghyuk Kim ◽  
Wonkyung Lee ◽  
Kunsoo Rhee ◽  
Soo Woong Kim ◽  
Jae-Seung Paick

The azoospermia factor c (AZFc) region of the Y chromosome consists of repetitive amplicons and is therefore highly susceptible to structural rearrangements, such as deletions and duplications. The b2/b3 deletion is a partial AZFc deletion that is conventionally determined by the selective absence of sY1191 in sequence-tagged site polymerase chain reaction (PCR) and is generally believed to retain two of the four deleted in azoospermia (DAZ) genes on the Y chromosome. In the present study we determined the copy number and expression of DAZ genes in sY1191-negative individuals. Using a DAZ dosage PCR assay and Southern blot analysis we evaluated the expression of four DAZ genes in five of six sY1191-negative individuals. Furthermore, cloning and immunoblot analyses revealed that three or more DAZ genes are expressed in sY1191-negative testes with germ cells. The results indicate that the selective absence of sY1191 not only means b2/b3 deletion with two DAZ genes, but also includes another AZFc configuration with four DAZ genes. These results exemplify the prevalence of variations in the AZFc region of the human Y chromosome.


2006 ◽  
Vol 85 (1) ◽  
pp. 229-231 ◽  
Author(s):  
Celia Ravel ◽  
Sandra Chantot-Bastaraud ◽  
Brahim El Houate ◽  
Jacqueline Mandelbaum ◽  
Jean-Pierre Siffroi ◽  
...  

2017 ◽  
Vol 10 (4) ◽  
pp. 256 ◽  
Author(s):  
JenabhaiB Chauhan ◽  
Mili Nailwal

2002 ◽  
pp. 801-806 ◽  
Author(s):  
C Foresta ◽  
A Bettella ◽  
E Moro ◽  
M Rossato ◽  
M Merico ◽  
...  

OBJECTIVE: The DAZ (deleted in azoospermia) gene family on the Y chromosome long arm is the major candidate for the AZFc (azoospermia factor c) phenotype of male infertility and it is expressed only in germ cells. The aim of the study was to assess Sertoli cell function in subjects with AZFc deletions. DESIGN: Case-control, prospective study. METHODS: We have studied six severely oligozoospermic subjects with AZFc-DAZ deletions, and looked whether they responded in terms of inhibin B production to a 1 month FSH treatment. These patients were compared with three groups of patients affected by different spermatogenic alterations not related to deletions on the Y chromosome. RESULTS: Although affected by severe testiculopathy, patients with AZFc-DAZ deletions had only slightly elevated FSH, and normal inhibin B plasma concentrations. Inhibin B responded normally during FSH treatment, supporting the hypothesis that Sertoli cells are not altered. On the contrary, other severe testiculopathies not related to Y chromosome deletions showed high FSH and low inhibin B concentrations, with no response to FSH treatment. In these cases the cause of the spermatogenic defect probably damaged both germ and Sertoli cells. Finally, idiopathic patients with a hormonal status similar to Y-deleted patients (slightly elevated FSH and normal inhibin B concentrations) did not respond to FSH treatment, suggesting that Sertoli cells were already at their maximal functional capability. CONCLUSIONS: These data confirm that Sertoli cell function is not damaged in patients with AZFc-DAZ deletions and that the strong reduction of germ cells does not affect the FSH-inhibin B feedback loop.


2019 ◽  
Vol 60 (3) ◽  
pp. 273-283 ◽  
Author(s):  
Maja Kuzmanovska ◽  
Predrag Noveski ◽  
Marija Terzic ◽  
Toso Plaseski ◽  
Katerina Kubelka-Sabit ◽  
...  

Andrologia ◽  
2016 ◽  
Vol 48 (9) ◽  
pp. 978-982 ◽  
Author(s):  
L. Alimardanian ◽  
K. Saliminejad ◽  
S. Razi ◽  
A. Ahani

Urology ◽  
2017 ◽  
Vol 102 ◽  
pp. 111-115 ◽  
Author(s):  
Yong-Sheng Zhang ◽  
Lin-Lin Li ◽  
Lin-Tao Xue ◽  
Hao Zhang ◽  
Yue-Ying Zhu ◽  
...  

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