College of Dentistry, Alkharj University, Alkharj, Kingdom of Saudi Arabia, India.
Eur J Hum Genet. 2011 Jan;19(1):23-9. doi: 10.1038/ejhg.2010.151. Epub 2010 Sep 8.
Microdeletions in azoospermia factor (AZF) region on distal Yq are associated with male infertility and spermatogenic failure due to intra-chromosomal homologous recombination between large nearly identical repeat amplicons and are found in ∼10% of azoospermic and severe oligozoospermic cases. Although AZFc is deleted in azoospermia or oligozoospermia, no definitive conclusion has been drawn for the role of partial AZFc deletions to spermatogenic failure. Therefore, this study is planned to investigate the role of gr/gr subdeletions in individuals with spermatogenic failure and to find its relationship with Y chromosome haplogroups (HGs) in infertile men from Indian population. It is a case-control study involving 236 azoospermic, 182 oligospermic and 240 healthy normozoospermic men. We found 18 gr/gr, 11 b1/b3 and 2 b2/b3 subdeletions in azoospermic patients and 12 gr/gr, 5 b1/b3 and 4 b2/b3 subdeletions in oligospermic patients. However, we also found seven gr/gr deletions in normozoospermic men. Seven patients each with spermatogenic arrest and oligospermia who carry gr/gr subdeletions have deleted DAZ3/DAZ4 genes. A total of 11 patients with sertoli cell-only syndrome (SCOS) and 5 oligospermic patients with gr/gr subdeletions also have DAZ1/DAZ2 genes deleted indicating that deletions of DAZ genes contributed differently to damage to spermatogenic process. L1 HG is found in patients showing b1/b3 subdeletions, whereas HG H1a2 and H1b were found in normozoospermic individuals with gr/gr subdeletions. Our results provide evidence of association between the occurrence of subdeletions and male infertility as well as the severity of the spermatogenic failure.
Y 染色体远端无精子因子(AZF)区的微缺失与染色体内部同源重组导致的大近同源重复扩增子之间的男性不育和生精失败有关,在无精子症和严重少精子症病例中约占 10%。虽然 AZFc 在无精子症或严重少精子症中缺失,但对于部分 AZFc 缺失对生精失败的作用尚未得出明确结论。因此,本研究计划研究 gr/gr 亚缺失在生精失败个体中的作用,并在印度人群中寻找其与 Y 染色体单倍群(HGs)的关系。这是一项涉及 236 名无精子症、182 名少精子症和 240 名健康正常精子症男性的病例对照研究。我们在无精子症患者中发现了 18 个 gr/gr、11 个 b1/b3 和 2 个 b2/b3 亚缺失,在少精子症患者中发现了 12 个 gr/gr、5 个 b1/b3 和 4 个 b2/b3 亚缺失。然而,我们也在正常精子症男性中发现了 7 个 gr/gr 缺失。7 名具有 gr/gr 亚缺失的生精阻滞和少精子症患者均缺失了 DAZ3/DAZ4 基因。总共 11 名患有唯支持细胞综合征(SCOS)和 5 名具有 gr/gr 亚缺失的少精子症患者也缺失了 DAZ1/DAZ2 基因,表明 DAZ 基因缺失对生精过程的损害程度不同。L1 HG 存在于具有 b1/b3 亚缺失的患者中,而 HG H1a2 和 H1b 存在于具有 gr/gr 亚缺失的正常精子症个体中。我们的结果提供了证据表明亚缺失的发生与男性不育以及生精失败的严重程度有关。