Zhang F, Li Z, Wen B, Jiang J, Shao M, Zhao Y, He Y, Song X, Qian J, Lu D, Jin L
State Key Laboratory of Genetic Engineering and Center for Anthropological Studies, School of Life Sciences, Fudan University, Shanghai, China.
Ann Hum Genet. 2006 May;70(Pt 3):304-13. doi: 10.1111/j.1529-8817.2005.00231.x.
The gene families in the AZFc region of the Y chromosome have been shown to be functionally important in human spermatogenesis. The gr/gr deletion, a partial AZFc deletion that reduces the copy numbers of all the AZFc gene families, was identified as a significant risk factor for spermatogenic impairment in Dutch, Spanish and Italians. However, the presence of this deletion in healthy French and Germans questioned its importance in male infertility. In this study, we have shown that the gr/gr deletion does not render an increased risk in Han Chinese. In fact, the gr/gr deletion is frequent (about 8%) in our survey of 886 East Asians from 8 ethnic groups. Furthermore, the DAZ1/DAZ2 deletion has been detected as the primary subtype of the gr/gr deletion in East Asians, though this doublet has been considered as crucial for normal spermatogenesis in Europeans. The different spermatogenic effects of various types of the partial AZFc deletion suggest that the functional difference between AZFc gene copies is a likely cause of inconsistent associations of the gr/gr deletion with spermatogenic impairment across populations.
Y染色体AZFc区域的基因家族已被证明在人类精子发生过程中具有重要功能。gr/gr缺失是一种部分AZFc缺失,它会减少所有AZFc基因家族的拷贝数,在荷兰人、西班牙人和意大利人中,该缺失被确定为精子发生受损的一个重要风险因素。然而,健康的法国人和德国人中存在这种缺失,这对其在男性不育中的重要性提出了质疑。在本研究中,我们表明gr/gr缺失在汉族人群中并不会增加风险。事实上,在我们对来自8个民族的886名东亚人的调查中,gr/gr缺失很常见(约8%)。此外,DAZ1/DAZ2缺失已被检测为东亚人中gr/gr缺失的主要亚型,尽管这种双重缺失在欧洲人眼中被认为对正常精子发生至关重要。各种类型的部分AZFc缺失产生的不同精子发生效应表明,AZFc基因拷贝之间的功能差异可能是导致gr/gr缺失在不同人群中与精子发生受损的关联不一致的原因。