McElreavey Ken, Quintana-Murci Lluís
Reproduction, Fertility and Populations, Institut Pasteur, 25 rue du Dr Roux, 75724 Paris Cedex 15, France.
Reprod Biomed Online. 2003 Jul-Aug;7(1):17-23. doi: 10.1016/s1472-6483(10)61723-3.
The human Y chromosome encodes genes that are essential for male sex determination, spermatogenesis and protection against Turner stigmata. In recent years mutations have been identified in Y-chromosome genes associated with these phenotypes and a series of microdeletions of the long arm of the Y have been defined that are specifically associated with male infertility. In parallel, the discovery of polymorphic markers on the Y, comprising of both slow-mutating binary markers and rapidly-mutating microsatellites, has enabled the high resolution definition of a large number of paternal lineages (haplogroups). These Y-chromosome haplogroups have been extensively used to trace population movements and understand human origins and histories, but recently a growing number of association studies have been performed aimed at assessing the relationship between the Y-chromosome background and Y-linked phenotypes such as infertility and male-specific cancers. These preliminary studies, comparing haplogroup distributions between case and control populations, are promising and suggest an association between different Y-chromosome lineages, sperm counts and prostate cancer. However, we highlight the need to extend these studies to other world populations. Increased sample numbers and a better haplogroup resolution using additional binary markers in association studies are necessary. By these approaches novel associations between Y-chromosome haplotypes and disease may be revealed and the degree to which selection is acting on the human Y chromosome may be determined.
人类Y染色体编码的基因对于男性性别决定、精子发生以及预防特纳综合征特征至关重要。近年来,已在与这些表型相关的Y染色体基因中鉴定出突变,并定义了一系列Y染色体长臂的微缺失,这些微缺失与男性不育症特别相关。与此同时,Y染色体上多态性标记的发现,包括缓慢突变的二元标记和快速突变的微卫星,使得能够高分辨率地定义大量父系谱系(单倍群)。这些Y染色体单倍群已被广泛用于追踪人口迁移以及了解人类起源和历史,但最近进行了越来越多的关联研究,旨在评估Y染色体背景与Y连锁表型(如不育症和男性特异性癌症)之间的关系。这些比较病例组和对照组人群中单倍群分布的初步研究很有前景,并表明不同的Y染色体谱系、精子数量和前列腺癌之间存在关联。然而,我们强调需要将这些研究扩展到其他世界人群。在关联研究中增加样本数量并使用额外的二元标记提高单倍群分辨率是必要的。通过这些方法,可能会揭示Y染色体单倍型与疾病之间的新关联,并确定选择作用于人类Y染色体的程度。