Kivisild Toomas
Department of Archaeology and Anthropology, University of Cambridge, Cambridge, CB2 1QH, UK.
Estonian Biocentre, 51010, Tartu, Estonia.
Hum Genet. 2017 May;136(5):529-546. doi: 10.1007/s00439-017-1773-z. Epub 2017 Mar 4.
High throughput sequencing methods have completely transformed the study of human Y chromosome variation by offering a genome-scale view on genetic variation retrieved from ancient human remains in context of a growing number of high coverage whole Y chromosome sequence data from living populations from across the world. The ancient Y chromosome sequences are providing us the first exciting glimpses into the past variation of male-specific compartment of the genome and the opportunity to evaluate models based on previously made inferences from patterns of genetic variation in living populations. Analyses of the ancient Y chromosome sequences are challenging not only because of issues generally related to ancient DNA work, such as DNA damage-induced mutations and low content of endogenous DNA in most human remains, but also because of specific properties of the Y chromosome, such as its highly repetitive nature and high homology with the X chromosome. Shotgun sequencing of uniquely mapping regions of the Y chromosomes to sufficiently high coverage is still challenging and costly in poorly preserved samples. To increase the coverage of specific target SNPs capture-based methods have been developed and used in recent years to generate Y chromosome sequence data from hundreds of prehistoric skeletal remains. Besides the prospects of testing directly as how much genetic change in a given time period has accompanied changes in material culture the sequencing of ancient Y chromosomes allows us also to better understand the rate at which mutations accumulate and get fixed over time. This review considers genome-scale evidence on ancient Y chromosome diversity that has recently started to accumulate in geographic areas favourable to DNA preservation. More specifically the review focuses on examples of regional continuity and change of the Y chromosome haplogroups in North Eurasia and in the New World.
高通量测序方法彻底改变了人类Y染色体变异的研究,它能从世界各地现存人群中数量不断增加的高覆盖度全Y染色体序列数据的背景下,提供从古代人类遗骸中获取的遗传变异的基因组尺度视图。古代Y染色体序列让我们首次得以激动地瞥见基因组中男性特异性区域的过去变异,并有机会基于此前从现存人群遗传变异模式得出的推断来评估模型。对古代Y染色体序列的分析具有挑战性,这不仅是因为与古代DNA研究普遍相关的问题,比如DNA损伤诱导的突变以及大多数人类遗骸中内源性DNA含量较低,还因为Y染色体的特殊性质,比如其高度重复的特性以及与X染色体的高度同源性。在保存不佳的样本中,对Y染色体独特映射区域进行鸟枪法测序以达到足够高的覆盖度仍然具有挑战性且成本高昂。为了提高特定目标单核苷酸多态性(SNP)的覆盖度,近年来已开发并使用了基于捕获的方法,以从数百具史前骨骼遗骸中生成Y染色体序列数据。除了直接测试在给定时间段内遗传变化与物质文化变化相伴程度的前景外,古代Y染色体测序还使我们能够更好地了解随着时间推移突变积累和固定的速率。本综述考虑了最近在有利于DNA保存的地理区域开始积累的关于古代Y染色体多样性的基因组尺度证据。更具体地说,本综述重点关注了欧亚大陆北部和新世界Y染色体单倍群的区域连续性和变化的例子。