Repping Sjoerd, van Daalen Saskia K M, Brown Laura G, Korver Cindy M, Lange Julian, Marszalek Janet D, Pyntikova Tatyana, van der Veen Fulco, Skaletsky Helen, Page David C, Rozen Steve
Howard Hughes Medical Institute, Whitehead Institute, and Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA.
Nat Genet. 2006 Apr;38(4):463-7. doi: 10.1038/ng1754. Epub 2006 Feb 26.
Although much structural polymorphism in the human genome has been catalogued, the kinetics of underlying change remain largely unexplored. Because human Y chromosomes are clonally inherited, it has been possible to capture their detailed relationships in a robust, worldwide genealogical tree. Examination of structural variation across this tree opens avenues for investigating rates of underlying mutations. We selected one Y chromosome from each of 47 branches of this tree and searched for large-scale variation. Four chromosomal regions showed extensive variation resulting from numerous large-scale mutations. Within the tree encompassed by the studied chromosomes, the distal-Yq heterochromatin changed length > or = 12 times, the TSPY gene array changed length > or = 23 times, the 3.6-Mb IR3/IR3 region changed orientation > or = 12 times and the AZFc region was rearranged > or = 20 times. After determining the total time spanned by all branches of this tree (approximately 1.3 million years or 52,000 generations), we converted these mutation counts to lower bounds on rates: > or = 2.3 x 10(-4), > or = 4.4 x 10(-4), > or = 2.3 x 10(-4) and > or = 3.8 x 10(-4) large-scale mutations per father-to-son Y transmission, respectively. Thus, high mutation rates have driven extensive structural polymorphism among human Y chromosomes. At the same time, we found limited variation in the copy number of Y-linked genes, which raises the possibility of selective constraints.
尽管人类基因组中许多结构多态性已被编目,但潜在变化的动力学在很大程度上仍未得到探索。由于人类Y染色体是克隆遗传的,因此有可能在一个强大的全球系谱树中捕捉它们的详细关系。检查这棵树上的结构变异为研究潜在突变率开辟了道路。我们从这棵树的47个分支中各选取了一条Y染色体,并搜索大规模变异。四个染色体区域显示出由大量大规模突变导致的广泛变异。在所研究染色体涵盖的树状结构中,Yq远端异染色质长度变化≥12次,TSPY基因阵列长度变化≥23次,3.6 Mb的IR3/IR3区域方向变化≥12次,AZFc区域重排≥20次。在确定了这棵树所有分支所跨越的总时间(约130万年或52000代)后,我们将这些突变计数转换为突变率的下限:每次父子Y染色体传递的大规模突变率分别≥2.3×10⁻⁴、≥4.4×10⁻⁴、≥2.3×10⁻⁴和≥3.8×10⁻⁴。因此,高突变率推动了人类Y染色体之间广泛的结构多态性。与此同时,我们发现Y连锁基因的拷贝数变化有限,这增加了存在选择性限制的可能性。