Fan Yuxin, Linardopoulou Elena, Friedman Cynthia, Williams Eleanor, Trask Barbara J
Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA.
Genome Res. 2002 Nov;12(11):1651-62. doi: 10.1101/gr.337602.
Human chromosome 2 was formed by the head-to-head fusion of two ancestral chromosomes that remained separate in other primates. Sequences that once resided near the ends of the ancestral chromosomes are now interstitially located in 2q13-2q14.1. Portions of these sequences had duplicated to other locations prior to the fusion. Here we present analyses of the genomic structure and evolutionary history of >600 kb surrounding the fusion site and closely related sequences on other human chromosomes. Sequence blocks that closely flank the inverted arrays of degenerate telomere repeats marking the fusion site are duplicated at many, primarily subtelomeric, locations. In addition, large portions of a 168-kb centromere-proximal block are duplicated at 9pter, 9p11.2, and 9q13, with 98%-99% average sequence identity. A 67-kb block on the distal side of the fusion site is highly homologous to sequences at 22qter. A third ~100-kb segment is 96% identical to a region in 2q11.2. By integrating data on the extent and similarity of these paralogous blocks, including the presence of phylogenetically informative repetitive elements, with observations of their chromosomal distribution in nonhuman primates, we infer the order of the duplications that led to their current arrangement. Several of these duplicated blocks may be associated with breakpoints of inversions that occurred during primate evolution and of recurrent chromosome rearrangements in humans.
人类2号染色体是由两条在其他灵长类动物中保持独立的祖先染色体头对头融合而成。曾经位于祖先染色体末端附近的序列现在位于2q13 - 2q14.1的间隙位置。这些序列的部分在融合之前已复制到其他位置。在这里,我们展示了对融合位点周围超过600 kb的基因组结构和进化历史以及其他人类染色体上密切相关序列的分析。紧邻标记融合位点的退化端粒重复序列反向阵列侧翼的序列块在许多主要是亚端粒的位置被复制。此外,一个168 kb着丝粒近端块的大部分在9pter、9p11.2和9q13处被复制,平均序列同一性为98% - 99%。融合位点远端的一个67 kb块与22qter处的序列高度同源。第三个约100 kb的片段与2q11.2中的一个区域有96% 的同一性。通过整合这些旁系同源块的范围和相似性数据,包括系统发育信息丰富的重复元件的存在,以及它们在非人类灵长类动物中的染色体分布观察结果,我们推断出导致它们当前排列的复制顺序。这些复制块中的几个可能与灵长类动物进化过程中发生的倒位断点以及人类反复出现的染色体重排有关。