Watanabe H, Fujiyama A, Hattori M, Taylor T D, Toyoda A, Kuroki Y, Noguchi H, BenKahla A, Lehrach H, Sudbrak R, Kube M, Taenzer S, Galgoczy P, Platzer M, Scharfe M, Nordsiek G, Blöcker H, Hellmann I, Khaitovich P, Pääbo S, Reinhardt R, Zheng H-J, Zhang X-L, Zhu G-F, Wang B-F, Fu G, Ren S-X, Zhao G-P, Chen Z, Lee Y-S, Cheong J-E, Choi S-H, Wu K-M, Liu T-T, Hsiao K-J, Tsai S-F, Kim C-G, OOta S, Kitano T, Kohara Y, Saitou N, Park H-S, Wang S-Y, Yaspo M-L, Sakaki Y
RIKEN, Genomic Sciences Center, Yokohama 230-0045, Japan.
Nature. 2004 May 27;429(6990):382-8. doi: 10.1038/nature02564.
Human-chimpanzee comparative genome research is essential for narrowing down genetic changes involved in the acquisition of unique human features, such as highly developed cognitive functions, bipedalism or the use of complex language. Here, we report the high-quality DNA sequence of 33.3 megabases of chimpanzee chromosome 22. By comparing the whole sequence with the human counterpart, chromosome 21, we found that 1.44% of the chromosome consists of single-base substitutions in addition to nearly 68,000 insertions or deletions. These differences are sufficient to generate changes in most of the proteins. Indeed, 83% of the 231 coding sequences, including functionally important genes, show differences at the amino acid sequence level. Furthermore, we demonstrate different expansion of particular subfamilies of retrotransposons between the lineages, suggesting different impacts of retrotranspositions on human and chimpanzee evolution. The genomic changes after speciation and their biological consequences seem more complex than originally hypothesized.
人类与黑猩猩的比较基因组研究对于缩小与人类独特特征(如高度发达的认知功能、双足行走或复杂语言的使用)相关的基因变化范围至关重要。在此,我们报告了黑猩猩22号染色体3330万个碱基对的高质量DNA序列。通过将整个序列与人类对应的21号染色体进行比较,我们发现该染色体除了近68000个插入或缺失外,还有1.44%由单碱基替换组成。这些差异足以在大多数蛋白质中产生变化。实际上,在231个编码序列(包括功能重要的基因)中,83%在氨基酸序列水平上存在差异。此外,我们证明了在这两个谱系中逆转录转座子特定亚家族的不同扩增,这表明逆转录转座对人类和黑猩猩进化有不同影响。物种形成后的基因组变化及其生物学后果似乎比最初假设的更为复杂。