Eichler Evan E, Sankoff David
Department of Genetics, Center for Human Genetics and Center for Computational Genomics, Case Western Reserve University School of Medicine and University Hospitals of Cleveland, Cleveland, OH 44106, USA.
Science. 2003 Aug 8;301(5634):793-7. doi: 10.1126/science.1086132.
Large-scale genome sequencing is providing a comprehensive view of the complex evolutionary forces that have shaped the structure of eukaryotic chromosomes. Comparative sequence analyses reveal patterns of apparently random rearrangement interspersed with regions of extraordinarily rapid, localized genome evolution. Numerous subtle rearrangements near centromeres, telomeres, duplications, and interspersed repeats suggest hotspots for eukaryotic chromosome evolution. This localized chromosomal instability may play a role in rapidly evolving lineage-specific gene families and in fostering large-scale changes in gene order. Computational algorithms that take into account these dynamic forces along with traditional models of chromosomal rearrangement show promise for reconstructing the natural history of eukaryotic chromosomes.
大规模基因组测序正在全面展现塑造真核生物染色体结构的复杂进化力量。比较序列分析揭示了明显随机重排的模式,这些重排穿插着基因组异常快速局部进化的区域。着丝粒、端粒、重复序列和散布重复序列附近的大量细微重排表明了真核生物染色体进化的热点。这种局部染色体不稳定性可能在快速进化的谱系特异性基因家族以及促进基因顺序的大规模变化中发挥作用。考虑到这些动态力量的计算算法以及传统的染色体重排模型,有望重建真核生物染色体的自然历史。