Stanyon R, Rocchi M, Capozzi O, Roberto R, Misceo D, Ventura M, Cardone M F, Bigoni F, Archidiacono N
Department of Animal Biology and Genetics, Laboratory of Anthropology, Via del Proconsolo 12, 50122, Florence, Italy.
Chromosome Res. 2008;16(1):17-39. doi: 10.1007/s10577-007-1209-z.
In 1992 the Japanese macaque was the first species for which the homology of the entire karyotype was established by cross-species chromosome painting. Today, there are chromosome painting data on more than 50 species of primates. Although chromosome painting is a rapid and economical method for tracking translocations, it has limited utility for revealing intrachromosomal rearrangements. Fortunately, the use of BAC-FISH in the last few years has allowed remarkable progress in determining marker order along primate chromosomes and there are now marker order data on an array of primate species for a good number of chromosomes. These data reveal inversions, but also show that centromeres of many orthologous chromosomes are embedded in different genomic contexts. Even if the mechanisms of neocentromere formation and progression are just beginning to be understood, it is clear that these phenomena had a significant impact on shaping the primate genome and are fundamental to our understanding of genome evolution. In this report we complete and integrate the dataset of BAC-FISH marker order for human syntenies 1, 2, 4, 5, 8, 12, 17, 18, 19, 21, 22 and the X. These results allowed us to develop hypotheses about the content, marker order and centromere position in ancestral karyotypes at five major branching points on the primate evolutionary tree: ancestral primate, ancestral anthropoid, ancestral platyrrhine, ancestral catarrhine and ancestral hominoid. Current models suggest that between-species structural rearrangements are often intimately related to speciation. Comparative primate cytogenetics has become an important tool for elucidating the phylogeny and the taxonomy of primates. It has become increasingly apparent that molecular cytogenetic data in the future can be fruitfully combined with whole-genome assemblies to advance our understanding of primate genome evolution as well as the mechanisms and processes that have led to the origin of the human genome.
1992年,日本猕猴成为首个通过跨物种染色体涂染确定其整个核型同源性的物种。如今,已有超过50种灵长类动物的染色体涂染数据。尽管染色体涂染是追踪易位的一种快速且经济的方法,但在揭示染色体内重排方面其效用有限。幸运的是,过去几年中细菌人工染色体荧光原位杂交(BAC-FISH)技术的应用使得在确定灵长类染色体上标记顺序方面取得了显著进展,现在已经有了一系列灵长类物种许多染色体的标记顺序数据。这些数据揭示了倒位现象,同时也表明许多直系同源染色体的着丝粒嵌入在不同的基因组环境中。即便新着丝粒形成和进化的机制才刚刚开始被理解,但很明显这些现象对塑造灵长类基因组产生了重大影响,并且对于我们理解基因组进化至关重要。在本报告中,我们完善并整合了人类同源染色体1、2、4、5、8、12、17、18、19、21、22以及X染色体的BAC-FISH标记顺序数据集。这些结果使我们能够针对灵长类进化树上五个主要分支点的祖先核型中的内容、标记顺序和着丝粒位置提出假设:灵长类祖先、类人猿祖先、阔鼻猴祖先、狭鼻猴祖先和人猿总科祖先。当前模型表明,物种间的结构重排通常与物种形成密切相关。比较灵长类细胞遗传学已成为阐明灵长类系统发育和分类学的重要工具。越来越明显的是,未来分子细胞遗传学数据可以与全基因组组装有效地结合起来,以推进我们对灵长类基因组进化以及导致人类基因组起源的机制和过程的理解。