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通过基因组精细定位对猿类和人类进行共线性比较。

Synteny comparison between apes and human using fine-mapping of the genome.

作者信息

de Pontbriand Alexandra, Wang Xiao-Ping, Cavaloc Yvon, Mattei Marie-Geneviève, Galibert Francis

机构信息

UMR 6061 CNRS Génétiques & Développement, Faculté de Médecine, Rennes, France.

出版信息

Genomics. 2002 Oct;80(4):395-401. doi: 10.1006/geno.2002.6847.

Abstract

Comparing the genomes of the great apes and human should provide novel information concerning the origins of humankind. Relative to the great apes, the human karyotype has one fewer chromosome pair, as human chromosome 2 derived from the telomeric fusion of two ancestral primate chromosomes. To identify the genomic rearrangements that accompanied human speciation, we initiated a comparative study between human, chimpanzee, and gorilla. Using the HAPPY mapping method, an acellular adaptation of the radiation hybrid method, we mapped a few hundred markers on the human, chimpanzee, and gorilla genomes. This allowed us to identify several chromosome rearrangements, in particular a pericentric inversion and a translocation. We precisely localized the synteny breakpoint that led to the formation of human chromosome 2. This breakpoint was confirmed by FISH mapping.

摘要

比较大猩猩和人类的基因组应该能提供有关人类起源的新信息。相对于大猩猩,人类的核型少了一对染色体,因为人类的2号染色体是由两条原始灵长类染色体的端粒融合而成的。为了确定伴随人类物种形成的基因组重排,我们启动了一项人类、黑猩猩和大猩猩之间的比较研究。我们使用HAPPY定位法(辐射杂种法的一种无细胞适应方法)在人类、黑猩猩和大猩猩基因组上定位了数百个标记。这使我们能够识别出几种染色体重排,特别是一个臂间倒位和一个易位。我们精确地定位了导致人类2号染色体形成的同线性断点。这个断点通过荧光原位杂交定位得到了证实。

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