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非人灵长类动物中米勒 - 迪克尔、史密斯 - 马吉尼斯和RARA基因座的染色体定位:对人类17号染色体进化的启示

Chromosome mapping of Miller-Diecker, Smith-Magenis and RARA loci in non-human primates: implications in the evolution of human chromosome 17.

作者信息

Sineo Luca, Romagno Daniela, Guarducci Silvia, Lapini Manuela, Giovannucci-Uzielli Maria Luisa, Chiarelli Brunetto

机构信息

Dipartimento di Biologia animale, Università degli Studi di Palermo, Italy.

出版信息

Genetica. 2002 Apr;114(3):275-80. doi: 10.1023/a:1016226213603.

Abstract

Molecular cytogenetics allows to verify chromosomal homologies previously hypothesised on the base of banding pattern comparison in different species. So far only the chromosome painting technique has been extensively used in studies of chromosomal evolution. This technique allows to detect only interchromosomal rearrangements. Human and Great Apes chromosomes basically differ by intrachromosomal rearrangements, in particular inversions; with chromosome painting it has just been possible to confirm the origin by fusion of human chromosome 2 and a reciprocal translocation in Gorilla, involving the homologous of chromosome 5 and 17. In order to verify intrachromosomal rearrangements in human chromosomal evolution, chromosome mapping of human loci in non-human primates is a useful approach. We mapped Miller-Diecker, Smith-Magenis and RARA loci localised on human chromosome 17, in Gorilla gorilla, Pongo pygmaeus, Macaca fascicularis and Cercopithecus aethiops. On the base of the obtained results it was possible to verify chromosomal rearrangements previously identified by banding, to achieve new informations about the controversial evolution of human chromosome 17, and to detect the occurrence of a paracentric inversion in the homologous in Cercopithecus aethiops.

摘要

分子细胞遗传学能够验证先前基于不同物种带型模式比较而假设的染色体同源性。到目前为止,只有染色体涂染技术在染色体进化研究中得到了广泛应用。该技术仅能检测染色体间的重排。人类和大猩猩的染色体基本差异在于染色体内重排,尤其是倒位;通过染色体涂染,仅能证实人类2号染色体由融合产生的起源以及大猩猩中涉及5号和17号染色体同源物的相互易位。为了验证人类染色体进化中的染色体内重排,在非人类灵长类动物中对人类基因座进行染色体定位是一种有用的方法。我们在大猩猩、红毛猩猩、食蟹猴和埃塞俄比亚猕猴中对位于人类17号染色体上的米勒 - 迪克克、史密斯 - 马吉尼斯和RARA基因座进行了定位。根据所得结果,有可能验证先前通过带型鉴定的染色体重排,获取有关人类17号染色体有争议进化的新信息,并检测到埃塞俄比亚猕猴同源染色体中发生的臂内倒位。

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