Koehler U, Bigoni F, Wienberg J, Stanyon R
Institute of Anthropology and Human Genetics, Munich, Germany.
Genomics. 1995 Nov 20;30(2):287-92. doi: 10.1006/geno.1995.9875.
We employed fluorescence in situ hybridization (FISH) of specific DNA libraries of all human chromosomes to establish homologies between the human karyotype and the karyotype of Hylobates concolor (2n = 52). Numerous intra- and interchromosomal rearrangements have led to a massive reorganization in the karyotype of H. concolor. There have been a minimum of 31 translocations. The 25 H. concolor autosomes are composed of 63-67 recognizable segments that show DNA homology to regions of the 22 human autosomes. Only 1 autosome, homologous to human chromosome 21, has not been involved in translocations. We compared the gene mapping data for H. concolor with our in situ hybridization and found that in most cases these data are confirmed by our results. H. concolor presents a case in a primate closely related to humans, in which chromosome morphology and synteny are highly disturbed in a manner similar to that encountered in rodents.
我们采用对所有人类染色体的特定DNA文库进行荧光原位杂交(FISH)的方法,来确定人类核型与白掌长臂猿(2n = 52)核型之间的同源性。大量的染色体内和染色体间重排导致了白掌长臂猿核型的大规模重组。至少发生了31次易位。白掌长臂猿的25条常染色体由63 - 67个可识别的片段组成,这些片段与22条人类常染色体区域显示出DNA同源性。只有1条与人类21号染色体同源的常染色体未参与易位。我们将白掌长臂猿的基因图谱数据与我们的原位杂交结果进行了比较,发现大多数情况下这些数据得到了我们结果的证实。白掌长臂猿是与人类密切相关的灵长类动物中的一个例子,其染色体形态和同线性受到高度干扰,方式类似于在啮齿动物中所遇到的情况。