Schmid M, Ott G, Haaf T, Scheres J M
Hum Genet. 1985;71(4):342-50. doi: 10.1007/BF00388461.
Lymphocyte cultures from man, gorilla, and chimpanzee were treated with 5-azacytidine and 5-azadeoxycytidine. These cytidine analogues induce common fragile sites in the chromosome bands 1q42 and 19q13 of man. A rare fragile site is induced by 5-azadeoxycytidine in the band 1q24. The optimum conditions required for inducing these new fragile sites were determined by a series of experiments. The common fragile site in human chromosome 1q42 also exists in the gorilla and chimpanzee in the homologous band 1p32. The fragile site in human chromosome 19q13 was demonstrated in the gorilla in the homologous chromosome band 20q13. These are the first examples found of evolutionary highly conserved fragile sites in homologous chromosome bands in related primate species. The interaction between 5-azacytidine, 5-azadeoxycytidine, and chromosomal DNA; the evolutionary conservation of genes located within or closely adjacent to the fragile sites in the chromosome 1 of Hominoidea; and the phylogenetic origin of the two new common fragile sites are discussed.
对来自人类、大猩猩和黑猩猩的淋巴细胞培养物用5-氮杂胞苷和5-氮杂脱氧胞苷进行处理。这些胞苷类似物在人类染色体带1q42和19q13中诱导常见的脆性位点。5-氮杂脱氧胞苷在带1q24中诱导出一个罕见的脆性位点。通过一系列实验确定了诱导这些新的脆性位点所需的最佳条件。人类染色体1q42中的常见脆性位点在大猩猩和黑猩猩的同源带1p32中也存在。人类染色体19q13中的脆性位点在大猩猩的同源染色体带20q13中得到证实。这些是在相关灵长类物种的同源染色体带中发现的进化上高度保守的脆性位点的首个例子。讨论了5-氮杂胞苷、5-氮杂脱氧胞苷与染色体DNA之间的相互作用;类人猿染色体1中脆性位点内或紧邻脆性位点的基因的进化保守性;以及两个新的常见脆性位点的系统发生起源。