Sánchez F, Natzle J E, Cleveland D W, Kirschner M W, McCarthy B J
Cell. 1980 Dec;22(3):845-54. doi: 10.1016/0092-8674(80)90561-9.
We have used cloned chicken cDNA sequences for alpha- and beta-tubulin to investigate tubulin gene organization in Drosophila melanogaster. Experiments using genomic Drosophila DNA from several sources indicate that there are at least four copies each of the alpha-tubulin gene and the beta-tubulin gene. In situ hybridization experiments show that both the alpha- and beta-tubulin multigene families have dispersed arrangements on the chromosome. Genes for alpha-tubulin have been localized at chromosomal bands 67C, 84B/C, 84D and 85E, while genes for beta-tubulin have been detected at bands 60A/B and 85D. alpha-Tubulin and beta-tubulin chicken cDNA sequences can be used to select a specific mRNA species from a complex mixture which translates in vitro into alpha- or beta-tubulin protein. RNA blot hybridization using the cloned chicken cDNA sequences as probes shows that the alpha- and beta-tubulin messages detected are clearly different in length, with the message for alpha-tubulin measuring approximately 2000 bases and the message for beta-tubulin containing approximately 1800 bases.
我们利用克隆的鸡α-和β-微管蛋白的cDNA序列来研究黑腹果蝇的微管蛋白基因组织。使用来自多个来源的果蝇基因组DNA进行的实验表明,α-微管蛋白基因和β-微管蛋白基因各自至少有四个拷贝。原位杂交实验表明,α-和β-微管蛋白多基因家族在染色体上呈分散排列。α-微管蛋白基因定位于染色体带67C、84B/C、84D和85E,而β-微管蛋白基因在带60A/B和85D处被检测到。鸡α-微管蛋白和β-微管蛋白的cDNA序列可用于从复杂混合物中选择特定的mRNA种类,该混合物在体外可翻译成α-或β-微管蛋白。使用克隆的鸡cDNA序列作为探针进行的RNA印迹杂交表明,检测到的α-和β-微管蛋白信使在长度上明显不同,α-微管蛋白信使约为2000个碱基,β-微管蛋白信使约含1800个碱基。