Scouras Z G, Milioni D, Yiangou M, Duchêne M, Domdey H
Department of Genetics, School of Biology, Faculty of Science, Aristotelian University of Thessaloniki, Greece.
Curr Genet. 1994 Jan;25(1):84-7. doi: 10.1007/BF00712973.
When the beta 1-, beta 2- and beta 3-tubulin-specific DNAs from Drosophila melanogaster were used as probes to recognize tubulin-specific sequences in the chromosomes of Drosophila auraria, they were found to hybridize to the same polytene band in region 32C of the 2L polytene chromosome. Three overlapping clones were isolated from a lambda EMBL3 genomic library of D. auraria, and they all contain beta-tubulin-specific sequences based on hybridization and partial-sequencing experiments of subcloned fragments. These clones hybridize in situ to the same polytene chromosome band in region 32C and they represent an approximately 35-kb fragment of genomic DNA.
当用来自黑腹果蝇的β1-、β2-和β3-微管蛋白特异性DNA作为探针,来识别金翼果蝇染色体中的微管蛋白特异性序列时,发现它们能与2L多线染色体32C区域的同一条多线带杂交。从金翼果蝇的λEMBL3基因组文库中分离出三个重叠克隆,根据亚克隆片段的杂交和部分测序实验,它们都含有β-微管蛋白特异性序列。这些克隆原位杂交到32C区域的同一条多线染色体带,它们代表了约35kb的基因组DNA片段。