黑腹果蝇reca样基因cDNA及基因组DNA的克隆。

Idengaku zasshi Pub Date : 1994-12-01 DOI:10.1266/jjg.69.663
E Akaboshi, Y Inoue, H Ryo
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引用次数: 27

摘要

从黑胃果蝇中分离到与酵母DMC1和RAD51基因同源的cDNA。酿酒酵母的DMC1和RAD51基因分别在减数分裂和减数分裂和有丝分裂过程中起着至关重要的作用,它们的基因产物彼此同源,并与大肠杆菌的RecA蛋白同源。这里克隆的cDNA包含一个开放的阅读框,编码336个氨基酸。对相应的基因组DNA片段进行序列分析,发现编码区与DMC1基因一样存在一个短内含子,而在RAD51基因中不存在。通过对唾液腺染色体的原位杂交,将reca样基因定位在第三条染色体的99D上。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cloning of the cDNA and genomic DNA that correspond to the recA-like gene of Drosophila melanogaster.

We have isolated a cDNA homologous to the yeast DMC1 and RAD51 genes from Drosophila melanogaster. The DMC1 and RAD51 genes of Saccharomyces cerevisiae are known to play crucial roles during meiosis and during both meiosis and mitosis, respectively, and their gene products are homologous to each other and to the RecA protein of Escherichia coli. The cDNA cloned here contains an open reading frame that encodes 336 amino acids. Sequence analysis of the corresponding genomic DNA fragment showed one short intron existing in the coding region as in the DMC1 gene, but not in the RAD51 gene. By in situ hybridization to the salivary gland chromosomes, the recA-like gene was cytologically mapped to 99D of the third chromosome.

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