Juan E, Papaceit M, Quintana A
Department de Genètica, Universitat de Barcelona, Spain.
J Mol Evol. 1994 May;38(5):455-67. doi: 10.1007/BF00178845.
The region of the genome of D. lebanonensis that contains the Adh gene and the downstream Adh-dup gene was sequenced. The structure of the two genes is the same as has been described for D. melanogaster. Adh has two promoters and Adh-dup has only one putative promoter. The levels of expression of the two genes in this species are dramatically different. Hybridizing the same Northern blots with a specific probe for Adh-dup, we did not find transcripts for this gene in D. lebanonensis. The level of Adh distal transcript in adults of D. lebanonensis is five times greater than that of D. melanogaster adults. The maximum levels of proximal transcript are attained at different larval stages in the two species, being three times higher in D. melanogaster late-second-instar larvae than in D. lebanonensis first-instar larvae. The level of Adh transcripts allowed us to determine distal and proximal initiation transcription sites, the position of the first intron, the use of two polyadenylation signals, and the heterogeneity of polyadenylation sites. Temporal and spatial expression profiles of the Adh gene of D. lebanonensis show qualitative differences compared with D. melanogaster. Adh and Adh-dup evolve differently as shown by the synonymous and nonsynonymous substitution rates for the coding region of both genes when compared across two species of the melanogaster group, two of the obscura group of the subgenus Sophophora and D. lebanonensis of the victoria group of the subgenus Scaptodrsophila. Synonymous rates for Adh are approximately half those for Adh-dup, while nonsynonymous rates for Adh are generally higher than those for Adh-dup. Adh shows 76.8% identities at the protein level and 70.2% identities at the nucleotide level while Adh-dup shows 83.7% identities at the protein level and 67.5% identities at the nucleotide level. Codon usage for Adh-dup is shown to be less biased than for Adh, which could explain the higher synonymous rates and the generally lower nonsynonymous substitution rates in Adh-dup compared with Adh. Phylogenetic trees reconstructed by distance matrix and parsimony methods show that Sophophora and Scaptodrosophila subgenera diverged shortly after the separation from the Drosophila subgenus.
对黎巴嫩果蝇基因组中包含乙醇脱氢酶(Adh)基因和下游Adh - dup基因的区域进行了测序。这两个基因的结构与黑腹果蝇中所描述的相同。Adh有两个启动子,而Adh - dup只有一个推定启动子。这两个基因在该物种中的表达水平差异显著。用针对Adh - dup的特异性探针与相同的Northern印迹杂交,我们在黎巴嫩果蝇中未发现该基因的转录本。黎巴嫩果蝇成虫中Adh远端转录本的水平比黑腹果蝇成虫高五倍。两种果蝇近端转录本的最高水平在不同幼虫阶段达到,黑腹果蝇二龄后期幼虫中的水平比黎巴嫩果蝇一龄幼虫中的高两倍。Adh转录本的水平使我们能够确定远端和近端起始转录位点、第一个内含子的位置、两个聚腺苷酸化信号的使用以及聚腺苷酸化位点的异质性。与黑腹果蝇相比,黎巴嫩果蝇Adh基因的时空表达谱显示出质的差异。当在黑腹果蝇组的两个物种、Sophophora亚属的obscura组的两个物种以及Scaptodrsophila亚属的victoria组的黎巴嫩果蝇之间进行比较时,Adh和Adh - dup的进化方式不同,这通过两个基因编码区的同义替换率和非同义替换率得以体现。Adh的同义替换率约为Adh - dup的一半,而Adh的非同义替换率通常高于Adh - dup。Adh在蛋白质水平上显示76.8%的同一性,在核苷酸水平上显示70.2%的同一性,而Adh - dup在蛋白质水平上显示83.7%的同一性,在核苷酸水平上显示67.5%的同一性。结果表明,Adh - dup的密码子使用偏好性低于Adh,这可以解释与Adh相比,Adh - dup中较高的同义替换率和通常较低的非同义替换率。通过距离矩阵和简约法重建的系统发育树表明,Sophophora亚属和Scaptodrosophila亚属在与Drosophila亚属分离后不久就分化了。