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邓氏果蝇中Adh-Adhr的部分特征及进化

Partial characterization and evolution of Adh-Adhr in Drosophila dunni.

作者信息

Colón-Parrilla Wilma V, Pérez-Chiesa Ivette

机构信息

Department of Biological Sciences, Faculty of General Studies, University of Puerto Rico, San Juan, P.R 00931-3323, USA.

出版信息

Biochem Genet. 2007 Apr;45(3-4):225-38. doi: 10.1007/s10528-006-9067-5. Epub 2007 Feb 28.

Abstract

We sequenced 2123 bp of the Adh-Adhr genomic region of Drosophila dunni of the cardini group from two cloned DNA PCR fragments and from two cDNA clones of an Adh transcript. This comprises the Adh coding region and introns, 3' UTR, intergenic sequence, and most of Adhr, which is 260 bp downstream of Adh. Both genes have the typical Drosophila melanogaster Adh structure of three exons and two introns, except for changes in the putative 8 bp sequence involved in downregulation within the 3' UTR of Adh. Two amino acid substitutions could explain the low activity previously reported for this enzyme in D. dunni: Thr --> Lys at position 191 and Val --> Thr at position 189. D. dunni's Adh has the lowest codon bias reported so far for Drosophila species, and based on analysis of the nucleotide substitution rate, it is less conserved than Adhr.

摘要

我们从两个克隆的DNA PCR片段和一个乙醇脱氢酶(Adh)转录本的两个互补DNA(cDNA)克隆中,对果蝇属卡迪尼组邓氏果蝇(Drosophila dunni)的Adh-Adhr基因组区域的2123碱基对进行了测序。这包括Adh编码区和内含子、3'非翻译区(UTR)、基因间序列,以及Adhr的大部分区域,Adhr位于Adh下游260碱基对处。除了Adh的3' UTR中参与下调的假定8碱基序列发生变化外,这两个基因都具有典型的黑腹果蝇(Drosophila melanogaster)Adh结构,即三个外显子和两个内含子。两个氨基酸取代可以解释先前报道的该酶在邓氏果蝇中活性较低的原因:第191位的苏氨酸(Thr)变为赖氨酸(Lys),第189位的缬氨酸(Val)变为苏氨酸(Thr)。邓氏果蝇的Adh具有迄今为止报道的果蝇物种中最低的密码子偏好性,并且根据核苷酸替代率分析,它比Adhr的保守性更低。

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