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地中海实蝇(Ceratitis capitata)中卵黄蛋白原基因簇:双翅目卵黄蛋白及其基因的序列和结构保守性

A cluster of vitellogenin genes in the Mediterranean fruit fly Ceratitis capitata: sequence and structural conservation in dipteran yolk proteins and their genes.

作者信息

Rina M, Savakis C

机构信息

Institute of Molecular Biology and Biotechnology, Foundation of Research and Technology, Heraklion, Crete, Greece.

出版信息

Genetics. 1991 Apr;127(4):769-80. doi: 10.1093/genetics/127.4.769.

Abstract

Four genes encoding the major egg yolk polypeptides of the Mediterranean fruit fly Ceratitis capitata, vitellogenins 1 and 2 (VG1 and VG2), were cloned, characterized and partially sequenced. The genes are located on the same region of chromosome 5 and are organized in pairs, each encoding the two polypeptides on opposite DNA strands. Restriction and nucleotide sequence analysis indicate that the gene pairs have arisen from an ancestral pair by a relatively recent duplication event. The transcribed part is very similar to that of the Drosophila melanogaster yolk protein genes Yp1, Yp2 and Yp3. The Vg1 genes have two introns at the same positions as those in D. melanogaster Yp3; the Vg2 genes have only one of the introns, as do D. melanogaster Yp1 and Yp2. Comparison of the five polypeptide sequences shows extensive homology, with 27% of the residues being invariable. The sequence similarity of the processed proteins extends in two regions separated by a nonconserved region of varying size. Secondary structure predictions suggest a highly conserved secondary structure pattern in the two regions, which probably correspond to structural and functional domains. The carboxy-end domain of the C. capitata proteins shows the same sequence similarities with triacyglycerol lipases that have been reported previously for the D. melanogaster yolk proteins. Analysis of codon usage shows significant differences between D. melanogaster and C. capitata vitellogenins with the latter exhibiting a less biased representation of synonymous codons.

摘要

克隆、鉴定并部分测序了编码地中海实蝇(Ceratitis capitata)主要卵黄多肽的四个基因,即卵黄原蛋白1和2(VG1和VG2)。这些基因位于5号染色体的同一区域,成对排列,每个基因在相反的DNA链上编码两种多肽。限制性酶切和核苷酸序列分析表明,这两个基因对是由一个祖先基因对通过相对较新的复制事件产生的。转录部分与黑腹果蝇(Drosophila melanogaster)卵黄蛋白基因Yp1、Yp2和Yp3的转录部分非常相似。Vg1基因在与黑腹果蝇Yp3相同的位置有两个内含子;Vg2基因只有其中一个内含子,黑腹果蝇的Yp1和Yp2也是如此。对这五种多肽序列的比较显示出广泛的同源性,27%的残基是不变的。加工后蛋白质的序列相似性在两个由大小不同的非保守区域隔开的区域中延伸。二级结构预测表明,这两个区域存在高度保守的二级结构模式,这可能对应于结构域和功能域。地中海实蝇蛋白质的羧基末端结构域与三酰甘油脂肪酶具有相同的序列相似性,这与之前报道的黑腹果蝇卵黄蛋白的情况相同。密码子使用分析表明,黑腹果蝇和地中海实蝇的卵黄原蛋白之间存在显著差异,后者同义密码子的偏向性较小。

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