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大鼠白细胞介素4基因的进化方面、结构及表达

Evolutionary aspects, structure, and expression of the rat interleukin 4 gene.

作者信息

Richter G, Blankenstein T, Diamantstein T

机构信息

Institut für Immunologie, Klinikum Steglitz, Freie Universität, Berlin, FRG.

出版信息

Cytokine. 1990 May;2(3):221-8. doi: 10.1016/1043-4666(90)90020-t.

DOI:10.1016/1043-4666(90)90020-t
PMID:1983334
Abstract

The rat interleukin 4 (IL 4) gene has been isolated from a genomic lambda phage library by cross-hybridization to the mouse IL 4 cDNA. Like the mouse and human counterparts, it exists as a single copy gene in the genome and consists of four exons. The overall structure of the IL 4 locus seems highly conserved. This is indicated by the low degree of restriction fragment length polymorphism in a number of laboratory and wild mice and by the conservation of the intron size between human, rat, and mouse IL 4 genes. Furthermore, evolutionary conserved elements are the promoter region, the position of cysteine residues and sequence motifs in the 3' untranslated regions that are believed to be involved in destabilization of the mRNA. In contrast, the predicted amino acid sequence of the rat IL 4 gene shows low homology (57%) with the mouse homologue. The divergence between mouse and rat IL 4 genes is even more pronounced in the carboxy-terminal region (47% homology in the last 68 amino acids). The ratio between replacement and silent mutations in the IL 4 genes of different species suggests a complex pattern of selective forces acting on the IL 4 gene, which includes both selection against and for amino acid substitutions in individual positions. The functional identity with IL 4 has been confirmed by expression of the gene and the demonstration of the ability to induce MHC class II antigen expression on spleen cells.

摘要

大鼠白细胞介素4(IL - 4)基因是通过与小鼠IL - 4 cDNA交叉杂交,从基因组λ噬菌体文库中分离得到的。与小鼠和人类的对应基因一样,它在基因组中以单拷贝基因形式存在,由四个外显子组成。IL - 4基因座的整体结构似乎高度保守。这体现在许多实验室小鼠和野生小鼠中限制片段长度多态性程度较低,以及人类、大鼠和小鼠IL - 4基因内含子大小的保守性上。此外,进化保守元件包括启动子区域、半胱氨酸残基的位置以及3'非翻译区的序列基序,这些被认为与mRNA的不稳定有关。相比之下,大鼠IL - 4基因的预测氨基酸序列与小鼠同源物的同源性较低(57%)。小鼠和大鼠IL - 4基因在羧基末端区域的差异更为明显(最后68个氨基酸中的同源性为47%)。不同物种IL - 4基因中替换突变与沉默突变的比例表明,作用于IL - 4基因的选择力模式复杂,其中包括对个别位置氨基酸替换的正向和负向选择。该基因的表达以及诱导脾细胞上MHC II类抗原表达能力的证明,证实了其与IL - 4的功能一致性。

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