杂交牛CD14基因的分子特征及SNP检测。

Molecular biology international Pub Date : 2011-01-01 Epub Date: 2011-10-25 DOI:10.4061/2011/507346
Aruna Pal, Arjava Sharma, T K Bhattacharya, P N Chatterjee, A K Chakravarty
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引用次数: 41

摘要

CD14是先天免疫的一个重要分子,可以对抗多种病原体。本文对杂交牛(Bos indicus×Bos taurus)的CD14基因进行了鉴定。CD14 cDNA的克隆和序列分析显示,全长1119个核苷酸的开放阅读框编码373个氨基酸蛋白和20个氨基酸信号肽。CB牛CD14基因与相应的哺乳动物同源基因具有较高的核苷酸同源性(59.3-98.1%)。在系统发育分析中,牛和水牛似乎是从一个共同的祖先分化出来的。在CB牛CD14基因中,新报道了包含17个氨基酸变化的25个snp,并检测到了突变热点位点。非同义取代超过同义取代表明该蛋白在家畜中通过正选择进化而来。根据氨基酸序列预测的蛋白质结构表明,CB牛CD14分子具有马蹄形结构。预测了LPS结合位点、LPS信号位点、富亮氨酸重复序列位点、推测的n -链糖基化位点、o -链糖基化位点、糖基磷脂酰肌醇锚位点、二硫桥、α螺旋、β链、富亮氨酸核输出信号位点、亮氨酸拉链位点和结构域连接位点。大多数亮氨酸和半胱氨酸残基在整个物种中保持保守。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Molecular Characterization and SNP Detection of CD14 Gene of Crossbred Cattle.

Molecular Characterization and SNP Detection of CD14 Gene of Crossbred Cattle.

Molecular Characterization and SNP Detection of CD14 Gene of Crossbred Cattle.

Molecular Characterization and SNP Detection of CD14 Gene of Crossbred Cattle.

CD14 is an important molecule for innate immunity that can act against a wide range of pathogens. The present paper has characterized CD14 gene of crossbred (CB) cattle (Bos indicus×Bos taurus). Cloning and sequence analysis of CD14 cDNA revealed 1119 nucleotide long open reading frame encoding 373 amino acids protein and 20 amino acids signal peptide. CB cattle CD14 gene exhibited a high percentage of nucleotide identity (59.3-98.1%) with the corresponding mammalian homologs. Cattle and buffalo appear to have diverged from a common ancestor in phylogenetic analysis. 25 SNPs with 17 amino acid changes were newly reported and the site for mutational hot-spot was detected in CB cattle CD14 gene. Non-synonymous substitutions exceeding synonymous substitutions indicate the evolution of this protein through positive selection among domestic animals. Predicted protein structures obtained from deduced amino acid sequence indicated CB cattle CD14 molecule to be a receptor with horse shoe-shaped structure. The sites for LPS binding, LPS signalling, leucine-rich repeats, putative N-linked glycosylation, O-linked glycosylation, glycosyl phosphatidyl inositol anchor, disulphide bridges, alpha helix, beta strand, leucine rich nuclear export signal, leucine zipper and domain linker were predicted. Most of leucine and cysteine residues remain conserved across the species.

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