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Copy number polymorphisms are not a common feature of innate immune genes.

机译:拷贝数多态性不是先天免疫基因的普遍特征。

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Extensive copy number polymorphism was recently reported for innate immunity-related alpha-defensin genes DEFA1 and DEFA3 and beta-defensin genes DEFB4, DEFB103, and DEFB104. To establish whether such polymorphisms are a common feature of innate immune genes we used quantitative real-time PCR to determine the copy numbers of seven genes whose products have important innate immune functions. The genes encoding lysozyme, lactoferrin, cathelicidin antimicrobial peptide (hCAP18/LL-37), cathepsin G, bactericidal/permeability-increasing protein, azurocidin (CAP37/heparin-binding protein), and neutrophil elastase were each found to be single copy per haploid genome. These findings, along with the recent observation that defensin genes DEFA4, DEFA5, DEFA6, and DEFB1 are single copy, suggest that copy number polymorphisms are not a common feature of the innate immune genome but are restricted to a small subset of innate immunity-related genes.
机译:最近报道了与先天性免疫相关的α-防御素基因DEFA1和DEFA3以及β-防御素基因DEFB4,DEFB103和DEFB104的广泛拷贝数多态性。为了确定这种多态性是否是先天免疫基因的共同特征,我们使用定量实时PCR来确定其产物具有重要先天免疫功能的七个基因的拷贝数。发现溶菌酶,乳铁蛋白,组织蛋白酶抗菌肽(hCAP18 / LL-37),组织蛋白酶G,杀菌/通透性增强蛋白,天青霉素(CAP37 /肝素结合蛋白)和嗜中性粒细胞弹性蛋白酶的基因每个单倍体均为单拷贝。基因组。这些发现以及最近关于防御素基因DEFA4,DEFA5,DEFA6和DEFB1是单拷贝的观察表明,拷贝数多态性不是先天免疫基因组的共同特征,而是局限于一小部分先天免疫相关基因。

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