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Baboon immunoglobulin constant region heavy chains: identification of four IGHG genes

机译:狒狒免疫球蛋白恒定区重链:四个IGHG基因的鉴定

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The increasing use of nonhuman primate models in biomedical research and especially in vaccine development requires the characterization of their immunoglobulin genes and corresponding products. Therefore, we sequenced, cloned and characterized the four immunoglobulin gamma chain constant region genes (IGHG) present in baboons. These four genes were designated IGHG1, IGHG2, IGHG3 and IGHG4 on the basis of sequence similarities with the four human genes encoding the IgG1, IgG2, IgG3 and IgG4 subclasses and the three known rhesus macaque IGHG genes. Specifically, the baboon IgG1, IgG2, IgG3 and IgG4 sequences exhibit 90.3%, 88.3%, 86.7% and 89.6% amino acid identity to their human counterpart. The percent of amino acid identity of baboon IgG1, IgG2 and IgG3 to the corresponding rhesus macaque sequences is 98.5, 93.1 and 94.4, respectively. Therefore, baboon and rhesus macaque IGHG genes are highly homologous to each other. The majority of differences existing between baboon and human sequences are clustered in the hinge region, with the upper hinge being the most diverse and containing several proline residues. Similar to rhesus macaques, the hinge regions of all baboon IGHG genes consist of a single exon, whereas in humans the IgG3 molecule is encoded by multiple exons. These results confirm the evolutionary instability of the hinge region and indicate that functional properties associated with the hinge regions of baboon and human IgG molecules might differ between the two species.
机译:非人类灵长类动物模型在生物医学研究中,尤其是在疫苗开发中的使用日益增加,要求对其免疫球蛋白基因和相应产物进行表征。因此,我们测序,克隆和表征狒狒中存在的四个免疫球蛋白γ链恒定区基因(IGHG)。根据与编码IgG1,IgG2,IgG3和IgG4亚类的四个人类基因以及三个已知的恒河猴IGHG基因的序列相似性,将这四个基因命名为IGHG1,IGHG2,IGHG3和IGHG4。具体地说,狒狒IgG1,IgG2,IgG3和IgG4序列与其人类对应物具有90.3%,88.3%,86.7%和89.6%的氨基酸同一性。狒狒IgG1,IgG2和IgG3与相应的猕猴序列的氨基酸同一性百分比分别为98.5、93.1和94.4。因此,狒狒和恒河猴的IGHG基因彼此高度同源。狒狒和人类序列之间存在的大多数差异集中在铰链区,上部铰链最多样化,并包含几个脯氨酸残基。与猕猴类似,所有狒狒IGHG基因的铰链区均由单个外显子组成,而在人类中,IgG3分子由多个外显子编码。这些结果证实了铰链区的进化不稳定性,并表明与狒狒和人IgG分子的铰链区相关的功能特性在这两个物种之间可能有所不同。

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