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牛免疫球蛋白λ轻链恒定区IGLC基因的特征分析

Characterization of the bovine immunoglobulin lambda light chain constant IGLC genes.

作者信息

Chen Limei, Li Min, Li Qing, Yang Xingyuan, An Xiaorong, Chen Yongfu

机构信息

State Key Laboratory for Agrobiotechnology, College of Biological Sciences, China Agricultural University, Beijing 100094, China.

出版信息

Vet Immunol Immunopathol. 2008 Aug 15;124(3-4):284-94. doi: 10.1016/j.vetimm.2008.04.012. Epub 2008 Apr 22.

Abstract

To characterize the bovine immunoglobulin lambda light chain constant region (IGLC) genes, we have isolated a bacterial artificial chromosome (BAC) clone by a PCR based approach from a bovine genomic DNA library, constructed using a genital ridge cell line derived from a male Holstein fetus. The positive BAC clone, containing the bovine IGLC genes, was fully sequenced and had a 138 kb insert. Sequence analysis revealed that the bovine immunoglobulin lambda light chain locus consisted of four joining-constant gene recombination units spanning approximately 20 kb DNA in length. A detailed examination of the recombination signal sequences, RNA splicing sites and coding sequences of the four joining-constant gene recombination units suggested that only two IGLC genes (IGLC2 and IGLC3) were functional while the IGLC1 and IGLC4 appeared to be pseudogenes. This conclusion was further confirmed by a series of RT-PCR amplifications, which also showed that among these four genes the IGLC3 was preferentially expressed in cattle. Phylogenetic analysis indicated that the bovine IGLC genes were more closely related to their equivalents in sheep and goats than that to other mammals.

摘要

为了表征牛免疫球蛋白λ轻链恒定区(IGLC)基因,我们采用基于PCR的方法从牛基因组DNA文库中分离出一个细菌人工染色体(BAC)克隆,该文库是使用来自雄性荷斯坦胎儿的生殖嵴细胞系构建的。包含牛IGLC基因的阳性BAC克隆经过了全序列测定,其插入片段长度为138 kb。序列分析表明,牛免疫球蛋白λ轻链基因座由四个连接恒定基因重组单元组成,跨度约为20 kb的DNA。对这四个连接恒定基因重组单元的重组信号序列、RNA剪接位点和编码序列进行详细检查后发现,只有两个IGLC基因(IGLC2和IGLC3)具有功能,而IGLC1和IGLC4似乎是假基因。一系列逆转录聚合酶链反应(RT-PCR)扩增进一步证实了这一结论,这些扩增还表明,在这四个基因中,IGLC3在牛中优先表达。系统发育分析表明,牛IGLC基因与其在绵羊和山羊中的对应基因的关系比与其他哺乳动物中的对应基因更为密切。

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