Characterisation of the human central MHC gene, BAT1: genomic structure and expression.

R J Allcock, P Price, S Gaudieri, C Leelayuwat, C S Witt, R L Dawkins
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引用次数: 18

Abstract

The BAT1 gene (D6S81E) encodes a member of the DEAD-box family of RNA-binding proteins, and lies in the central MHC. This region contains genes which affect susceptibility to immunopathological diseases. A 14-kb section of the human MHC containing the BAT1 gene and a further 5-kb telomeric of BAT1 was sequenced using DNA from individuals homozygous for HLA-A1, B8, DR3 and HLA- A1, B57, DR7. Analysis of our sequences and the previously reported human cDNA sequence showed that the expressed sequence of the 8.1 and 57.1 haplotypes is identical with only minor substitutions in the introns. Phylogenetic analysis suggests BAT1 may be a translation initiation factor. Screening of cells and tissues for BAT1 mRNA suggests an abundant member of a family of proteins expressed in multiple cell types, notably macrophages and hepatocytes. Expression was independent of MHC haplotype, consistent with the lack of sequence polymorphism.

人类中心MHC基因BAT1的特征:基因组结构和表达。
BAT1基因(D6S81E)编码rna结合蛋白DEAD-box家族的一个成员,位于MHC中心。该区域包含影响免疫病理疾病易感性的基因。利用HLA-A1、B8、DR3和HLA-A1、B57、DR7纯合个体的DNA,对含有BAT1基因的14kb人MHC片段和BAT1基因的5kb端粒进行了测序。结果表明,8.1和57.1单倍型的表达序列完全相同,内含子中只有少量的替换。系统发育分析表明BAT1可能是翻译起始因子。细胞和组织中BAT1 mRNA的筛选表明,BAT1 mRNA是一个在多种细胞类型中表达的蛋白家族的丰富成员,特别是巨噬细胞和肝细胞。表达与MHC单倍型无关,与序列多态性缺失一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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