Vidal S, Belouchi A M, Cellier M, Beatty B, Gros P
Department of Biochemistry, McGill University, Montréal, Québéc, Canada.
Mamm Genome. 1995 Apr;6(4):224-30. doi: 10.1007/BF00352405.
The mouse Nramp1 gene was initially identified by positional cloning as a candidate for the host resistance locus Bcg on mouse Chromosome (Chr) 1. Subsequent studies have shown that Nramp is a small gene family of at least three members in the mouse genome. We report the isolation and characterization of a cDNA clone corresponding to the second member of the human NRAMP family, NRAMP2. Predicted amino acid sequence analysis of the NRAMP2 polypeptide identifies a polytopic membrane protein highly homologous to NRAMP1, with 66% identical residues (80% overall homology), resulting in identical predicted secondary structures for the two proteins. Sequence conservation is particularly high in the predicted transmembrane domains (90%), suggesting that these regions play a key role in the structural and functional aspects common to both proteins. As opposed to its NRAMP1 counterpart, whose expression is restricted to phagocytic cells, Northern blotting analyses indicate that NRAMP2 mRNA transcripts are expressed at low levels in all tissues analyzed. Fluorescence in situ hybridization has identified 12q13 as the chromosomal location for human NRAMP2.
小鼠Nramp1基因最初通过定位克隆被鉴定为小鼠1号染色体(Chr)上宿主抗性位点Bcg的候选基因。随后的研究表明,Nramp是小鼠基因组中一个至少由三个成员组成的小基因家族。我们报道了与人类NRAMP家族第二个成员NRAMP2相对应的cDNA克隆的分离和特性分析。对NRAMP2多肽的预测氨基酸序列分析确定了一种与Nramp1高度同源的多结构域膜蛋白,有66%的相同残基(总体同源性为80%),导致这两种蛋白质的预测二级结构相同。在预测的跨膜结构域中序列保守性特别高(90%),表明这些区域在两种蛋白质共有的结构和功能方面起关键作用。与其Nramp1对应物不同,Nramp1的表达仅限于吞噬细胞,Northern印迹分析表明,NRAMP2 mRNA转录本在所有分析的组织中均低水平表达。荧光原位杂交已确定12q13为人NRAMP2的染色体定位。