Walensky L D, Shi Z T, Blackshaw S, DeVries A C, Demas G E, Gascard P, Nelson R J, Conboy J G, Rubin E M, Snyder S H, Mohandas N
Department of Neuroscience The Johns Hopkins School of Medicine Baltimore, Maryland 21205, USA.
Curr Biol. 1998 Nov 19;8(23):1269-72. doi: 10.1016/s0960-9822(07)00536-2.
The erythrocyte membrane cytoskeletal protein 4.1 (4.1R) is a structural protein that confers stability and flexibility to erythrocytes via interactions with the cytoskeletal proteins spectrin and F-actin and with the band 3 and glycophorin C membrane proteins. Mutations in 4.1R can cause hereditary elliptocytosis, a disease characterized by a loss of the normal discoid morphology of erythrocytes, resulting in hemolytic anemia [1]. Different isoforms of the 4.1 protein have been identified in a wide variety of nonerythroid tissues by immunological methods [2-5]. The variation in molecular weight of these different 4.1 isoforms, which range from 30 to 210 kDa [6], has been attributed to complex alternative splicing of the 4.1R gene [7]. We recently identified two new 4.1 genes: one is generally expressed throughout the body (4. 1G) [8] and the other is expressed in central and peripheral neurons (4.1N) [9]. Here, we examined 4.1R expression by in situ hybridization analysis and found that 4.1R was selectively expressed in hematopoietic tissues and in specific neuronal populations. In the brain, high levels of 4.1R were discretely localized to granule cells in the cerebellum and dentate gyrus. We generated mice that lacked 4.1R expression; these mice had deficits in movement, coordination, balance and learning, in addition to the predicted hematological abnormalities. The neurobehavioral findings are consistent with the distribution of 4.1R in the brain, suggesting that 4.1R performs specific functions in the central nervous system.
红细胞膜细胞骨架蛋白4.1(4.1R)是一种结构蛋白,它通过与细胞骨架蛋白血影蛋白和F-肌动蛋白以及带3和血型糖蛋白C膜蛋白相互作用,赋予红细胞稳定性和柔韧性。4.1R中的突变可导致遗传性椭圆形红细胞增多症,这是一种以红细胞正常盘状形态丧失为特征的疾病,可导致溶血性贫血[1]。通过免疫学方法已在多种非红细胞组织中鉴定出4.1蛋白的不同同工型[2-5]。这些不同的4.1同工型分子量在30至210 kDa之间[6],其分子量变化归因于4.1R基因的复杂可变剪接[7]。我们最近鉴定出两个新的4.1基因:一个在全身普遍表达(4.1G)[8],另一个在中枢和外周神经元中表达(4.1N)[9]。在这里,我们通过原位杂交分析检测了4.1R的表达,发现4.1R在造血组织和特定神经元群体中选择性表达。在大脑中,高水平的4.1R离散地定位于小脑和齿状回的颗粒细胞中。我们培育出缺乏4.1R表达的小鼠;这些小鼠除了有预测的血液学异常外,还存在运动、协调、平衡和学习方面的缺陷。神经行为学研究结果与4.1R在大脑中的分布一致,表明4.1R在中枢神经系统中发挥特定功能。