Huang Hua, Zhao PengXiang, Arimatsu Kei, Tabeta Koichi, Yamazaki Kazuhisa, Krieg Lara, Fu Emily, Zhang Tian, Du Xin
Department of Medicine, University of California, San Diego, La Jolla, California 92093.
G3 (Bethesda). 2013 Oct 3;3(10):1687-95. doi: 10.1534/g3.113.007013.
Linkage between transmembrane proteins and the spectrin-based cytoskeleton is necessary for membrane elasticity of red blood cells. Mutations of the proteins that mediate this linkage result in various types of hemolytic anemia. Here we report a novel N-ethyl-N-nitrosourea-induced mutation of ankyrin-1, named hema6, which causes hereditary spherocytosis in mice through a mild reduction of protein expression. The causal mutation was traced to a single nucleotide transition located deep into intron 13 of gene Ank1. In vitro minigene splicing assay revealed two abnormally spliced transcripts containing cryptic exons from fragments of Ank1 intron 13. The inclusion of cryptic exons introduced a premature termination codon, which leads to nonsense-mediated decay of the mutant transcripts in vivo. Hence, in homozygous mice, only wild-type ankyrin-1 is expressed, albeit at 70% of the level in wild-type mice. Heterozygotes display a similar hereditary spherocytosis phenotype stemming from intermediate protein expression level, indicating the haploinsufficiency of the mutation. Weakened linkage between integral transmembrane protein, band 3, and underlying cytoskeleton was observed in mutant mice as the result of reduced high-affinity binding sites provided by ankyrin-1. Hema6 is the only known mouse mutant of Ank1 allelic series that expresses full-length canonical ankyrin-1 at a reduced level, a fact that makes it particularly useful to study the functional impact of ankyrin-1 quantitative deficiency.
跨膜蛋白与血影蛋白为基础的细胞骨架之间的连接对于红细胞的膜弹性是必要的。介导这种连接的蛋白质发生突变会导致各种类型的溶血性贫血。在此,我们报告一种由N-乙基-N-亚硝基脲诱导的锚蛋白-1新突变,命名为hema6,它通过轻度降低蛋白质表达在小鼠中引起遗传性球形红细胞增多症。致病突变追溯到位于Ank1基因第13内含子深处的单个核苷酸转换。体外小基因剪接试验揭示了两个异常剪接的转录本,它们包含来自Ank1第13内含子片段的隐蔽外显子。隐蔽外显子的包含引入了一个提前终止密码子,这导致体内突变转录本的无义介导衰变。因此,在纯合小鼠中,仅表达野生型锚蛋白-1,尽管其水平为野生型小鼠的70%。杂合子由于中间蛋白质表达水平而表现出类似的遗传性球形红细胞增多症表型,表明该突变的单倍剂量不足。由于锚蛋白-1提供的高亲和力结合位点减少,在突变小鼠中观察到整合跨膜蛋白带3与下层细胞骨架之间的连接减弱。Hema6是Ank1等位基因系列中唯一已知的小鼠突变体,它以降低的水平表达全长经典锚蛋白-1,这一事实使其对于研究锚蛋白-1定量缺陷的功能影响特别有用。