McMahon A P, Giebelhaus D H, Champion J E, Bailes J A, Lacey S, Carritt B, Henchman S K, Moon R T
Differentiation. 1987;34(1):68-78. doi: 10.1111/j.1432-0436.1987.tb00052.x.
Several overlapping cDNA clones encompassing 2760 nucleotides of the alpha-subunit of a human non-erythroid spectrin (termed fodrin) were isolated from a human lung fibroblast cDNA library. DNA and RNA blot analyses indicated that a single copy alpha-fodrin gene encodes a 9-kb transcript. The cDNA clones were sequenced, and all were found to contain long open reading frames. The overlapping regions were identical except for a 60-nucleotide inframe insertion at position 1133 in the composite sequence. This result suggests that at least two distinct transcripts exist in fibroblast cells. The chromosomal location of human alpha-fodrin was assigned to 1p34-1p36.1 by hybridization to somatic cell hybrids, and it is thus distinct from that of human alpha-spectrin which has been mapped to 1q22-1q25. Alignment of the composite 919 amino acids of the predicted protein sequence of human alpha-fodrin with that of human alpha-spectrin indicated that alpha-fodrin has a similar 106-amino-acid repeating structure, which is homologous with alpha-spectrin repeats 7-15. Repeats 10 and 11 are anomalous in sequence and structure from other repeats. A comparison of nucleic acid and amino acid homologies between alpha-spectrin and the alpha-fodrin of several vertebrates indicated that human non-erythroid alpha-fodrin and the common alpha-subunit of erythroid and non-erythroid cells of non-mammalian vertebrates are closely related (90%-96% amino acid homology), whereas alpha-fodrin is only distantly related to the erythroid-specific alpha-spectrin subunit of mammals (55%-59% amino acid homology). These data suggest that mammalian erythroid alpha-spectrin evolved by duplication and rapid divergence from an ancestral alpha-fodrin-like gene.
从人肺成纤维细胞cDNA文库中分离出几个重叠的cDNA克隆,这些克隆包含人非红细胞血影蛋白(称为 fodrin)α亚基的2760个核苷酸。DNA和RNA印迹分析表明,单个拷贝的α-fodrin基因编码一个9kb的转录本。对cDNA克隆进行测序,发现它们都含有长开放阅读框。除了复合序列中第1133位有一个60个核苷酸的框内插入外,重叠区域是相同的。这一结果表明,成纤维细胞中至少存在两种不同的转录本。通过与体细胞杂种杂交,将人α-fodrin的染色体定位到1p34 - 1p36.1,因此它与已定位到1q22 - 1q25的人α-血影蛋白不同。将人α-fodrin预测蛋白序列的919个复合氨基酸与人α-血影蛋白的序列进行比对,表明α-fodrin具有相似的106个氨基酸的重复结构,与α-血影蛋白的7 - 15个重复序列同源。重复序列10和11在序列和结构上与其他重复序列不同。对几种脊椎动物的α-血影蛋白和α-fodrin之间的核酸和氨基酸同源性进行比较表明,人非红细胞α-fodrin与非哺乳动物脊椎动物红细胞和非红细胞的共同α亚基密切相关(氨基酸同源性为90% - 96%),而α-fodrin与哺乳动物红细胞特异性α-血影蛋白亚基的关系较远(氨基酸同源性为55% - 59%)。这些数据表明,哺乳动物红细胞α-血影蛋白是通过从一个祖先α-fodrin样基因的复制和快速分化而进化的。