Watanabe T
Animal Breeding and Reproduction, Graduate School of Agriculture, Hokkaido University, Sapporo, Japan.
Cytogenet Genome Res. 2007;117(1-4):370-5. doi: 10.1159/000103200.
The Mx gene was originally found in laboratory mice in an infection experiment using influenza virus (Lindermann, 1962). Almost all of the mouse strains in that experiment died from the infection, and only the A2G strain had resistance to the virus. This resistant character was shown to be inherited as a single autosomal dominant trait (Lindermann et al., 1963; Lindermann, 1964; Haller et al., 1979). A congenic mouse strain was established by introducing the Mx+ allele of the A2G resistant strain into the Mx- sensitive inbred strain BALB/c (Staeheli et al., 1984). By immunizing parental BALB/c mice with extracts of interferon (IFN)-treated cultured cells from congenic BALB/c-Mx+ mice, a specific antibody against Mx protein was obtained (Horisberger et al., 1983; Staeheli et al., 1985). The Mx protein was detected in the nucleus of IFN-alpha/beta-treated mouse cells by immunofluorescence using the anti-Mx antibody (Dreiding et al., 1985). Thereafter, by using the antibody as an indicator, cDNA encoding the Mx protein was cloned from a cDNA library constructed from IFN-treated cells of congenic BALB/c-Mx+ mice (Staeheli et al., 1986a). IFN-treated Mx+ mouse cells contained a 3.5-kb Mx mRNA in the Northern blot, while Mx- cells failed to express the transcript. The functional Mx+ gene from an A2G mouse was found to contain 14 exons and encode 631 amino acids. The Mx- allelic mouse strains were found to be missing sequence of exons 9 through 11 or to contain a point mutation that converts lysine at position 389 to a stop codon (Staeheli et al., 1988). If these polymorphisms of the Mx gene could be detected in domestic animals, it would be possible to produce breeds that show resistance to infectious diseases.
Mx基因最初是在一项使用流感病毒的感染实验中,于实验小鼠体内发现的(林德曼,1962年)。在该实验中,几乎所有的小鼠品系都死于感染,只有A2G品系对病毒具有抗性。这种抗性特征被证明是作为单一常染色体显性性状遗传的(林德曼等人,1963年;林德曼,1964年;哈勒等人,1979年)。通过将A2G抗性品系的Mx+等位基因导入Mx-敏感近交系BALB/c,建立了一个同源基因小鼠品系(施泰利等人,1984年)。用来自同源BALB/c-Mx+小鼠的干扰素(IFN)处理的培养细胞提取物免疫亲代BALB/c小鼠,获得了一种针对Mx蛋白的特异性抗体(霍里斯伯格等人,1983年;施泰利等人,1985年)。使用抗Mx抗体通过免疫荧光在IFN-α/β处理的小鼠细胞的细胞核中检测到了Mx蛋白(德赖丁等人,1985年)。此后,以该抗体为指标,从由同源BALB/c-Mx+小鼠的IFN处理细胞构建的cDNA文库中克隆了编码Mx蛋白的cDNA(施泰利等人,1986a)。在Northern印迹中,IFN处理的Mx+小鼠细胞含有一个3.5 kb的Mx mRNA,而Mx-细胞未能表达该转录本。发现来自A2G小鼠的功能性Mx+基因包含14个外显子,编码631个氨基酸。发现Mx-等位基因小鼠品系缺失外显子9至11的序列,或含有一个将第389位赖氨酸转换为终止密码子的点突变(施泰利等人,1988年)