Sugaya Kimihiko, Hongo Etsuko, Tsuji Hideo
Radiation Hazards Research Group, National Institute of Radiological Sciences, 4-9-1, Anagawa, Inage-ku, Chiba 263-8555, Japan.
Exp Cell Res. 2005 May 15;306(1):242-51. doi: 10.1016/j.yexcr.2005.02.017. Epub 2005 Mar 20.
Temperature-sensitive CHO-K1 mutant cell line tsTM18 exhibits chromosomal instability and cell cycle arrest at S and G2 phases with decreased DNA synthesis at the nonpermissive temperature, 39 degrees C. To identify the causative mutation, we fused tsTM18 cells with normal human cells to generate hybrids carrying fragments of human chromosomes. Analysis of chromosome content of temperature-resistant transformants and introduction of a bacterial artificial chromosome containing part of human chromosome 9 led to isolation of the human SMU1 gene. Comparison of sequences of the Smu1 gene from wild-type and mutant cells revealed that the mutant phenotype is caused by a G-to-A transition that yields a gly-to-arg substitution at position 489 in hamster Smu1. The substituted glycine is located in the WD-repeat domain of Smu1. Single-stranded DNA accumulated in the nuclei of mutant cells at 39 degrees C. Furthermore, cdc2 kinase was not activated during G2 phase, and there was no chromosome segregation due to incomplete assembly of the spindle during M phase. Thus, Smu1 appears to be involved directly or indirectly in DNA replication, activation of cdc2 kinase, spindle assembly, and maintenance of chromosome integrity, reflecting the important roles of Smu1 in cellular function.
温度敏感型CHO-K1突变细胞系tsTM18在39℃的非允许温度下表现出染色体不稳定性以及在S期和G2期的细胞周期停滞,同时DNA合成减少。为了鉴定致病突变,我们将tsTM18细胞与正常人细胞融合以产生携带人类染色体片段的杂种细胞。对耐温转化体的染色体含量进行分析,并导入包含人类9号染色体部分片段的细菌人工染色体,从而分离出人类SMU1基因。对野生型和突变细胞的Smu1基因序列进行比较,结果显示突变表型是由一个G到A的转换导致的,该转换在仓鼠Smu1的第489位产生了一个甘氨酸到精氨酸的替换。被替换的甘氨酸位于Smu1的WD重复结构域中。在39℃时,单链DNA在突变细胞的细胞核中积累。此外,在G2期cdc2激酶未被激活,并且在M期由于纺锤体组装不完全而没有染色体分离。因此,Smu1似乎直接或间接地参与了DNA复制、cdc2激酶的激活、纺锤体组装以及染色体完整性的维持,这反映了Smu1在细胞功能中的重要作用。