Wong T C, Ayata M, Hirano A, Yoshikawa Y, Tsuruoka H, Yamanouchi K
Department of Microbiology, University of Washington School of Medicine, Seattle 98195.
J Virol. 1989 Dec;63(12):5464-8. doi: 10.1128/JVI.63.12.5464-5468.1989.
The matrix (M) genes of Yamagata-1 strain subacute sclerosing panencephalitis virus passaged in African green monkey kidney cells and human neuroblastoma cells displayed strikingly nonrandom sequence divergence. The genes of both substrains shared a large number of uridine (U) to cytidine (C) transitions, but the latter contained numerous additional U to C changes in a localized region. Over 90% of the additional mutations were identical to the hypermutated nucleotides in the M gene found in a measles inclusion body encephalitis case. The nonrandom nature, the apparent host dependency, and the abrupt boundaries of these mutations suggest that these mutations might be caused by an extrinsic biased mutational activity rather than intrinsic polymerase errors. This mutational activity might account for the extraordinarily high C to U ratios in the non-protein-coding regions of both the M and fusion genes of wild-type measles virus.
在非洲绿猴肾细胞和人神经母细胞瘤细胞中传代的山形-1株亚急性硬化性全脑炎病毒的基质(M)基因显示出明显的非随机序列差异。两个亚株的基因都有大量的尿苷(U)到胞苷(C)的转变,但后者在一个局部区域含有许多额外的U到C的变化。超过90%的额外突变与在一例麻疹包涵体脑炎病例中发现的M基因中的超突变核苷酸相同。这些突变的非随机性质、明显的宿主依赖性以及突变的突然边界表明,这些突变可能是由外在的偏向性突变活性而非内在的聚合酶错误引起的。这种突变活性可能解释了野生型麻疹病毒M基因和融合基因非编码区中异常高的C到U比率。