Dyall-Smith M L, Holmes I H
Nucleic Acids Res. 1984 May 11;12(9):3973-82. doi: 10.1093/nar/12.9.3973.
The dsRNA gene segment coding for the major outer shell glycoprotein of a human rotavirus (Hu/Australia/5/77, serotype 2) was converted into DNA and cloned into the PstI site of the plasmid pBR322. The cloned gene was sequenced and found to be 1062 bp long with one long open reading frame capable of coding for a protein 326 amino-acids. When this gene sequence was compared to the published sequences of the corresponding genes of two animal rotaviruses, SA11 (simian) and UK (bovine), all three were found to be closely related (74-78%). The predicted amino-acid sequences of the three genes were also highly conserved (75-86%), despite the fact that the three viruses belong to different serotypes.
编码人轮状病毒(Hu/澳大利亚/5/77,血清型2)主要外壳糖蛋白的双链RNA基因片段被转化为DNA,并克隆到质粒pBR322的PstI位点。对克隆的基因进行测序,发现其长度为1062 bp,有一个长开放阅读框,能够编码一个326个氨基酸的蛋白质。当将该基因序列与两种动物轮状病毒SA11(猿猴)和UK(牛)的相应基因的已发表序列进行比较时,发现这三者密切相关(74-78%)。尽管这三种病毒属于不同血清型,但这三个基因的预测氨基酸序列也高度保守(75-86%)。