Wesley R D
United States Department of Agriculture, Agricultural Research Service, National Animal Disease Center, Ames, Iowa.
Adv Exp Med Biol. 1990;276:301-6. doi: 10.1007/978-1-4684-5823-7_41.
The E2-peplomer protein gene of the virulent Miller strain of transmissible gastroenteritis virus (TGEV) was sequenced from cDNA clones and compared to the E2 gene sequence of the avirulent Purdue strain. Sequence comparisons indicate that most amino acid differences occur in the N-terminal half of the E2-peplomer which represents the most exposed region of the protein. In addition, analysis of an incompletely sequenced open reading frame (ORF) to the immediate 5' side of the E2 gene indicates extensive sequence homology with the infectious bronchitis virus (IBV) F2 gene which is thought to encode a RNA polymerase.
从cDNA克隆中对传染性胃肠炎病毒(TGEV)强毒株米勒株的E2纤突蛋白基因进行测序,并与无毒力的普渡株的E2基因序列进行比较。序列比较表明,大多数氨基酸差异出现在E2纤突蛋白的N端一半区域,该区域是该蛋白最暴露的区域。此外,对E2基因紧邻5'端的一个测序不完全的开放阅读框(ORF)的分析表明,其与传染性支气管炎病毒(IBV)的F2基因有广泛的序列同源性,F2基因被认为编码一种RNA聚合酶。