Smith G A, Young P L, Mattick J S
Pathology Branch, Queensland Department of Primary Industries, Yeerongpilly, Australia.
J Gen Virol. 1990 Oct;71 ( Pt 10):2417-24. doi: 10.1099/0022-1317-71-10-2417.
On the basis of their restriction endonuclease digestion patterns, four Australian bovine herpesvirus type 1 (BHV-1) isolates were classified as belonging to the BHV-1.2a subtypes. The thymidine kinase (TK) genes of all four BHV-1.2a isolates were located on a 3.5 kb SalI restriction fragment. This is in contrast to North American and European BHV-1.1 isolates whose TK genes are contained on a 2.6 to 2.8 kb SalI fragment. The restriction fragments containing the TK genes were cloned into phagemid vectors and their sequences determined using the dideoxynucleotide chain termination method. The BHV-1.2a isolates possessed identical TK gene sequences, which differed from previously published TK sequences for the LA and 6660 BHV-1.1 strains. In addition to five single base alterations, there were six separate base insertions which resulted in two major frameshifts which spanned an area of 72 amino acids or 20% of the expressed TK gene product. The predicted amino acid sequence exhibited a higher degree of similarity to other herpesvirus TKs, suggesting that previously published TK gene sequences may have been incorrect. The present nucleotide sequence and corresponding amino acid composition reinforces previous observations concerning regions of herpesvirus TK amino acid conservation and should assist in future studies into the evolution and functional domains of herpesvirus TKs.
根据其限制性内切酶消化模式,四种澳大利亚1型牛疱疹病毒(BHV-1)分离株被归类为属于BHV-1.2a亚型。所有四种BHV-1.2a分离株的胸苷激酶(TK)基因位于一个3.5 kb的SalI限制性片段上。这与北美和欧洲的BHV-1.1分离株形成对比,后者的TK基因包含在一个2.6至2.8 kb的SalI片段上。含有TK基因的限制性片段被克隆到噬菌粒载体中,并使用双脱氧核苷酸链终止法确定其序列。BHV-1.2a分离株具有相同的TK基因序列,这与先前发表的LA和6660 BHV-1.1株的TK序列不同。除了五个单碱基改变外,还有六个单独的碱基插入,导致两个主要的移码,跨越72个氨基酸的区域或所表达的TK基因产物的20%。预测的氨基酸序列与其他疱疹病毒TK表现出更高程度的相似性,表明先前发表的TK基因序列可能不正确。目前的核苷酸序列和相应的氨基酸组成强化了先前关于疱疹病毒TK氨基酸保守区域的观察结果,并应有助于未来对疱疹病毒TK的进化和功能域的研究。