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与1型单纯疱疹病毒胸苷激酶和UL24基因同源的马立克氏病病毒2型基因的鉴定及DNA序列分析

Identification and DNA sequence analysis of the Marek's disease virus serotype 2 genes homologous to the thymidine kinase and UL24 genes of herpes simplex virus type 1.

作者信息

Shimojima Y, Jang H K, Ono M, Maeda K, Tohya Y, Mikami T

机构信息

Department of Veterinary Microbiology, Faculty of Agriculture, University of Tokyo, Japan.

出版信息

Virus Genes. 1997;14(1):81-7. doi: 10.1023/a:1007943624997.

DOI:10.1023/a:1007943624997
PMID:9208458
Abstract

The thymidine kinase (TK) gene has been used as a safe and convenient locus for expression of heterologous proteins in some alphaherpesviruses including herpesvirus of turkeys (HVT) antigenically related to Marek's disease virus (MDV) serotypes 1 (MDV1) and 2 (MDV2). In MDV2 strain HPRS 24 genome, genes equivalent to the TK and UL24 homologues of herpes simplex virus type 1 were identified and sequenced. The MDV2 UL24 gene overlaps the 5' end of the TK gene in a head-to-head orientation. The predicted region encoding for the MDV2 TK gene is 1,056 nucleotides, corresponding to a polypeptide of 352 amino acids in length. Putative nucleotide- and thymidine-binding sites were identified within the predicted amino acid sequence. The predicted region encoding for the UL24 gene is 948 nucleotides, corresponding to a polypeptide of 316 amino acids in length. By northern blot analyses using MDV2 TK- and UL24-specific DNA probes, four transcripts of approximately 7.8, 5.0, 3.5, and 1.1 kb for the TK gene, and a transcript of 3.8 kb for the UL24 gene were detected in MDV2-infected cells. Alignment of the amino acid sequence of MDV2 TK homologue with those published for TK homologues of other MDV serotypes showed 73.9% (MDV1 vs. MDV2), 58.2% (MDV1 vs. HVT), and 56.8% (MDV2 vs. HVT) identities. Comparison to other alphaherpesvirus TK homologues revealed amino acid sequence homologies varying from 34.5% to 27.8%. The putative MDV2 UL24 homologous protein had identity with the well conserved five motifs among alphaherpesviruses.

摘要

胸苷激酶(TK)基因已被用作在一些α疱疹病毒中表达异源蛋白的安全且便捷的位点,这些病毒包括与马立克氏病病毒(MDV)血清型1(MDV1)和2(MDV2)抗原相关的火鸡疱疹病毒(HVT)。在MDV2毒株HPRS 24基因组中,鉴定并测序了与单纯疱疹病毒1型的TK和UL24同源物等效的基因。MDV2 UL24基因以头对头的方向与TK基因的5'端重叠。预测的编码MDV2 TK基因的区域为1056个核苷酸,对应于长度为352个氨基酸的多肽。在预测的氨基酸序列中鉴定出了推定的核苷酸结合位点和胸苷结合位点。预测的编码UL24基因的区域为948个核苷酸,对应于长度为316个氨基酸的多肽。通过使用MDV2 TK和UL24特异性DNA探针的Northern印迹分析,在MDV2感染的细胞中检测到TK基因的约7.8、5.0、3.5和1.1 kb的四种转录本,以及UL24基因的3.8 kb的转录本。MDV2 TK同源物的氨基酸序列与其他MDV血清型的TK同源物已发表的序列比对显示,同一性分别为73.9%(MDV1与MDV2)、58.2%(MDV1与HVT)和56.8%(MDV2与HVT)。与其他α疱疹病毒TK同源物的比较显示氨基酸序列同源性在34.5%至27.8%之间变化。推定的MDV2 UL24同源蛋白与α疱疹病毒中五个保守的基序具有同一性。

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本文引用的文献

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J Vet Med Sci. 1996 Nov;58(11):1057-66. doi: 10.1292/jvms.58.11_1057.
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Virus Genes. 1996;12(2):185-8. doi: 10.1007/BF00572957.
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Temporal regulation of herpes simplex virus type 1 UL24 mRNA expression via differential polyadenylation.通过差异多聚腺苷酸化对单纯疱疹病毒1型UL24 mRNA表达进行时间调控。
Virology. 1996 Apr 1;218(1):204-13. doi: 10.1006/viro.1996.0180.
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