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痘苗病毒主要包膜抗原p37K编码基因的一个orf病毒同源物的鉴定与表征。

Identification and characterization of an orf virus homologue of the vaccinia virus gene encoding the major envelope antigen p37K.

作者信息

Sullivan J T, Mercer A A, Fleming S B, Robinson A J

机构信息

Health Research Council Virus Research Unit, University of Otago, Dunedin, New Zealand.

出版信息

Virology. 1994 Aug 1;202(2):968-73. doi: 10.1006/viro.1994.1420.

Abstract

DNA sequence analysis of a 1.55-kb region located 10 kb from the left end of the orf virus NZ-2 strain (OV NZ2) genome revealed an open reading frame, B2L, encoding a protein with a predicted molecular weight of 41.67 kDa. This protein (p42K) shows 42% amino acid sequence identity to the vaccinia virus (VAC) major envelope antigen p37K. In addition, p42K shows homology to a protein encoded by molluscum contagiosum virus (42.8% identity) and another encoded by fowlpox virus (38.3% identity). These proteins are themselves homologues of the VAC p37K. B2L is actively transcribed after the onset of DNA replication and S1 nuclease analysis mapped the 5' end of the transcript to within the sequence TAAATG. A VAC recombinant capable of expressing the p42K gene was constructed and used as an antigen in radioimmune precipitations and lymphocyte transformation assays. These assays demonstrated that OV p42K is one of a limited number of OV proteins to which sheep mount a strong antibody response and which stimulate lymphocytes derived from draining lymph nodes following a natural infection with OV NZ2.

摘要

对痘苗病毒NZ - 2株(OV NZ2)基因组左端10 kb处一个1.55 kb区域进行的DNA序列分析,揭示了一个开放阅读框B2L,其编码一种预测分子量为41.67 kDa的蛋白质。该蛋白质(p42K)与痘苗病毒(VAC)主要包膜抗原p37K的氨基酸序列一致性为42%。此外,p42K与传染性软疣病毒编码的一种蛋白质具有同源性(一致性为42.8%),还与禽痘病毒编码的另一种蛋白质具有同源性(一致性为38.3%)。这些蛋白质本身就是VAC p37K的同源物。B2L在DNA复制开始后被积极转录,S1核酸酶分析将转录本的5'端定位在序列TAAATG内。构建了一种能够表达p42K基因的VAC重组体,并将其用作放射免疫沉淀和淋巴细胞转化试验中的抗原。这些试验表明,OV p42K是绵羊产生强烈抗体反应的有限数量的OV蛋白质之一,并且在自然感染OV NZ2后能刺激引流淋巴结来源的淋巴细胞。

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