Rodríguez-Cerezo E, Shaw J G
Department of Plant Pathology, University of Kentucky, Lexington 40546.
Virology. 1991 Dec;185(2):572-9. doi: 10.1016/0042-6822(91)90527-i.
The existence of two viral RNA-encoded proteins in cells infected with tobacco vein mottling potyvirus (TVMV) has been demonstrated. One of the proteins (named 34K) maps at the N-terminus of the TVMV polyprotein and the other (42K) between the helper component and cylindrical inclusion proteins; both had previously been predicted in the consensus potyviral genetic map. The 34K and 42K coding regions of TVMV were cloned separately in a bacterial expression vector and the proteins were isolated from transformed Escherichia coli. These were used to raise polyclonal antibodies which reacted specifically with proteins of the expected size in immunoblots of extracts of TVMV-infected tobacco leaves and protoplasts. In addition to 42K, the anti-42K serum detected similar amounts of a second protein of apparent size 37 kDa that was absent in 42K-expressing bacteria. Both 34K and 42K were present predominantly in membrane-enriched fractions of extracts of TVMV-infected tobacco leaves. Computer analysis of the deduced amino acid sequence of 42K suggests that this viral protein may be an integral transmembrane protein.
已证实,在感染烟草脉斑驳马铃薯Y病毒(TVMV)的细胞中存在两种病毒RNA编码蛋白。其中一种蛋白(命名为34K)位于TVMV多聚蛋白的N端,另一种(42K)位于辅助成分和柱状内含体蛋白之间;这两种蛋白此前在马铃薯Y病毒属的共有遗传图谱中已被预测到。TVMV的34K和42K编码区分别克隆到一个细菌表达载体中,并从转化的大肠杆菌中分离出这两种蛋白。用这些蛋白制备多克隆抗体,该抗体在TVMV感染的烟草叶片和原生质体提取物的免疫印迹中能与预期大小的蛋白发生特异性反应。除了42K,抗42K血清还检测到等量的另一种表观大小为37 kDa的蛋白,该蛋白在表达42K的细菌中不存在。34K和42K主要存在于TVMV感染的烟草叶片提取物的富含膜的组分中。对42K推导的氨基酸序列进行计算机分析表明,这种病毒蛋白可能是一种整合跨膜蛋白。