Willems L, Gatot J S, Mammerickx M, Portetelle D, Burny A, Kerkhofs P, Kettmann R
Molecular Biology, Faculty of Agronomy, Gembloux, Belgium.
J Virol. 1995 Jul;69(7):4137-41. doi: 10.1128/JVI.69.7.4137-4141.1995.
The bovine leukemia virus (BLV) transmembrane protein (gp30) contains three YXXL motifs at its carboxyterminal end. Two of these motifs have been implicated in vitro in signal transduction pathways from the external to the intracellular compartment. In order to analyze the biological relevance of these motifs in vivo, recombinant BLV proviruses were constructed. A mutation of the tyrosine residue of the second YXXL motif completely destroyed the infectious potential of the virus in sheep. In contrast, the tyrosine of the first motif appeared to be dispensable for infectivity. However, the propagation of the recombinant virus within the animal was greatly impaired (as demonstrated by PCR and enzyme-linked immunosorbent assay). These recombinant BLVs thus exhibit an attenuated phenotype. Altogether, our data demonstrate the importance of the YXXL motifs of the BLV transmembrane protein for in vivo infection and viral propagation.
牛白血病病毒(BLV)跨膜蛋白(gp30)在其羧基末端含有三个YXXL基序。其中两个基序在体外与从细胞外到细胞内区室的信号转导途径有关。为了分析这些基序在体内的生物学相关性,构建了重组BLV前病毒。第二个YXXL基序的酪氨酸残基发生突变完全破坏了该病毒在绵羊中的感染潜力。相反,第一个基序的酪氨酸对于感染性似乎是可有可无的。然而,重组病毒在动物体内的传播受到极大损害(通过聚合酶链反应和酶联免疫吸附测定证明)。因此,这些重组BLV表现出减毒表型。总之,我们的数据证明了BLV跨膜蛋白的YXXL基序对于体内感染和病毒传播的重要性。