Koch W, Zimmermann W, Oliff A, Friedrich R
J Virol. 1984 Mar;49(3):828-40. doi: 10.1128/JVI.49.3.828-840.1984.
We sequenced the envelope (env) gene and 3' long terminal repeat of a Friend mink cell focus-inducing virus (F-MCFV). We also sequenced the gp70 coding regions for two cDNA clones of another F-MCFV. The deduced amino acid sequence of the env gene products of both F-MCFVs were compared to the corresponding sequences of other MCFVs and of ecotropic viruses. The env polypeptides of the different viruses showed long stretches of homology in the carboxy-terminal half of gp70 and in p15env ("constant region"). The amino-terminal half of gp70 was very similar in all MCFVs, but showed extensive variations relative to the ecotropic viruses ("differential region"). This differential region in all MCFVs is of endogeneous origin. We show evidence that this region carries determinants for ecotropic or polytropic host range. No indication could be found that the env gene products determine the histological type of disease caused by particular MCFVs. When the long terminal repeats of F-MCFV and Friend murine leukemia virus were compared with those of other viruses causing either lymphatic leukemia or erythroleukemia, several nucleotides were localized which might determine the histological type of disease caused by these viruses.
我们对一种弗氏水貂细胞灶性诱导病毒(F-MCFV)的包膜(env)基因和3'长末端重复序列进行了测序。我们还对另一种F-MCFV的两个cDNA克隆的gp70编码区进行了测序。将两种F-MCFV的env基因产物推导的氨基酸序列与其他MCFV和嗜亲性病毒的相应序列进行了比较。不同病毒的env多肽在gp70的羧基末端一半和p15env(“恒定区”)中显示出长片段的同源性。所有MCFV中gp70的氨基末端一半非常相似,但相对于嗜亲性病毒显示出广泛的变异(“差异区”)。所有MCFV中的这个差异区起源于内源性。我们提供的证据表明,该区域携带嗜亲性或多嗜性宿主范围的决定因素。未发现env基因产物决定特定MCFV引起的疾病组织学类型的迹象。当将F-MCFV和弗氏鼠白血病病毒的长末端重复序列与其他引起淋巴白血病或红白血病的病毒的长末端重复序列进行比较时,定位了几个可能决定这些病毒引起的疾病组织学类型的核苷酸。