Donoghue D J, Rothenberg E, Hopkins N, Baltimore D, Sharp P A
Cell. 1978 Aug;14(4):959-70. doi: 10.1016/0092-8674(78)90350-1.
The dual host range virus HIX has been previously characterized as an envelope gene recombinant between Moloney murine leukemia virus (Mo-MuLV) and an unidentified xenotropic murine leukemia virus. Using long reverse transcripts of Mo-MuLV, a region of nonhomology has been mapped by electron microscopic analysis of heteroduplexes formed with HIX 35S virion RNA. In this nonhomology region, the Mo-MuLV cDNA strand measured approximately 900 nucleotides, mapping between 1.6 and 2.5 kilobases from the 3' end. In a previous study, hybridization of Mo-MuLV 21S RNA with Mo-MuLV cDNA resulted in the formation of different heteroduplex structures diagnostic of a noncontiguously coded leader sequence at the 5' end of the 21S RNA. Following hybridization of poly(A)+ HIX 21S RAN with 8.2 kb Mo-MuLV cDNA, analogous heteroduplex structures were observed exhibiting the Mo-MuLV:HIX substitution loop in the DNA:RNA segment of the molecules. This analysis permitted more precise mapping of the nonhomology region with respect to the splice point in the 21S presumptive glycoprotein mRNA. The mapping of this nonhomology region in HIX virus provides an internal visual marker for the 3' end of the genome which may prove useful in future analyses of other deletion or substitution derivatives of Mo-MuLV.
双宿主范围病毒HIX先前已被鉴定为莫洛尼鼠白血病病毒(Mo-MuLV)与一种未鉴定的嗜异性鼠白血病病毒之间的包膜基因重组体。利用Mo-MuLV的长反转录产物,通过对与HIX 35S病毒粒子RNA形成的异源双链体进行电子显微镜分析,绘制了一个非同源区域。在这个非同源区域中,Mo-MuLV cDNA链大约有900个核苷酸,位于从3'端起1.6至2.5千碱基之间。在先前的一项研究中,Mo-MuLV 21S RNA与Mo-MuLV cDNA杂交导致形成了不同的异源双链体结构,这些结构可诊断出21S RNA 5'端存在非连续编码的前导序列。在用聚腺苷酸加尾的HIX 21S RNA与8.2 kb Mo-MuLV cDNA杂交后,观察到了类似的异源双链体结构,在分子的DNA:RNA片段中呈现出Mo-MuLV:HIX替代环。该分析使得能够更精确地绘制非同源区域相对于21S推定糖蛋白mRNA剪接位点的图谱。在HIX病毒中绘制这个非同源区域为基因组的3'端提供了一个内部可视标记,这在未来对Mo-MuLV的其他缺失或替代衍生物的分析中可能会很有用。