Shealy D J, Mosser A G, Rueckert R R
J Virol. 1980 May;34(2):431-7. doi: 10.1128/JVI.34.2.431-437.1980.
Virions of Rous-associated virus type 61 contain a previously unrecognized p19-related protein, called p19f, which comigrates with gag protein p12 during electrophoresis in sodium dodecyl sulfate-polyacrylamide gels but can be separated by gel filtration chromatography in 6 M guanidine hydrochloride. It is shown that the existence of p19f accounts for the earlier inability to order p27 and p12 by the pactamycin mapping procedure. Remapping with pactamycin by using methods which take this new protein into account yielded a gag gene order of NH2-p219-p27-p12-p15-COOH. It also confirmed earlier positions for the env and pol genes and placed unclassified protein p10 near a translational initiation site. The pactamycin-derived mapping position of p12 differs from reports based on tryptic analysis. An analysis of procedural shortcomings emphasizes the need for more definitive determinations of the avian gag gene order.
罗氏相关病毒61型的病毒粒子含有一种以前未被识别的与p19相关的蛋白质,称为p19f,它在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳过程中与gag蛋白p12迁移率相同,但在6M盐酸胍中通过凝胶过滤色谱法可将它们分离。结果表明,p19f的存在解释了早期通过嘌呤霉素定位程序无法确定p27和p12顺序的原因。通过考虑这种新蛋白质的方法用嘌呤霉素重新定位,得到的gag基因顺序为NH2-p219-p27-p12-p15-COOH。它还证实了env和pol基因的早期位置,并将未分类的蛋白质p10置于翻译起始位点附近。嘌呤霉素衍生的p12定位与基于胰蛋白酶分析的报告不同。对程序缺陷的分析强调了对禽gag基因顺序进行更明确测定的必要性。