Abrell J W, Reitz M S, Gallo R C
J Virol. 1975 Dec;16(6):1566-74. doi: 10.1128/JVI.16.6.1566-1574.1975.
DNA polymerases purified by the same procedure from four mammalian RNA viruses, simian sarcoma virus type 1, gibbon ape lymphoma virus, Mason-Pfizer monkey virus, and Rauscher murine leukemia virus are capable of transcribing heteropolymeric regions of viral 70S RNA without any other primer. In this reconstituted system the enzymes from simian sarcoma virus type 1, Mason-Pfizer monkey virus, and Rauscher murine leukemia virus transcribe viral 70S RNA almost as efficiently as the DNA polymerase from the avian myeloblastosis virus, but gibbon ape lymphoma virus DNA polymerase is approximately three-to fivefold less efficient. Although there is a substantial difference among the sizes of these DNA polymerases (160,000 daltons for the avian myeloblastosis virus enzyme, 110,000 daltons for the Mason-Pfizer monkey virus enzyme, and 70,000 daltons for the mammalian type C viral polymerases), the ability to transcribe viral 70S RNA is a characteristic common to these enzymes.
通过相同程序从四种哺乳动物RNA病毒(1型猿猴肉瘤病毒、长臂猿淋巴瘤病毒、梅森- Pfizer猴病毒和劳氏鼠白血病病毒)中纯化得到的DNA聚合酶,能够在没有任何其他引物的情况下转录病毒70S RNA的异聚区域。在这个重组系统中,1型猿猴肉瘤病毒、梅森- Pfizer猴病毒和劳氏鼠白血病病毒的酶转录病毒70S RNA的效率几乎与禽成髓细胞瘤病毒的DNA聚合酶相同,但长臂猿淋巴瘤病毒DNA聚合酶的效率约低三到五倍。尽管这些DNA聚合酶的大小存在显著差异(禽成髓细胞瘤病毒酶为160,000道尔顿,梅森- Pfizer猴病毒酶为110,000道尔顿,哺乳动物C型病毒聚合酶为70,000道尔顿),但转录病毒70S RNA的能力是这些酶共有的特征。