Benz E W, Dina D
Proc Natl Acad Sci U S A. 1979 Jul;76(7):3294-8. doi: 10.1073/pnas.76.7.3294.
Moloney murine sarcoma virus (MSV) virions incubated under optimal conditions were shown to support extensive synthesis of double-stranded DNA. The major product, a 5950-base-pair (6-kilobase-pair DNA) double-stranded DNA, was characterized by cleavage with restriction endonucleases and shown to contain a 600-nucleotide-long direct repeat at both ends of the MSV genome. Linear DNA molecules made in vivo shortly after infection were compared to the linear double-stranded DNA synthesized in vitro. The restriction maps of both viral DNA products were indistinguishable. The 600-base-pair repeat results in a progeny DNA molecule that is longer than the parental MSV genomic RNA. The generation of this repeat must involve a mechanism that allows the viral reverse transcriptase (RNA-dependent DNA nucleotidyltransferase) to copy 5'- and 3'-terminal genomic (+) strand sequences twice.
在最佳条件下孵育的莫洛尼鼠肉瘤病毒(MSV)病毒粒子被证明能支持双链DNA的大量合成。主要产物是一种5950个碱基对(6千碱基对DNA)的双链DNA,通过限制性内切酶切割进行表征,并显示在MSV基因组两端都含有一个600个核苷酸长的直接重复序列。将感染后不久在体内产生的线性DNA分子与体外合成的线性双链DNA进行比较。两种病毒DNA产物的限制性图谱无法区分。600个碱基对的重复导致子代DNA分子比亲本MSV基因组RNA长。这种重复序列的产生必定涉及一种机制,该机制允许病毒逆转录酶(RNA依赖性DNA核苷酸转移酶)将5'和3'末端基因组(+)链序列复制两次。