McCutchan T, Singer M, Rosenberg M
J Biol Chem. 1979 May 10;254(9):3592-7.
In an effort to characterize sites of recombination between SV40 and monkey DNA, we have determined the primary sequence of a large portion of the SV40 variant, designated 1103. This virus contains DNA sequences derived both from the wild type SV40 genome and from the permissive monkey cell in which the virus was propagated. Further, the monkey sequences included in the defective genome are homologous to both highly repeated monkey DNA (alpha component) and sequences that are infrequently repeated in the monkey genome. The regions of the 1103 genome where DNA sequences were determined include 1) the segments of the variant that surround joints connecting SV40 and monkey sequences, 2) the segment that contains the joint between monkey sequences of high and low reiteration frequency, and 3) the DNA segment of the variant that is homologous to monkey alpha component DNA. Comparison of the data obtained from the sequences analysis of the SV40 variants 1103 and CVP8/1/P2 (EcoRI res) (described in Wakamiya, T., McCutchan, T., Rosenberg, M., and Singer, M. (1979) J. Biol. Chem 254, 3584-3591) reveals certain similarities between the two that may be involved in eukaryotic recombination and defective variant formation.
为了确定SV40与猴DNA之间的重组位点,我们测定了大部分SV40变体(命名为1103)的一级序列。这种病毒包含源自野生型SV40基因组以及病毒在其中繁殖的允许性猴细胞的DNA序列。此外,缺陷基因组中包含的猴序列与高度重复的猴DNA(α组分)以及在猴基因组中不常重复的序列均具有同源性。测定了DNA序列的1103基因组区域包括:1)围绕连接SV40和猴序列的接头的变体片段;2)包含高低重复频率猴序列之间接头的片段;3)与猴α组分DNA同源的变体DNA片段。对从SV40变体1103和CVP8/1/P2(EcoRI酶切)(如Wakamiya, T., McCutchan, T., Rosenberg, M., and Singer, M. (1979) J. Biol. Chem 254, 3584 - 3591所述)的序列分析中获得的数据进行比较,揭示了两者之间某些可能与真核生物重组和缺陷变体形成有关的相似性。