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九个转化的啮齿动物细胞系中整合的猴病毒40 DNA的自发重排。

Spontaneous rearrangement of integrated simian virus 40 DNA in nine transformed rodent cell lines.

作者信息

Gurney T, Gurney E G

机构信息

Department of Biology, University of Utah, Salt Lake City 84112.

出版信息

J Virol. 1989 Jan;63(1):165-74. doi: 10.1128/JVI.63.1.165-174.1989.

DOI:10.1128/JVI.63.1.165-174.1989
PMID:2562813
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC247669/
Abstract

Frequencies of spontaneous DNA rearrangement within or near integrated simian virus 40 (SV40) DNA were measured in four transformed mouse and rat cell lines of independent origin and in five clones of the SV40-transformed mouse line SVT2. Rearrangements were detected as polymorphisms of restriction enzyme fragment length in subclones of the lines. At least 17% of the subclones of each line had detectable rearrangements. The rate of rearrangement was calculated to be at least 5 x 10(-3) events per cell per division. No rearrangements were detected in sequences of an immunoglobulin gene, part of the coding region of the mouse protein p53, and five proto-oncogenes. The possible role of recombination between duplicated segments of integrated SV40 DNA in generating rearrangements was studied in the five SVT2 clones, which differed in the number of duplications within a single SV40 DNA segment. The SVT2 clone that had no duplications, M3, became rearranged further at least as frequently as did closely related lines with one, two, or three duplications. Another line in this group that had one small duplication, X1, had a much higher frequency of rearrangement than did the others; integrated SV40 DNA of X1 became mostly rearranged within 100 cell divisions. The examples of M3 and X1 suggested that the high rate of rearrangement characteristic of integrated SV40 DNA was influenced more by the presence of particular sequences within or near integrated SV40 DNA than by the number or extent of duplicated sequences.

摘要

在四个独立起源的转化小鼠和大鼠细胞系以及猿猴病毒40(SV40)转化的小鼠细胞系SVT2的五个克隆中,测量了整合的SV40 DNA内部或附近自发DNA重排的频率。重排被检测为细胞系亚克隆中限制性酶切片段长度的多态性。每个细胞系至少17%的亚克隆有可检测到的重排。计算得出重排率至少为每细胞每分裂5×10⁻³次事件。在免疫球蛋白基因序列、小鼠蛋白p53编码区的一部分以及五个原癌基因中未检测到重排。在五个SVT2克隆中研究了整合的SV40 DNA重复片段之间的重组在产生重排中的可能作用,这五个克隆在单个SV40 DNA片段内的重复数量上有所不同。没有重复的SVT2克隆M3,其进一步重排的频率至少与具有一、二或三个重复的密切相关细胞系一样高。该组中另一个有一个小重复的细胞系X1,其重排频率比其他细胞系高得多;X1的整合SV40 DNA在100次细胞分裂内大多发生了重排。M3和X1的例子表明,整合的SV40 DNA重排率高的特征更多地受整合的SV40 DNA内部或附近特定序列的存在影响,而不是受重复序列的数量或范围影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57c/247669/40d5c24029ec/jvirol00068-0189-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57c/247669/a1e69680c9f3/jvirol00068-0185-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57c/247669/1e229f2c649e/jvirol00068-0186-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57c/247669/d3e16f11cd5b/jvirol00068-0188-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57c/247669/504fbb6b2e12/jvirol00068-0188-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57c/247669/ce438149197b/jvirol00068-0189-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57c/247669/40d5c24029ec/jvirol00068-0189-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57c/247669/a1e69680c9f3/jvirol00068-0185-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57c/247669/1e229f2c649e/jvirol00068-0186-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57c/247669/d3e16f11cd5b/jvirol00068-0188-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57c/247669/504fbb6b2e12/jvirol00068-0188-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57c/247669/ce438149197b/jvirol00068-0189-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57c/247669/40d5c24029ec/jvirol00068-0189-b.jpg

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本文引用的文献

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Elimination of Mycoplasma hyorhinis infections from four cell lines.从四种细胞系中清除猪鼻支原体感染。
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Two types of deletion within integrated viral sequences mediate reversion of simian virus 40-transformed mouse cells.整合病毒序列内的两种缺失类型介导了猿猴病毒40转化的小鼠细胞的回复突变。
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