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用于诱变研究的基于瞬时SV40的穿梭载体的开发:问题与解决方案。

The development of transient SV40 based shuttle vectors for mutagenesis studies: problems and solutions.

作者信息

Seidman M

机构信息

Molecular Biology Department, Otsuka Pharmaceutical Co., Ltd., Rockville, MD 20850.

出版信息

Mutat Res. 1989 Mar-May;220(2-3):55-60. doi: 10.1016/0165-1110(89)90010-9.

DOI:10.1016/0165-1110(89)90010-9
PMID:2538741
Abstract

Shuttle-vector plasmids would appear to provide a powerful technology for studying mutagenesis in mammalian (including human) cells. Recently, as described in this and other papers in this volume, several shuttle-vector systems have been described and applied. The development of the first shuttle vectors for these purposes was hindered by two major problems. The first of these was the 'poison' sequence present in many pBR322 based vectors. The second was the problem of spontaneous mutagenesis associated with transfection of the plasmids into mammalian cells. Effective solutions for both problems have been devised, and it is now possible to experimentally address a variety of questions concerning mutagenesis and repair in mammalian cells.

摘要

穿梭载体质粒似乎为研究哺乳动物(包括人类)细胞中的诱变作用提供了一种强大的技术。最近,正如本卷中这篇论文及其他论文所描述的,已经报道并应用了几种穿梭载体系统。用于这些目的的首批穿梭载体的开发受到两个主要问题的阻碍。第一个问题是许多基于pBR322的载体中存在的“毒性”序列。第二个问题是与将质粒转染到哺乳动物细胞中相关的自发诱变问题。针对这两个问题都已设计出有效的解决方案,现在有可能通过实验解决有关哺乳动物细胞诱变和修复的各种问题。

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1
The development of transient SV40 based shuttle vectors for mutagenesis studies: problems and solutions.用于诱变研究的基于瞬时SV40的穿梭载体的开发:问题与解决方案。
Mutat Res. 1989 Mar-May;220(2-3):55-60. doi: 10.1016/0165-1110(89)90010-9.
2
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Shuttle vectors for studying mutagenesis in mammalian cells.用于研究哺乳动物细胞诱变的穿梭载体。
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Analysis of mutations occurring during replication of a SV40 shuttle vector in mammalian cells.SV40穿梭载体在哺乳动物细胞中复制期间发生的突变分析。
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From simian virus 40 to transient shuttle vectors in mutagenesis studies.从猴病毒40到诱变研究中的瞬时穿梭载体。
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Studies on direct and indirect effects of DNA damage on mutagenesis in monkey cells using an SV40-based shuttle vector.使用基于SV40的穿梭载体对猴细胞中DNA损伤对诱变的直接和间接影响的研究。
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J Gen Virol. 1992 Jun;73 ( Pt 6):1533-6. doi: 10.1099/0022-1317-73-6-1533.

引用本文的文献

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Induction of frameshift and base pair substitution mutations by the major DNA adduct of the endogenous carcinogen malondialdehyde.内源性致癌物丙二醛的主要DNA加合物诱导移码和碱基对替代突变。
Proc Natl Acad Sci U S A. 2003 Nov 25;100(24):14247-52. doi: 10.1073/pnas.2332176100. Epub 2003 Nov 5.
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Mutagenicity of a unique thymine-thymine dimer or thymine-thymine pyrimidine pyrimidone (6-4) photoproduct in mammalian cells.独特的胸腺嘧啶 - 胸腺嘧啶二聚体或胸腺嘧啶 - 胸腺嘧啶嘧啶酮(6 - 4)光产物在哺乳动物细胞中的诱变性。
Nucleic Acids Res. 1996 May 15;24(10):1837-40. doi: 10.1093/nar/24.10.1837.
3
Ultraviolet-induced mutations in Cockayne syndrome cells are primarily caused by cyclobutane dimer photoproducts while repair of other photoproducts is normal.
科凯恩综合征细胞中的紫外线诱导突变主要由环丁烷二聚体光产物引起,而其他光产物的修复则是正常的。
Proc Natl Acad Sci U S A. 1993 Aug 1;90(15):7260-4. doi: 10.1073/pnas.90.15.7260.
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Protein oxidative damage is associated with life expectancy of houseflies.蛋白质氧化损伤与家蝇的寿命相关。
Proc Natl Acad Sci U S A. 1993 Aug 1;90(15):7255-9. doi: 10.1073/pnas.90.15.7255.
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Mutagenesis in monkey cells of a vector containing a single d(GPG) cis-diamminedichloroplatinum(II) adduct placed on codon 13 of the human H-ras proto-oncogene.在猴细胞中对一种载体进行诱变,该载体在人H-ras原癌基因的第13密码子处含有单个d(GPG)顺式二氯二氨合铂(II)加合物。
Nucleic Acids Res. 1994 Jul 11;22(13):2519-24. doi: 10.1093/nar/22.13.2519.
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Mutagenic specificities of four stereoisomeric benzo[c]phenanthrene dihydrodiol epoxides.四种立体异构的苯并[c]菲二氢二醇环氧化物的诱变特异性。
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