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多瘤病毒调控区突变体在不同小鼠细胞系中的复制顺式优势

Replicative cis-advantage of polyomavirus regulatory region mutants in different murine cell lines.

作者信息

De Simone V, Amati P

出版信息

J Virol. 1987 May;61(5):1615-20. doi: 10.1128/JVI.61.5.1615-1620.1987.

DOI:10.1128/JVI.61.5.1615-1620.1987
PMID:3033287
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC254143/
Abstract

To determine the relative growth advantages of polyomavirus regulatory region mutants selected from Friend leukemic and neuroblastoma cells persistently infected with polyomavirus A2 wild type, different murine cell lines, some of which are capable of further differentiation in vitro, were used as hosts in mixed infection and transfection. The tests allowed the determination, through the measurement of cis-advantage in replication, of the most effective polyomavirus regulatory region constitutions for a given cell line and, in some cases, for specific stages of cell differentiation. Furthermore, different domains of the viral regulatory region were shown to have different effects--positive, neutral, or negative--depending on the host analyzed.

摘要

为了确定从持续感染多瘤病毒A2野生型的Friend白血病细胞和神经母细胞瘤细胞中筛选出的多瘤病毒调控区突变体的相对生长优势,将不同的鼠细胞系(其中一些能够在体外进一步分化)用作混合感染和转染的宿主。通过测量复制中的顺式优势,这些试验能够确定对于给定细胞系以及某些情况下对于细胞分化的特定阶段而言最有效的多瘤病毒调控区组成。此外,病毒调控区的不同结构域根据所分析的宿主表现出不同的作用——正向、中性或负向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a73/254143/bd9d5b3a7694/jvirol00096-0328-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a73/254143/e0af03c62f44/jvirol00096-0327-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a73/254143/52dd8f7af896/jvirol00096-0327-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a73/254143/bd9d5b3a7694/jvirol00096-0328-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a73/254143/e0af03c62f44/jvirol00096-0327-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a73/254143/52dd8f7af896/jvirol00096-0327-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a73/254143/bd9d5b3a7694/jvirol00096-0328-a.jpg

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Replicative cis-advantage of polyomavirus regulatory region mutants in different murine cell lines.多瘤病毒调控区突变体在不同小鼠细胞系中的复制顺式优势
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2
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本文引用的文献

1
An SV40 "enhancer trap" incorporates exogenous enhancers or generates enhancers from its own sequences.一个SV40“增强子陷阱”包含外源性增强子或从其自身序列产生增强子。
Cell. 1984 Apr;36(4):983-92. doi: 10.1016/0092-8674(84)90048-5.
2
Polyomavirus growth and persistence in Friend erythroleukemic cells.多瘤病毒在弗氏红白血病细胞中的生长与持续存在
J Virol. 1984 Feb;49(2):566-71. doi: 10.1128/JVI.49.2.566-571.1984.
3
Polyomavirus origin for DNA replication comprises multiple genetic elements.多瘤病毒DNA复制的起源包含多个遗传元件。
成年小鼠肾脏对急性多瘤病毒感染变得易感,并在细胞损伤和再生时重新激活持续性感染。
J Virol. 1993 Mar;67(3):1424-32. doi: 10.1128/JVI.67.3.1424-1432.1993.
4
Mutations of polyomavirus VP1 allow in vitro growth in undifferentiated cells and modify in vivo tissue replication specificity.多瘤病毒VP1的突变允许其在未分化细胞中进行体外生长,并改变体内组织复制特异性。
J Virol. 1994 Feb;68(2):1196-9. doi: 10.1128/JVI.68.2.1196-1199.1994.
5
Protein recognition sites in polyomavirus enhancer: formation of a novel site for NF-1 factor in an enhancer mutant and characterization of a site in the enhancer D domain.多瘤病毒增强子中的蛋白质识别位点:增强子突变体中NF-1因子新位点的形成及增强子D结构域中一个位点的特征分析
EMBO J. 1990 Mar;9(3):947-55. doi: 10.1002/j.1460-2075.1990.tb08193.x.
6
Genetic analysis of the enhancer requirements for polyomavirus DNA replication in mice.小鼠多瘤病毒DNA复制增强子需求的遗传分析
J Virol. 1990 Feb;64(2):476-85. doi: 10.1128/JVI.64.2.476-485.1990.
7
Relationship of eukaryotic DNA replication to committed gene expression: general theory for gene control.真核生物DNA复制与特定基因表达的关系:基因控制的一般理论
Microbiol Rev. 1991 Sep;55(3):512-42. doi: 10.1128/mr.55.3.512-542.1991.
8
E1A represses wild-type and F9-selected polyomavirus DNA replication by a mechanism not requiring depression of large tumor antigen transcription.E1A通过一种不需要抑制大肿瘤抗原转录的机制来抑制野生型和F9选择的多瘤病毒DNA复制。
J Virol. 1991 Jun;65(6):2921-8. doi: 10.1128/JVI.65.6.2921-2928.1991.
9
Mutations in the VP1 coding region of polyomavirus determine differentiating stage specificity.多瘤病毒VP1编码区的突变决定分化阶段特异性。
J Virol. 1992 Dec;66(12):7153-8. doi: 10.1128/JVI.66.12.7153-7158.1992.
J Virol. 1983 Sep;47(3):586-99. doi: 10.1128/JVI.47.3.586-599.1983.
4
DNA replication origin of polyoma virus: early proximal boundary.多瘤病毒的DNA复制起点:早期近端边界
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Sequence repeats in a polyoma virus DNA region important for gene expression.多瘤病毒DNA区域中对基因表达重要的序列重复。
J Virol. 1983 Jul;47(1):233-7. doi: 10.1128/JVI.47.1.233-237.1983.
6
Papovaviral persistent infections.乳头多瘤空泡病毒持续性感染
Microbiol Rev. 1982 Dec;46(4):384-425. doi: 10.1128/mr.46.4.384-425.1982.
7
The pUC plasmids, an M13mp7-derived system for insertion mutagenesis and sequencing with synthetic universal primers.pUC质粒,一种源自M13mp7的用于插入诱变和使用合成通用引物进行测序的系统。
Gene. 1982 Oct;19(3):259-68. doi: 10.1016/0378-1119(82)90015-4.
8
Polyoma mutants that productively infect F9 embryonal carcinoma cells do not rescue wild-type polyoma in F9 cells.能有效感染F9胚胎癌细胞的多瘤病毒突变体无法拯救F9细胞中的野生型多瘤病毒。
Proc Natl Acad Sci U S A. 1982 Mar;79(5):1479-83. doi: 10.1073/pnas.79.5.1479.
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A region of the polyoma virus genome between the replication origin and late protein coding sequences is required in cis for both early gene expression and viral DNA replication.多瘤病毒基因组中位于复制起点和晚期蛋白编码序列之间的区域对于早期基因表达和病毒DNA复制而言,在顺式作用中是必需的。
Nucleic Acids Res. 1981 Dec 11;9(23):6231-50. doi: 10.1093/nar/9.23.6231.
10
Expression of polyoma early functions in mouse embryonal carcinoma cells depends on sequence rearrangements in the beginning of the late region.
Cell. 1980 Jun;20(2):393-9. doi: 10.1016/0092-8674(80)90625-x.