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危机前的小鼠细胞在54千道尔顿磷蛋白的量以及对猿猴病毒40转化的易感性方面表现出菌株特异性共变。

Pre-crisis mouse cells show strain-specific covariation in the amount of 54-kilodalton phosphoprotein and in susceptibility to transformation by simian virus 40.

作者信息

Chen S, Blanck G, Pollack R E

出版信息

Proc Natl Acad Sci U S A. 1983 Sep;80(18):5670-4. doi: 10.1073/pnas.80.18.5670.

DOI:10.1073/pnas.80.18.5670
PMID:6310588
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC384320/
Abstract

We have used several inbred mouse strains to examine the role of the 54-kilodalton (kDa) cellular phosphoprotein in transformation by the papovavirus simian virus 40. We have measured the endogenous 54-kDa phosphoprotein in cells obtained from these inbred mouse strains. To study the effect of passage, cell cultures were measured for amount of the 54-kDa phosphoprotein at the 2nd and 12th passages. In the absence of any transforming agent, the amount of endogenous 54-kDa phosphoprotein in early pre-crisis mouse cells varied in a strain-specific way. Transformation frequency varied coordinately with endogenous 54-kDa expression. Mouse strains whose cells produced a high level of endogenous 54-kDa phosphoprotein on passage did not further increase its expression after simian virus 40 transformation.

摘要

我们使用了几种近交系小鼠品系来研究54千道尔顿(kDa)细胞磷蛋白在多瘤病毒猿猴病毒40转化过程中的作用。我们测量了从这些近交系小鼠品系获得的细胞中的内源性54-kDa磷蛋白。为了研究传代的影响,在第2代和第12代时测量细胞培养物中54-kDa磷蛋白的量。在没有任何转化剂的情况下,早期危机前小鼠细胞中内源性54-kDa磷蛋白的量以品系特异性方式变化。转化频率与内源性54-kDa表达协同变化。其细胞在传代时产生高水平内源性54-kDa磷蛋白的小鼠品系在猿猴病毒40转化后不会进一步增加其表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9abe/384320/7d949bb23fc8/pnas00644-0226-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9abe/384320/14b1a3c7dfc1/pnas00644-0224-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9abe/384320/a3ccb8d99b7c/pnas00644-0225-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9abe/384320/7d949bb23fc8/pnas00644-0226-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9abe/384320/14b1a3c7dfc1/pnas00644-0224-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9abe/384320/a3ccb8d99b7c/pnas00644-0225-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9abe/384320/7d949bb23fc8/pnas00644-0226-a.jpg

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1
Pre-crisis mouse cells show strain-specific covariation in the amount of 54-kilodalton phosphoprotein and in susceptibility to transformation by simian virus 40.危机前的小鼠细胞在54千道尔顿磷蛋白的量以及对猿猴病毒40转化的易感性方面表现出菌株特异性共变。
Proc Natl Acad Sci U S A. 1983 Sep;80(18):5670-4. doi: 10.1073/pnas.80.18.5670.
2
Quantitation and characterization of a species-specific and embryo stage-dependent 55-kilodalton phosphoprotein also present in cells transformed by simian virus 40.一种也存在于被猿猴病毒40转化的细胞中的、物种特异性且依赖胚胎阶段的55千道尔顿磷蛋白的定量与特性分析。
Proc Natl Acad Sci U S A. 1981 Nov;78(11):6953-7. doi: 10.1073/pnas.78.11.6953.
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6
Cell growth and differentiation in vitro in mouse macrophages transformed by a tsA mutant of simian virus 40. I. Cellular response in proliferative and phagocytic activities to the shift of temperature differs depending on the culture state in mouse bone marrow cells transformed by the tsA640 mutant of simian virus 40.由猿猴病毒40的tsA突变体转化的小鼠巨噬细胞的体外细胞生长与分化。I. 经猿猴病毒40的tsA640突变体转化的小鼠骨髓细胞中,增殖和吞噬活性的细胞反应随温度变化而不同,这取决于培养状态。
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Genomic landscapes of endogenous retroviruses unveil intricate genetics of conventional and genetically-engineered laboratory mouse strains.内源性逆转录病毒的基因组图谱揭示了传统和基因工程实验室小鼠品系的复杂遗传学特征。
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Secreted phosphoprotein markers for neoplastic transformation of human epithelial and fibroblastic cells.用于人类上皮细胞和成纤维细胞肿瘤转化的分泌型磷蛋白标志物。
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Sensitivity of simian virus 40-transformed C57BL/6 mouse embryo fibroblasts to lysis by murine natural killer cells.猿猴病毒40转化的C57BL/6小鼠胚胎成纤维细胞对鼠自然杀伤细胞裂解的敏感性。
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Fate of viral DNA in nonpermissive cells infected with simian virus 40.被猴病毒40感染的非允许细胞中病毒DNA的命运
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本文引用的文献

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Quantitative studies of the growth of mouse embryo cells in culture and their development into established lines.对培养的小鼠胚胎细胞生长及其发育成既定细胞系的定量研究。
J Cell Biol. 1963 May;17(2):299-313. doi: 10.1083/jcb.17.2.299.
2
A 53-kilodalton protein common to chemically and virally transformed cells shows extensive sequence similarities between species.一种在化学转化和病毒转化细胞中常见的53千道尔顿蛋白质在不同物种间显示出广泛的序列相似性。
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p53 transformation-related protein: detection by monoclonal antibody in mouse and human cells.
小鼠p53细胞肿瘤抗原的基因和假基因位于不同的染色体上。
Mol Cell Biol. 1984 Aug;4(8):1638-40. doi: 10.1128/mcb.4.8.1638-1640.1984.
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SV40 transformation of Swiss 3T3 cells can cause a stable reduction in the calcium requirement for growth.猿猴病毒40(SV40)对瑞士3T3细胞的转化可导致细胞生长所需钙含量的稳定降低。
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Oligomerization of oncoprotein p53.癌蛋白p53的寡聚化
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Overproduction of protein p53 contributes to simian virus 40-mediated transformation.蛋白质p53的过度产生有助于猿猴病毒40介导的转化。
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Structural prerequisites of simian virus 40 large T antigen for the maintenance of cell transformation.猿猴病毒40大T抗原维持细胞转化的结构前提条件。
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p53转化相关蛋白:在小鼠和人类细胞中通过单克隆抗体进行检测
Proc Natl Acad Sci U S A. 1981 Mar;78(3):1695-9. doi: 10.1073/pnas.78.3.1695.
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Transforming activity of human tumor DNAs.人类肿瘤DNA的转化活性。
Proc Natl Acad Sci U S A. 1981 Feb;78(2):1181-4. doi: 10.1073/pnas.78.2.1181.
5
Nonlytic simian virus 40-specific 100K phosphoprotein is associated with anchorage-independent growth in simian virus 40-transformed and revertant mouse cell lines.非裂解性猿猴病毒40特异性100K磷蛋白与猿猴病毒40转化及回复的小鼠细胞系中的不依赖贴壁生长有关。
Mol Cell Biol. 1981 Nov;1(11):994-1006. doi: 10.1128/mcb.1.11.994-1006.1981.
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Isolation of a transforming sequence from a human bladder carcinoma cell line.从人膀胱癌细胞系中分离出一个转化序列。
Cell. 1982 May;29(1):161-9. doi: 10.1016/0092-8674(82)90100-3.
7
Quantitation and characterization of a species-specific and embryo stage-dependent 55-kilodalton phosphoprotein also present in cells transformed by simian virus 40.一种也存在于被猿猴病毒40转化的细胞中的、物种特异性且依赖胚胎阶段的55千道尔顿磷蛋白的定量与特性分析。
Proc Natl Acad Sci U S A. 1981 Nov;78(11):6953-7. doi: 10.1073/pnas.78.11.6953.
8
Three different human tumor cell lines contain different oncogenes.三种不同的人类肿瘤细胞系含有不同的癌基因。
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Detection of a common feature in several human tumor cell lines--a 53,000-dalton protein.在几种人类肿瘤细胞系中检测到一种共同特征——一种53,000道尔顿的蛋白质。
Proc Natl Acad Sci U S A. 1981 Jan;78(1):41-5. doi: 10.1073/pnas.78.1.41.
10
Activation of a cellular onc gene by promoter insertion in ALV-induced lymphoid leukosis.禽白血病病毒诱导的淋巴细胞白血病中,启动子插入激活细胞癌基因。
Nature. 1981 Apr 9;290(5806):475-80. doi: 10.1038/290475a0.