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v-sis 转化细胞中 c-Jun、Jun-B、Jun-D 和 Egr-1 的磷酸化转化特异性模式。

Transformation-specific pattern of phosphorylation of c-Jun, Jun-B, Jun-D and Egr-1 in v-sis transformed cells.

作者信息

Grover-Bardwick A, Adamson E, Mercola D

机构信息

San Diego Regional Cancer Center, CA 92161.

出版信息

Carcinogenesis. 1994 Aug;15(8):1667-74. doi: 10.1093/carcin/15.8.1667.

DOI:10.1093/carcin/15.8.1667
PMID:8055649
Abstract

The degree of phosphorylation of c-Jun, Jun-B, Jun-D and Egr-1 transcription factors was examined during normal growth and during a prolonged period of defined transformation of NIH-3T3 cells which conditionally express v-sis [Mercola, D. et al. (1992) Oncogene, 7, 1793-1803]. During the asynchronous growth of normal cells phosphorylation of all factors was low and constant at all stages of growth from low density (c. 25 x 10(3) cells/cm2) through log-phase of growth to saturation density (c. 100 x 10(3) cells/cm2). Upon induction of v-sis, a marked and coordinate increase in phosphorylation occurred for c-Jun, Jun-B and Egr-1 to approximately 320%, 230% and 420% respectively above basal levels which was stable for the 2.5 day transformation period. The phosphorylation of Jun-D increased to over 600% and, after about 20 h, steadily declined to near basal levels at 54 h post-induction. Moreover, at any time phosphorylation and v-sis expression were fully reversible upon removal of the inducer. It appears that increased phosphorylation of the Jun family members and Egr-1 is not necessary for normal growth of NIH-3T3 but is dependent upon the expression of v-sis. Thus, normal and transformed cells may be distinguished. For c-Jun, the v-sis enhanced phosphorylation occurs at serines 63 and 73 and is required for transformation by several oncogenes [Smeal, T. et al. (1992) Mol. Cell. Biol., 12, 3507-3513]. The results described here show that the phosphorylation of additional factors is a stable and specific correlate of transformation which have have regulatory significance during transformation.

摘要

在正常生长期间以及在条件性表达v-sis的NIH-3T3细胞的长期特定转化过程中,检测了c-Jun、Jun-B、Jun-D和Egr-1转录因子的磷酸化程度[梅科拉,D.等人(1992年),《癌基因》,7,1793 - 1803]。在正常细胞的异步生长过程中,从低密度(约25×10³个细胞/cm²)到对数生长期再到饱和密度(约100×10³个细胞/cm²)的所有生长阶段,所有因子的磷酸化水平都很低且恒定。诱导v-sis表达后,c-Jun、Jun-B和Egr-1的磷酸化显著且协同增加,分别比基础水平高出约320%、230%和420%,在2.5天的转化期内保持稳定。Jun-D的磷酸化增加到超过600%,并且在诱导后约20小时,在诱导后54小时稳步下降至接近基础水平。此外,在任何时候,去除诱导剂后磷酸化和v-sis表达都是完全可逆的。似乎Jun家族成员和Egr-1的磷酸化增加对于NIH-3T3细胞的正常生长不是必需的,而是依赖于v-sis的表达。因此,可以区分正常细胞和转化细胞。对于c-Jun,v-sis增强的磷酸化发生在丝氨酸63和73位点,并且是几种癌基因转化所必需的[斯米尔,T.等人(1992年),《分子细胞生物学》,12,3507 - 3513]。这里描述的结果表明,其他因子的磷酸化是转化的稳定且特异性的相关指标,在转化过程中具有调节意义。

相似文献

1
Transformation-specific pattern of phosphorylation of c-Jun, Jun-B, Jun-D and Egr-1 in v-sis transformed cells.v-sis 转化细胞中 c-Jun、Jun-B、Jun-D 和 Egr-1 的磷酸化转化特异性模式。
Carcinogenesis. 1994 Aug;15(8):1667-74. doi: 10.1093/carcin/15.8.1667.
2
Suppression of v-sis-dependent transformation by the transcription factor, Egr-1.转录因子Egr-1对v-sis依赖性转化的抑制作用。
Oncogene. 1994 May;9(5):1367-77.
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Protein kinase C-zeta reverts v-raf transformation of NIH-3T3 cells.蛋白激酶C-ζ可逆转NIH-3T3细胞的v-raf转化。
Genes Dev. 1996 Jun 15;10(12):1455-66. doi: 10.1101/gad.10.12.1455.
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Imbalanced expression of cellular nuclear oncogenes caused by v-sis/PDGF-2.由v-sis/血小板衍生生长因子-2导致的细胞核癌基因表达失衡。
Oncogene. 1991 Sep;6(9):1531-7.
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Platelet-derived growth factor (PDGF) B and A homodimers transform murine fibroblasts depending on the genetic background of the cell.血小板衍生生长因子(PDGF)B和A同二聚体根据细胞的遗传背景转化小鼠成纤维细胞。
J Biol Chem. 1994 Dec 2;269(48):30604-8.
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Raf revertant cells resist transformation by non-nuclear oncogenes and are deficient in the induction of early response genes by TPA and serum.Raf回复细胞对非核癌基因介导的转化具有抗性,并且在佛波酯(TPA)和血清诱导早期反应基因方面存在缺陷。
Oncogene. 1993 Feb;8(2):361-70.
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Oncoprotein-mediated signalling cascade stimulates c-Jun activity by phosphorylation of serines 63 and 73.癌蛋白介导的信号级联反应通过丝氨酸63和73的磷酸化刺激c-Jun活性。
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Rapid effects of triiodothyronine on immediate-early gene expression in Schwann cells.三碘甲状腺原氨酸对雪旺细胞即刻早期基因表达的快速影响。
Glia. 2001 Aug;35(2):81-9. doi: 10.1002/glia.1073.
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Antiproliferative effects of heparin on normal and transformed NIH/3T3 fibroblasts.肝素对正常及转化的NIH/3T3成纤维细胞的抗增殖作用。
Cell Biol Int. 1993 Aug;17(8):781-6. doi: 10.1006/cbir.1993.1140.
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Reversible transformation by v-sis: a model cell line for analysis of transformation by antisense methods.由v-sis介导的可逆转化:一种用于通过反义方法分析转化的模型细胞系。
Antisense Res Dev. 1991 Fall;1(3):289-95.

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