Grover-Bardwick A, Adamson E, Mercola D
San Diego Regional Cancer Center, CA 92161.
Carcinogenesis. 1994 Aug;15(8):1667-74. doi: 10.1093/carcin/15.8.1667.
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.
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。