Zerial M, Toschi L, Ryseck R P, Schuermann M, Müller R, Bravo R
European Molecular Biology Laboratory, Heidelberg, FRG.
EMBO J. 1989 Mar;8(3):805-13. doi: 10.1002/j.1460-2075.1989.tb03441.x.
We have identified a gene, fos B, encoding a nuclear protein of 338 amino acids presenting a 70% homology with c-fos, whose expression is activated during G0/G1 transition. Growth factor stimulation of quiescent cells leads to a rapid and transient accumulation of fos B mRNA, with kinetics similar to those of c-fos. The induction of fos B mRNA levels is in part due to a dramatic increase in the transcription of the gene. The half-life of fos B mRNA is in the order of 10-15 min. Both transcriptional activation and mRNA stability are substantially increased in the presence of protein synthesis inhibitors. Immunoprecipitation studies showed that fos B as c-fos protein, forms a complex in vitro with c-jun and jun B proteins in the absence of a target binding sequence. Gel retardation assays demonstrated that fos B protein positively influences the binding of c-jun and jun B proteins to an AP-1 binding consensus sequence, suggesting that fos B protein plays a role in control of gene expression.
我们已经鉴定出一个基因,即fos B,它编码一种由338个氨基酸组成的核蛋白,与c-fos具有70%的同源性,其表达在G0/G1期转换过程中被激活。对静止细胞的生长因子刺激导致fos B mRNA迅速且短暂地积累,其动力学与c-fos相似。fos B mRNA水平的诱导部分归因于该基因转录的显著增加。fos B mRNA的半衰期约为10 - 15分钟。在存在蛋白质合成抑制剂的情况下,转录激活和mRNA稳定性均显著增加。免疫沉淀研究表明,与c-fos蛋白一样,fos B蛋白在体外无靶结合序列时能与c-jun和jun B蛋白形成复合物。凝胶阻滞试验表明,fos B蛋白对c-jun和jun B蛋白与AP-1结合共有序列的结合有正向影响,这表明fos B蛋白在基因表达调控中发挥作用。