Yoshida T, Sato H, Iba H
Department of Tumor Virus Research, University of Tokyo, Japan.
Biochem Biophys Res Commun. 1991 Jan 31;174(2):934-9. doi: 10.1016/0006-291x(91)91508-a.
The RNA transcript and the gene product of a newly isolated fos-related gene, fra-2, were analyzed in growth-arrested and growth-stimulated chicken embryo fibroblasts (CEF). In the growth-arrested cells, a small amount of 6.8 kilobase (kb) fra-2 transcript was synthesized and several species (40-46 kilodaltons (kd) of hypophosphorylated fra-2 gene products (Fra-2) were detected. After the growth stimulation, two species of fra-2 transcripts of 6.8 kb and 5.7 kb were transiently induced. Compared with c-fos mRNA, expression of these fra-2 mRNAs was significantly prolonged, in good agreement with the previous analysis on the synthetic rate of Fos and Fra-2 proteins. Upon growth stimulation, Fra-2 undergoes more extensive phosphorylation on serine residues to form a 46 kd band, possibly owing to the protein kinase activity induced by serum.
在生长停滞和生长刺激的鸡胚成纤维细胞(CEF)中分析了新分离的fos相关基因fra-2的RNA转录本和基因产物。在生长停滞的细胞中,合成了少量6.8千碱基(kb)的fra-2转录本,并检测到几种低磷酸化的fra-2基因产物(Fra-2)(40-46千道尔顿(kd))。生长刺激后,短暂诱导出6.8 kb和5.7 kb的两种fra-2转录本。与c-fos mRNA相比,这些fra-2 mRNA的表达显著延长,这与先前对Fos和Fra-2蛋白合成速率的分析结果高度一致。生长刺激后,Fra-2在丝氨酸残基上发生更广泛的磷酸化,形成46 kd的条带,这可能归因于血清诱导的蛋白激酶活性。