Planck S R, Listerud M D, Buckley S D
Oregon Health Sciences University, Portland 97201.
Nucleic Acids Res. 1988 Dec 23;16(24):11663-73. doi: 10.1093/nar/16.24.11663.
The levels of mRNA encoding hnRNP core protein A1 have been compared in quiescent and proliferating Rat-1 embryonic fibroblasts. Northern blot hybridization analyses using probes made from an A1 cDNA clone, lambda HDP-182, isolated by Cobianchi et al. (J. Biol. Chem. 261:3536-2543 (1986] indicated that three sizes of poly A + RNAs, 1.6, 2.0, & 4.0 kb, have extensive sequence homology. The levels of all three A1 RNA species are responsive to the proliferation state of the cells. Stimulation of quiescent Rat-1 cells with serum or epidermal growth factor resulted in a 2- to 5-fold increase in the levels of each of these three RNAs that was evident after 2 hours and reached a peak after about 8 hours. Addition of the protein synthesis inhibitor, cycloheximide, along with epidermal growth factor completely blocked the upsurge in A1 RNA levels. Thus, the A1 RNA species are not primary transcriptional targets of epidermal growth factor but do show an induction pattern similar to mRNAs encoding some glycolytic enzymes.
在静止和增殖的大鼠-1胚胎成纤维细胞中,对编码hnRNP核心蛋白A1的mRNA水平进行了比较。使用由Cobianchi等人(《生物化学杂志》261:3536 - 2543 [1986])分离的A1 cDNA克隆λHDP - 182制备的探针进行的Northern印迹杂交分析表明,三种大小的多聚腺苷酸+RNA,即1.6、2.0和4.0 kb,具有广泛的序列同源性。所有这三种A1 RNA种类的水平都对细胞的增殖状态有反应。用血清或表皮生长因子刺激静止的大鼠-1细胞,导致这三种RNA各自的水平增加2至5倍,2小时后明显增加,约8小时后达到峰值。同时添加蛋白质合成抑制剂环己酰亚胺和表皮生长因子完全阻断了A1 RNA水平的升高。因此,A1 RNA种类不是表皮生长因子的主要转录靶点,但确实显示出与编码某些糖酵解酶的mRNA相似的诱导模式。