Linzer D I, Nathans D
Proc Natl Acad Sci U S A. 1983 Jul;80(14):4271-5. doi: 10.1073/pnas.80.14.4271.
A cDNA plasmid library has been constructed from the poly(A)+ RNA present in BALB/c3T3 cells after serum stimulation. Of 3,500 clones tested, approximately 0.5% contained inserts corresponding to mRNAs present at higher levels in serum-stimulated BALB/c 3T3 cell cultures than in quiescent cultures. Most of these RNA species increased 2- to 5-fold, and the kinetics of increase for various RNAs differed. One clone (28H6) hybridized to a 1-kilobase RNA species that is present at barely detectable levels in resting cells but is increased at least 15- to 20-fold after serum stimulation, reaching a maximal level coincident with the onset of DNA synthesis. This RNA was at a high level in proliferating cells but decreased rapidly as cells reached confluence. 28H6 RNA was also increased in resting cells infected with simian virus 40 or stimulated with platelet-derived growth factor.
已从血清刺激后的BALB/c3T3细胞中存在的聚腺苷酸加尾(poly(A)+)RNA构建了一个cDNA质粒文库。在测试的3500个克隆中,约0.5%含有与在血清刺激的BALB/c 3T3细胞培养物中比在静止培养物中水平更高的mRNA相对应的插入片段。这些RNA种类中的大多数增加了2至5倍,并且各种RNA的增加动力学有所不同。一个克隆(28H6)与一种1千碱基的RNA种类杂交,该RNA在静止细胞中仅以难以检测的水平存在,但在血清刺激后至少增加15至20倍,在DNA合成开始时达到最高水平。这种RNA在增殖细胞中处于高水平,但随着细胞达到汇合状态而迅速下降。28H6 RNA在感染猿猴病毒40的静止细胞或用血小板衍生生长因子刺激的静止细胞中也增加。