Bandman E
Mol Biol Rep. 1977 Dec;3(6):421-8. doi: 10.1007/BF00808383.
The stability of mRNA has been measured in 3T3 cells in the resting and the growing states, and also during the transition from the resting to the growing state. Pulse labled poly (A)+ mRNA chased with uridine and cytidine supplemented growth medium decayed with a half-life of 6.5 hr in the resting state, 26 hr during the transition from the resting to the growing condition, and 18 hr during serum-stimulated growth. The half-life of poly(A)+ mRNA determined by steady state labeling yielded similar results in resting and serum-stimulated 3T3 cells. Thus during the transition from resting to serum-stimulated growth in 3T3 cells poly(A)+ mRNA becomes more stable.
已在处于静止状态和生长状态的3T3细胞中,以及从静止状态向生长状态转变的过程中,对mRNA的稳定性进行了测定。用补充有尿苷和胞苷的生长培养基进行脉冲标记的聚腺苷酸(poly(A)+)mRNA,在静止状态下以6.5小时的半衰期衰减,在从静止状态向生长状态转变的过程中半衰期为26小时,在血清刺激生长期间半衰期为18小时。通过稳态标记测定的聚腺苷酸(poly(A)+)mRNA的半衰期,在静止和血清刺激的3T3细胞中产生了相似的结果。因此,在3T3细胞从静止状态向血清刺激生长状态转变的过程中,聚腺苷酸(poly(A)+)mRNA变得更加稳定。