Ramagopal S, Marcus A
J Cell Physiol. 1979 Mar;98(3):603-11. doi: 10.1002/jcp.1040980318.
RNA synthesis has been investigated in resting and growing cells of a culture of Scarlet rose. The rates of messenger RNA (mRNA) and ribosomal RNA (rRNA) synthesis are five- and ten-fold higher, respectively, in the growing culture. In stationary phase cultures, newly synthesized 26S and 18S rRNA do not appear in the cytoplasm in equimolar amounts. Rather, the 26S/18S ratio of [3H]-uridine labeled rRNA of stationary cells ranged from 0.9 to 1.3 while the ratio of the corresponding fraction from growing cells was 1.6 to 2.0. A similar result was obtained when cells were labeled with [3H-CH3] methionine. Pulse chase experiments demonstrated that the nascent pre-rRNA in resting cells could be chased into polysomes. These data are interpreted to indicate that a major part of the regulation of rRNA synthesis in stationary cells is at the level of the processing of the rRNA transcript.
对 Scarlet rose 培养物中静止和生长细胞的 RNA 合成进行了研究。在生长培养物中,信使 RNA(mRNA)和核糖体 RNA(rRNA)的合成速率分别高出五倍和十倍。在稳定期培养物中,新合成的 26S 和 18S rRNA 不会以等摩尔量出现在细胞质中。相反,静止细胞中 [3H]-尿苷标记的 rRNA 的 26S/18S 比值在 0.9 至 1.3 之间,而生长细胞中相应部分的比值为 1.6 至 2.0。当用 [3H-CH3] 甲硫氨酸标记细胞时,也得到了类似的结果。脉冲追踪实验表明,静止细胞中新生的前体 rRNA 可以追踪到多核糖体中。这些数据被解释为表明静止细胞中 rRNA 合成调控的主要部分在于 rRNA 转录本的加工水平。