Mangiarotti Giorgio, Schlessinger David
Department of Microbiology, Washington University School of Medicine St. Louis, Mo. 63110, U.S.A.
J Mol Biol. 1967 Nov 14;29(3):395-418. doi: 10.1016/0022-2836(67)90107-6. Epub 2004 Oct 27.
During a continuous label with [H]uracil of fragile cells in exponential growth, all or very nearly all the hybridizable mRNA of the cells can be observed in polyribosomes during zonal sedimentation in sucrose gradients. In contrast, all the newly formed rRNA appears to be free of polyribosomes until it is part of complete ribosomal subunits. The separation of the two major classes of newly formed RNA permits the direct observation of the growth with time of mRNA molecules, of ribosomal subunits and of polyribosomes. A complete chain of ribosomal RNA forms in one to two minutes; completion of either a 30 s or 50 s ribosome requires a minimum of about five minutes more. The specific activities of free ribosomal subunits and those that are present in polyribosomes increase at identical rates, consistent with very rapid exchange of the two classes. Before any new subunits are finished, the H-labeled RNA in polyribosomes is the cellular mRNA, which can therefore be extracted and observed separated from ribosomal RNA. Assuming that their sedimentation rates in sucrose gradients are related to molecular weights as are those of ribosomal rRNA and that no degradation occurs dining extraction, most of the molecules of mRNA are large enough to code for only one or two protein chains of 30,000 molecular weight. The kinetics of entry of all the new mRNA into polyribosomes is in agreement with the view that a polyribosome forms as the corresponding messenger RNA is synthesized, over a period of at least a minute. 3% of the total cellular RNA in these cultures (doubling time 120 minutes) is mRNA, with an average chemical lifetime of 11 to 12·5 minutes.
在对处于指数生长期的脆弱细胞进行连续的[H]尿嘧啶标记过程中,在蔗糖梯度中进行区带沉降时,可在多核糖体中观察到细胞的所有或几乎所有可杂交的mRNA。相比之下,所有新形成的rRNA在成为完整核糖体亚基的一部分之前似乎都游离于多核糖体之外。新形成的两类RNA的分离使得能够直接观察mRNA分子、核糖体亚基和多核糖体随时间的生长情况。完整的核糖体RNA链在一到两分钟内形成;形成一个30S或50S核糖体至少还需要大约五分钟。游离核糖体亚基和多核糖体中存在的核糖体亚基的比活性以相同的速率增加,这与两类亚基之间非常快速的交换一致。在任何新的亚基完成之前,多核糖体中H标记的RNA就是细胞mRNA,因此可以提取并与核糖体RNA分离进行观察。假设它们在蔗糖梯度中的沉降速率与核糖体rRNA的沉降速率一样与分子量相关,并且在提取过程中不发生降解,那么大多数mRNA分子足够大,只能编码一两条分子量为30,000的蛋白质链。所有新mRNA进入多核糖体的动力学与这样一种观点一致,即多核糖体是在相应信使RNA合成的过程中形成的,这个过程至少持续一分钟。在这些培养物(倍增时间为120分钟)中,细胞总RNA的3%是mRNA,其平均化学半衰期为11至12.5分钟。