Glibetic M, Larson D E, Sienna N, Bachellerie J P, Sells B H
Department of Molecular Biology and Genetics, University of Guelph, Ontario, Canada.
Exp Cell Res. 1992 Sep;202(1):183-9. doi: 10.1016/0014-4827(92)90418-8.
Differentiation of proliferating rat L6 myoblasts to syncytial multinucleated myotubes results in a significant downshift in the rate of U3 snRNA gene transcription, paralleling the decrease in rRNA synthesis previously documented. Coordinate production of U3 snRNA and rRNA during the differentiation process adds further support for a role of U3 snRNA in ribosome biogenesis. Despite the dramatic decrease in U3 snRNA transcription during differentiation, a corresponding drop in the cellular level of U3 snRNA does not occur. In myotubes, the amount of U3 snRNA is regulated at the post-transcriptional level in which there is a significant accumulation of U3 snRNA in the cytoplasm of myotubes. This intracellular redistribution of U3 snRNA may significantly affect the entire process of rRNA maturation or result from the decrease in ribosome production accompanying terminal differentiation of myoblasts.
增殖的大鼠L6成肌细胞分化为多核的肌管会导致U3 snRNA基因转录速率显著下降,这与之前记录的rRNA合成减少情况相似。在分化过程中U3 snRNA和rRNA的协同产生进一步支持了U3 snRNA在核糖体生物发生中的作用。尽管在分化过程中U3 snRNA转录显著减少,但U3 snRNA的细胞水平并未相应下降。在肌管中,U3 snRNA的量在转录后水平受到调节,其中U3 snRNA在肌管细胞质中大量积累。U3 snRNA的这种细胞内重新分布可能会显著影响rRNA成熟的整个过程,或者是由于成肌细胞终末分化伴随的核糖体产生减少所致。