McEntee C M, Cantwell R, Thomas L C, Hudson A P
Dept. Microbiology and Immunology, Medical College of Pennsylvania, Philadelphia.
Biochem Biophys Res Commun. 1989 Oct 16;164(1):362-9. doi: 10.1016/0006-291x(89)91727-0.
The nuclear-mitochondrial stringent response was examined in isonuclear rho+, 21S rRNA-containing rho-, and rho o strains of S. cerevisiae. By 30 min after nutritional downshift, nuclear rDNA transcription falls to 15% of control levels congruently in all strains, as assayed via whole-cell RNA or by hybrid selection of specific double-labeled transcripts. Both in vivo and in vitro, the mitochondrial stringent response is identical between the rho- strain and its parental rho+ strain, and in both, the kinetics and magnitude of the organellar response mirror those of the nuclear response. The data show that mitochondrial transcription and protein synthesis are not required for stringent regulation of either nuclear or mitochondrial rDNA transcription.
在酿酒酵母的同核 rho+、含 21S rRNA 的 rho-和 rho o 菌株中检测了核-线粒体严谨反应。营养条件下调 30 分钟后,通过全细胞 RNA 或特异性双标记转录本的杂交筛选测定,所有菌株中的核 rDNA 转录均一致降至对照水平的 15%。在体内和体外,rho-菌株与其亲本 rho+菌株的线粒体严谨反应相同,并且在这两种情况下,细胞器反应的动力学和幅度都反映了核反应的动力学和幅度。数据表明,核或线粒体 rDNA 转录的严谨调节不需要线粒体转录和蛋白质合成。