Dong H, Kirsebom L A, Nilsson L
Department of Molecular Biology, Uppsala University Biomedical Center, Sweden.
J Mol Biol. 1996 Aug 23;261(3):303-8. doi: 10.1006/jmbi.1996.0461.
We have studied the expression of 4.5 S RNA and M1 RNA, the catalytic subunit of Escherchia coli RNase P, under various growth conditions. Both RNA species increase in abundance as a function of growth rate. There are roughly 450 molecules of 4.5 S RNA and 80 molecules of M1 RNA per cell at 0.4 doubling per hour, and this is increased to 5300 and 1060 molecules per cell, respectively, at 2.7 doublings per hour. Deletion of both relA and spoT, the two genes that are responsible for synthesis of ppGpp, does not affect the rate of synthesis of either RNA species. However, deletion of fis renders the expression of 4.5 S RNA independent of growth rate, but has little effect on the expression of M1 RNA. These data suggest that the expression of both 4.5 S RNA and M1 RNA genes are growth-rate regulated, but not through the same mechanism. The growth-rate dependent accumulation of 4.5 S RNA depends on FIS-mediated trans-activation, whereas that of M1 RNA is not governed by ppGpp or by FIS.
我们研究了大肠杆菌核糖核酸酶P的催化亚基4.5S RNA和M1 RNA在各种生长条件下的表达情况。这两种RNA的丰度均随生长速率的增加而增加。在每小时0.4次倍增时,每个细胞中约有450个4.5S RNA分子和80个M1 RNA分子,而在每小时2.7次倍增时,这一数量分别增加到每个细胞5300个和1060个分子。负责合成ppGpp的relA和spoT这两个基因的缺失,并不影响这两种RNA的合成速率。然而,fis基因的缺失使4.5S RNA的表达与生长速率无关,但对M1 RNA的表达影响不大。这些数据表明,4.5S RNA和M1 RNA基因的表达均受生长速率调控,但调控机制不同。4.5S RNA依赖生长速率的积累取决于FIS介导的反式激活,而M1 RNA的积累则不受ppGpp或FIS的调控。