Trivedi A, Vilalta A, Gopalan S, Johnson D L
Department of Molecular Pharmacology, Schools of Pharmacy and Medicine, University of Southern California, Los Angeles 90033, USA.
Mol Cell Biol. 1996 Dec;16(12):6909-16. doi: 10.1128/MCB.16.12.6909.
We have investigated the role of the TATA-binding protein (TBP) in modulating RNA polymerase (Pol) III gene activity. Epitope-tagged TBP (e-TBP) was both transiently and stably transfected in Drosophila Schneider S-2 cells to increase the total cellular level of TBP. Analysis of the transcripts synthesized from cotransfected tRNA and U6 RNA genes revealed that both types of RNA Pol III promoters were substantially stimulated by an increase in e-TBP in a dose-dependent manner. Furthermore, a TBP-dependent increase in the levels of endogenous tRNA transcripts was produced in the stable line induced to express the e-TBP. We further determined whether the ability of increased TBP to induce RNA Pol III gene expression was due to a direct effect of increased TBP complexes on RNA Pol III gene promoters or an indirect consequence of enhanced expression of RNA Pol II genes. A TBP expression plasmid (e-TBP332), containing a mutation within the highly conserved carboxy-terminal domain, was both transiently and stably transfected into S-2 cells. e-TBP332 augmented the transcription from two RNA Pol II gene promoters indistinguishably from that observed when e-TBP was expressed. In contrast, e-TBP332 was completely defective in its ability to stimulate either the tRNA or U6 RNA gene promoters. In addition, increasing levels of a truncated TBP protein containing only the carboxy-terminal region failed to induce either the tRNA or U6 RNA gene promoter, whereas it retained its ability to stimulate an RNA Pol II promoter. Thus, the TBP-dependent increase in RNA Pol II gene activity is not sufficient for enhanced RNA Pol III gene transcription; rather, a direct effect on RNA Pol III promoters is required. Furthermore, these results provide the first direct evidence that the amino-terminal region of TBP is important for the formation or function of TBP-containing complexes utilized by TATA-less and TATA-containing RNA Pol III promoters. Together, these studies demonstrate that TBP is limiting for the expression of both classes of RNA Pol III promoters in Drosophila cells and implicate an important role for TBP in regulating RNA Pol III gene expression.
我们研究了TATA结合蛋白(TBP)在调节RNA聚合酶(Pol)III基因活性中的作用。将表位标记的TBP(e-TBP)瞬时和稳定转染到果蝇Schneider S-2细胞中,以提高细胞内TBP的总水平。对共转染的tRNA和U6 RNA基因合成的转录本进行分析发现,两种类型的RNA Pol III启动子均受到e-TBP增加的显著刺激,且呈剂量依赖性。此外,在诱导表达e-TBP的稳定细胞系中,内源性tRNA转录本水平出现了TBP依赖性增加。我们进一步确定,TBP增加诱导RNA Pol III基因表达的能力,是由于TBP复合物增加对RNA Pol III基因启动子的直接作用,还是RNA Pol II基因表达增强的间接结果。将一个在高度保守的羧基末端结构域内含有突变的TBP表达质粒(e-TBP332)瞬时和稳定转染到S-2细胞中。e-TBP332增强了两个RNA Pol II基因启动子的转录,与表达e-TBP时观察到的情况无明显差异。相比之下,e-TBP332在刺激tRNA或U6 RNA基因启动子的能力上完全缺陷。此外,仅包含羧基末端区域的截短TBP蛋白水平增加,未能诱导tRNA或U6 RNA基因启动子,而它保留了刺激RNA Pol II启动子的能力。因此,RNA Pol II基因活性的TBP依赖性增加不足以增强RNA Pol III基因转录;相反,需要对RNA Pol III启动子有直接作用。此外,这些结果提供了首个直接证据,表明TBP的氨基末端区域对于无TATA和含TATA的RNA Pol III启动子所利用的含TBP复合物的形成或功能很重要。总之,这些研究表明,TBP对果蝇细胞中两类RNA Pol III启动子的表达具有限制作用,并暗示TBP在调节RNA Pol III基因表达中起重要作用。