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野生型和突变型启动子在体内外对TFIIIB70过表达的差异反应。

A differential response of wild type and mutant promoters to TFIIIB70 overexpression in vivo and in vitro.

作者信息

Sethy-Coraci I, Moir R D, López-de-León A, Willis I M

机构信息

Department of Biochemistry, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

出版信息

Nucleic Acids Res. 1998 May 15;26(10):2344-52. doi: 10.1093/nar/26.10.2344.

Abstract

TFIIIB, the initiation factor for transcription by RNA polymerase III (pol III) is, in yeast, composed of three subunits: TBP, TFIIIB70/Brf1 and TFIIIB90. To determine the extent to which each of these subunits is limiting for pol III transcription, the effect of overexpressing each subunit was assessed on the expression of wild-type and promoter mutant pol III genes both in vivo and in vitro . In vivo , we find that the synthesis of wild-type pol III genes is not limited to a significant extent by the level of any TFIIIB subunit. There is, however, a two-fold increase in the synthesis of the promoter mutant gene, sup9-e A19-supS1 , in strains overexpressing TFIIIB70. The findings suggest that overexpression of TFIIIB70has a differential effect on the expression of pol III genes with strong versus weak promoters. In vitro transcription assays support this conclusion and reveal an inverse correlation between the transcriptional response to TFIIIB70overexpression and promoter strength. The individual TFIIIB subunits are nuclear by immunofluorescence and are calculated to have nuclear concentrations in the low micromolar range. In comparison, the factors are diluted 100-fold or more in whole cell extracts. This dilution accounts for the generally limiting nature of TFIIIB70in pol III gene transcription in vitro.

摘要

TFIIIB是RNA聚合酶III(pol III)转录的起始因子,在酵母中由三个亚基组成:TBP、TFIIIB70/Brf1和TFIIIB90。为了确定这些亚基中的每一个对pol III转录的限制程度,在体内和体外评估了过表达每个亚基对野生型和启动子突变型pol III基因表达的影响。在体内,我们发现野生型pol III基因的合成在很大程度上不受任何TFIIIB亚基水平的限制。然而,在过表达TFIIIB70的菌株中,启动子突变基因sup9-e A19-supS1的合成增加了两倍。这些发现表明,TFIIIB70的过表达对具有强启动子和弱启动子的pol III基因的表达有不同的影响。体外转录分析支持这一结论,并揭示了对TFIIIB70过表达的转录反应与启动子强度之间的负相关。通过免疫荧光检测,单个TFIIIB亚基定位于细胞核,计算得出其在细胞核中的浓度处于低微摩尔范围内。相比之下,在全细胞提取物中这些因子被稀释了100倍或更多。这种稀释解释了TFIIIB70在体外pol III基因转录中通常具有的限制性质。

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