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A growth-dependent transcription initiation factor (TIF-IA) interacting with RNA polymerase I regulates mouse ribosomal RNA synthesis.

机译:与RNA聚合酶I相互作用的依赖生长的转录起始因子(TIF-IA)调节小鼠核糖体RNA的合成。

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摘要

Control of mouse ribosomal RNA synthesis in response to extracellular signals is mediated by TIF-IA, a regulatory factor whose amount or activity correlates with cell proliferation. Factor TIF-IA interacts with RNA polymerase I (pol I), thus converting it into a transcriptionally active holoenzyme, which is able to initiate specifically at the rDNA promoter in the presence of the other auxiliary transcription initiation factors, designated TIF-IB, TIF-IC and UBF. With regard to several criteria, the growth-dependent factor TIF-IA behaves like a bacterial sigma factor: (i) it associates physically with pol I, (ii) it is required for initiation of transcription, (iii) it is present in limiting amounts and (iv) under certain salt conditions, it is chromatographically separable from the polymerase. In addition, evidence is presented that dephosphorylation of pol I abolishes in vitro transcription initiation from the ribosomal gene promoter without significantly affecting the polymerizing activity of the enzyme at nonspecific templates. The involvement of both a regulatory factor and post-translational modification of the transcribing enzyme provides an efficient and versatile mechanism of rDNA transcription regulation which enables the cell to adapt ribosome synthesis rapidly to a variety of extracellular signals.
机译:响应细胞外信号的小鼠核糖体RNA合成的控制是由TIF-IA介导的,TIF-IA是一种调节因子,其数量或活性与细胞增殖相关。因子TIF-IA与RNA聚合酶I(pol I)相互作用,从而将其转化为转录活性全酶,能够在存在其他辅助转录起始因子(称为TIF-IB,TIF)的情况下在rDNA启动子上特异性起始-IC和UBF。关于几个标准,生长依赖性因子TIF-IA的行为类似于细菌sigma因子:(i)与pol I物理结合,(ii)转录启动所必需,(iii)存在于限制中和(iv)在某些盐条件下,可从色谱上与聚合酶分离。另外,有证据表明,pol I的去磷酸化消除了核糖体基因启动子的体外转录起始,而没有显着影响该酶在非特异性模板上的聚合活性。转录酶的调节因子和翻译后修饰的参与提供了rDNA转录调节的有效且通用的机制,使细胞能够将核糖体合成快速适应各种细胞外信号。

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