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多个酵母核糖体DNA基因的转录需要Uaf30将上游激活因子(UAF)靶向到启动子。

Transcription of multiple yeast ribosomal DNA genes requires targeting of UAF to the promoter by Uaf30.

作者信息

Hontz Robert D, French Sarah L, Oakes Melanie L, Tongaonkar Prasad, Nomura Masayasu, Beyer Ann L, Smith Jeffrey S

机构信息

Department of Biochemistry and Molecular Genetics, University of Virginia Health System, School of Medicine, Charlottesville, VA 22908, USA.

出版信息

Mol Cell Biol. 2008 Nov;28(21):6709-19. doi: 10.1128/MCB.00703-08. Epub 2008 Sep 2.

Abstract

Upstream activating factor (UAF) is a multisubunit complex that functions in the activation of ribosomal DNA (rDNA) transcription by RNA polymerase I (Pol I). Cells lacking the Uaf30 subunit of UAF reduce the rRNA synthesis rate by approximately 70% compared to wild-type cells and produce rRNA using both Pol I and Pol II. Miller chromatin spreads demonstrated that even though there is an overall reduction in rRNA synthesis in uaf30 mutants, the active rDNA genes in such strains are overloaded with polymerases. This phenotype was specific to defects in Uaf30, as mutations in other UAF subunits resulted in a complete absence of rDNA genes with high or even modest Pol densities. The lack of Uaf30 prevented UAF from efficiently binding to the rDNA promoter in vivo, leading to an inability to activate a large number of rDNA genes. The relatively few genes that did become activated were highly transcribed, apparently to compensate for the reduced rRNA synthesis capacity. The results show that Uaf30p is a key targeting factor for the UAF complex that facilitates activation of a large proportion of rDNA genes in the tandem array.

摘要

上游激活因子(UAF)是一种多亚基复合物,在RNA聚合酶I(Pol I)激活核糖体DNA(rDNA)转录过程中发挥作用。与野生型细胞相比,缺乏UAF的Uaf30亚基的细胞将rRNA合成速率降低了约70%,并且使用Pol I和Pol II两者来产生rRNA。Miller染色质铺展显示,尽管uaf30突变体中rRNA合成总体减少,但此类菌株中的活性rDNA基因却被聚合酶过度负载。这种表型是Uaf30缺陷所特有的,因为其他UAF亚基的突变导致完全不存在具有高或中等Pol密度的rDNA基因。Uaf30的缺失阻止了UAF在体内有效结合rDNA启动子,导致无法激活大量rDNA基因。相对少数被激活的基因被高度转录,显然是为了补偿降低的rRNA合成能力。结果表明,Uaf30p是UAF复合物的关键靶向因子,有助于激活串联阵列中大部分rDNA基因。

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