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核糖体基因转录的物种特异性:一种与人类RNA聚合酶I相关的因子可阻止小鼠核糖体DNA的转录。

Species specificity of ribosomal gene transcription: a factor associated with human RNA polymerase I prevents transcription of mouse rDNA.

作者信息

Eberhard D, Grummt I

机构信息

Division of Molecular Biology of the Cell II, German Cancer Research Center, Heidelberg, Germany.

出版信息

DNA Cell Biol. 1996 Feb;15(2):167-73. doi: 10.1089/dna.1996.15.167.

Abstract

An intrinsic property of class I gene transcription by RNA polymerase I (Pol I) is the species specificity of the initiation reaction. Previous studies have demonstrated that species-specific rDNA promoter recognition is brought about by a TBP-TAF complex, termed TIF-IB in mouse and SL1 in man. We have compared the ability of affinity-purified TIF-IB and SL1 to direct transcription from the homologous rDNA template both in a reconstituted transcription system and in nuclear extracts prepared from mouse and human cells. We show that Pol I from both species and the individual transcription factors, with the exception of TIF-IB/SL1, are functionally interchangeable in the reconstituted transcription system containing purified proteins. In nuclear extracts, however, species-specific differences are obvious. Whereas SL1 reprograms a heterologous mouse extract to recognize the human promoter, TIF-IB fails to reprogram a human extract unless it is complemented with mouse Pol I. Crude human, but not mouse, Pol I exhibits species-specific differences that disappear after purification. We propose that in extracts and less purified fractions human Pol I exists as 'holoenzyme' containing associated protein(s) that prevent assembly of TIF-IB-directed initiation complexes at the murine rDNA promoter.

摘要

RNA聚合酶I(Pol I)进行的I类基因转录的一个内在特性是起始反应的物种特异性。先前的研究表明,物种特异性的核糖体DNA(rDNA)启动子识别是由一种TBP-TAF复合物介导的,在小鼠中称为TIF-IB,在人类中称为SL1。我们比较了亲和纯化的TIF-IB和SL1在重组转录系统以及从小鼠和人类细胞制备的核提取物中指导同源rDNA模板转录的能力。我们发现,在含有纯化蛋白质的重组转录系统中,除了TIF-IB/SL1外,来自这两个物种的Pol I和各个转录因子在功能上是可互换的。然而,在核提取物中,物种特异性差异很明显。虽然SL1可以使异源小鼠提取物重新编程以识别人类启动子,但TIF-IB除非与小鼠Pol I互补,否则无法使人类提取物重新编程。未经纯化的人类Pol I(而非小鼠Pol I)表现出物种特异性差异,纯化后这些差异消失。我们提出,在提取物和纯化程度较低的组分中,人类Pol I以“全酶”形式存在,其中含有相关蛋白质,这些蛋白质会阻止TIF-IB指导的起始复合物在小鼠rDNA启动子处组装。

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