The composition of the RNA polymerase I transcription machinery switches from initiation to elongation mode

被引:25
作者
Bier, M
Fath, S
Tschochner, H
机构
[1] Univ Regensburg, Inst Biol 3, D-93053 Regensburg, Germany
[2] Biochem Zentrum Heidelberg, D-69120 Heidelberg, Germany
来源
FEBS LETTERS | 2004年 / 564卷 / 1-2期
关键词
ribosome synthesis; nucleolus; rDNA; in vitro transcription; promoter; RNA polymerase I; Rrn3p; Saccharomyces cerevisiae;
D O I
10.1016/S0014-5793(04)00311-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The amounts of RNA polymerase I (Pol I) and basal rDNA transcription factors were determined in yeast whole cell extracts. A 17-fold excess of Pol I was found compared to the Pol I-specific initiation factors upstream activating factor (UAF) and core factor (CF) which underlines that both initiation factors interact with a minor fraction of Pol I when rDNA transcription is active. Surprisingly, Rrn3p, another Pol I-specific initiation factor, is more abundant in cell lysates than UAF and CF. Our analyses revealed that a large fraction of cellular Rrn3p is not associated with Pol I. However, the amount of initiation-active Rrn3p which forms a stable complex with Pol I corresponds to the levels of UAF and CF which have been shown to bind the promoter. Initiation-active Rrn3p dissociates from the template during or immediately after Pol I has switched from initiation to elongation. Our data support a model in which the elongating Pol I leaves the initiation factors UAF, CF and Rrn3p close by the promoter. (C) 2004 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:41 / 46
页数:6
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