Yang Q, Radebaugh C A, Kubaska W, Geiss G K, Paule M R
Department of Biochemistry and Molecular Biology, Colorado State University, Fort Collins 80523, USA.
Nucleic Acids Res. 1995 Nov 11;23(21):4345-52. doi: 10.1093/nar/23.21.4345.
The intergenic spacer (IGS) of Acanthamoeba castellanii rRNA genes contains repeated elements which are weak enhancers for transcription by RNA polymerase I. A protein, EBF, was identified and partially purified which binds to the enhancers and to several other sequences within the IGS, but not to other DNA fragments, including the rRNA core promoter. No consensus binding sequence could be discerned in these fragments and bound factor is in rapid equilibrium with unbound. EBF has functional characteristics similar to vertebrate upstream binding factors (UBF). Not only does it bind to the enhancer and other IGS elements, but it also stimulates binding of TIF-IB, the fundamental transcription initiation factor, to the core promoter and stimulates transcription from the promoter. Attempts to identify polypeptides with epitopes similar to rat or Xenopus laevis UBF suggest that structurally the protein from A.castellanii is not closely related to vertebrate UBF.
卡氏棘阿米巴rRNA基因的基因间隔区(IGS)含有重复元件,这些元件是RNA聚合酶I转录的弱增强子。一种名为EBF的蛋白质被鉴定并部分纯化,它能与增强子以及IGS内的其他几个序列结合,但不与包括rRNA核心启动子在内的其他DNA片段结合。在这些片段中无法识别出一致的结合序列,结合的因子与未结合的因子处于快速平衡状态。EBF具有与脊椎动物上游结合因子(UBF)相似的功能特性。它不仅能与增强子和其他IGS元件结合,还能刺激基本转录起始因子TIF-IB与核心启动子的结合,并刺激启动子的转录。试图鉴定具有与大鼠或非洲爪蟾UBF相似表位的多肽,结果表明卡氏棘阿米巴的这种蛋白质在结构上与脊椎动物的UBF没有密切关系。