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Oct-2促进功能性起始前复合体的组装,并且在启动子处对于多轮转录是持续必需的。

Oct-2 facilitates functional preinitiation complex assembly and is continuously required at the promoter for multiple rounds of transcription.

作者信息

Arnosti D N, Merino A, Reinberg D, Schaffner W

机构信息

Institute of Molecular Biology II, University of Zürich, Switzerland.

出版信息

EMBO J. 1993 Jan;12(1):157-66. doi: 10.1002/j.1460-2075.1993.tb05641.x.

Abstract

Octamer factor 2 (Oct-2, OTF-2, NF-A2) is an 'upstream' promoter factor that binds to the octamer motif (ATGCAAAT) implicated in control of immunoglobulin gene transcription in B-lymphocytes. We have studied the role of Oct-2 in the process of transcription initiation in vitro using both nuclear extracts and purified basal transcription factors. Oct-2 specifically stimulates transcription from octamer-containing promoters in both systems. Thus, Oct-2 is a 'true activator', rather than merely an 'anti-repressor' counteracting the effect of histones. In order-of-addition experiments, Oct-2 is required early, together with TFIID, to allow formation of a preinitiation complex. Oct-2 cannot functionally interact with cloned TATA binding protein (TBP) but rather requires 'coactivators' found in the TFIID fraction. In single-round transcription experiments, early competition for Oct-2 by an octamer oligonucleotide is deleterious, but no effect is seen after assembly of a complete preinitiation complex. However, for multiple rounds of transcription, Oct-2 is continuously required at the promoter; this result argues against a 'hit-and-run' mechanism whereby the activator becomes dispensible after organizing a TFIID-promoter complex. In agreement with our previous studies in vivo, the N-terminal glutamine-rich activation domain of Oct-2 is required for full activity in vitro, indicating that this domain directly interacts with basal transcription factors.

摘要

八聚体因子2(Oct-2、OTF-2、NF-A2)是一种“上游”启动子因子,可与八聚体基序(ATGCAAAT)结合,该基序与B淋巴细胞中免疫球蛋白基因转录的控制有关。我们使用核提取物和纯化的基础转录因子,在体外研究了Oct-2在转录起始过程中的作用。在这两个系统中,Oct-2都能特异性地刺激含八聚体启动子的转录。因此,Oct-2是一种“真正的激活因子”,而不仅仅是一种抵消组蛋白作用的“抗抑制因子”。在添加顺序实验中,Oct-2需要与TFIID一起在早期存在,以允许形成预起始复合物。Oct-2不能与克隆的TATA结合蛋白(TBP)发生功能相互作用,而是需要在TFIID组分中发现的“共激活因子”。在单轮转录实验中,八聚体寡核苷酸对Oct-2的早期竞争是有害的,但在完整的预起始复合物组装后则没有影响。然而,对于多轮转录,启动子处持续需要Oct-2;这一结果与“打了就跑”机制相悖,在该机制中,激活因子在组织TFIID-启动子复合物后就变得可有可无。与我们之前在体内的研究一致,Oct-2的N端富含谷氨酰胺的激活结构域在体外发挥完全活性是必需的,这表明该结构域直接与基础转录因子相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cb8/413187/2802ff361415/emboj00073-0169-a.jpg

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