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构巢曲霉多聚体CCAAT结合复合物AnCF通过其hapB亚基基因进行负向自我调节。

The Aspergillus nidulans multimeric CCAAT binding complex AnCF is negatively autoregulated via its hapB subunit gene.

作者信息

Steidl S, Hynes M J, Brakhage A A

机构信息

Institut für Mikrobiologie und Genetik, Technische Universität Darmstadt, Schnittspahnstrasse 10, Darmstadt, D-64287, Germany.

出版信息

J Mol Biol. 2001 Mar 2;306(4):643-53. doi: 10.1006/jmbi.2001.4412.

Abstract

Cis-acting CCAAT elements are frequently found in eukaryotic promoter regions. Many of them are bound by conserved multimeric complexes. In the fungus Aspergillus nidulans the respective complex was designated AnCF (A. nidulans CCAAT binding factor). AnCF is composed of at least three subunits designated HapB, HapC and HapE. Here, we show that the promoter regions of the hapB genes in both A. nidulans and Aspergillus oryzae contain two inversely oriented, conserved CCAAT boxes (box alpha and box beta). Electrophoretic mobility shift assays (EMSAs) using both nuclear extracts and the purified, reconstituted AnCF complex indicated that AnCF binding in vitro to these boxes occurs in a non-mutually exclusive manner. Western and Northern blot analyses showed that steady-state levels of HapB protein as well as hapB mRNA were elevated in hapC and hapE deletion mutants, suggesting a repressing effect of AnCF on hapB expression. Consistently, in a hapB deletion background the hapB-lacZ expression level was elevated compared with the expression in the wild-type. This was further supported by overexpression of hapB using an inducible alcA-hapB construct. Induction of alcA-hapB expression strongly repressed the expression of a hapB-lacZ gene fusion. However, mutagenesis of box beta led to a fivefold reduced expression of a hapB-lacZ gene fusion compared with the expression derived from a wild-type hapB-lacZ fusion. These results indicate that (i) box beta is an important positive cis-acting element in hapB regulation, (ii) AnCF does not represent the corresponding positive trans-acting factor and (iii) that AnCF is involved in repression of hapB.

摘要

顺式作用的CCAAT元件常见于真核生物启动子区域。其中许多元件与保守的多聚体复合物结合。在真菌构巢曲霉中,相应的复合物被命名为AnCF(构巢曲霉CCAAT结合因子)。AnCF由至少三个亚基组成,分别命名为HapB、HapC和HapE。在此,我们表明构巢曲霉和米曲霉中hapB基因的启动子区域都含有两个反向排列的保守CCAAT框(α框和β框)。使用核提取物以及纯化的、重组的AnCF复合物进行的电泳迁移率变动分析(EMSA)表明,AnCF在体外与这些框的结合并非相互排斥。蛋白质免疫印迹和Northern印迹分析表明,在hapC和hapE缺失突变体中,HapB蛋白以及hapB mRNA的稳态水平升高,这表明AnCF对hapB表达具有抑制作用。一致地,在hapB缺失背景下,hapB - lacZ的表达水平相较于野生型有所升高。使用可诱导的alcA - hapB构建体对hapB进行过表达进一步支持了这一点。诱导alcA - hapB表达强烈抑制了hapB - lacZ基因融合体的表达。然而,β框的诱变导致hapB - lacZ基因融合体的表达相较于野生型hapB - lacZ融合体降低了五倍。这些结果表明:(i)β框是hapB调控中一个重要的正向顺式作用元件;(ii)AnCF并非相应的正向反式作用因子;(iii)AnCF参与了对hapB的抑制。

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