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弗拉菲,粗糙脉孢菌分生孢子形成的主要调节因子,直接激活一个受发育调控的疏水蛋白基因。

Fluffy, the major regulator of conidiation in Neurospora crassa, directly activates a developmentally regulated hydrophobin gene.

作者信息

Rerngsamran Panan, Murphy Michael B, Doyle Sharon A, Ebbole Daniel J

机构信息

Program for the Biology of Filamentous Fungi, Department of Plant Pathology and Microbiology, Texas A&M University, College Station, TX 77843, USA.

出版信息

Mol Microbiol. 2005 Apr;56(1):282-97. doi: 10.1111/j.1365-2958.2005.04544.x.

Abstract

The fluffy (fl) gene of Neurospora crassa is required for asexual sporulation and encodes an 88 kDa polypeptide containing a typical fungal Zn2Cys6 DNA-binding motif. Identification of genes regulated by fl will provide insight into how fungi regulate growth during morphogenesis. As a step towards identifying the target genes on which FL may act, we sought to define target sequences to which the FL protein binds. The DNA binding domain of FL was expressed in Escherichia coli as a fusion with glutathione S-transferase (GST) and purified using glutathione-sepharose affinity chromatography. The DNA binding sites were selected and amplified by means of a polymerase chain reaction (PCR)-mediated random-site selection method involving affinity bead-binding and gel mobility shift analysis. Sequencing and comparison of the selected clones suggested that FL binds to the motif 5'-CGG(N)9CCG-3'. A potential binding site was found in the promoter region of the eas (ccg-2) gene, which encodes a fungal hydrophobin. In vitro competitive binding assays revealed a preferred binding site for FL in the eas promoter, 5'-CGGAAGTTTC CTCCG-3', which is located 1498 bp upstream of the eas translation initiation codon. In vivo experiments using a foreign DNA sequence tag also confirmed that this sequence resides in a region required for FL regulation. In addition, yeast one hybrid experiments demonstrated that the C-terminal portion of FL functions in transcriptional activation. Transcriptional profiling was used to identify additional potential targets for regulation by fl.

摘要

粗糙脉孢菌的蓬松(fl)基因是无性孢子形成所必需的,它编码一种88 kDa的多肽,该多肽含有典型的真菌Zn2Cys6 DNA结合基序。鉴定受fl调控的基因将有助于深入了解真菌在形态发生过程中如何调节生长。作为鉴定FL可能作用的靶基因的第一步,我们试图确定FL蛋白结合的靶序列。FL的DNA结合结构域在大肠杆菌中作为与谷胱甘肽S-转移酶(GST)的融合蛋白表达,并使用谷胱甘肽-琼脂糖亲和色谱法进行纯化。通过聚合酶链反应(PCR)介导的随机位点选择方法,结合亲和珠结合和凝胶迁移率变动分析,选择并扩增DNA结合位点。对所选克隆的测序和比较表明,FL与基序5'-CGG(N)9CCG-3'结合。在编码真菌疏水蛋白的eas(ccg-2)基因的启动子区域发现了一个潜在的结合位点。体外竞争性结合试验揭示了eas启动子中FL的优先结合位点5'-CGGAAGTTTC CTCCG-3',该位点位于eas翻译起始密码子上游1498 bp处。使用外源DNA序列标签的体内实验也证实该序列位于FL调控所需的区域。此外,酵母单杂交实验表明FL的C末端部分在转录激活中起作用。转录谱分析用于鉴定fl调控的其他潜在靶标。

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