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里氏木霉中纤维素分解和木聚糖分解基因的转录激活因子XYR1特异性结合位点的鉴定

Identification of specific binding sites for XYR1, a transcriptional activator of cellulolytic and xylanolytic genes in Trichoderma reesei.

作者信息

Furukawa Takanori, Shida Yosuke, Kitagami Naoki, Mori Kazuki, Kato Masashi, Kobayashi Tetsuo, Okada Hirofumi, Ogasawara Wataru, Morikawa Yasushi

机构信息

Department of Bioengineering, Nagaoka University of Technology, Nagaoka, Niigata, Japan.

出版信息

Fungal Genet Biol. 2009 Aug;46(8):564-74. doi: 10.1016/j.fgb.2009.04.001. Epub 2009 Apr 23.

Abstract

The transcriptional activator XYR1 is the central regulator that governs cellulolytic and xylanolytic gene expression in Trichoderma reesei. However, despite its biological importance, relatively little is known about its functional binding sequences. In the present study, we investigated the binding characteristics and specific target for XYR1 by using DNase I footprinting analysis and electrophoretic mobility shift assays. We demonstrate that XYR1 can interact not only with the 5'-GGCTAA-3' motif but also with several 5'-GGC(A/T)(3)-3' motifs. In silico analysis revealed that the 5'-GGC(A/T)(3)-3' motifs are widespread as single site in 5'-upstream region of all the XYR1-regulated genes. Furthermore, we defined the important nucleotides within the binding site that contribute to specific interaction with XYR1. Our results suggest that, together with the inverted repeat motifs, the single 5'-GGC(A/T)(4)-3' motifs play important roles as functional XYR1-binding sites in the regulation of cellulase and xylanase gene expression in T. reesei.

摘要

转录激活因子XYR1是里氏木霉中调控纤维素分解和木聚糖分解基因表达的核心调节因子。然而,尽管其具有生物学重要性,但对其功能结合序列的了解相对较少。在本研究中,我们通过DNA酶I足迹分析和电泳迁移率变动分析,研究了XYR1的结合特性和特定靶点。我们证明XYR1不仅可以与5'-GGCTAA-3'基序相互作用,还可以与几个5'-GGC(A/T)(3)-3'基序相互作用。电子分析表明,5'-GGC(A/T)(3)-3'基序在所有XYR1调控基因的5'-上游区域中作为单个位点广泛存在。此外,我们确定了结合位点内有助于与XYR1特异性相互作用的重要核苷酸。我们的结果表明,与反向重复基序一起,单个5'-GGC(A/T)(4)-3'基序在里氏木霉纤维素酶和木聚糖酶基因表达调控中作为功能性XYR1结合位点发挥重要作用。

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