The Penicillium chrysogenum tom1 Gene a Major Target of Transcription Factor MAT1-1-1 Encodes a Nuclear Protein Involved in Sporulation.

IF 2.1 Q3 MYCOLOGY Frontiers in fungal biology Pub Date : 2022-07-14 eCollection Date: 2022-01-01 DOI:10.3389/ffunb.2022.937023
Barbara Ramšak, Ulrich Kück
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Abstract

Fungal mating-type loci (MAT) encode transcription factors (TFs) MAT1-1-1 and MAT1-2-1, which govern sexual reproduction as well as other developmental processes. In Penicillium chrysogenum, the major producer of the beta-lactam antibiotic penicillin, a recent chromatin immunoprecipitation followed by sequencing (ChIP-seq) analysis identified 254 genes as direct targets of MAT1-1-1, many of which encode thus far uncharacterized proteins. Here, we characterized one of the major targets of MAT1-1-1, the tom1 gene, which encodes a protein highly conserved within the group of Eurotiomycetes fungi. Using fluorescence microscopy, we demonstrated binding of MAT1-1-1 to the tom1 promoter by reporter gene analysis. Extensive electrophoretic mobility shift assays (EMSAs) further showed that the promoter sequence of tom1 is bound in vitro by both MAT1-1-1 and MAT1-2-1. This indicated an interaction between the two TFs, which was verified by yeast two-hybrid analysis. The sequence of tom1 carries a nuclear localization sequence, and indeed its nuclear localization was verified by fluorescence microscopy. The in vivo function of tom1 was investigated using tom1 deletion strains, as well as a complementing strain where the wild-type tom1 gene was reintroduced. We found a clear sporulation defect in the deletion strain, which became more evident when the fungi were grown at an elevated temperature of 31°C.

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产黄青霉tom1基因是转录因子MAT1-1-1的主要靶点,编码一种参与孢子产生的核蛋白。
真菌交配型基因座(MAT)编码转录因子(TF)MAT1-1-1和MAT1-2-1,它们控制有性生殖和其他发育过程。在β-内酰胺抗生素青霉素的主要生产商产黄青霉中,最近的染色质免疫沉淀和测序(ChIP-seq)分析确定254个基因是MAT1-1-1的直接靶标,其中许多基因编码迄今为止未鉴定的蛋白质。在这里,我们描述了MAT1-1-1的主要靶标之一,tom1基因,它编码一种在欧洲真菌群中高度保守的蛋白质。使用荧光显微镜,我们通过报告基因分析证明了MAT1-1-1与tom1启动子的结合。广泛的电泳迁移率转移分析(EMSA)进一步表明,tom1的启动子序列在体外与MAT1-1-1和MAT1-2-1结合。这表明两种TF之间存在相互作用,酵母双杂交分析证实了这一点。tom1的序列带有核定位序列,事实上,它的核定位已通过荧光显微镜进行了验证。使用tom1缺失菌株以及重新引入野生型tom1基因的补充菌株来研究tom1的体内功能。我们在缺失菌株中发现了明显的孢子形成缺陷,当真菌在31°C的高温下生长时,这种缺陷变得更加明显。
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2.70
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审稿时长
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