Allgemeine und Molekulare Botanik, Ruhr-Universität Bochum, 44780 Bochum, Germany.
Mikrobiologisches Institut - Klinische Mikrobiologie, Immunologie und Hygiene, Universitätsklinikum Erlangen und Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg, 91054 Erlangen, Germany.
G3 (Bethesda). 2021 Feb 9;11(2). doi: 10.1093/g3journal/jkaa012.
Mating-type transcription factors are master regulators of sexually related signal transduction pathways in fungi; however, their recognition of specific DNA sequences from target genes is widely undetermined. Here, we identified and characterized the DNA-binding sequence of the MAT1-1-1 alpha-box domain transcription factor from the human pathogen Aspergillus fumigatus. In order to explore MAT1-1-1 DNA-binding targets, we used the previously reported MAT1-1-1 binding motif from Penicillium chrysogenum, in a bioinformatics approach. We identified 18 A. fumigatus genes carrying the MAT1.1 sequence in their upstream region, among them genes for the α-pheromone precursor (PpgA), G-protein-coupled pheromone receptor (PreA), and for TomA, an unidentified protein. To validate our prediction further, quantification of transcript levels showed a decrease in expression of ppgA, tomA, and others in a MAT1-1 deletion strain. For a functional analysis of the binding sites, truncated variants of the A. fumigatus MAT1-1-1 gene were introduced into Escherichia coli for heterologous expression. The yield of recombinant protein was further optimized for the AfMAT1-1-178-235 variant that harbors an extended alpha-box domain. AfMAT1-1-178-235 bound to a subset of the most strongly upregulated genes: ppgA, preA, and tomA. The DNA-binding specificity was confirmed by testing mutated binding sequences, as well as performing competition experiments with specific and non-specific sequences. Finally, equilibrium dissociation constants of 1.83 ± 0.1 and 1.45 ± 0.26 µM were determined for AfMAT1-1-178-235 and fusion protein GST-AfMAT1-1-178-235. Collectively, these findings provide further insights into AfMAT1-1-1-mediated gene expression and imply that alpha-box domain regulators from other members of Eurotiales control fungal development in a conserved manner.
交配型转录因子是真菌中与性相关的信号转导途径的主要调节剂;然而,它们对靶基因特定 DNA 序列的识别在很大程度上还不清楚。在这里,我们从人类病原体烟曲霉中鉴定并描述了 MAT1-1-1α-盒结构域转录因子的 DNA 结合序列。为了探索 MAT1-1-1 DNA 结合靶标,我们使用了之前从青霉属报道的 MAT1-1-1 结合基序,采用了一种生物信息学方法。我们在 18 个携带 MAT1.1 序列的烟曲霉基因中发现了它们的上游区域,其中包括α-信息素前体(PpgA)、G 蛋白偶联信息素受体(PreA)和 TomA(一个未鉴定的蛋白)的基因。为了进一步验证我们的预测,我们发现 MAT1-1 缺失株中 ppgA、tomA 和其他基因的转录水平下降。为了对结合位点进行功能分析,我们将烟曲霉 MAT1-1-1 基因的截断变体导入大肠杆菌进行异源表达。进一步优化了含有扩展α-盒结构域的 AfMAT1-1-178-235 变体的重组蛋白产量。AfMAT1-1-178-235 与一组表达最强上调的基因结合:ppgA、preA 和 tomA。通过测试突变结合序列以及使用特异性和非特异性序列进行竞争实验,证实了 DNA 结合特异性。最后,确定了 AfMAT1-1-178-235 和融合蛋白 GST-AfMAT1-1-178-235 的平衡解离常数分别为 1.83±0.1 和 1.45±0.26μM。总的来说,这些发现进一步深入了解了 AfMAT1-1-1 介导的基因表达,并暗示来自其他粪壳菌目的α-盒结构域调节剂以保守的方式控制真菌的发育。