{"title":"基因调控网络资源有助于预测烟曲霉生物合成基因簇的反式作用调控因子。","authors":"Hye-Won Seo, Jin Woo Bok, Nancy P Keller","doi":"10.1128/mbio.03874-24","DOIUrl":null,"url":null,"abstract":"<p><p>The field of secondary metabolism has greatly benefitted from computational advances in recent years. This has been particularly true for fungal natural product studies. Strides in genome mining have led to the identification of an extraordinary number of secondary metabolite biosynthetic gene clusters (BGCs) across the fungal Kingdom and metabologenomic platforms can group BGCs into gene cluster families and link them to initial chemical structures. Missing are computational applications focused on identifying BGC regulatory networks. Here, we applied the new online gene regulatory network resource, GRAsp (<u>G</u>ene <u>R</u>egulation of <i><u>Asp</u>ergillus fumigatus</i>), to identify unknown and unpredictable BGC trans-acting transcriptional/metabolite production modules. GRAsp correctly predicted a two-component regulatory module composed of the transcription factors (TFs), RogA (<u>r</u>egulation <u>o</u>f <u>g</u>liotoxin) and HsfA, which negatively regulate the gliotoxin BGC and are also involved in gliotoxin self-protection. RogA functions through the repression of <i>gliZ,</i> the pathway-specific gliotoxin TF, and HsfA functions by activating <i>rogA</i> expression. Furthermore, GRAsp identified TFs that regulate the production of two BGCs lacking pathway-specific TFs, the helvolic acid and fumitremorgin BGCs, respectively. Finally, the known TF, NsdD, was predicted and found to regulate the hexadehydroastechrome BGC. These advances highlight the power of inference algorithms to uncover unpredictable networks in specialized metabolite synthesis.IMPORTANCEToxic secondary metabolites are virulence factors of the opportunistic fungal pathogen <i>Aspergillus fumigatus,</i> yet the transcriptional networks regulating secondary metabolite production remain elusive. Uncovering novel regulators without any prior information is challenging. Computational programs have gained prominence in the field of secondary metabolite research due to their accuracy and ability to handle vast amounts of data, including DNA, RNA, and protein data. In this study, a newly developed online computer platform, Gene Regulation of <i>A. fumigatus</i>, was used to identify five regulators involved in the production of several <i>A. fumigatus</i> toxins, including gliotoxin, helvolic acid, fumitremorgin, and hexadehydroastechrome. This work illustrates the potential for discovering new trans-acting regulators and mechanisms of secondary metabolite regulation through the examination of computational gene regulatory networks.</p>","PeriodicalId":18315,"journal":{"name":"mBio","volume":" ","pages":"e0387424"},"PeriodicalIF":4.7000,"publicationDate":"2025-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11898546/pdf/","citationCount":"0","resultStr":"{\"title\":\"Gene regulatory network resource aids in predicting trans-acting regulators of biosynthetic gene clusters in <i>Aspergillus fumigatus</i>.\",\"authors\":\"Hye-Won Seo, Jin Woo Bok, Nancy P Keller\",\"doi\":\"10.1128/mbio.03874-24\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The field of secondary metabolism has greatly benefitted from computational advances in recent years. This has been particularly true for fungal natural product studies. Strides in genome mining have led to the identification of an extraordinary number of secondary metabolite biosynthetic gene clusters (BGCs) across the fungal Kingdom and metabologenomic platforms can group BGCs into gene cluster families and link them to initial chemical structures. Missing are computational applications focused on identifying BGC regulatory networks. Here, we applied the new online gene regulatory network resource, GRAsp (<u>G</u>ene <u>R</u>egulation of <i><u>Asp</u>ergillus fumigatus</i>), to identify unknown and unpredictable BGC trans-acting transcriptional/metabolite production modules. GRAsp correctly predicted a two-component regulatory module composed of the transcription factors (TFs), RogA (<u>r</u>egulation <u>o</u>f <u>g</u>liotoxin) and HsfA, which negatively regulate the gliotoxin BGC and are also involved in gliotoxin self-protection. RogA functions through the repression of <i>gliZ,</i> the pathway-specific gliotoxin TF, and HsfA functions by activating <i>rogA</i> expression. Furthermore, GRAsp identified TFs that regulate the production of two BGCs lacking pathway-specific TFs, the helvolic acid and fumitremorgin BGCs, respectively. Finally, the known TF, NsdD, was predicted and found to regulate the hexadehydroastechrome BGC. These advances highlight the power of inference algorithms to uncover unpredictable networks in specialized metabolite synthesis.IMPORTANCEToxic secondary metabolites are virulence factors of the opportunistic fungal pathogen <i>Aspergillus fumigatus,</i> yet the transcriptional networks regulating secondary metabolite production remain elusive. Uncovering novel regulators without any prior information is challenging. Computational programs have gained prominence in the field of secondary metabolite research due to their accuracy and ability to handle vast amounts of data, including DNA, RNA, and protein data. In this study, a newly developed online computer platform, Gene Regulation of <i>A. fumigatus</i>, was used to identify five regulators involved in the production of several <i>A. fumigatus</i> toxins, including gliotoxin, helvolic acid, fumitremorgin, and hexadehydroastechrome. This work illustrates the potential for discovering new trans-acting regulators and mechanisms of secondary metabolite regulation through the examination of computational gene regulatory networks.</p>\",\"PeriodicalId\":18315,\"journal\":{\"name\":\"mBio\",\"volume\":\" \",\"pages\":\"e0387424\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2025-03-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11898546/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"mBio\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1128/mbio.03874-24\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/2/18 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"mBio","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/mbio.03874-24","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/18 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
近年来,计算技术的进步极大地促进了次级代谢领域的发展。对于真菌天然产物的研究尤其如此。基因组挖掘的进展已经导致真菌王国中大量次生代谢物生物合成基因簇(BGCs)的鉴定,代谢基因组学平台可以将BGCs分组到基因簇家族中并将它们与初始化学结构联系起来。缺失的是专注于识别BGC监管网络的计算应用。在此,我们应用新的在线基因调控网络资源GRAsp (gene Regulation of Aspergillus fumigatus)来识别未知和不可预测的BGC反式转录/代谢物产生模块。GRAsp正确预测了一个由转录因子(tf)、胶质毒素调控因子RogA和HsfA组成的双组分调控模块,该模块负向调控胶质毒素BGC,并参与胶质毒素的自我保护。RogA通过抑制gliZ(通路特异性胶质毒素TF)发挥作用,HsfA通过激活RogA表达发挥作用。此外,GRAsp还发现了两种缺乏途径特异性TFs的BGCs,分别是helvolic acid和fumitremorgin BGCs,它们可以调节BGCs的产生。最后,预测了已知的TF NsdD,并发现它调节六氢星形色素BGC。这些进展突出了推理算法在揭示特殊代谢物合成中不可预测的网络方面的力量。有毒次生代谢物是条件真菌病原体烟曲霉的毒力因子,但调控次生代谢物产生的转录网络仍然难以捉摸。在没有任何事先信息的情况下发现新的监管机构是具有挑战性的。计算程序由于其准确性和处理大量数据(包括DNA、RNA和蛋白质数据)的能力,在次级代谢物研究领域获得了突出地位。本研究利用新开发的在线计算机平台“烟曲霉基因调控”(Gene Regulation of fumigatus),鉴定了参与烟曲霉毒素(包括胶质毒素、helvolic acid、fumitremorgin和hexadehydroastechrome)产生的5个调控因子。这项工作说明了通过计算基因调控网络的研究发现新的反式作用调控因子和次生代谢物调控机制的潜力。
Gene regulatory network resource aids in predicting trans-acting regulators of biosynthetic gene clusters in Aspergillus fumigatus.
The field of secondary metabolism has greatly benefitted from computational advances in recent years. This has been particularly true for fungal natural product studies. Strides in genome mining have led to the identification of an extraordinary number of secondary metabolite biosynthetic gene clusters (BGCs) across the fungal Kingdom and metabologenomic platforms can group BGCs into gene cluster families and link them to initial chemical structures. Missing are computational applications focused on identifying BGC regulatory networks. Here, we applied the new online gene regulatory network resource, GRAsp (Gene Regulation of Aspergillus fumigatus), to identify unknown and unpredictable BGC trans-acting transcriptional/metabolite production modules. GRAsp correctly predicted a two-component regulatory module composed of the transcription factors (TFs), RogA (regulation of gliotoxin) and HsfA, which negatively regulate the gliotoxin BGC and are also involved in gliotoxin self-protection. RogA functions through the repression of gliZ, the pathway-specific gliotoxin TF, and HsfA functions by activating rogA expression. Furthermore, GRAsp identified TFs that regulate the production of two BGCs lacking pathway-specific TFs, the helvolic acid and fumitremorgin BGCs, respectively. Finally, the known TF, NsdD, was predicted and found to regulate the hexadehydroastechrome BGC. These advances highlight the power of inference algorithms to uncover unpredictable networks in specialized metabolite synthesis.IMPORTANCEToxic secondary metabolites are virulence factors of the opportunistic fungal pathogen Aspergillus fumigatus, yet the transcriptional networks regulating secondary metabolite production remain elusive. Uncovering novel regulators without any prior information is challenging. Computational programs have gained prominence in the field of secondary metabolite research due to their accuracy and ability to handle vast amounts of data, including DNA, RNA, and protein data. In this study, a newly developed online computer platform, Gene Regulation of A. fumigatus, was used to identify five regulators involved in the production of several A. fumigatus toxins, including gliotoxin, helvolic acid, fumitremorgin, and hexadehydroastechrome. This work illustrates the potential for discovering new trans-acting regulators and mechanisms of secondary metabolite regulation through the examination of computational gene regulatory networks.
期刊介绍:
mBio® is ASM''s first broad-scope, online-only, open access journal. mBio offers streamlined review and publication of the best research in microbiology and allied fields.