{"title":"The Cys2-His2 zinc finger transcription factor NsdC regulates hyphal branching, conidiation and mycelial pellet morphology in Aspergillus oryzae","authors":"Hui Ting Chu , Naazneen Sofeo , Jasmin Jebarani Jebamony , Prakash Arumugam","doi":"10.1016/j.fgb.2025.104019","DOIUrl":null,"url":null,"abstract":"<div><div>Hyper-branching morphology boosts protein production in filamentous fungi as protein secretion occurs predominantly at the actively growing apical hyphal tip. However, mechanisms regulating hyphal morphology in fungi remain poorly characterized. In this paper, we report that the Cys2-His2 Zinc finger transcription factor NsdC negatively regulates both conidiation and hyphal branching in <em>Aspergillus oryzae.</em> The <em>∆nsdC A. oryzae</em> mutants produced 10-fold more conidia than the wild type (WT) strain and overexpressed BrlA which is the master transcription factor for the conidiation pathway. The mutant also produced hyphae that were more branched in comparison to the WT strain. Analysis of macro-morphology of <em>∆nsdC</em> mutant strain expressing human lysozyme in protein production medium (5 × DPY) revealed that it formed large mycelial clumps compared to compact pellets in the WT strain. However, lysozyme secretion in the ∆<em>nsdC</em> mutants was comparable to the WT strain, indicating that hyper-branching does not necessarily result in increased protein secretion. Our results also demonstrate that NsdC is a critical regulator of conidiation, hyphal branching and mycelial macro-morphology in <em>A. oryzae</em>.</div></div>","PeriodicalId":55135,"journal":{"name":"Fungal Genetics and Biology","volume":"180 ","pages":"Article 104019"},"PeriodicalIF":2.3000,"publicationDate":"2025-06-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fungal Genetics and Biology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S108718452500060X","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0
Abstract
Hyper-branching morphology boosts protein production in filamentous fungi as protein secretion occurs predominantly at the actively growing apical hyphal tip. However, mechanisms regulating hyphal morphology in fungi remain poorly characterized. In this paper, we report that the Cys2-His2 Zinc finger transcription factor NsdC negatively regulates both conidiation and hyphal branching in Aspergillus oryzae. The ∆nsdC A. oryzae mutants produced 10-fold more conidia than the wild type (WT) strain and overexpressed BrlA which is the master transcription factor for the conidiation pathway. The mutant also produced hyphae that were more branched in comparison to the WT strain. Analysis of macro-morphology of ∆nsdC mutant strain expressing human lysozyme in protein production medium (5 × DPY) revealed that it formed large mycelial clumps compared to compact pellets in the WT strain. However, lysozyme secretion in the ∆nsdC mutants was comparable to the WT strain, indicating that hyper-branching does not necessarily result in increased protein secretion. Our results also demonstrate that NsdC is a critical regulator of conidiation, hyphal branching and mycelial macro-morphology in A. oryzae.
丝状真菌的超分支形态促进了蛋白质的产生,因为蛋白质的分泌主要发生在活跃生长的顶端菌丝尖端。然而,真菌菌丝形态的调节机制仍不清楚。本文报道了Cys2-His2锌指转录因子NsdC对米曲霉分生和菌丝分支均有负调控作用。∆nsdC A. oryzae突变体产生的分生孢子数是野生型(WT)的10倍,并且过表达分生途径的主要转录因子BrlA。与WT菌株相比,突变体也产生了更多分支的菌丝。表达人溶菌酶的∆nsdC突变菌株在蛋白生产培养基(5 × DPY)中的宏观形态分析显示,与WT菌株的致密球相比,它形成了较大的菌丝团块。然而,∆nsdC突变体的溶菌酶分泌与WT菌株相当,这表明超分支不一定会导致蛋白质分泌增加。我们的研究结果还表明,NsdC是米孢霉分生、菌丝分支和菌丝宏观形态的关键调节因子。
期刊介绍:
Fungal Genetics and Biology, formerly known as Experimental Mycology, publishes experimental investigations of fungi and their traditional allies that relate structure and function to growth, reproduction, morphogenesis, and differentiation. This journal especially welcomes studies of gene organization and expression and of developmental processes at the cellular, subcellular, and molecular levels. The journal also includes suitable experimental inquiries into fungal cytology, biochemistry, physiology, genetics, and phylogeny.
Fungal Genetics and Biology publishes basic research conducted by mycologists, cell biologists, biochemists, geneticists, and molecular biologists.
Research Areas include:
• Biochemistry
• Cytology
• Developmental biology
• Evolutionary biology
• Genetics
• Molecular biology
• Phylogeny
• Physiology.