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学者姓名：OLSSON JAN OLOF STEFAN
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Abstract ：
The Myb family of transcription factors (TFs) is a large and functionally diverse group found in all eukaryotes. Its role in fungi remains poorly studied, despite the fact that it is thought to play a role in the pathogenicity of fungal pathogens. In this study, we have characterized the functional role of a Myb family TF called MoMyb13 in the rice blast fungus, Magnaporthe oryzae. MoMyb13 has orthologues only in ascomycete fungi, making it of special interest. Localization experiments confirmed that MoMyb13 is located in the nuclei, as expected for a TF. Phenotypic analysis showed that MoMyb13 mutants exhibited reduced growth, white instead of dark colonies, formed no conidia and, consequently, no conidial appressoria. The mutants completely lost pathogenicity, despite being able to form dark hyphal appressoria at their hyphae ends. Furthermore, the mutant colonies lost hydrophobicity and had significantly reduced expression of the hydrophobin MPG1 that MoMyb13 appears to regulate. However, overexpression of MPG1 in the mutants restored hydrophobicity, but not pathogenicity. Stress assay showed that the mutants were more sensitive to SDS, CR, and H2O2, but more tolerant to NaCl and SOR. In summary, our study revealed the crucial function of MoMyb13 in the growth, conidiation, hydrophobicity, stress response, and pathogenicity of M. oryzae. MoMyb13 is thus needed in the late and very early stages of infection for the spreading of the fungus to other plants and the early establishment of infection in other plants.
Keyword ：
functional characterization functional characterization Magnaporthe oryzae Magnaporthe oryzae Myb Myb transcription factor transcription factor
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| GB/T 7714 | Li, Ya , Zheng, Xiuxia , Pei, Mengtian et al. Functional Analysis of MoMyb13, a Myb Transcription Factor Involved in Regulating Growth, Conidiation, Hydrophobicity, and Pathogenicity of Magnaporthe oryzae [J]. | AGRONOMY-BASEL , 2024 , 14 (2) . |
| MLA | Li, Ya et al. "Functional Analysis of MoMyb13, a Myb Transcription Factor Involved in Regulating Growth, Conidiation, Hydrophobicity, and Pathogenicity of Magnaporthe oryzae" . | AGRONOMY-BASEL 14 . 2 (2024) . |
| APA | Li, Ya , Zheng, Xiuxia , Pei, Mengtian , Chen, Mengting , Zhang, Shengnan , Liang, Chenyu et al. Functional Analysis of MoMyb13, a Myb Transcription Factor Involved in Regulating Growth, Conidiation, Hydrophobicity, and Pathogenicity of Magnaporthe oryzae . | AGRONOMY-BASEL , 2024 , 14 (2) . |
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The initial stage of rice blast fungus, Magnaporthe oryzae, infection, before 36 h postinoculation, is a critical timespan for deploying pathogen effectors to overcome the host's defences and ultimately cause the disease. However, how this process is regulated at the transcription level remains largely unknown. This study functionally characterized two M. oryzae Early Infection-induced Transcription Factor genes (MOEITF1 and MOEITF2) and analysed their roles in this process. Target gene deletion and mutant phenotype analysis showed that the mutants Delta moeitf1 and Delta moeitf2 were only defective for infection growth but not for vegetative growth, asexual/sexual sporulation, conidial germination, and appressoria formation. Gene expression analysis of 30 putative effectors revealed that most effector genes were down-regulated in mutants, implying a potential regulation by the transcription factors. Artificial overexpression of two severely down-regulated effectors, T1REP and T2REP, in the mutants partially restored the pathogenicity of Delta moeitf1 and Delta moeitf2, respectively, indicating that these are directly regulated. Yeast one-hybrid assay and electrophoretic mobility shift assay indicated that Moeitf1 specifically bound the T1REP promoter and Moeitf2 specifically bound the T2REP promoter. Both T1REP and T2REP were predicted to be secreted during infection, and the mutants of T2REP were severely reduced in pathogenicity. Our results indicate crucial roles for the fungal-specific Moeitf1 and Moeitf2 transcription factors in regulating an essential step in M. oryzae early establishment after penetrating rice epidermal cells, highlighting these as possible targets for disease control.
Keyword ：
early infection process early infection process effectors effectors expression expression Magnaporthe oryzae Magnaporthe oryzae transcription factors transcription factors
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| GB/T 7714 | Cao, Yiyang , Chen, Jia , Xie, Xuze et al. Characterization of two infection-induced transcription factors of Magnaporthe oryzae reveals their roles in regulating early infection and effector expression [J]. | MOLECULAR PLANT PATHOLOGY , 2022 , 23 (8) : 1200-1213 . |
| MLA | Cao, Yiyang et al. "Characterization of two infection-induced transcription factors of Magnaporthe oryzae reveals their roles in regulating early infection and effector expression" . | MOLECULAR PLANT PATHOLOGY 23 . 8 (2022) : 1200-1213 . |
| APA | Cao, Yiyang , Chen, Jia , Xie, Xuze , Liu, Shenghua , Jiang, Yue , Pei, Mengtian et al. Characterization of two infection-induced transcription factors of Magnaporthe oryzae reveals their roles in regulating early infection and effector expression . | MOLECULAR PLANT PATHOLOGY , 2022 , 23 (8) , 1200-1213 . |
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Background: Trichoderma reesei has extraordinary potential for high-level protein production at large scales, and it need to be further explored through genetic engineering tools to obtain a thorough understanding of its cellular physiology. Understanding the genetic factors involved in the intrinsic regulatory network is crucial; without this information, there would be restrictions in expressing genes of interest. Past and present studies are concentrated on the application and expansion of novel expression systems using synthetic biology concepts. These approaches involve either using previously established promoters that are strong or genetically engineered promoters. Genomic and transcriptomic methods have also been employed to isolate strong promoters and expression systems such as light-inducible expression systems, copper-inducible expression systems, L-methionine inducible promoters, and Tet-On expression system etc. Aims of review: In this review, we will highlight various research endeavors related to tunable and constitutive promoters; the role of different promoters in homologous and heterologous protein expression; the identification of innovative promoters, and strategies that may be beneficial for future research aimed at improving and enhancing protein expression in T. reesei. Key scientific concepts of the review: The characterization of new promoters and implementation of novel expression systems that will result in a significant extension of the molecular toolbox that is accessible for the genetic engineering of innovative strains of T. reesei. Genetically engineered strong inducible promoters such as Pcbh1 through replacement of transcriptional repressors (cre1, ace1) with transcriptional activators (xyr1, ace2, ace3, hap2/3/5) and synthetic expression systems can result in elevated production of endoglucanases (EGLs), beta-glucosidases (BGLs), and cellobiohydrolases (CBHs). Strong constitutive promoters such as Pcdna1 can be converted into genetically engineered synthetic hybrid promoters by integrating the activation region of strong inducible promoters, which can allow the induction and expression of cellulases even on repressing media. More efforts are necessary to identify innovative promoters and novel expression strategies for the enhanced expression of desirable proteins at industrial scales.
Keyword ：
Constitutive promoters Constitutive promoters Inducible promoters Inducible promoters Innovative promoters Innovative promoters Repressible promoters Repressible promoters Transcription factors Transcription factors Trichoderma reesei Trichoderma reesei
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| GB/T 7714 | Adnan, Muhammad , Ma, Xuekun , Olsson, Stefan et al. Promoter regulation and genetic engineering strategies for enhanced cellulase expression in Trichoderma reesei [J]. | MICROBIOLOGICAL RESEARCH , 2022 , 259 . |
| MLA | Adnan, Muhammad et al. "Promoter regulation and genetic engineering strategies for enhanced cellulase expression in Trichoderma reesei" . | MICROBIOLOGICAL RESEARCH 259 (2022) . |
| APA | Adnan, Muhammad , Ma, Xuekun , Olsson, Stefan , Wang, Juan , Liu, Gang . Promoter regulation and genetic engineering strategies for enhanced cellulase expression in Trichoderma reesei . | MICROBIOLOGICAL RESEARCH , 2022 , 259 . |
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| GB/T 7714 | Adnan, Muhammad , Ma, Xuekun , Olsson, Stefan et al. Promoter regulation and genetic engineering strategies for enhanced cellulase expression in Trichoderma reesei (vol 259, 127011, 2022) [J]. | MICROBIOLOGICAL RESEARCH , 2022 , 261 . |
| MLA | Adnan, Muhammad et al. "Promoter regulation and genetic engineering strategies for enhanced cellulase expression in Trichoderma reesei (vol 259, 127011, 2022)" . | MICROBIOLOGICAL RESEARCH 261 (2022) . |
| APA | Adnan, Muhammad , Ma, Xuekun , Olsson, Stefan , Wang, Juan , Liu, Gang . Promoter regulation and genetic engineering strategies for enhanced cellulase expression in Trichoderma reesei (vol 259, 127011, 2022) . | MICROBIOLOGICAL RESEARCH , 2022 , 261 . |
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In nature, fungal endophytes often have facultative endohyphal bacteria (FEB). Can a model plant pathogenic fungus have them, and does it affect their phenotype? We constructed a growth system/microcosm to allow an F. graminearum isolate to grow through natural soil and then re-isolated it on a gentamicin-containing medium, allowing endohyphal growth of bacteria while killing other bacteria. F. graminearum PH-1 labelled with a His1mCherry gene staining the fungal nuclei fluorescent red was used to confirm the re-isolation of the fungus. Most new re-isolates contained about 10 16SrRNA genes per fungal mCherry gene determined by qPCR. The F. graminearum + FEB holobiont isolates containing the bacteria were sub-cultured several times, and their bacterial contents were stable. Sequencing the bacterial 16SrRNA gene from several Fg-FEB holobiont isolates revealed endophytic bacteria known to be capable of nitrogen fixation. We tested the pathogenicity of one common Fg-FEB holobiont association, F. graminearum + Stenatrophomonas maltophilia, and found increased pathogenicity. The 16SrRNA gene load per fungal His1mCherry gene inside the wheat stayed the same as previously found in vitro. Finally, strong evidence was found for Fg-S. maltophilia symbiotic nitrogen fixation benefitting the fungus.
Keyword ：
facultative endohyphal bacteria facultative endohyphal bacteria fungal-bacterial interaction fungal-bacterial interaction gentamicin gentamicin new enrichment and isolation technique new enrichment and isolation technique symbiotic nitrogen fixation symbiotic nitrogen fixation
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| GB/T 7714 | Ali, Hina , Pei, Mengtian , Li, Hongchen et al. The Wheat Head Blight Pathogen Fusarium graminearum Can Recruit Collaborating Bacteria from Soil [J]. | CELLS , 2022 , 11 (19) . |
| MLA | Ali, Hina et al. "The Wheat Head Blight Pathogen Fusarium graminearum Can Recruit Collaborating Bacteria from Soil" . | CELLS 11 . 19 (2022) . |
| APA | Ali, Hina , Pei, Mengtian , Li, Hongchen , Fang, Wenqin , Mao, Hongkun , Khan, Hamid Ali et al. The Wheat Head Blight Pathogen Fusarium graminearum Can Recruit Collaborating Bacteria from Soil . | CELLS , 2022 , 11 (19) . |
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The rice pathogen Magnaporthe oryzae causes severe losses to rice production. Previous studies have shown that the protein kinase MoCK2 is essential for pathogenesis, and this ubiquitous eukaryotic protein kinase might affect several processes in the fungus that are needed for infection. To better understand which cellular processes are affected by MoCK2 activity, we performed a detailed transcriptome sequencing analysis of deletions of the MoCK2 b1 and b2 components in relation to the background strain Ku80 and connected this analysis with the abundance of substrates for proteins in a previous pulldown of the essential CKa subunit of CK2 to estimate the effects on proteins directly interacting with CK2. The results showed that MoCK2 seriously affected carbohydrate metabolism, fatty acid metabolism, amino acid metabolism, and the related transporters and reduced acetyl-CoA production. CK2 phosphorylation can affect the folding of proteins and especially the effective formation of protein complexes by intrinsically disordered or mitochondrial import by destabilizing soluble alpha helices. The upregulated genes found in the pulldown of the b1 and b2 mutants indicate that proteins directly interacting with CK2 are compensatorily upregulated depending on their pulldown. A similar correlation was found for mitochondrial proteins. Taken together, the classes of proteins and the changes in regulation in the b1 and b2 mutants suggest that CK2 has a central role in mitochondrial metabolism, secondary metabolism, and reactive oxygen species (ROS) resistance, in addition to its previously suggested role in the formation of new ribosomes, all of which are processes central to efficient nonself responses as innate immunity. IMPORTANCE The protein kinase CK2 is highly expressed and essential for plants, animals, and fungi, affecting fatty acid-related metabolism. In addition, it directly affects the import of essential mitochondrial proteins into mitochondria. These effects mean that CK2 is essential for lipid metabolism and mitochondrial function and, as shown previously, is crucial for making new translation machinery proteins. Taken together, our new results combined with previously reported results indicate that CK2 is an essential protein necessary for the capacities to launch efficient innate immunity responses and withstand the negative effects of such responses necessary for general resistance against invading bacteria and viruses as well as to interact with plants, withstand plant immunity responses, and kill plant cells.
Keyword ：
acetyl-CoA acetyl-CoA Magnaporthe oryzae Magnaporthe oryzae mitochondria mitochondria MoCK2 MoCK2 transcriptome analysis transcriptome analysis
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| GB/T 7714 | Zhang, Lianhu , Shan, Chonglei , Zhang, Yifan et al. Transcriptome Analysis of Protein Kinase MoCK2, which Affects Acetyl-CoA Metabolism and Import of CK2-Interacting Mitochondrial Proteins into Mitochondria in the Rice Blast Fungus Magnaporthe oryzae [J]. | MICROBIOLOGY SPECTRUM , 2022 , 10 (6) . |
| MLA | Zhang, Lianhu et al. "Transcriptome Analysis of Protein Kinase MoCK2, which Affects Acetyl-CoA Metabolism and Import of CK2-Interacting Mitochondrial Proteins into Mitochondria in the Rice Blast Fungus Magnaporthe oryzae" . | MICROBIOLOGY SPECTRUM 10 . 6 (2022) . |
| APA | Zhang, Lianhu , Shan, Chonglei , Zhang, Yifan , Miao, Wenjing , Bing, Xiaoli , Kuang, Weigang et al. Transcriptome Analysis of Protein Kinase MoCK2, which Affects Acetyl-CoA Metabolism and Import of CK2-Interacting Mitochondrial Proteins into Mitochondria in the Rice Blast Fungus Magnaporthe oryzae . | MICROBIOLOGY SPECTRUM , 2022 , 10 (6) . |
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Polar growth during appressorium formation is vital for the penetration peg formation in the rice blast fungus, Magnaporthe oryzae. Previous research has shown that the Sln1-septin-exocyst complex, localized at the base of the appressorium in contact with the leaf surface, forms a ring structure that influences growth polarity and affects penetration peg formation, and is necessary for pathogenicity. Our previous research showed CK2 proteins assemble another ring structure positioned perpendicular to the Sln1-septin-exocyst complex. Our research showed that the CK2 ring needs to become correctly assembled for penetration peg function and subsequent plant infection. In the present study, we found that the ring structures of CK2 are absent in the appressorium of Delta MoSep3 septin deletion mutants lacking the septin ring of the Sln1-septin-exocyst complex. Sln1 affects the septin proteins that recruit the exocyst complex that localizes as another ring at the appressorium's bottom. Destruction of the exocyst complex by mutation also causes incorrect localization of the CK2 ring structure. In conclusion, CK2 probably takes part in reestablishing the appressorium' spolarity growth necessary for penetration peg formation. We can also conclude that the correct localization and assembly of one or more CK2 ring structures in the appressorium depend on the initial assembly of the Sln1-septin-exocyst complex two rings at the base of the appressorium.
Keyword ：
appressorium appressorium CK2 CK2 exocyst exocyst penetration peg penetration peg septin ring septin ring
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| GB/T 7714 | Zhang, Lianhu , Cai, Yan , Li, Yunxi et al. MoSep3 and MoExo70 are needed for MoCK2 ring assembly essential for appressorium function in the rice blast fungus, Magnaporthe oryzae [J]. | MOLECULAR PLANT PATHOLOGY , 2021 , 22 (9) : 1159-1164 . |
| MLA | Zhang, Lianhu et al. "MoSep3 and MoExo70 are needed for MoCK2 ring assembly essential for appressorium function in the rice blast fungus, Magnaporthe oryzae" . | MOLECULAR PLANT PATHOLOGY 22 . 9 (2021) : 1159-1164 . |
| APA | Zhang, Lianhu , Cai, Yan , Li, Yunxi , Zhang, Tian , Wang, Baohua , Lu, Guodong et al. MoSep3 and MoExo70 are needed for MoCK2 ring assembly essential for appressorium function in the rice blast fungus, Magnaporthe oryzae . | MOLECULAR PLANT PATHOLOGY , 2021 , 22 (9) , 1159-1164 . |
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In eukaryotic organisms, the 5-oxoprolinase is one of the six key enzymes in the gamma-glutamyl cycle that is involved in the biosynthetic pathway of glutathione (GSH, an antioxidative tripeptide counteracting the oxidative stress). To date, little is known about the biological functions of the 5-oxoprolinase in filamentous phytopathogenic fungi. In this study, we investigated the 5-oxoprolinase in Fusarium graminearum for the first time. In F. graminearum, two paralogous genes (FgOXP1 and FgOXP2) were identified to encode the 5-oxoprolinase while only one homologous gene encoding the 5-oxoprolinase could be found in other filamentous phytopathogenic fungi or Saccharomyces cerevisiae. Deletion of FgOXP1 or FgOXP2 in F. graminearum led to significant defects in its virulence on wheat. This is likely caused by an observed decreased deoxynivalenol (DON, a mycotoxin) production in the gene deletion mutant strains as DON is one of the best characterized virulence factors of F. graminearum. The FgOXP2 deletion mutant strains were also defective in conidiation and sexual reproduction while the FgOXP1 deletion mutant strains were normal for those phenotypes. Double deletion of FgOXP1 and FgOXP2 led to more severe defects in conidiation, DON production and virulence on plants, suggesting that both FgOXP1 and FgOXP2 play a role in fungal development and plant colonization. Although transformation of MoOXP1into Delta Fgoxp1 was able to complement Delta Fgoxp1, transformation of MoOXP1 into Delta Fgoxp2 failed to restore its defects in sexual development, DON production and pathogenicity. Taken together, these results suggest that FgOXP1 and FgOXP2 are likely to have been functionally diversified and play significant roles in fungal development and full virulence in F. graminearum.
Keyword ：
DON production DON production Fungal virulence Fungal virulence Fusarium graminearum Fusarium graminearum Sexual reproduction Sexual reproduction The 5-oxoprolinase The 5-oxoprolinase The gamma-glutamyl cycle The gamma-glutamyl cycle
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| GB/T 7714 | Yang, Piao , Chen, Yunyun , Wu, Huiming et al. The 5-oxoprolinase is required for conidiation, sexual reproduction, virulence and deoxynivalenol production of Fusarium graminearum [J]. | CURRENT GENETICS , 2018 , 64 (1) : 285-301 . |
| MLA | Yang, Piao et al. "The 5-oxoprolinase is required for conidiation, sexual reproduction, virulence and deoxynivalenol production of Fusarium graminearum" . | CURRENT GENETICS 64 . 1 (2018) : 285-301 . |
| APA | Yang, Piao , Chen, Yunyun , Wu, Huiming , Fang, Wenqin , Liang, Qifu , Zheng, Yangling et al. The 5-oxoprolinase is required for conidiation, sexual reproduction, virulence and deoxynivalenol production of Fusarium graminearum . | CURRENT GENETICS , 2018 , 64 (1) , 285-301 . |
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Endosomal sorting machineries regulate the transport of their cargoes among intracellular compartments. However, the molecular nature of such intracellular trafficking processes in pathogenic fungal development and pathogenicity remains unclear. Here, we dissect the roles and molecular mechanisms of two sorting nexin proteins and their cargoes in endosomal recycling in Fusarium graminearum using high-resolution microscopy and high-throughput co-immunoprecipitation strategies. We show that the sorting nexins, FgSnx41 and FgSnx4, interact with each other and assemble into a functionally interdependent heterodimer through their respective BAR domains. Further analyses demonstrate that the dimer localizes to the early endosomal membrane and coordinates endosomal sorting. The small GTPase FgRab5 regulates the correct localization of FgSnx41-FgSnx4 and is consequently required for its trafficking function. The protein FgSnc1 is a cargo of FgSnx41-FgSnx4 and regulates the fusion of secreted vesicles with the fungal growing apex and plasma membrane. In the absence of FgSnx41 or FgSnx4, FgSnc1 is mis-sorted and degraded in the vacuole, and null deletion of either component causes defects in the fungal polarized growth and virulence. Overall, for the first time, our results reveal the mechanism of FgSnc1 endosomal recycling by FgSnx41-FgSnx4 heterodimer which is essential for polarized growth and pathogenicity in F.graminearum.
Keyword ：
endosomal sorting endosomal sorting FgSnx41-FgSnx4 FgSnx41-FgSnx4 Fusarium graminearum Fusarium graminearum pathogenicity pathogenicity polarized growth polarized growth recycling recycling
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| GB/T 7714 | Zheng, Wenhui , Lin, Yahong , Fang, Wenqin et al. The endosomal recycling of FgSnc1 by FgSnx41-FgSnx4 heterodimer is essential for polarized growth and pathogenicity in Fusarium graminearum [J]. | NEW PHYTOLOGIST , 2018 , 219 (2) : 654-671 . |
| MLA | Zheng, Wenhui et al. "The endosomal recycling of FgSnc1 by FgSnx41-FgSnx4 heterodimer is essential for polarized growth and pathogenicity in Fusarium graminearum" . | NEW PHYTOLOGIST 219 . 2 (2018) : 654-671 . |
| APA | Zheng, Wenhui , Lin, Yahong , Fang, Wenqin , Zhao, Xu , Lou, Yi , Wang, Guanghui et al. The endosomal recycling of FgSnc1 by FgSnx41-FgSnx4 heterodimer is essential for polarized growth and pathogenicity in Fusarium graminearum . | NEW PHYTOLOGIST , 2018 , 219 (2) , 654-671 . |
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Jacalin-related lectins (JRLs) are widely distributed carbohydrate-binding proteins in the plant kingdom, which play key roles in development and pathogen defense. In this study, we profiled evolutionary trajectory of JRLs family in 30 plant species and identified domain diversification and recombination leading to different responsive patterns of JRLs in rice during defense against rice blast. All of 30 plant species analyzed in our study have two types of JRLs by containing either a single jacalin or repeated jacalin domains, while chimeric jacalins exist in more than half of the species, especially in the Poaceae family. Moreover, Poaceae species have evolved two types of unique chimeric JRLs by fusing the jacalin domain(s) with dirigent or NB_ARC domain, some of which positively regulate plant immunity. Seven Poaceae-specific JRLs are found in the rice genome. We further found expression of rice JRLs, including four Poaceae-specific JRLs, are induced by Magnaporthe oryzae infections at either early or late infection stages. Overall, the results present the evolutionary trajectory of JRLs in plant and highlight essential roles of Poaceae specific JRLs against pathogen attacks in rice.
Keyword ：
infection responses infection responses jacalin-related lectins jacalin-related lectins Magnaporthe oryzae Magnaporthe oryzae Oryza sativa Oryza sativa phylogeny phylogeny
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| GB/T 7714 | Han Yi-juan , Zhong Zhen-hui , Song Lin-lin et al. Evolutionary analysis of plant jacalin-related lectins (JRLs) family and expression of rice JRLs in response to Magnaporthe oryzae [J]. | JOURNAL OF INTEGRATIVE AGRICULTURE , 2018 , 17 (6) : 1252-1266 . |
| MLA | Han Yi-juan et al. "Evolutionary analysis of plant jacalin-related lectins (JRLs) family and expression of rice JRLs in response to Magnaporthe oryzae" . | JOURNAL OF INTEGRATIVE AGRICULTURE 17 . 6 (2018) : 1252-1266 . |
| APA | Han Yi-juan , Zhong Zhen-hui , Song Lin-lin , Stefan, Olsson , Wang Zong-hua , Lu Guo-long . Evolutionary analysis of plant jacalin-related lectins (JRLs) family and expression of rice JRLs in response to Magnaporthe oryzae . | JOURNAL OF INTEGRATIVE AGRICULTURE , 2018 , 17 (6) , 1252-1266 . |
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