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Characterization of Plant Defensin (PDF) Genes in Banana (Musa acuminata) Reveals the Antifungal Ability of MaPDF2.2 to Fusarium Wilt Pathogens SCIE
期刊论文 | 2025 , 11 (5) | HORTICULTURAE
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Abstract :

Plant defensin (PDF/DEF), an important pathogenesis-related protein which widely exists in plants, displays broad-spectrum antifungal activities. To date, however, reports on the banana PDFs are very limited. In this study, we identified, cloned, and characterized the five Class I PDFs (MaPDF2.1 similar to MaPDF2.5) in banana (Musa acuminata). Further, their expression in root, corm, leaf, and fruit were studied. MaPDFs exhibited quite different expression patterns in different organs, with MaPDF2.2 as the only member expressing in all the tested organs, and its expression levels in all organs were the highest among all MaPDFs. The MaPDF2.2 expression could be significantly upregulated by both low- and high-temperature stresses but significantly downregulated by the inoculations of plant growth promoting endophytic fungus Serendipita indica and banana Fusarium wilt (FW) pathogen Fusarium oxysporum f. sp. cubense (Foc) Tropical race 4 (FocTR4). Moreover, the S. indica pre-colonization could significantly alleviate the suppression of FocTR4 on MaPDF2.2, suggesting that this MaPDF might contribute greatly to the S. indica-enhanced FW resistance. By using tobacco leaf transient overexpression, the function of MaPDF2.2 was investigated. Its overexpression significantly inhibited the infection of Foc race 1 (Foc1) and FocTR4 in tobacco leaves. Furthermore, in vitro antifungal ability assays revealed that the recombinant His-MaPDF2.2 protein could significantly inhibit the growth of Foc1 and FocTR4, as well as the pigment accumulation of Foc1. Our study revealed the sequence and expression characteristics of banana PDFs and demonstrated the antifungal ability of MaPDF2.2 to FW pathogens.

Keyword :

antifungal ability antifungal ability banana Fusarium wilt banana Fusarium wilt gene expression analysis gene expression analysis plant defensin plant defensin prokaryotic expression prokaryotic expression

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GB/T 7714 Li, Ruide , Wang, Bin , Wu, Huan et al. Characterization of Plant Defensin (PDF) Genes in Banana (Musa acuminata) Reveals the Antifungal Ability of MaPDF2.2 to Fusarium Wilt Pathogens [J]. | HORTICULTURAE , 2025 , 11 (5) .
MLA Li, Ruide et al. "Characterization of Plant Defensin (PDF) Genes in Banana (Musa acuminata) Reveals the Antifungal Ability of MaPDF2.2 to Fusarium Wilt Pathogens" . | HORTICULTURAE 11 . 5 (2025) .
APA Li, Ruide , Wang, Bin , Wu, Huan , Cheng, Chunzhen . Characterization of Plant Defensin (PDF) Genes in Banana (Musa acuminata) Reveals the Antifungal Ability of MaPDF2.2 to Fusarium Wilt Pathogens . | HORTICULTURAE , 2025 , 11 (5) .
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A NAC Transcription Factor TuNAC69 Contributes to ANK-NLR-WRKY NLR-Mediated Stripe Rust Resistance in the Diploid Wheat Triticum urartu SCIE
期刊论文 | 2022 , 23 (1) | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
WoS CC Cited Count: 15
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Stripe rust is one of the most devastating diseases in wheat. Nucleotide-binding site (NBS) and leucine-rich repeat (LRR) domain receptors (NLRs) recognize pathogenic effectors and trigger plant immunity. We previously identified a unique NLR protein YrU1 in the diploid wheat Triticum urartu, which contains an N-terminal ANK domain and a C-terminal WRKY domain and confers disease resistance to stripe rust fungus Puccinia striiformis f. sp. Tritici (Pst). However, how YrU1 functions in disease resistance is not clear. In this study, through the RNA-seq analysis, we found that the expression of a NAC member TuNAC69 was significantly up-regulated after inoculation with Pst in the presence of YrU1. TuNAC69 was mainly localized in the nucleus and showed transcriptional activation in yeast. Knockdown TuNAC69 in diploid wheat Triticum urartu PI428309 that contains YrU1 by virus-induced gene silencing reduced the resistance to stripe rust. In addition, overexpression of TuNAC69 in Arabidopsis enhanced the resistance to powdery mildew Golovinomyces cichoracearum. In summary, our study indicates that TuNAC69 participates in the immune response mediated by NLR protein YrU1, and likely plays an important role in disease resistance to other pathogens.

Keyword :

NLR NLR plant immunity plant immunity stripe rust stripe rust TuNAC69 TuNAC69 YrU1 YrU1

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GB/T 7714 Xu, Yang , Zou, Shenghao , Zeng, Hao et al. A NAC Transcription Factor TuNAC69 Contributes to ANK-NLR-WRKY NLR-Mediated Stripe Rust Resistance in the Diploid Wheat Triticum urartu [J]. | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES , 2022 , 23 (1) .
MLA Xu, Yang et al. "A NAC Transcription Factor TuNAC69 Contributes to ANK-NLR-WRKY NLR-Mediated Stripe Rust Resistance in the Diploid Wheat Triticum urartu" . | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES 23 . 1 (2022) .
APA Xu, Yang , Zou, Shenghao , Zeng, Hao , Wang, Wei , Wang, Bin , Wang, Huan et al. A NAC Transcription Factor TuNAC69 Contributes to ANK-NLR-WRKY NLR-Mediated Stripe Rust Resistance in the Diploid Wheat Triticum urartu . | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES , 2022 , 23 (1) .
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Identification and characterization of early Fusarium wilt responsive mRNAs and long non-coding RNAs in banana root using high-throughput sequencing SCIE
期刊论文 | 2021 , 11 (1) | SCIENTIFIC REPORTS
WoS CC Cited Count: 3
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Fusarium wilt disease, caused by Fusarium oxysporum f.sp. cubense (Foc), has been recognized as the most devastating disease to banana. The regulatory role of long non-coding RNAs (lncRNAs) in plant defense has been verified in many plant species. However, the understanding of their role during early FocTR4 (Foc tropical race 4) infection stage is very limited. In this study, lncRNA sequencing was used to reveal banana root transcriptome profile changes during early FocTR4 infection stages. Quantitative real time PCR (qRT-PCR) was performed to confirm the expression of eight differentially expressed (DE) lncRNAs (DELs) and their predicted target genes (DETs), and three DE genes (DEGs). Totally, 12,109 lncRNAs, 36,519 mRNAs and 2642 novel genes were obtained, of which 1398 (including 78 DELs, 1220 DE known genes and 100 DE novel genes) were identified as FocTR4 responsive DE transcripts. Gene function analysis revealed that most DEGs were involved in biosynthesis of secondary metabolites, plant-pathogen interaction, plant hormone signal transduction, phenylalanine metabolism, phenylpropanoid biosynthesis, alpha-linolenic acid metabolism and so on. Coincidently, many DETs have been identified as DEGs in previous transcriptome studies. Moreover, many DETs were found to be involved in ribosome, oxidative phosphorylation, lipoic acid metabolism, ubiquitin mediated proteolysis, N-glycan biosynthesis, protein processing in endoplasmic reticulum and DNA damage response pathways. QRT-PCR result showed the expression patterns of the selected transcripts were mostly consistent with our lncRNA sequencing data. Our present study showed the regulatory role of lncRNAs on known biotic and abiotic stress responsive genes and some new-found FocTR4 responsive genes, which can provide new insights into FocTR4-induced changes in the banana root transcriptome during the early pathogen infection stage.

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GB/T 7714 Cheng, Chunzhen , Liu, Fan , Tian, Na et al. Identification and characterization of early Fusarium wilt responsive mRNAs and long non-coding RNAs in banana root using high-throughput sequencing [J]. | SCIENTIFIC REPORTS , 2021 , 11 (1) .
MLA Cheng, Chunzhen et al. "Identification and characterization of early Fusarium wilt responsive mRNAs and long non-coding RNAs in banana root using high-throughput sequencing" . | SCIENTIFIC REPORTS 11 . 1 (2021) .
APA Cheng, Chunzhen , Liu, Fan , Tian, Na , Mensah, Raphael Anue , Sun, Xueli , Liu, Jiapeng et al. Identification and characterization of early Fusarium wilt responsive mRNAs and long non-coding RNAs in banana root using high-throughput sequencing . | SCIENTIFIC REPORTS , 2021 , 11 (1) .
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The Endophytic Fungus Piriformospora indica Reprograms Banana to Cold Resistance SCIE
期刊论文 | 2021 , 22 (9) | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
WoS CC Cited Count: 44
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Banana (Musa spp.), one of the most important fruits worldwide, is generally cold sensitive. In this study, by using the cold-sensitive banana variety Tianbaojiao (Musa acuminate) as the study material, we investigated the effects of Piriformospora indica on banana cold resistance. Seedlings with and without fungus colonization were subjected to 4 degrees C cold treatment. The changes in plant phenotypes, some physiological and biochemical parameters, chlorophyll fluorescence parameters, and the expression of eight cold-responsive genes in banana leaves before and after cold treatment were measured. Results demonstrated that P. indica colonization reduced the contents of malondialdehyde (MDA) and hydrogen peroxide (H2O2) but increased the activities of superoxide dismutase (SOD) and catalase (CAT) and the contents of soluble sugar (SS) and proline. Noteworthily, the CAT activity and SS content in the leaves of P. indica-colonized banana were significant (p < 0.05). After 24 h cold treatment, the decline in maximum photochemistry efficiency of photosystem II (F-v/F-m), photochemical quenching coefficient (qP), efficient quantum yield [Y(II)], and photosynthetic electron transport rate (ETR) in the leaves of P. indica-colonized banana was found to be lower than in the non-inoculated controls (p < 0.05). Moreover, although the difference was not significant, P. indica colonization increased the photochemical conversion efficiency and electron transport rate and alleviated the damage to the photosynthetic reaction center of banana leaves under cold treatment to some extent. Additionally, the expression of the most cold-responsive genes in banana leaves was significantly induced by P. indica during cold stress (p < 0.05). It was concluded that P. indica confers banana with enhanced cold resistance by stimulating antioxidant capacity, SS accumulation, and the expression of cold-responsive genes in leaves. The results obtained from this study are helpful for understanding the P. indica-induced cold resistance in banana.

Keyword :

antioxidant enzymes antioxidant enzymes banana cold resistance banana cold resistance cold-responsive genes cold-responsive genes endophytic fungus endophytic fungus soluble sugar soluble sugar

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GB/T 7714 Li, Dan , Bodjrenou, David Mahoudjro , Zhang, Shuting et al. The Endophytic Fungus Piriformospora indica Reprograms Banana to Cold Resistance [J]. | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES , 2021 , 22 (9) .
MLA Li, Dan et al. "The Endophytic Fungus Piriformospora indica Reprograms Banana to Cold Resistance" . | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES 22 . 9 (2021) .
APA Li, Dan , Bodjrenou, David Mahoudjro , Zhang, Shuting , Wang, Bin , Pan, Hong , Yeh, Kai-Wun et al. The Endophytic Fungus Piriformospora indica Reprograms Banana to Cold Resistance . | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES , 2021 , 22 (9) .
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Genome-wide identification and expression pattern analysis of lipoxygenase gene family in banana SCIE
期刊论文 | 2021 , 11 (1) | SCIENTIFIC REPORTS
WoS CC Cited Count: 33
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The LOX genes have been identified and characterized in many plant species, but studies on the banana LOX genes are very limited. In this study, we respectively identified 18 MaLOX, 11 MbLOX, and 12 MiLOX genes from the Musa acuminata, M. balbisiana and M. itinerans genome data, investigated their gene structures and characterized the physicochemical properties of their encoded proteins. Banana LOXs showed a preference for using and ending with G/C and their encoded proteins can be classified into 9-LOX, Type I 13-LOX and Type II 13-LOX subfamilies. The expansion of the MaLOXs might result from the combined actions of genome-wide, tandem, and segmental duplications. However, tandem and segmental duplications contribute to the expansion of MbLOXs. Transcriptome data based gene expression analysis showed that MaLOX1, 4, and 7 were highly expressed in fruit and their expression levels were significantly regulated by ethylene. And 11, 12 and 7 MaLOXs were found to be low temperature-, high temperature-, and Fusarium oxysporum f. sp. Cubense tropical race 4 (FocTR4)-responsive, respectively. MaLOX8, 9 and 13 are responsive to all the three stresses, MaLOX4 and MaLOX12 are high temperature- and FocTR4-responsive; MaLOX6 and MaLOX17 are significantly induced by low temperature and FocTR4; and the expression of MaLOX7 and MaLOX16 are only affected by high temperature. Quantitative real-time PCR (qRT-PCR) analysis revealed that the expression levels of several MaLOXs are regulated by MeJA and FocTR4, indicating that they can increase the resistance of banana by regulating the JA pathway. Additionally, the weighted gene co-expression network analysis (WGCNA) of MaLOXs revealed 3 models respectively for 5 (MaLOX7-11), 3 (MaLOX6, 13, and 17), and 1 (MaLOX12) MaLOX genes. Our findings can provide valuable information for the characterization, evolution, diversity and functionality of MaLOX, MbLOX and MiLOX genes and are helpful for understanding the roles of LOXs in banana growth and development and adaptations to different stresses.

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GB/T 7714 Liu, Fan , Li, Hua , Wu, Junwei et al. Genome-wide identification and expression pattern analysis of lipoxygenase gene family in banana [J]. | SCIENTIFIC REPORTS , 2021 , 11 (1) .
MLA Liu, Fan et al. "Genome-wide identification and expression pattern analysis of lipoxygenase gene family in banana" . | SCIENTIFIC REPORTS 11 . 1 (2021) .
APA Liu, Fan , Li, Hua , Wu, Junwei , Wang, Bin , Tian, Na , Liu, Jiapeng et al. Genome-wide identification and expression pattern analysis of lipoxygenase gene family in banana . | SCIENTIFIC REPORTS , 2021 , 11 (1) .
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Identification, Characterization and Expression Analysis of Anthocyanin Biosynthesis-related bHLH Genes in Blueberry (Vaccinium corymbosum L.) SCIE
期刊论文 | 2021 , 22 (24) | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
WoS CC Cited Count: 20
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Basic helix-loop-helix proteins (bHLHs) play very important roles in the anthocyanin biosynthesis of many plant species. However, the reports on blueberry anthocyanin biosynthesis-related bHLHs were very limited. In this study, six anthocyanin biosynthesis-related bHLHs were identified from blueberry genome data through homologous protein sequence alignment. Among these blueberry bHLHs, VcAN1, VcbHLH42-1, VcbHLH42-2 and VcbHLH42-3 were clustered into one group, while VcbHLH1-1 and VcbHLH1-2 were clustered into the other group. All these bHLHs were of the bHLH-MYC_N domain, had DNA binding sites and reported conserved amino acids in the bHLH domain, indicating that they were all G-box binding proteins. Protein subcellular location prediction result revealed that all these bHLHs were nucleus-located. Gene structure analysis showed that VcAN1 gDNA contained eight introns, while all the others contained seven introns. Many light-, phytohormone-, stress- and plant growth and development-related cis-acting elements and transcription factor binding sites (TFBSs) were identified in their promoters, but the types and numbers of cis-elements and TFBSs varied greatly between the two bHLH groups. Quantitative real-time PCR results showed that VcAN1 expressed highly in old leaf, stem and blue fruit, and its expression increased as the blueberry fruit ripened. Its expression in purple podetium and old leaf was respectively significantly higher than in green podetium and young leaf, indicating that VcAN1 plays roles in anthocyanin biosynthesis regulation not only in fruit but also in podetium and leaf. VcbHLH1-1 expressed the highest in young leaf and stem, and the lowest in green fruit. The expression of VcbHLH1-1 also increased as the fruit ripened, and its expression in blue fruit was significantly higher than in green fruit. VcbHLH1-2 showed high expression in stem but low expression in fruit, especially in red fruit. Our study indicated that the anthocyanin biosynthesis regulatory functions of these bHLHs showed certain spatiotemporal specificity. Additionally, VcAN1 might be a key gene controlling the anthocyanin biosynthesis in blueberry, whose function is worth exploring further for its potential applications in plant high anthocyanin breeding.

Keyword :

anthocyanin anthocyanin basic helix-loop-helix protein (bHLH) basic helix-loop-helix protein (bHLH) blueberry blueberry expression regulation expression regulation gene expression gene expression

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GB/T 7714 Zhang, Yongyan , Liu, Fan , Wang, Bin et al. Identification, Characterization and Expression Analysis of Anthocyanin Biosynthesis-related bHLH Genes in Blueberry (Vaccinium corymbosum L.) [J]. | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES , 2021 , 22 (24) .
MLA Zhang, Yongyan et al. "Identification, Characterization and Expression Analysis of Anthocyanin Biosynthesis-related bHLH Genes in Blueberry (Vaccinium corymbosum L.)" . | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES 22 . 24 (2021) .
APA Zhang, Yongyan , Liu, Fan , Wang, Bin , Wu, Huan , Wu, Junwei , Liu, Jiapeng et al. Identification, Characterization and Expression Analysis of Anthocyanin Biosynthesis-related bHLH Genes in Blueberry (Vaccinium corymbosum L.) . | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES , 2021 , 22 (24) .
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自主出题模式在高校遗传学双语教学中的应用
期刊论文 | 2021 , (08) , 161-164 | 教育教学论坛
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遗传学是生物类专业的一门重要专业基础课,学科内容发展迅速,开展双语教学对学生紧跟国际发展趋势和学科前沿,提升国际竞争力具有重要意义。然而,学生在学习过程中面临教学内容难和英语学习难的两大问题,如何在教学中激发学生的学习兴趣,发挥学生的主体地位,提高教学效果是课程改革需要考虑的问题。可在多元化评价方式中采用学生自主出题的模式,并在两届本科生中试验教学,取得了良好的效果,极大地激发了学生学习的兴趣,培养了学生的自主学习能力和创新能力以及双语学习能力。

Keyword :

双语教学 双语教学 教学改革 教学改革 自主出题 自主出题 遗传学 遗传学

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GB/T 7714 郑燕 , 崔凯 , 汪斌 . 自主出题模式在高校遗传学双语教学中的应用 [J]. | 教育教学论坛 , 2021 , (08) : 161-164 .
MLA 郑燕 et al. "自主出题模式在高校遗传学双语教学中的应用" . | 教育教学论坛 08 (2021) : 161-164 .
APA 郑燕 , 崔凯 , 汪斌 . 自主出题模式在高校遗传学双语教学中的应用 . | 教育教学论坛 , 2021 , (08) , 161-164 .
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Regulation of Morphology, Aflatoxin Production, and Virulence of Aspergillus flavus by the Major Nitrogen Regulatory Gene areA SCIE
期刊论文 | 2019 , 11 (12) | TOXINS
WoS CC Cited Count: 26
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Aspergillus flavus is a renowned plant, animal and human pathogen. areA is a global nitrogen regulatory gene of the GATA transcription factor family, shown to be the major nitrogen regulator. In this study, we identified areA in A. flavus and studied its function. The AreA protein contained a signatory zinc finger domain, which is extremely conserved across fungal species. Gene deletion (Delta areA) and over-expression (OE::areA) strains were constructed by homologous recombination to elucidate the role of areA in A. flavus. The Delta areA strain was unable to efficiently utilize secondary nitrogen sources for growth of A. flavus, and it had poorly developed conidiophores, when observed on complete medium, resulting in the production of significantly less conidia than the wild-type strain (WT). Aflatoxin B1 (AFB1) production was reduced in Delta areA compared with the WT strain in most conditions tested, and Delta areA had impaired virulence in peanut seeds. areA also played important roles in the sensitivity of A. flavus to osmotic, cell wall and oxidative stresses. Hence, areA was found to be important for the growth, aflatoxin production and pathogenicity of A. flavus. This work sheds light on the function of areA in the regulation of the nitrogen metabolism of A. flavus, and consequently aims at providing new ways for controlling the crossover pathogen, A. flavus.

Keyword :

aflatoxins aflatoxins AreA AreA Aspergillus flavus Aspergillus flavus glutamine glutamine nitrogen metabolism nitrogen metabolism

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GB/T 7714 Fasoyin, Opemipo Esther , Yang, Kunlong , Qiu, Mengguang et al. Regulation of Morphology, Aflatoxin Production, and Virulence of Aspergillus flavus by the Major Nitrogen Regulatory Gene areA [J]. | TOXINS , 2019 , 11 (12) .
MLA Fasoyin, Opemipo Esther et al. "Regulation of Morphology, Aflatoxin Production, and Virulence of Aspergillus flavus by the Major Nitrogen Regulatory Gene areA" . | TOXINS 11 . 12 (2019) .
APA Fasoyin, Opemipo Esther , Yang, Kunlong , Qiu, Mengguang , Wang, Bin , Wang, Sen , Wang, Shihua . Regulation of Morphology, Aflatoxin Production, and Virulence of Aspergillus flavus by the Major Nitrogen Regulatory Gene areA . | TOXINS , 2019 , 11 (12) .
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Carbon catabolite repression gene creA regulates morphology, aflatoxin biosynthesis and virulence in Aspergillus flavus SCIE
期刊论文 | 2018 , 115 , 41-51 | FUNGAL GENETICS AND BIOLOGY
WoS CC Cited Count: 68
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Carbon catabolite repression (CCR) is a very important mechanism employed in the utilization of carbon as an energy source, required for the regulation of growth, development and secondary metabolite production in fungi. Despite the wide study of this mechanism in fungi, little is known about the major CCR gene creA in A. fiavus. Hence, we report identification of A. fiavus carbon catabolite repression gene creA, which is responsible for the repression of secondary carbon sources. Gene deletion and over-expression was employed to explicate the role of creA in the morphology, pathogenicity, and secondary metabolite production in A. flavus. We investigated these factors using three carbon sources including glucose, sucrose and maltose. Gene deletion mutant (Delta creA) had a significant growth defect on complete medium and minimal medium containing maltose. Conidia production in Delta creA was significantly impaired irrespective of the carbon source available, while sclerotia production was significantly increased, compared to wild type (WT) and over-expression strain (OE::creA). Importantly, Delta creA produced insignificant amount of aflatoxin in complete medium, and its ability to colonize hosts was also impaired. Concisely, we showed that creA played an important role in the morphology, pathogenicity and secondary metabolite production of A. fiavus.

Keyword :

Aflatoxin Aflatoxin Aspergillus flavus Aspergillus flavus Carbon catabolite repression Carbon catabolite repression creA creA

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GB/T 7714 Fasoyin, Opemipo Esther , Wang, Bin , Qiu, Mengguang et al. Carbon catabolite repression gene creA regulates morphology, aflatoxin biosynthesis and virulence in Aspergillus flavus [J]. | FUNGAL GENETICS AND BIOLOGY , 2018 , 115 : 41-51 .
MLA Fasoyin, Opemipo Esther et al. "Carbon catabolite repression gene creA regulates morphology, aflatoxin biosynthesis and virulence in Aspergillus flavus" . | FUNGAL GENETICS AND BIOLOGY 115 (2018) : 41-51 .
APA Fasoyin, Opemipo Esther , Wang, Bin , Qiu, Mengguang , Han, Xiaoyun , Chung, Kuang-Ren , Wang, Shihua . Carbon catabolite repression gene creA regulates morphology, aflatoxin biosynthesis and virulence in Aspergillus flavus . | FUNGAL GENETICS AND BIOLOGY , 2018 , 115 , 41-51 .
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SBP-box/SPL基因在植物表皮毛发育中的作用 CSCD PKU
期刊论文 | 2017 , 46 (02) , 121-128 | 福建农林大学学报(自然科学版)
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植物表皮毛作为表皮细胞的特有组织在分类、减少热量和水分散失、抵御昆虫和微生物侵害方面发挥作用,同时也是生长发育时相转换的一个重要指标.而且表皮毛在提高产量等农艺性状方面也发挥重要作用,如棉花纤维组织的产量和品质.SBP-box/SPL基因是植物特有的一个较小的基因家族,在生长发育多个方面扮演重要角色,涉及花期、育性、果实成熟、蓝光信号传导、器官大小等性状.其中,在调控植物"年龄"相关的时相转换中作用明显.本文对表皮毛发育调控中SPL基因功能、涉及的microRNA,及它们与其他表皮毛发育调控途径的关系进行综述,以期为植物表皮毛发育的深入研究及应用奠定基础.

Keyword :

microRNA microRNA SBP-box/SPL基因 SBP-box/SPL基因 发育调控 发育调控 植物表皮毛 植物表皮毛

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GB/T 7714 汪斌 , 林格格 , 宋海冰 et al. SBP-box/SPL基因在植物表皮毛发育中的作用 [J]. | 福建农林大学学报(自然科学版) , 2017 , 46 (02) : 121-128 .
MLA 汪斌 et al. "SBP-box/SPL基因在植物表皮毛发育中的作用" . | 福建农林大学学报(自然科学版) 46 . 02 (2017) : 121-128 .
APA 汪斌 , 林格格 , 宋海冰 , 陈壬杰 , 兰涛 . SBP-box/SPL基因在植物表皮毛发育中的作用 . | 福建农林大学学报(自然科学版) , 2017 , 46 (02) , 121-128 .
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