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1.
PLoS One ; 13(12): e0199851, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-30589839

RESUMO

The WRKY proteins constitute a large family of transcription factors that have been known to play a wide range of regulatory roles in multiple biological processes. Over the past few years, many reports have focused on analysis of evolution and biological function of WRKY genes at the whole genome level in different plant species. However, little information is known about WRKY genes in melon (Cucumis melo L.). In the present study, a total of 56 putative WRKY genes were identified in melon, which were randomly distributed on their respective chromosomes. A multiple sequence alignment and phylogenetic analysis using melon, cucumber and watermelon predicted WRKY domains indicated that melon WRKY proteins could be classified into three main groups (I-III). Our analysis indicated that no recent duplication events of WRKY genes were detected in melon, and strong purifying selection was observed among the 85 orthologous pairs of Cucurbitaceae species. Expression profiles of CmWRKY derived from RNA-seq data and quantitative RT-PCR (qRT-PCR) analyses showed distinct expression patterns in various tissues, and the expression of 16 CmWRKY were altered following powdery mildew infection in melon. Besides, we also found that a total of 24 WRKY genes were co-expressed with 11 VQ family genes in melon. Our comparative genomic analysis provides a foundation for future functional dissection and understanding the evolution of WRKY genes in cucurbitaceae species, and will promote powdery mildew resistance study in melon.


Assuntos
Cucumis melo , Resistência à Doença/genética , Evolução Molecular , Regulação da Expressão Gênica , Doenças das Plantas/genética , Proteínas de Plantas , Fatores de Transcrição , Cucumis melo/genética , Cucumis melo/metabolismo , Genes de Plantas , Proteínas de Plantas/biossíntese , Proteínas de Plantas/genética , Especificidade da Espécie , Fatores de Transcrição/biossíntese , Fatores de Transcrição/genética
2.
PLoS One ; 12(7): e0181843, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28750081

RESUMO

The basic/helix-loop-helix (bHLH) proteins constitute a superfamily of transcription factors that are known to play a range of regulatory roles in eukaryotes. Over the past few decades, many bHLH family genes have been well-characterized in model plants, such as Arabidopsis, rice and tomato. However, the bHLH protein family in peanuts has not yet been systematically identified and characterized. Here, 132 and 129 bHLH proteins were identified from two wild ancestral diploid subgenomes of cultivated tetraploid peanuts, Arachis duranensis (AA) and Arachis ipaensis (BB), respectively. Phylogenetic analysis indicated that these bHLHs could be classified into 19 subfamilies. Distribution mapping results showed that peanut bHLH genes were randomly and unevenly distributed within the 10 AA chromosomes and 10 BB chromosomes. In addition, 120 bHLH gene pairs between the AA-subgenome and BB-subgenome were found to be orthologous and 101 of these pairs were highly syntenic in AA and BB chromosomes. Furthermore, we confirmed that 184 bHLH genes expressed in different tissues, 22 of which exhibited tissue-specific expression. Meanwhile, we identified 61 bHLH genes that may be potentially involved in peanut-specific subterranean. Our comprehensive genomic analysis provides a foundation for future functional dissection and understanding of the regulatory mechanisms of bHLH transcription factors in peanuts.


Assuntos
Arachis/embriologia , Arachis/genética , Fatores de Transcrição Hélice-Alça-Hélice Básicos/genética , Genoma de Planta , Família Multigênica , Sementes/embriologia , Sementes/genética , Motivos de Aminoácidos , Sequência de Aminoácidos , Fatores de Transcrição Hélice-Alça-Hélice Básicos/química , Fatores de Transcrição Hélice-Alça-Hélice Básicos/metabolismo , Cromossomos de Plantas/genética , Análise por Conglomerados , Sequência Conservada/genética , DNA de Plantas/metabolismo , Perfilação da Expressão Gênica , Regulação da Expressão Gênica no Desenvolvimento , Regulação da Expressão Gênica de Plantas , Loci Gênicos , Íntrons/genética , Filogenia , Domínios Proteicos , Alinhamento de Sequência , Homologia de Sequência do Ácido Nucleico , Sintenia/genética
3.
Sci Rep ; 5: 16689, 2015 Nov 20.
Artigo em Inglês | MEDLINE | ID: mdl-26584639

RESUMO

In open beef feedlot systems, more than 50% of dietary nitrogen (N) is lost as ammonia (NH3). Here we report an effective and economically-viable method to mitigate NH3 emissions by the application of lignite. We constructed two cattle pens (20 × 20 m) to determine the effectiveness of lignite in reducing NH3 emissions. Twenty-four steers were fed identical commercial rations in each pen. The treatment pen surface was dressed with 4.5 kg m(-2) lignite dry mass while no lignite was applied in the control pen. We measured volatilised NH3 concentrations using Ecotech EC9842 NH3 analysers in conjunction with a mass balance method to calculate NH3 fluxes. Application of lignite decreased NH3 loss from the pen by approximately 66%. The cumulative NH3 losses were 6.26 and 2.13 kg N head(-1) in the control and lignite treatment, respectively. In addition to the environmental benefits of reduced NH3 losses, the value of retained N nutrient in the lignite treated manure is more than $37 AUD head(-1) yr(-1), based on the current fertiliser cost and estimated cost of lignite application. We show that lignite application is a cost-effective method to reduce NH3 loss from cattle feedlots.


Assuntos
Amônia/análise , Ração Animal/análise , Carvão Mineral/estatística & dados numéricos , Abrigo para Animais , Amônia/metabolismo , Criação de Animais Domésticos/economia , Criação de Animais Domésticos/métodos , Animais , Bovinos , Carvão Mineral/economia , Análise Custo-Benefício , Ecossistema , Esterco/análise , Nitrogênio/análise , Nitrogênio/metabolismo
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