Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 5 de 5
Filtrar
1.
Plant Mol Biol ; 88(1-2): 85-99, 2015 May.
Artigo em Inglês | MEDLINE | ID: mdl-25800365

RESUMO

Cytochrome P450s are among the largest protein coding gene families in plant genomes. However, majority of the genes remain uncharacterized. Here, we report the characterization of dss1, a rice mutant showing dwarfism and reduced grain size. The dss1 phenotype is caused by a non-synonymous point mutation we identified in DSS1, which is member of a P450 gene cluster located on rice chromosome 3 and corresponds to the previously reported CYP96B4/SD37 gene. Phenotypes of several dwarf mutants characterized in rice are associated with defects in the biosynthesis or perception of the phytohormones gibberellins (GAs) and brassinosteroids (BRs). However, both GA and BR failed to rescue the dss1 phenotype. Hormone profiling revealed the accumulation of abscisic acid (ABA) and ABA metabolites, as well as significant reductions in GA19 and GA53 levels, precursors of the bioactive GA1, in the mutant. The dss1 contents of cytokinin and auxins were not significantly different from wild-type plants. Consistent with the accumulation of ABA and metabolites, germination and early growth was delayed in dss1, which also exhibited an enhanced tolerance to drought. Additionally, expressions of members of the DSS1/CYP96B gene cluster were regulated by drought stress and exogenous ABA. RNA-seq-based transcriptome profiling revealed, among others, that cell wall-related genes and genes involved in lipid metabolism were up- and down-regulated in dss1, respectively. Taken together, these findings suggest that DSS1 mediates growth and stress responses in rice by fine-tuning GA-to-ABA balance, and might as well play a role in lipid metabolism.


Assuntos
Sistema Enzimático do Citocromo P-450/metabolismo , Secas , Oryza/enzimologia , Oryza/crescimento & desenvolvimento , Proteínas de Plantas/metabolismo , Estresse Fisiológico , Ácido Abscísico/metabolismo , Sequência de Aminoácidos , Mapeamento Cromossômico , Cromossomos de Plantas/genética , Clonagem Molecular , Sistema Enzimático do Citocromo P-450/química , Sistema Enzimático do Citocromo P-450/genética , Retículo Endoplasmático/metabolismo , Perfilação da Expressão Gênica , Regulação da Expressão Gênica de Plantas , Genes de Plantas , Giberelinas/metabolismo , Dados de Sequência Molecular , Família Multigênica , Mutação/genética , Oryza/genética , Oryza/fisiologia , Fenótipo , Proteínas de Plantas/química , Proteínas de Plantas/genética
2.
Mol Genet Genomics ; 290(2): 611-22, 2015 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-25367283

RESUMO

Lesion mimic mutants (LMMs) provide a useful tool to study defense-related programmed cell death (PCD) in plants. Although a number of LMMs have been identified in multiple species, most of the candidate genes are yet to be isolated. Here, we report the identification and characterization of a novel rice (Oryza sativa L.) lesion mimic resembling (lmr) mutant, and cloning of the corresponding LMR gene. The LMR locus was initially delineated to 1.2 Mb region on chromosome 6, which was further narrowed down to 155-kb using insertions/deletions (INDELs) and cleavage amplified polymorphic sequence markers developed in this study. We sequenced the open reading frames predicted within the candidate genomic region, and identified a G-A base substitution causing a premature translation termination in a gene that encodes an ATPase associated with various cellular activities type (AAA-type) protein. RNA interference transgenic lines with reduced LMR transcripts exhibited the lesion mimic phenotype similar to that of lmr plants. Furthermore, expression of the wild-type LMR in the mutant background complemented the lesion phenotype, confirming that the mutation identified in LMR is responsible for the mutant phenotype. The pathogenesis-related (PR) genes PBZ1 and PR1 were induced in lmr, which also showed enhanced resistance to rice blast (Magnaporthe oryzae) and bacterial blight (Xanthomonas oryzae pv. oryzae), suggesting LMR is a negative regulator of cell death in rice. The identification of lmr and cloning of the corresponding LMR gene provide an additional resource for the study of PCD in plants.


Assuntos
Adenosina Trifosfatases/genética , Oryza/enzimologia , Folhas de Planta/enzimologia , Proteínas de Plantas/genética , Adenosina Trifosfatases/biossíntese , Sequência de Aminoácidos , Cloroplastos/enzimologia , Clonagem Molecular , Resistência à Doença , Estudos de Associação Genética , Ligação Genética , Dados de Sequência Molecular , Oryza/genética , Fenótipo , Filogenia , Folhas de Planta/genética , Proteínas de Plantas/biossíntese , Transporte Proteico , Análise de Sequência de DNA
3.
New Phytol ; 202(1): 116-131, 2014 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-24350905

RESUMO

The significance of plastid terminal oxidase (PTOX) in phytoene desaturation and chloroplast function has been demonstrated using PTOX-deficient mutants, particularly in Arabidopsis. However, studies on its role in monocots are lacking. Here, we report cloning and characterization of the rice (Oryza sativa) PTOX1 gene. Using Ecotype Targeting Induced Local Lesions IN Genomes (EcoTILLING) and TILLING as forward genetic tools, we identified the causative mutation of an EMS mutant characterized by excessive tillering, semi-dwarfism and leaf variegation that corresponded to the PTOX1 gene. The tillering and semi-dwarf phenotypes of the ptox1 mutant are similar to phenotypes of known strigolactone (SL)-related rice mutants, and both phenotypic traits could be rescued by application of the synthetic SL GR24. The ptox1 mutant accumulated phytoene in white leaf sectors with a corresponding deficiency in ß-carotene, consistent with the expected function of PTOX1 in promoting phytoene desaturase activity. There was also no accumulation of the carotenoid-derived SL ent-2'-epi-5-deoxystrigol in root exudates. Elevated concentrations of auxin were detected in the mutant, supporting previous observations that SL interaction with auxin is important in shoot branching control. Our results demonstrate that PTOX1 is required for both carotenoid and SL synthesis resulting in SL-deficient phenotypes in rice.


Assuntos
Compostos Heterocíclicos com 3 Anéis/metabolismo , Lactonas/metabolismo , Mutação/genética , Oryza/enzimologia , Oxirredutases/genética , Plastídeos/enzimologia , Ácido Abscísico/metabolismo , Sequência de Aminoácidos , Arabidopsis/genética , Proteínas de Arabidopsis/genética , Carotenoides/metabolismo , Clonagem Molecular , Genes de Plantas/genética , Teste de Complementação Genética , Marcadores Genéticos , Ácidos Indolacéticos/metabolismo , Modelos Biológicos , Dados de Sequência Molecular , Mutagênese/genética , Oryza/genética , Oxirredutases/química , Oxirredutases/deficiência , Fenótipo , Filogenia , Mapeamento Físico do Cromossomo , Proteínas de Plantas/química , Proteínas de Plantas/genética , Proteínas de Plantas/metabolismo , Plastídeos/genética , Polimorfismo Genético , Análise de Sequência de Proteína
4.
J Nutr Sci Vitaminol (Tokyo) ; 65(Supplement): S196-S199, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31619629

RESUMO

The BADH1 was characterized by investigating its association to aroma, drought and salinity stress through sequence and gene expression analysis using the selected aromatic rice accessions from Central Luzon State University, Philippines. Polymorphisms including SNPs, were observed in genomic analysis between the resistant check and the susceptible varieties during saline condition. On the other hand, BADH1 transcript level in tolerant varieties revealed that during salt treatment, the salt tolerant check Pokkali and moderately salt tolerant accession Leyte Special have increased transcript level compared to non-treated saline condition relative to actin. The downstream investigation of the BADH1 using genomic and transcriptomic approach is important information to elucidate the molecular mechanism of fragrance development among aromatic rice in CLSU and its response to abiotic stresses.


Assuntos
Betaína-Aldeído Desidrogenase/genética , Oryza/genética , Secas , Expressão Gênica , Filipinas , Polimorfismo de Nucleotídeo Único/genética , Águas Salinas , Análise de Sequência , Estresse Fisiológico/genética
5.
Genes Genet Syst ; 87(3): 169-79, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22976392

RESUMO

The rice (Oryza sativa L.) lesion mimic and senescence (lms) EMS-mutant, identified in a japonica cultivar Hitomebore, is characterized by a spontaneous lesion mimic phenotype during its vegetative growth, an accelerated senescence after flowering, and enhanced resistance to rice blast (Magnaporthe oryzae). To isolate the OsLMS gene, we crossed the lms mutant to Kasalath (indica), and used mutant F(2) plants to initially map the candidate region to about 322-kb on the long arm of chromosome 2. Illumina whole-genome re-sequencing of the mutant and aligning the reads to Hitomebore reference sequence within the candidate region delineated by linkage analysis identified a G to A nucleotide substitution. The mutation corresponded to the exon-intron splicing junction of a novel gene that encodes a carboxyl-terminal domain (CTD) phosphatase domain and two double stranded RNA binding motifs (dsRBM) containing protein. By PCR amplification, we confirmed that the mutation causes splicing error that is predicted to introduce a premature stop codon. RNA interference (RNAi) transgenic lines with suppressed expression of LMS gene exhibited the lesion mimic phenotype, confirming that the mutation identified in LMS is responsible for the mutant phenotype. OsLMS shares a moderate amino-acid similarity to the Arabidopsis FIERY2/CPL1 gene, which is known to control many plant processes such as stress response and development. Consistence with this similarity, the lms mutant shows sensitivity to cold stress at the early growth stage, suggesting that LMS is a negative regulator of stress response in rice.


Assuntos
Oryza , RNA de Cadeia Dupla , Genes de Plantas , Mutação , Oryza/genética , Fenótipo , Proteínas de Plantas/genética
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA