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1.
Int J Mol Sci ; 20(1)2019 Jan 08.
Artigo em Inglês | MEDLINE | ID: mdl-30626061

RESUMO

As a promising energy plant for biodiesel, Jatropha curcas is a tropical and subtropical shrub and its growth is affected by one of major abiotic stress, chilling. Therefore, we adopt the phosphoproteomic analysis, physiological measurement and ultrastructure observation to illustrate the responsive mechanism of J. curcas seedling under chilling (4 °C) stress. After chilling for 6 h, 308 significantly changed phosphoproteins were detected. Prolonged the chilling treatment for 24 h, obvious physiological injury can be observed and a total of 332 phosphoproteins were examined to be significantly changed. After recovery (28 °C) for 24 h, 291 phosphoproteins were varied at the phosphorylation level. GO analysis showed that significantly changed phosphoproteins were mainly responsible for cellular protein modification process, transport, cellular component organization and signal transduction at the chilling and recovery periods. On the basis of protein-protein interaction network analysis, phosphorylation of several protein kinases, such as SnRK2, MEKK1, EDR1, CDPK, EIN2, EIN4, PI4K and 14-3-3 were possibly responsible for cross-talk between ABA, Ca2+, ethylene and phosphoinositide mediated signaling pathways. We also highlighted the phosphorylation of HOS1, APX and PIP2 might be associated with response to chilling stress in J. curcas seedling. These results will be valuable for further study from the molecular breeding perspective.


Assuntos
Temperatura Baixa , Jatropha/metabolismo , Jatropha/fisiologia , Fosfoproteínas/metabolismo , Proteínas de Plantas/metabolismo , Proteômica/métodos , Plântula/metabolismo , Estresse Fisiológico , Motivos de Aminoácidos , Sequência de Aminoácidos , Ontologia Genética , Jatropha/ultraestrutura , Anotação de Sequência Molecular , Fosfopeptídeos/metabolismo , Fosfoproteínas/química , Fosforilação , Folhas de Planta/metabolismo , Folhas de Planta/ultraestrutura , Proteínas de Plantas/química , Mapas de Interação de Proteínas , Plântula/anatomia & histologia , Plântula/fisiologia , Plântula/ultraestrutura
2.
J Proteomics ; 143: 346-352, 2016 06 30.
Artigo em Inglês | MEDLINE | ID: mdl-26924298

RESUMO

UNLABELLED: The inner integument of Jatropha curcas seeds is a non-photosynthetic tissue that acts primarily as a conduit for the delivery of nutrients to the embryo and endosperm. In this study we performed a histological and transmission electron microscopy analysis of the inner integument in stages prior to fertilization to 25days after pollination, to establish the structural changes associated with the plastid to gerontoplast transition. This study showed that plastids are subjected to progressive changes, which include the dismantling of the internal membrane system, matrix degradation and the formation of stromule-derived vesicles. A proteome analysis of gerontoplasts isolated from the inner integument at 25days after pollination, resulted in the identification of 1923 proteins, which were involved in a myriad of metabolic functions, such as synthesis of amino acids and fatty acids. Among the identified proteins, were also a number of hydrolases (peptidases, lipases and carbohydrases), which presumably are involved in the ordered dismantling of this organelle to provide additional sources of nutrients for the growing embryo and endosperm. The dataset we provide here may provide a foundation for the study of the proteome changes associated with the plastid to gerontoplast transition in non-photosynthetic tissues. SIGNIFICANCE: We describe ultrastructural features of gerontoplasts isolated from the inner integument of developing seeds of Jatropha curcas, together with a deep proteome analysis of these gerontoplasts. This article explores a new aspect of the biology of plastids, namely the ultrastructural and proteome changes associated with the transition plastid to gerontoplast in a non-photosynthetic tissue.


Assuntos
Jatropha/embriologia , Proteoma/análise , Jatropha/química , Jatropha/ultraestrutura , Microscopia Eletrônica de Transmissão , Plastídeos/química , Plastídeos/ultraestrutura , Proteômica/métodos , Sementes/química , Sementes/ultraestrutura
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