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1.
Plant Physiol ; 180(2): 986-997, 2019 06.
Artigo em Inglês | MEDLINE | ID: mdl-30967482

RESUMO

In plants, male sterility is an important agronomic trait, especially in hybrid crop production. Many factors are known to affect crop male sterility, but it remains unclear whether Suc transporters (SUTs) participate directly in this process. Here, we identified and functionally characterized the cucumber (Cucumis sativus) CsSUT1, a typical plasma membrane-localized energy-dependent high-affinity Suc-H+ symporter. CsSUT1 is expressed in male flowers and encodes a protein that is localized primarily in the tapetum, pollen, and companion cells of the phloem of sepals, petals, filaments, and pedicel. The male flowers of CsSUT1-RNA interference (RNAi) lines exhibited a decrease in Suc, hexose, and starch content, relative to those of the wild type, during the later stages of male flower development, a finding that was highly associated with male sterility. Transcriptomic analysis revealed that numerous genes associated with sugar metabolism, transport, and signaling, as well as with auxin signaling, were down-regulated, whereas most myeloblastosis (MYB) transcription factor genes were up-regulated in these CsSUT1-RNAi lines relative to wild type. Our findings demonstrate that male sterility can be induced by RNAi-mediated down-regulation of CsSUT1 expression, through the resultant perturbation in carbohydrate delivery and subsequent alteration in sugar and hormone signaling and up-regulation of specific MYB transcription factors. This knowledge provides a new approach for bioengineering male sterility in crop plants.


Assuntos
Metabolismo dos Carboidratos/genética , Cucumis sativus/genética , Regulação para Baixo , Regulação da Expressão Gênica de Plantas , Proteínas de Membrana Transportadoras/metabolismo , Infertilidade das Plantas/genética , Proteínas de Plantas/metabolismo , Membrana Celular/metabolismo , Regulação para Baixo/genética , Genes de Plantas , Ácidos Indolacéticos/metabolismo , Proteínas de Membrana/metabolismo , Proteínas de Membrana Transportadoras/genética , Floema/metabolismo , Floema/ultraestrutura , Proteínas de Plantas/genética , Pólen/genética , Pólen/ultraestrutura , Interferência de RNA , Transdução de Sinais , Fatores de Transcrição/metabolismo
2.
Micron ; 70: 7-20, 2015 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-25541480

RESUMO

Tobraviruses, like other (+) stranded RNA viruses of plants, replicate their genome in cytoplasm and use such usual membranous structures like endoplasmic reticulum. Based on the ultrastructural examination of Tobacco rattle virus (TRV)-infected potato and tobacco leaf tissues, in this work we provide evidence of the participation of not only the membranous and vesicular ER structures but also other cell organelles during the viral infection cycle. Non-capsidated TRV PSG particles (potato isolate from the Netherlands) (long and short forms) were observed inside the nucleus while the presence of TRV capsid protein (CP) was detected in the nucleus caryolymph and within the nucleolus area. Both capsidated and non-capsidated viral particles were localized inside the strongly disorganized chloroplasts and mitochondria. The electron-dense TRV particles were connected with vesicular structures of mitochondria as well as with chloroplasts in both potato and tobacco tissues. At 15-30 days after infection, vesicles filled with TRV short particles were visible in mitochondria revealing the expanded cristae structures. Immunodetection analysis revealed the TRV PSG CP epitope inside chloroplast with disorganized thylakoids structure as well as in mitochondria of different tobacco and potato tissues. The ultrastructural analysis demonstrated high dynamics of the main cell organelles during the TRV PSG-Solanaceous plants interactions. Moreover, our results suggest a relationship between organelle changes and different stages of virus infection cycle and/or particle formation.


Assuntos
Retículo Endoplasmático/ultraestrutura , Organelas/ultraestrutura , Organelas/virologia , Doenças das Plantas/virologia , Vírus de Plantas/fisiologia , Vírus de RNA/fisiologia , Proteínas do Capsídeo/isolamento & purificação , Núcleo Celular/ultraestrutura , Núcleo Celular/virologia , Cloroplastos/ultraestrutura , Cloroplastos/virologia , Retículo Endoplasmático/virologia , Células do Mesofilo/ultraestrutura , Células do Mesofilo/virologia , Microscopia Eletrônica de Transmissão , Mitocôndrias/ultraestrutura , Mitocôndrias/virologia , Floema/ultraestrutura , Floema/virologia , Folhas de Planta/virologia , Vírus de Plantas/ultraestrutura , Vírus de RNA/ultraestrutura , Solanum tuberosum/virologia , Nicotiana/virologia
3.
Microsc Res Tech ; 77(8): 647-52, 2014 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-24861363

RESUMO

Lavandula dentata L. is an aromatic plant used in folk medicine for different purposes and, for this reason, phytochemical surveys have been carried out in the search for bioactive substances aiming to support its uses. Since there is little knowledge on the structural aspects of L. dentata, this work has studied the anatomical characters of the leaf and stem using light and scanning electron microscopy, in order to assist the species identification. As a result, there are different types of trichomes: capitate glandular with uni- or bicellular head, peltate glandular with multicellular head, and branched non-glandular. The leaf is hypostomatic showing diacytic stomata. The epidermis is uniseriate and coated with striate cuticle. The mesophyll is dorsiventral and the midrib is concave-convex and traversed by a single collateral vascular bundle. The stem is quadrangular and has alternating strands of collenchyma and cortical parenchyma as well as a typical endodermis in the cortex. The phloem and xylem cylinders are traversed by narrow rays and there is an incomplete sclerenchymatic sheath adjoining the phloem. These results are a novelty for the species and contribute to distinguish it from other lavenders.


Assuntos
Lavandula/ultraestrutura , Plantas Medicinais/ultraestrutura , Lavandula/anatomia & histologia , Microscopia Eletrônica de Varredura , Floema/ultraestrutura , Folhas de Planta/anatomia & histologia , Folhas de Planta/ultraestrutura , Caules de Planta/anatomia & histologia , Caules de Planta/ultraestrutura , Estômatos de Plantas/ultraestrutura , Plantas Medicinais/anatomia & histologia , Tricomas/ultraestrutura , Xilema/ultraestrutura
4.
J Virol ; 83(11): 5419-29, 2009 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-19297484

RESUMO

Poleroviruses are restricted to vascular phloem tissues from which they are transmitted by their aphid vectors and are not transmissible mechanically. Phloem limitation has been attributed to the absence of virus proteins either facilitating movement or counteracting plant defense. The polerovirus capsid is composed of two forms of coat protein, the major P3 protein and the minor P3/P5 protein, a translational readthrough of P3. P3/P5 is required for insect transmission and acts in trans to facilitate long-distance virus movement in phloem tissue. Specific potato leafroll virus mutants lacking part or all of the P5 domain moved into and infected nonvascular mesophyll tissue when the source-sink relationship of the plant (Solanum sarrachoides) was altered by pruning, with the progeny virus now being transmissible mechanically. However, in a period of months, a phloem-specific distribution of the virus was reestablished in the absence of aphid transmission. Virus from the new phloem-limited infection showed compensatory mutations that would be expected to restore the production of full-length P3/P5 as well as the loss of mechanical transmissibility. The data support our hypothesis that phloem limitation in poleroviruses presumably does not result from a deficiency in the repertoire of virus genes but rather results from P3/P5 accumulation under selection in the infected plant, with the colateral effect of facilitating transmission by phloem-feeding aphid vectors.


Assuntos
Proteínas do Capsídeo/metabolismo , Luteoviridae/metabolismo , Floema/virologia , Doenças das Plantas/virologia , Sequência de Aminoácidos , Sequência de Bases , Proteínas do Capsídeo/química , Proteínas do Capsídeo/genética , Genoma Viral/genética , Luteoviridae/genética , Luteoviridae/ultraestrutura , Microscopia Eletrônica de Transmissão , Dados de Sequência Molecular , Mutação/genética , Floema/crescimento & desenvolvimento , Floema/ultraestrutura , Solanum/crescimento & desenvolvimento , Solanum/ultraestrutura , Solanum/virologia
5.
Biosci Biotechnol Biochem ; 71(11): 2759-65, 2007 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-17986772

RESUMO

SaPIN2a, a plant proteinase inhibitor from nightshade (Solanum americanum), was located to the enucleate sieve elements (SEs) of phloem. The expressed SaPIN2a in transgenic lettuce showed inhibition of plant endogenous trypsin- and chymotrypsin-like activities, suggesting that SaPIN2a can regulate proteolysis in plant cells. To further investigate the physiological role of SaPIN2a, we produced transgenic nightshade and lettuce plants overexpressing SaPIN2a from the cauliflower mosaic virus (CaMV) 35S promoter using Agrobacterium-mediated transformation. Overexpression of SaPIN2a in transgenic plants was demonstrated by northern blot and western blot analysis. SaPIN2a-overexpressing transgenic nightshade plants showed significantly lower height than wild-type plants. Transmission electron microscopy analysis showed that chloroplast-like organelles with thylakoids, which are not present in enucleate SEs of wild-type plants, were present in the enucleate SEs of SaPIN2a-overexpressing transgenic plants. This finding is discussed in terms of the possible role played by SaPIN2a in the regulation of proteolysis in SEs.


Assuntos
Cloroplastos/ultraestrutura , Lactuca/genética , Lactuca/ultraestrutura , Plantas Geneticamente Modificadas/genética , Plantas Geneticamente Modificadas/ultraestrutura , Inibidores de Serina Proteinase/fisiologia , Caulimovirus/genética , Microscopia Eletrônica de Transmissão , Organelas/ultraestrutura , Floema/química , Floema/ultraestrutura , Regiões Promotoras Genéticas , Rhizobium/genética , Inibidores de Serina Proteinase/análise , Inibidores de Serina Proteinase/genética , Solanum/genética , Tilacoides/ultraestrutura
6.
New Phytol ; 173(3): 495-508, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17244044

RESUMO

We examined the subcellular cadmium (Cd) localization in roots and leaves of wild-type Arabidopsis thaliana (ecotype Columbia) exposed to environmentally relevant Cd concentrations. Energy-dispersive X-ray microanalysis (EDXMA) was performed on high-pressure frozen and freeze-substituted tissues. In the root cortex, Cd was associated with phosphorus (Cd/P) in the apoplast and sulfur (Cd/S) in the symplast, suggesting phosphate and phytochelatin sequestration, respectively. In the endodermis, sequestration of Cd/S was present as fine granular deposits in the vacuole and as large granular deposits in the cytoplasm. In the central cylinder, symplastic accumulation followed a distinct pattern illustrating the importance of passage cells for the uptake of Cd. In the apoplast, a shift of Cd/S granular deposits from the middle lamella towards the plasmalemma was observed. Large amounts of precipitated Cd in the phloem suggest retranslocation from the shoot. In leaves, Cd was detected in tracheids but not in the mesophyll tissue. Extensive symplastic and apoplastic sequestration in the root parenchyma combined with retranslocation via the phloem confirms the excluder strategy of Arabidopsis thaliana.


Assuntos
Arabidopsis/metabolismo , Cádmio/metabolismo , Folhas de Planta/metabolismo , Raízes de Plantas/metabolismo , Arabidopsis/efeitos dos fármacos , Arabidopsis/crescimento & desenvolvimento , Arabidopsis/ultraestrutura , Cádmio/toxicidade , Floema/citologia , Floema/efeitos dos fármacos , Floema/ultraestrutura , Fósforo/metabolismo , Epiderme Vegetal/efeitos dos fármacos , Epiderme Vegetal/ultraestrutura , Folhas de Planta/efeitos dos fármacos , Folhas de Planta/ultraestrutura , Raízes de Plantas/efeitos dos fármacos , Raízes de Plantas/ultraestrutura , Frações Subcelulares , Enxofre/metabolismo , Xilema/efeitos dos fármacos , Xilema/ultraestrutura
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