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1.
Sci Rep ; 10(1): 17574, 2020 10 16.
Artigo em Inglês | MEDLINE | ID: mdl-33067553

RESUMO

Grapevine (Vitis vinifera L.) is a crop of major economic importance. However, grapevine yield is guaranteed by the massive use of pesticides to counteract pathogen infections. Under temperate-humid climate conditions, downy mildew is a primary threat for viticulture. Downy mildew is caused by the biotrophic oomycete Plasmopara viticola Berl. & de Toni, which can attack grapevine green tissues. In lack of treatments and with favourable weather conditions, downy mildew can devastate up to 75% of grape cultivation in one season and weaken newly born shoots, causing serious economic losses. Nevertheless, the repeated and massive use of some fungicides can lead to environmental pollution, negative impact on non-targeted organisms, development of resistance, residual toxicity and can foster human health concerns. In this manuscript, we provide an innovative approach to obtain specific pathogen protection for plants. By using the yeast two-hybrid approach and the P. viticola cellulose synthase 2 (PvCesA2), as target enzyme, we screened a combinatorial 8 amino acid peptide library with the aim to identify interacting peptides, potentially able to inhibit PvCesa2. Here, we demonstrate that the NoPv1 peptide aptamer prevents P. viticola germ tube formation and grapevine leaf infection without affecting the growth of non-target organisms and without being toxic for human cells. Furthermore, NoPv1 is also able to counteract Phytophthora infestans growth, the causal agent of late blight in potato and tomato, possibly as a consequence of the high amino acid sequence similarity between P. viticola and P. infestans cellulose synthase enzymes.


Assuntos
Aptâmeros de Peptídeos/farmacologia , Glucosiltransferases/antagonistas & inibidores , Oomicetos/efeitos dos fármacos , Doenças das Plantas/terapia , Proteínas de Plantas/antagonistas & inibidores , Proteínas Citotóxicas Formadoras de Poros/farmacologia , Sequência de Aminoácidos , Celulose/biossíntese , Glucosiltransferases/química , Oomicetos/enzimologia , Oomicetos/ultraestrutura , Biblioteca de Peptídeos , Fotossíntese , Phytophthora infestans/efeitos dos fármacos , Phytophthora infestans/enzimologia , Phytophthora infestans/ultraestrutura , Doenças das Plantas/parasitologia , Folhas de Planta/efeitos dos fármacos , Folhas de Planta/enzimologia , Proteínas de Plantas/química , Alinhamento de Sequência , Homologia de Sequência de Aminoácidos , Solanum tuberosum , Técnicas do Sistema de Duplo-Híbrido , Vitis
2.
Nature ; 488(7412): 535-9, 2012 Aug 23.
Artigo em Inglês | MEDLINE | ID: mdl-22914168

RESUMO

As an essential macroelement for all living cells, phosphorus is indispensable in agricultural production systems. Natural phosphorus reserves are limited, and it is therefore important to develop phosphorus-efficient crops. A major quantitative trait locus for phosphorus-deficiency tolerance, Pup1, was identified in the traditional aus-type rice variety Kasalath about a decade ago. However, its functional mechanism remained elusive until the locus was sequenced, showing the presence of a Pup1-specific protein kinase gene, which we have named phosphorus-starvation tolerance 1 (PSTOL1). This gene is absent from the rice reference genome and other phosphorus-starvation-intolerant modern varieties. Here we show that overexpression of PSTOL1 in such varieties significantly enhances grain yield in phosphorus-deficient soil. Further analyses show that PSTOL1 acts as an enhancer of early root growth, thereby enabling plants to acquire more phosphorus and other nutrients. The absence of PSTOL1 and other genes-for example, the submergence-tolerance gene SUB1A-from modern rice varieties underlines the importance of conserving and exploring traditional germplasm. Introgression of this quantitative trait locus into locally adapted rice varieties in Asia and Africa is expected to considerably enhance productivity under low phosphorus conditions.


Assuntos
Adaptação Fisiológica/genética , Oryza/enzimologia , Oryza/fisiologia , Fósforo/deficiência , Proteínas Quinases/metabolismo , Cruzamento , Secas , Genes de Plantas/genética , Genoma de Planta/genética , Dados de Sequência Molecular , Oryza/classificação , Oryza/genética , Proteínas de Plantas/genética , Proteínas de Plantas/metabolismo , Raízes de Plantas/enzimologia , Raízes de Plantas/genética , Raízes de Plantas/crescimento & desenvolvimento , Plantas Geneticamente Modificadas , Proteínas Quinases/genética , Locos de Características Quantitativas/genética
3.
Plant J ; 31(5): 589-99, 2002 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-12207649

RESUMO

The mutants irt1-1 and irt1-2 of Arabidopsis thaliana were identified among a collection of T-DNA-tagged lines on the basis of a decrease in the effective quantum yield of photosystem II. The mutations responsible interfere with expression of IRT1, a nuclear gene that encodes the metal ion transporter IRT1. In irt1 mutants, photosensitivity and chlorophyll fluorescence parameters, as well as abundance and composition of the photosynthetic apparatus, are significantly altered. Additional effects of the mutation under greenhouse conditions, including chlorosis and a drastic reduction in growth rate and fertility, are compatible with a deficiency in iron transport. Propagation of irt1 plants on media supplemented with additional quantities of iron salts restores almost all aspects of wild-type behaviour. The irt2-1 mutant, which carries an En insertion in the highly homologous IRT2 gene of Arabidopsis thaliana, was identified by reverse genetics and shows no symptoms of iron deficiency. This, together with the finding that irt1-1 can be complemented by 35S::IRT1 but not by 35S::IRT2, demonstrates that, although the products of the two genes are closely related, only AtIRT1 is required for iron homeostasis under physiological conditions.


Assuntos
Proteínas de Arabidopsis/metabolismo , Arabidopsis/fisiologia , Proteínas de Transporte de Cátions/metabolismo , Ferro/metabolismo , Fotossíntese/fisiologia , Proteínas de Plantas , Alelos , Arabidopsis/genética , Proteínas de Arabidopsis/genética , Proteínas de Transporte/genética , Proteínas de Transporte/metabolismo , Proteínas de Transporte de Cátions/genética , Elementos de DNA Transponíveis/genética , Regulação da Expressão Gênica de Plantas , Homeostase , Transporte de Íons/fisiologia , Complexos de Proteínas Captadores de Luz , Mutagênese Insercional , Mutação , Fenótipo , Fotossíntese/genética , Complexo de Proteínas do Centro de Reação Fotossintética/genética , Complexo de Proteínas do Centro de Reação Fotossintética/metabolismo , Complexo de Proteína do Fotossistema II , Pigmentos Biológicos/metabolismo , Folhas de Planta/genética , Folhas de Planta/fisiologia
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