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Phytophthora parasitica is an important oomycete that causes disease in a variety of plants, dimethomorph fungicides being specific for oomycetes. The aim of this study was to use RNA-seq to rapidly discover the mechanism by which dimethomorph acts in the treatment of P. parasitica. We found that the expression of 832 genes changed significantly after the dimethomorph treatment, including 365 up-regulated genes and 467 down-regulated genes. According to the Gene Ontology (GO) enrichment analysis, pathway enrichment and verification test results, the following conclusions are obtained: (i) the treatment of P. parasitica with dimethomorph causes changes in the expression levels of genes associated with the cell wall and cell wall synthesis; (ii) dimethomorph treatment results in reduced permeability of the cell membrane and changes in the expression of certain transport-related proteins; (iii) dimethomorph treatment increased reactive oxygen species and reduced the expression of genes related to the control of oxidative stress. Phytophthora parasitica es un importante oomiceto que origina enfermedades en una variedad de plantas; el fungicida dimetomorf es específico contra oomicetos. El objetivo de este estudio fue utilizar la tecnología de RNA-seq para descubrir rápidamente el mecanismo por el que el dimetomorf actúa en el tratamiento de P. parasitica. Descubrimos que la expresión de 832 genes se modificaba significativamente tras el tratamiento con dimetomorf, incluyendo 365 genes que son sobrerregulados y 467 genes que son subrregulados. El análisis de enriquecimiento de ontología de genes (GO), análisis de enriquecimiento de las vías y pruebas de verificación permitieron extraer las conclusiones siguientes: 1) el tratamiento de P. parasitica con dimetomorf origina cambios en los niveles de expresión de los genes relacionados con la pared celular y su síntesis; 2) el tratamiento con dimetomorf origina una reducción de la permeabilidad de la membrana celular, así como cambios en la expresión de ciertas proteínas relacionadas con el transporte, y 3) el tratamiento con dimetomorf incrementó las especies reactivas del oxígeno y redujo la expresión de los genes relacionados con el control del estrés oxidativo.

Residual antibiotics can enter soil and water bodies through organic fertilizers with food safety risk via plants absorption, while how do plant growth and quinolone accumulation respond to residual antibiotics levels in soil or water is not clear. Hydroponic experiment in greenhouse was conducted with floating seedlings of tobacco as model plant to investigate the responses of quinolone antibiotics accumulation and plant growth to different levels of ciprofloxacin (CIP) and norfloxacin (NOR). Results showed that CIP and NOR inhibited the growth of tobacco seedlings. The plant height, stem circumference, maximum leaf width, and maximum leaf area of tobacco seedlings were significantly decreased. So as to the plant biomass of leaves, stems, and roots. Accumulation of CIP in the tobacco seedlings in the T3 was 1.1 times that of the tobacco seedlings in the T1, NOR in the T4 was 1.2 times that of the tobacco seedlings in the T1. And the higher the concentration, the more significant the inhibitory effect. Both antibiotics can be absorbed and accumulated by tobacco seedlings. Additionally, the inhibitory effect of CIP was greater than that of NOR.

Phytophthora parasitica is an important oomycete that causes disease in a variety of plants, dimethomorph fungicides being specific for oomycetes. The aim of this study was to use RNA-seq to rapidly discover the mechanism by which dimethomorph acts in the treatment of P. parasitica. We found that the expression of 832 genes changed significantly after the dimethomorph treatment, including 365 up-regulated genes and 467 down-regulated genes. According to the Gene Ontology (GO) enrichment analysis, pathway enrichment and verification test results, the following conclusions are obtained: (i) the treatment of P. parasitica with dimethomorph causes changes in the expression levels of genes associated with the cell wall and cell wall synthesis; (ii) dimethomorph treatment results in reduced permeability of the cell membrane and changes in the expression of certain transport-related proteins; (iii) dimethomorph treatment increased reactive oxygen species and reduced the expression of genes related to the control of oxidative stress.

Cadmium (Cd) of tobacco is a pollutant that is extremely toxic to the health of humans. Protein plant cadmium resistance 8 gene has been characterized to increase the plant Cd resistance. In present experiment, the complete mRNA sequence of tobacco protein plant cadmium resistance 8 gene was amplified using the rapid amplification of cDNA ends methods. The full-length tobacco protein plant cadmium resistance 8 gene mRNA was 887bp containing an 555 bp open reading frame, which encodes a protein of 184 amino acids. BLAST analysis revealed that tobacco protein plant cadmium resistance 8 protein shares high homology with the protein plant cadmium resistance 8 of potato (81%), Lycopersicon esculentum (80%), Eutrema salsugineum (60%), Capsella rubella (58%) and thale cress (57%). Results also showed that tobacco protein plant cadmium resistance 8 gene has a closer genetic relationship with the protein plant cadmium resistance 8 gene of Lycopersicon esculentum . The expression profile was studied and the results indicated that tobacco protein plant cadmium resistance 8 gene was highly expressed in root, moderately expressed in stem, and hardly expressed in flower and leaf. These results established the primary foundation of utilizing tobacco protein plant cadmium resistance 8 gene to decrease the cadmium content of tobacco and benefit the health of humans in the future.

The complete mRNA sequence of one tobacco (Nicotiana tabacum) gene-leucine aminopeptidase was amplified through rapid amplification of cDNA ends (RACE) method. The full-length mRNA was 2,051 bp containing an 1,584-bp open reading frame, which encodes a protein of 527 amino acids. Sequence analysis revealed that the deduced tobacco leucine aminopeptidase protein shares high homology with the leucine aminopeptidase of wine grape (84 %), populus trichocarpa (79 %), thale cress (77 %), and triticum urartu (74 %). Results also showed that tobacco leucine aminopeptidase gene has a close genetic relationship with the leucine aminopeptidase gene of wine grape. The expression profile was studied and result indicated that tobacco leucine aminopeptidase gene was differentially expressed in detected tobacco tissues including leaf, stem, root, and flower. Our experiment established the foundation for further research on this tobacco gene.

The complete mRNA sequence of one tobacco ( Nicotiana tabacum ) gene- apoplastic invertase, was amplified using the rapid amplification of cDNA ends methods based on some tobacco ESTs. The full-length tobacco apoplastic invertase gene mRNA was 1,985bp containing an 1,740 bp open reading frame, which encodes a protein of 579 amino acids. Sequence analysis revealed that the apoplastic invertase of tobacco shares high homology with the apoplastic invertase of potato (82%), Lycopersicon esculentum ( 81%) and Lycopersicon pennellii (78%). Results also showed that tobacco apoplastic invertase gene has a closer genetic relationship with the apoplastic invertase gene of Lycopersicon esculentum . The prediction of transmembrane helices showed that tobacco apoplastic invertase might be a transmembrane protein. The expression profile was studied and the results indicated that tobacco apoplastic invertase gene was differentially expressed in detected tobacco tissues including leaf, stem, root and flower. Our experiment established the foundation for further research on this tobacco gene.