The effect of slow-release fertilizer application on reducing the fertilization times of ratooning rice was explored by carrying out plot experiments using different slow-release fertilizer formulas.The results showed...The effect of slow-release fertilizer application on reducing the fertilization times of ratooning rice was explored by carrying out plot experiments using different slow-release fertilizer formulas.The results showed that compared with conventional fertilization of farmers(TCK),there were no significant differences in plant heights of the first rice crop and ratoon rice crop and the number of tillers was slightly increased,by applying different ratios and types of slow-release fertilizers,indicating that reducing fertilization times did not affect rice growth.Compared with the TCK,the yields of treatments T1,T2,T3 and T4 of slow-release fertilizers increased to a certain extent.The yield of the first rice crop increased by 14.7%,16.7%,23.5% and 17.5%,respectively,the yields of the ratoon rice crop increased by 6.3%,5.8%,7.4% and 8.1%,respectively,and the yields of the two rice crops increased between 10.8% and 16.1%,indicating that reasonable combined application of slow-release nitrogen and fast-acting nitrogen fertilizer could meet the nutrient requirements of ratooning rice at different growth stages,and the application of slow-release fertilizers could reduce the fertilization times of ratooning rice.Based on the combination of rice yield and slow-release fertilizer cost in the first rice crop and ratoon rice crop,the T 3 formula was preferred,that is,urea-formaldehyde slow-release nitrogen fertilizer was used as the base and tillering fertilizer,and polyurethane-coated slow-release nitrogen fertilizer was used as the panicle-sprouting fertilizer.展开更多
DNA methyltransferase 3A (Dnmt3a), a de novo methyltransferase, has attracted a great deal of attention for its important role played in tumorigenesis. We have previously demonstrated that melanoma is unable to grow i...DNA methyltransferase 3A (Dnmt3a), a de novo methyltransferase, has attracted a great deal of attention for its important role played in tumorigenesis. We have previously demonstrated that melanoma is unable to grow in-vivo in conditions of Dnmt3a depletion in a mouse model. In this study, we cultured the Dnmt3a depletion B16 melanoma (Dnmt3a-D) cell line to conduct a comparative analysis of protein expression con-comitant with Dnmt3a depletion in a melanoma cell line. After two-dimensional separation, by gel electro-phoresis and liquid chromatography, combined with mass spectrometry analysis (1DE-LC-MS/MS), the re-sults demonstrated that 467 proteins were up-regulated and 535 proteins were down-regulated in the Dnmt3a-D cell line compared to the negative control (NC) cell line. The Genome Ontology (GO) and KEGG pathway were used to further analyze the altered proteins. KEGG pathway analysis indicated that the MAPK signaling pathway exhibited a greater alteration in proteins, an interesting finding due to the close relation-ship with tumorigenesis. The results strongly suggested that Dnmt3a potentially controls the process of tu-morigenesis through the regulation of the proteins (JNK1, p38α, ERK1, ERK2, and BRAF) involved in tu-mor-related pathways, such as the MAPK signaling pathway and melanoma pathway.展开更多
基金Supported by National Key Research and Development Project(No.2018YFD0301302).
文摘The effect of slow-release fertilizer application on reducing the fertilization times of ratooning rice was explored by carrying out plot experiments using different slow-release fertilizer formulas.The results showed that compared with conventional fertilization of farmers(TCK),there were no significant differences in plant heights of the first rice crop and ratoon rice crop and the number of tillers was slightly increased,by applying different ratios and types of slow-release fertilizers,indicating that reducing fertilization times did not affect rice growth.Compared with the TCK,the yields of treatments T1,T2,T3 and T4 of slow-release fertilizers increased to a certain extent.The yield of the first rice crop increased by 14.7%,16.7%,23.5% and 17.5%,respectively,the yields of the ratoon rice crop increased by 6.3%,5.8%,7.4% and 8.1%,respectively,and the yields of the two rice crops increased between 10.8% and 16.1%,indicating that reasonable combined application of slow-release nitrogen and fast-acting nitrogen fertilizer could meet the nutrient requirements of ratooning rice at different growth stages,and the application of slow-release fertilizers could reduce the fertilization times of ratooning rice.Based on the combination of rice yield and slow-release fertilizer cost in the first rice crop and ratoon rice crop,the T 3 formula was preferred,that is,urea-formaldehyde slow-release nitrogen fertilizer was used as the base and tillering fertilizer,and polyurethane-coated slow-release nitrogen fertilizer was used as the panicle-sprouting fertilizer.
文摘DNA methyltransferase 3A (Dnmt3a), a de novo methyltransferase, has attracted a great deal of attention for its important role played in tumorigenesis. We have previously demonstrated that melanoma is unable to grow in-vivo in conditions of Dnmt3a depletion in a mouse model. In this study, we cultured the Dnmt3a depletion B16 melanoma (Dnmt3a-D) cell line to conduct a comparative analysis of protein expression con-comitant with Dnmt3a depletion in a melanoma cell line. After two-dimensional separation, by gel electro-phoresis and liquid chromatography, combined with mass spectrometry analysis (1DE-LC-MS/MS), the re-sults demonstrated that 467 proteins were up-regulated and 535 proteins were down-regulated in the Dnmt3a-D cell line compared to the negative control (NC) cell line. The Genome Ontology (GO) and KEGG pathway were used to further analyze the altered proteins. KEGG pathway analysis indicated that the MAPK signaling pathway exhibited a greater alteration in proteins, an interesting finding due to the close relation-ship with tumorigenesis. The results strongly suggested that Dnmt3a potentially controls the process of tu-morigenesis through the regulation of the proteins (JNK1, p38α, ERK1, ERK2, and BRAF) involved in tu-mor-related pathways, such as the MAPK signaling pathway and melanoma pathway.
