Chinese cabbage has a high annual demand in China.However,clubroot disease caused by the infection of Plasmodiophora brassicae seriously affects its yield.Transcriptome analysis identified a root meristem growth facto...Chinese cabbage has a high annual demand in China.However,clubroot disease caused by the infection of Plasmodiophora brassicae seriously affects its yield.Transcriptome analysis identified a root meristem growth factor 6(BrRGF6)as significantly up-regulated in Chinese cabbage roots infected with Plasmodiophora brassicae.Quantitative reverse-transcription polymerase chain reaction and in situ hybridization analysis showed higher BrRGF6 expression in susceptible materials than in resistant materials.After Plasmodiophora brassicae infection,BrRGF6 expression was significantly up-regulated,especially in susceptible materials.Gene function analysis showed that the roots of Arabidopsis mutant rgf6 grew faster than the wild-type,and delayed the infection progress of Plasmodiophora brassicae.A Protein,nuclear transcription factor Y subunit C(BrNF-YC),was screened from yeast two-hybrid library of Chinese cabbage induced by Plasmodiophora brassicae,and verified to interact with BrRGF6 by yeast two-hybrid co-transfer.Yeast one-hybrid andβGlucuronidase activity analysis showed that BrNF-YC could directly bind to and strongly activate the promoter of BrRGF6.Transgenic verification showed that BrRGF6 or BrNF-YC silenced Chinese cabbage significantly decreased the expression of BrRGF6,accelerated root development,and reduced incidence of clubroot disease.However,after overexpression of BrRGF6 or BrNF-YC,the phenotype showed a reverse trend.Therefore,BrRGF6 silencing accelerated root growth and enhanced resistance to clubroot disease,which was regulated by BrNF-YC.展开更多
Mulberry(Mori Fructus),a highly promising functional food,has long exhibited multiple therapeutic effects as a tonic in traditional Chinese food and pharmacology.Polysaccharides have been regarded as the pivotal pharm...Mulberry(Mori Fructus),a highly promising functional food,has long exhibited multiple therapeutic effects as a tonic in traditional Chinese food and pharmacology.Polysaccharides have been regarded as the pivotal pharmacological ingredient in mulberry.In this study,structural characterization and bioactivities of polysaccharides from mulberry(PFM-3)were determined.The results showed that PFM-3 was a pyranose containing carboxyl group,which was mainly composed of glucose(Glc)and a small amount of mannose(Man)and fucose(Fuc).The molecular weight of PFM-3 was 96.17 kDa,and the surface of PFM-3 was compact and uniform crack.PFM-3 markedly decreased lipid accumulation,triglyceride(TG)and low density lipoprotein cholesterin(LDL-C)on hyperlipidemia human hepatocellular carcinoma(HepG2)cells.PFM-3 recovered nuclear morphometry and mitochondrial membrane potential(MMP),enhanced the activity of glutathione peroxidase(GPx)and decreased cell arrest in G2 phase on oxidative stress HepG2 cells.In addition,PFM-3 promoted the decline of tumor necrosis factor-α(TNF-α)and the augment of interleukin-10(IL-10)secretion on inflammatory mouse leukemia cells of monocyte macrophage(RAW 264.7).This work provides a certificate that PFM-3 could markedly improve cellular lipid accumulation,endogenous antioxidant defense capacity and inflammation levels to further use for treatment and amelioration of related diseases.展开更多
基金supported by grants from the National Natural Science Foundation of China[grant number 31972412,32272717].
文摘Chinese cabbage has a high annual demand in China.However,clubroot disease caused by the infection of Plasmodiophora brassicae seriously affects its yield.Transcriptome analysis identified a root meristem growth factor 6(BrRGF6)as significantly up-regulated in Chinese cabbage roots infected with Plasmodiophora brassicae.Quantitative reverse-transcription polymerase chain reaction and in situ hybridization analysis showed higher BrRGF6 expression in susceptible materials than in resistant materials.After Plasmodiophora brassicae infection,BrRGF6 expression was significantly up-regulated,especially in susceptible materials.Gene function analysis showed that the roots of Arabidopsis mutant rgf6 grew faster than the wild-type,and delayed the infection progress of Plasmodiophora brassicae.A Protein,nuclear transcription factor Y subunit C(BrNF-YC),was screened from yeast two-hybrid library of Chinese cabbage induced by Plasmodiophora brassicae,and verified to interact with BrRGF6 by yeast two-hybrid co-transfer.Yeast one-hybrid andβGlucuronidase activity analysis showed that BrNF-YC could directly bind to and strongly activate the promoter of BrRGF6.Transgenic verification showed that BrRGF6 or BrNF-YC silenced Chinese cabbage significantly decreased the expression of BrRGF6,accelerated root development,and reduced incidence of clubroot disease.However,after overexpression of BrRGF6 or BrNF-YC,the phenotype showed a reverse trend.Therefore,BrRGF6 silencing accelerated root growth and enhanced resistance to clubroot disease,which was regulated by BrNF-YC.
基金This work was supported by the Joint Project of the National Natural Science Foundation of China[Grant No.U20A20400]the Liaoning Provincial Natural Science Foundation Regional Joint Fund Project[2020-MZLH34]+1 种基金Shenyang Young and Middle-aged Science and Technology Innovation Leading Talents Project[RC200495]Shenyang Science and Technology Innovation Platform Project[21-103-0-14,21-104-0-28].
文摘Mulberry(Mori Fructus),a highly promising functional food,has long exhibited multiple therapeutic effects as a tonic in traditional Chinese food and pharmacology.Polysaccharides have been regarded as the pivotal pharmacological ingredient in mulberry.In this study,structural characterization and bioactivities of polysaccharides from mulberry(PFM-3)were determined.The results showed that PFM-3 was a pyranose containing carboxyl group,which was mainly composed of glucose(Glc)and a small amount of mannose(Man)and fucose(Fuc).The molecular weight of PFM-3 was 96.17 kDa,and the surface of PFM-3 was compact and uniform crack.PFM-3 markedly decreased lipid accumulation,triglyceride(TG)and low density lipoprotein cholesterin(LDL-C)on hyperlipidemia human hepatocellular carcinoma(HepG2)cells.PFM-3 recovered nuclear morphometry and mitochondrial membrane potential(MMP),enhanced the activity of glutathione peroxidase(GPx)and decreased cell arrest in G2 phase on oxidative stress HepG2 cells.In addition,PFM-3 promoted the decline of tumor necrosis factor-α(TNF-α)and the augment of interleukin-10(IL-10)secretion on inflammatory mouse leukemia cells of monocyte macrophage(RAW 264.7).This work provides a certificate that PFM-3 could markedly improve cellular lipid accumulation,endogenous antioxidant defense capacity and inflammation levels to further use for treatment and amelioration of related diseases.