Flower color is an essential trait in ornamental plant breeding. Lycoris longituba is a popular ornamental plant native to central eastern China. The decrease in anthocyanin accumulation causes L. longituba petal colo...Flower color is an essential trait in ornamental plant breeding. Lycoris longituba is a popular ornamental plant native to central eastern China. The decrease in anthocyanin accumulation causes L. longituba petal color fading during flower development, which considerably affects the ornamental value of L. longituba. However, mechanisms underlying anthocyanin biosynthesis inhibition during L. longituba petal development remain unclear. In this study, three LlDFR genes were confirmed to be involved in anthocyanin biosynthesis and LlDFRc exerted the strongest promoting effect on anthocyanin accumulation. According to the correlation analysis results, LlbHLH12 exhibited the strongest negative correlation with LlDFRc. Quantitative real-time PCR analysis showed that LlbHLH12 was highly expressed during the medium bud and full bloom stages of flower development. LlbHLH12 was identified as a member of subgroup XII of bHLH transcription factor family. Subcellular localization and transcriptional activation ability assay revealed that LlbHLH12 was located in the nucleus without transcriptional activation activity. Overexpression of LlbHLH12 in Nicotiana tabacum and L. longituba inhibited anthocyanin accumulation by suppressing the expression of anthocyanin biosynthetic pathway genes. Furthermore, yeast one-hybrid, dual-luciferase, and β-glucuronidase activity assays showed that LlbHLH12 directly bound to the promoters of LlPAL and LlDFRc and suppressed their expression to inhibit anthocyanin biosynthesis. Overall, our study identified a novel bHLH repressor negatively regulating anthocyanin biosynthesis and provided new insights into the molecular mechanisms underlying color fading in L. longituba petals.展开更多
A novel sesquiterpenoid was isolated from the whole plant of Glechoma longituba. Its structure was elucidated as 1, 8-epoxy-7（11）-germacren-5-one-12, 8-olide 1 on the basis of spectral evidences.
To obtain a primary overview of gene diversity and expression pattern inLycoris longituba, 4,992 ESTs (Expressed Sequence Tags) from L. longituba bud were se-quenced and4,687 cleaned ESTs were used for gene expression...To obtain a primary overview of gene diversity and expression pattern inLycoris longituba, 4,992 ESTs (Expressed Sequence Tags) from L. longituba bud were se-quenced and4,687 cleaned ESTs were used for gene expression analysis. Clustered by the PHRAP program, 967contigs and 1,343 singlets were obtained. Blast search showed that 179 contigs and 227 singlets(totally 1,066 ESTs) had homologues in GenBank and 3,621 ESTs were novel.展开更多
Aims Most plants are clonal in nature.Clonal ramets can share water,nutrients and photosynthate,especially when they experience patchy resources.Patch contrast(i.e.a difference in resources among patches)and patch dir...Aims Most plants are clonal in nature.Clonal ramets can share water,nutrients and photosynthate,especially when they experience patchy resources.Patch contrast(i.e.a difference in resources among patches)and patch direction(i.e.source–sink relations)are among the basic attributes of spatial patchiness.Here,I hypothesize that young established ramets in nutrient-rich patches support old ramets in nutrient-poor patches when ramets are subjected to different patch contrasts and patch directions.Methods In a greenhouse experiment,old and young ramets of Glechoma longituba were grown in four combinations consisting of patch contrast and patch direction.Minus patch direction refers to a patch combination in which parent ramets grow in nutrient-rich patches while connected daughter ramets grow in nutrient-poor ones and plus patch direction is the opposite direction.Imeasured photosynthesis and fluorescence traits,harvested all ramets,took morphological measures,weighed their dry mass and determined their nutrient uptake and use.Important Findings For parental ramets of G.longituba,patch contrast and patch direction and their interactions had no significant effects on net photosynthetic rate,maximal fluorescence yield,photochemical quenching(quenching refers to any process which decreases the fluorescence intensity of a given substance),non-photochemical quenching,nutrient uptake,biomass and stolon weight ratio.Patch direction alone significantly affected root weight ratio.Large patch contrast enhanced N use efficiency(NUE)and P use efficiency(PUE);plus patch direction decreased NUE,but increased PUE;the patch contrast by patch direction interaction affected PUE and K use efficiency(KUE).There were significant interactions between patch direction and patch contrast on PUE and KUE.It is concluded that soil nutrient patchiness may influence nutrient use strategies,but not nutrient uptake,photosynthesis and growth of parent ramets of G.longituba connected to daughter ramets,and that patch contrast and patch direction jointly affect PUE and KUE.展开更多
基金supported by the National Natural Science Foundation of China(Grant Nos.31870695,32071828)the Priority Academic Program Development of Jiangsu Higher Education Institutions(PAPD).
文摘Flower color is an essential trait in ornamental plant breeding. Lycoris longituba is a popular ornamental plant native to central eastern China. The decrease in anthocyanin accumulation causes L. longituba petal color fading during flower development, which considerably affects the ornamental value of L. longituba. However, mechanisms underlying anthocyanin biosynthesis inhibition during L. longituba petal development remain unclear. In this study, three LlDFR genes were confirmed to be involved in anthocyanin biosynthesis and LlDFRc exerted the strongest promoting effect on anthocyanin accumulation. According to the correlation analysis results, LlbHLH12 exhibited the strongest negative correlation with LlDFRc. Quantitative real-time PCR analysis showed that LlbHLH12 was highly expressed during the medium bud and full bloom stages of flower development. LlbHLH12 was identified as a member of subgroup XII of bHLH transcription factor family. Subcellular localization and transcriptional activation ability assay revealed that LlbHLH12 was located in the nucleus without transcriptional activation activity. Overexpression of LlbHLH12 in Nicotiana tabacum and L. longituba inhibited anthocyanin accumulation by suppressing the expression of anthocyanin biosynthetic pathway genes. Furthermore, yeast one-hybrid, dual-luciferase, and β-glucuronidase activity assays showed that LlbHLH12 directly bound to the promoters of LlPAL and LlDFRc and suppressed their expression to inhibit anthocyanin biosynthesis. Overall, our study identified a novel bHLH repressor negatively regulating anthocyanin biosynthesis and provided new insights into the molecular mechanisms underlying color fading in L. longituba petals.
基金the National Natural Science Foundation of China [No. 30460150] the Previous Special Research Program of Significant Foundation Research 2004CCA03800.
文摘A novel sesquiterpenoid was isolated from the whole plant of Glechoma longituba. Its structure was elucidated as 1, 8-epoxy-7（11）-germacren-5-one-12, 8-olide 1 on the basis of spectral evidences.
基金Hi-tech Research &Development Program of China (863 Program, No. 2002AA241051) and Science & Technology Program for Agriculture Development of Shanghai.
文摘To obtain a primary overview of gene diversity and expression pattern inLycoris longituba, 4,992 ESTs (Expressed Sequence Tags) from L. longituba bud were se-quenced and4,687 cleaned ESTs were used for gene expression analysis. Clustered by the PHRAP program, 967contigs and 1,343 singlets were obtained. Blast search showed that 179 contigs and 227 singlets(totally 1,066 ESTs) had homologues in GenBank and 3,621 ESTs were novel.
基金National Natural Science Foundation of China(40435014).
文摘Aims Most plants are clonal in nature.Clonal ramets can share water,nutrients and photosynthate,especially when they experience patchy resources.Patch contrast(i.e.a difference in resources among patches)and patch direction(i.e.source–sink relations)are among the basic attributes of spatial patchiness.Here,I hypothesize that young established ramets in nutrient-rich patches support old ramets in nutrient-poor patches when ramets are subjected to different patch contrasts and patch directions.Methods In a greenhouse experiment,old and young ramets of Glechoma longituba were grown in four combinations consisting of patch contrast and patch direction.Minus patch direction refers to a patch combination in which parent ramets grow in nutrient-rich patches while connected daughter ramets grow in nutrient-poor ones and plus patch direction is the opposite direction.Imeasured photosynthesis and fluorescence traits,harvested all ramets,took morphological measures,weighed their dry mass and determined their nutrient uptake and use.Important Findings For parental ramets of G.longituba,patch contrast and patch direction and their interactions had no significant effects on net photosynthetic rate,maximal fluorescence yield,photochemical quenching(quenching refers to any process which decreases the fluorescence intensity of a given substance),non-photochemical quenching,nutrient uptake,biomass and stolon weight ratio.Patch direction alone significantly affected root weight ratio.Large patch contrast enhanced N use efficiency(NUE)and P use efficiency(PUE);plus patch direction decreased NUE,but increased PUE;the patch contrast by patch direction interaction affected PUE and K use efficiency(KUE).There were significant interactions between patch direction and patch contrast on PUE and KUE.It is concluded that soil nutrient patchiness may influence nutrient use strategies,but not nutrient uptake,photosynthesis and growth of parent ramets of G.longituba connected to daughter ramets,and that patch contrast and patch direction jointly affect PUE and KUE.
基金This work was supported by the National Natural ScienceFoundation of China(30460150)the Previous Special Research ProgramofSignificant Fundation Research(2004CCA03800)
