Leaves from three_year_old solar greenhouse nectarine trees ( Prunus persica L. var. nectarina Ait. “Zao Hong Yan”) were used as materials in this study. It was the first time that the ultrastructural charact...Leaves from three_year_old solar greenhouse nectarine trees ( Prunus persica L. var. nectarina Ait. “Zao Hong Yan”) were used as materials in this study. It was the first time that the ultrastructural characteristics of phloem tissues of source leaves were observed and compared in normal and weak light intensities using the transmission electron microscopy. Results showed that the average diameters of companion cells (CC) and sieve elements (SE) of all kinds of veins were bigger in normal than that in weak light intensity, indicating that light could influence the cell development and growth. Dense cytoplasm with abundant mitochondria, endoplasmic reticulums, multivesicular bodies, vesicles and plastids were observed in normal light intensity. On the contrary, CC with small vacuolar structures and few mitochondrias, endoplasmic reticulums were shown in weak light. Misalignment of grana thylakoid margins of nectarine leaves also was seen in weak light. The sieve pores of SEs were obstructed in weak light. Chloroplasts with numerous starch grains and few mitochondrias were noticed in the mesophyll cell (MES) surrounding the bundle sheath in weak light. The storage of starch grains appeared to result from an unbalance between photosynthate production and export of photosynthates. This observation provided a strong support to the point that most leaves export the most of assimilates in the light time. Plasmodesmal densities between SE/CC, CC/PP (phloem parenchyma cell), PP/PP and PP/BSC (bundle_sheath cell) decreased in weak light. Plasmodesmata were observed between CC/SE (NS) (nacreous_walled sieve element), PP/BSC in branch veins in normal light intensity, but not in weak light. Thus apoplasmic pathway may be the main mode of transport of assimilates in weak light, however symplasmic pathway may be the main mode of transport of assimilates in normal light intensity. These results demonstrated that the solar greenhouse nectarine trees could be adapted to the weak light via the ultrastructure variation of phloem tissues of the source leaves.展开更多
The development, cytological characters and ultrastructure of phloem ganglion in the nodal region of Phyllostachys edulis (Carr.) H. de Lehaie, a most economically important bamboo, were investigated and the possi...The development, cytological characters and ultrastructure of phloem ganglion in the nodal region of Phyllostachys edulis (Carr.) H. de Lehaie, a most economically important bamboo, were investigated and the possible physiological function of this special structure was proposed. The phloem ganglion derived directly from procambium is situated at the sites where the vascular bundle forks and is present in pairs. The phloem ganglion is spindle_like in appearance and usually consists of 4 to 6 layers. Two kinds of cells in the ganglion could be distinguished. In the middle, there are two layers of filiform cells with pointed ends so that there are no normal sieve plates. Nevertheless, there are many pits on the lateral wall of the filiform cells. The other type of cells located at both ends of the spindle which possess an intermediate form between the filiform cell and the normal sieve tube. The walls of these cells towards the filiform cells are strongly convex forming a special sieve plate. Ultrastructure study showed that cells in the ganglion are connected by enriched plasmodesma. During early differentiation, the paramural body and the ingrowth of cell wall could be observed. It indicates that the cells of phloem ganglion have the character of transfer cells. The organelles in the mature cells are mainly plastids with abundant accumulation of proteins of crystalline structure. The above_mentioned results suggest that the physiological function of the phloem ganglion is closely related with substance transport.展开更多
The fast growth of Tetracentron sinense is a potential valuable timber resource, but whether its anatomy and chemical components are suitable for timber is unknown. We used light microscopy and SEM to examine the anat...The fast growth of Tetracentron sinense is a potential valuable timber resource, but whether its anatomy and chemical components are suitable for timber is unknown. We used light microscopy and SEM to examine the anatomical structure and FITR to measure the chemical components of the phloem and xylem of this tree. Radial variations in growth ring width and tracheid dimensions were also evaluated. The sieve tube, phloem parenchyma cell and sclereids clusters were the main cells in phloem, and the tracheid was the fundamental cell in xylem. An unusual tracheid type, fiber-tracheids or vessel-liked elements was visible. Wood rays nonstoried, uniseriate and multiseriate, including heterogeneous II, occasionally I, and usually 3-6 cells wide. The mean growth-ring width was 2.53 +/- 0.46 mm, and the percentage of late wood was over 60%. For radial variation, growth-ring width increased at an early growth stage, and reached the largest increment during years 11-15, then decreased. The maximum growth-ring width was 5.313 mm. During late growth (60-85 years), trees also maintained a high radial growth increment. Radial variation in the percentage of late wood was uniform, about 50-70%, throughout the growth years. Growth patterns in the length and width of early and late wood were similar as the trees aged. From the FTIR results, the chemical components differed significantly between xylem and phloem, hemicellulose in particular was higher in the xylem than in the phloem, where it was apparently absent. All of these suggest that the composition of phloem in T. sinense is very similar to that of hardwood, and it has higher growth ratio and uniform wood properties.展开更多
Phloem is the woody tissue for the storage and long-distance transport of organic matter in vascular bundles.To reveal the process of secondary phloem development and differentiation in Pinus massoniana,the structure ...Phloem is the woody tissue for the storage and long-distance transport of organic matter in vascular bundles.To reveal the process of secondary phloem development and differentiation in Pinus massoniana,the structure of the secondary phloem and the distribution of cell inclusions were observed by histochemical staining,spontaneous fluorescence of phenolic substances and cell segregation.Based on tissue development and differentiation characteristics of P.massoniana secondary phloem,the secondary phloem development was divided into seven stages:the functional phloem stage;the sieve cell lignification stage;the phloem ray bending stage;the parenchyma cell dedifferentiation and division stage;the dedifferentiated parenchyma cell population formation stage;the periderm alteration stage,and the rhytidome stage.An analysis of cell morphology and inclusion distribution characteristics showed that the sieve cells were deformed during lignification,the quantities of parenchyma and resin ducts increased with development and the crystal content in cells,as well as the levels of sugars and lipids in phloem parenchyma cells,increased with development.The results indicate that the P.massoniana phloem first lost longitudinal transport function and then increased its secretory,storage and mechanical functions.Ultimately,the parenchyma differentiated into the cortex and periderm,and the tissue outside the new periderm lignified to form the rhytidome,which fully developed into the protective tissue of the stem.展开更多
Phloem loading and transport of sugar from leaves to sink tissues such as fruits are crucial for yield formation.Camellia oleifera is an evergreen horticultural crop with high value;however,its low production limits t...Phloem loading and transport of sugar from leaves to sink tissues such as fruits are crucial for yield formation.Camellia oleifera is an evergreen horticultural crop with high value;however,its low production limits the development of the C.oleifera industry.In this study,using a combination of ultrastructural observation,fluorescence loss in photobleaching(FLIP)and inhibitor treatment,we revealed that C.oleifera leaves mainly adopt a symplastic loading route from mesophyll cells to the surrounding vascular bundle cells in minor veins.HPLC assays showed that sucrose is the main sugar transported and only a small amount of raffinose or stachyose was detected in petioles,supporting a passive symplastic loading route in C.oleifera leaves.Compared to leaves grown this year(LT),the carbohydrate synthesis capacity in leaves grown last year(LL)was decreased while LL retained more soluble sugar,suggesting a decrease in transport capacity with leaf ageing.TEM and tissue staining showed that a reduction in plasmodesmata density leads to a decline in the degree of cellular coupling and is responsible for the weakening transport capacity in older leaves.RNA-seq revealed several differentially expressed genes(DEGs)including CoPDCB1-1,CoSUT1 and CoSWEET12,which are likely involved in the regulation of phloem loading and sugar transport.An expression correlation network is constructed between PD-callose binding protein genes,sugar transporter genes and senescence-associated genes.Collectively,this study provides the evidence of the passive symplastic phloem loading pathway in C.oleifera leaves and constructs the correlation between sugar transport and leaf ageing.展开更多
Salinity is a serious challenge for agriculture production by limiting the arable land.Rice is a major staple food crop but very sensitive to salt stress.In this study,we used Arabidopsis for the functional characteri...Salinity is a serious challenge for agriculture production by limiting the arable land.Rice is a major staple food crop but very sensitive to salt stress.In this study,we used Arabidopsis for the functional characterization of a rice F-box gene LOC_Os04g48270(OsPP12-A13)under salinity stress.OsPP12-A13 is a nuclear-localized protein that is strongly upregulated under salinity stress in rice and showed the highest expression in the stem,followed by roots and leaves.Two types of transgenic lines for OsPP12-A13 were generated,including constitutive tissue over-expression using the CaMV35S promoter and phloem specific over-expression using the pSUC2 promoter.Both types of transgenic plants showed salinity tolerance at the seedling stage through higher germination percentage and longer root length,as compared to control plants under salt stress in MS medium.Both the transgenic plants also exhibited salt tolerance at the reproductive stage through higher survival rate,plant dry biomass,and seed yield per plant as compared to control plants.Determination of Na+concentration in leaves,stem and roots of salt-stressed transgenic plants showed that Na^(+) concentration was less in leaf and stem as compared to roots.The opposite was observed in wild type stressed plants,suggesting that OsPP12-A13 may be involved in Na+transport from root to leaf.Transgenic plants also displayed less ROS levels and higher activities of peroxidase and glutathione S-transferase along with upregulation of their corresponding genes as compared to control plants which further indicated a role of OsPP12-A13 in maintaining ROS homeostasis under salt stress.Further,the non-significant difference between the transgenic lines obtained from the two vectors highlighted that OsPP12-A13 principally works in the phloem.Taken together,this study showed that OsPP12-A13 improves salt tolerance in rice,possibly by affecting Na^(+) transport and ROS homeostasis.展开更多
Hyhrid rice has greatly contributed to rice production inChina. But concurrently a dramatic upsurge of rice plant-hopper occurred, particularly for the whitebacked plant-hopper (WBPH), Sogatella furcifera. It has beco...Hyhrid rice has greatly contributed to rice production inChina. But concurrently a dramatic upsurge of rice plant-hopper occurred, particularly for the whitebacked plant-hopper (WBPH), Sogatella furcifera. It has become animportant economic insect pest of hybrid rice, although ithad only been a minor herbivore of rice before nation-wideexploitation of hybrid rice.展开更多
Plant jasmonoyl-L-isoleucine(JA-Ile)is a major defense signal against insect feeding,but whether or how insect salivary effectors suppress JA-Ile synthesis and thus facilitate viral transmission in the plant phloem re...Plant jasmonoyl-L-isoleucine(JA-Ile)is a major defense signal against insect feeding,but whether or how insect salivary effectors suppress JA-Ile synthesis and thus facilitate viral transmission in the plant phloem remains elusive.Insect carboxylesterases(CarEs)are the third major family of detoxification enzymes.Here,we identify a new leafhopper CarE,CarE10,that is specifically expressed in salivary glands and is secreted into the rice phloem as a saliva component.Leafhopper CarE10 directly binds to rice jasmonate resistant 1(JAR1)and promotes its degradation by the proteasome system.Moreover,the direct association of CarE10 with JAR1 clearly impairs JAR1 enzyme activity for conversion of JA to JA-Ile in an in vitro JAIle synthesis system.A devastating rice reovirus activates and promotes the co-secretion of virions and CarE10 via virus-induced vesicles into the saliva-storing salivary cavities of the leafhopper vector and ultimately into the rice phloem to establish initial infection.Furthermore,a virus-mediated increase in CarE10 secretion or overexpression of CarE10 in transgenic rice plants causes reduced levels of JAR1 and thus suppresses JA-Ile synthesis,promoting host attractiveness to insect vectors and facilitating initial viral transmission.Our findings provide insight into how the insect salivary protein CarE10 suppresses host JA-Ile synthesis to promote initial virus transmission in the rice phloem.展开更多
The accumulation of Cd by rice poses significant health risks.Foliar fertilizationwith Zn can reduce grain Cd contents in rice grown in Cd-contaminated soils.However,atmospheric deposition on leaves is another vector ...The accumulation of Cd by rice poses significant health risks.Foliar fertilizationwith Zn can reduce grain Cd contents in rice grown in Cd-contaminated soils.However,atmospheric deposition on leaves is another vector of Cd contamination,and it remains unclear how Zn application affects the allocation of such Cd.We conducted an experiment where the flag leaves of rice plants were treated with solutions with various Zn concentrations and a constant Cd concentration.The 111Cd stable isotope was used to trace the flux of foliarapplied Cd.Higher levels of foliar-applied Zn enhanced Cd efflux and grain allocation.This is attributed to limited sequestration of foliar-applied Cd in the leaf cell symplasm and increased Cd desorption from leaf cell walls when a high Zn^(2+)concentration occurs in the apoplast.Nonionic Zn oxide nanoparticlesmitigated these effects.Additionally,the expressions of OsLCT1 and OsZIP7 in flag leaves and OsHMA2 and OsZIP7 in the uppermost nodes were upregulated under high-Zn^(2+)treatment,which may facilitate Cd phloem loading and grain allocation.Caution is advised in using foliar Zn in areas with high atmospheric Cd due to potential grain-contamination risks.展开更多
Resistance of the melon line TGR-1551 to the aphid Aphis gossypii is based on preventing aphids from ingesting phloem sap. In electrical penetration graphs （EPGs）, this resistance has been characterized with A. goss...Resistance of the melon line TGR-1551 to the aphid Aphis gossypii is based on preventing aphids from ingesting phloem sap. In electrical penetration graphs （EPGs）, this resistance has been characterized with A. gossypii showing unusually long phloem salivation periods （waveform El） mostly followed by pathway activities （waveform C） or if followed by phloem ingestion （waveform E2）, ingestion was not sustained for more than 10 min. Stylectomy with aphids on susceptible and resistant plants was performed during EPG recording while the stylet tips were phloem inserted. This was followed by dissection of the penetrated leaf section, plant tissue fixation, resin embedding, and ultrathin sectioning for transmission electron microscopic observation in order to study the resistance mechanism in the TGR. The most obvious aspect appeared to be the coagulation of phloem proteins inside the stylet canals and the punctured sieve elements. Stylets of 5 aphids per genotype were amputated during sieve element （SE） salivation （El） and SE ingestion （E2）. Cross-sections of stylet bundles in susceptible melon plants showed that the contents of the stylet canals were totally clear and also, no coagulated phloem proteins occurred in their punctured sieve elements. In contrast, electron-dense coagulations were found in both locations in the resistant plants. Due to calcium binding, aphid saliva has been hypothesized to play an essential role in preventing/suppressing such coagulations that cause occlusion of sieves plate and in the food canal of the aphid＇s stylets. Doubts about this role of E 1 salivation are discussed on the basis of our results.展开更多
In response to phosphate(Pi) deficiency, it has been shown that micro-RNAs(miRNAs) and mRNAs are transported through the phloem for delivery to sink tissues. Growing evidence also indicates that long noncoding RNAs(ln...In response to phosphate(Pi) deficiency, it has been shown that micro-RNAs(miRNAs) and mRNAs are transported through the phloem for delivery to sink tissues. Growing evidence also indicates that long noncoding RNAs(lncRNAs) are critical regulators of Pi homeostasis in plants. However, whether lncRNAs are present in and move through the phloem, in response to Pi deficiency, remains to be established. Here, using cucumber as a model plant, we show that lncRNAs are enriched in the phloem translocation stream and respond,systemically, to an imposed Pi-stress. A well-known lncRNA, IPS1, the target mimic(TM) of miRNA399,accumulates to a high level in the phloem, but is not responsive to early Pi deficiency. An additional 24 miRNA TMs were also detected in the phloem translocation stream; among them miRNA171 TMs and miR166 TMs were induced in response to an imposed Pi stress.Grafting studies identified 22 lncRNAs which move systemically into developing leaves and root tips. A CU-rich PTB motif was further identified in these mobile lncRNAs. Our findings revealed that lncRNAs respond to Pi deficiency, non-cell-autonomously, and may act as systemic signaling agents to coordinate early Pi deficiency signaling, at the whole-plant level.展开更多
The plant sucrose transporter SUT1 （from Solanum tuberosum, S. lycopersicum, or Zea mays） exhibits redoxdependent dimerization and targeting if heterologously expressed in S. cerevisiae （Krtigel et al., 2008）. It ...The plant sucrose transporter SUT1 （from Solanum tuberosum, S. lycopersicum, or Zea mays） exhibits redoxdependent dimerization and targeting if heterologously expressed in S. cerevisiae （Krtigel et al., 2008）. It was also shown that SUT1 is present in motile vesicles when expressed in tobacco cells and that its targeting to the plasma membrane is reversible. StSUT1 is internalized in the presence of brefeldin A （BFA） in yeast, plant cells, and in mature sieve elements as confirmed by immunolocalization. These results were confirmed here and the dynamics of intracellular SUT1 localization were further elucidated. Inhibitor studies revealed that vesicle movement of SUT1 is actin-dependent. BFA-mediated effects might indicate that anterograde vesicle movement is possible even in mature sieve elements, and could involve components of the cytoskeleton that were previously thought to be absent in SEs. Our results are in contradiction to this old dogma of plant physiology and the potential of mature sieve elements should therefore be re-evaluated. In addition, SUT1 internalization was found to be dependent on the plasma membrane lipid composition. SUT1 belongs to the detergent-resistant membrane （DRM） fraction in planta and is targeted to membrane raft-like microdomains when expressed in yeast （Kr（igel et al,, 2008）, Here, SUT1-GFP expression in different yeast mutants, which were unable to perform en- docytosis and/or raft formation, revealed a strong link between SUT1 raft localization, the sterol composition and mem- brane potential of the yeast plasma membrane, and the capacity of the SUT1 protein to be internalized by endocytosis. The results provide new insight into the regulation of sucrose transport and the mechanism of endocytosis in plant cells.展开更多
In plants, the phloem is the component of the vascular system that delivers nutrients and transmits signals from mature leaves to developing sink tissues. Recent studies have identified proteins, mRNA, and small RNA w...In plants, the phloem is the component of the vascular system that delivers nutrients and transmits signals from mature leaves to developing sink tissues. Recent studies have identified proteins, mRNA, and small RNA within the phloem sap of several plant species. It is now of considerable interest to elucidate the biological functions of these potential long-distance signal agents, to further our understanding of how plants coordinate their developmental programs at the whole-plant level. In this study, we developed a strategy for the functional analysis of phloem-mobile mRNA by focusing on IAA transcripts, whose mobility has previously been reported in melon （Cucumis melo cv. Hale＇s Best Jumbo）. Indoleacetic acid （IAA） proteins are key transcriptional regulators of auxin signaling, and are involved in a broad range of developmental processes including root development. We used a combination of vasculature-enriched sampling and hetero-grafting techniques to identify IAA18 and IAA28 as phloemmobile transcripts in the model plant Arabidopsis thaliana. Micro-grafting experiments were used to confirm that these IAA transcripts, which are generated in vascular tissues of mature leaves, are then transported into the root system where they negatively regulate lateral root formation. Based on these findings, we present a model in which auxin distribution, in combination with phloem-mobile Aux/IAA transcripts, can determine the sites of auxin action.展开更多
We investigated the role of the ＂sieve tube-companion cell complex＂ lining the tube periphery, particularly the microfilament and microtubule, in assisting the pushing of phloem sap flow. We made a simple phloem tra...We investigated the role of the ＂sieve tube-companion cell complex＂ lining the tube periphery, particularly the microfilament and microtubule, in assisting the pushing of phloem sap flow. We made a simple phloem transport system with a living radish plant, in which the conducting channel was exposed for local treatment with chemicals that are effective in modulating protoplasmic movement （acetylcholine, （ACh） a neurotransmitter in animals and insects; cytochalasin B, （CB） a specific inhibitor of many cellular responses that are mediated by microfilament systems and amiprophos-methyl, （APM） a specific inhibitor of many cellular responses that are mediated by microtubule systems）. Their effects on phloem transport were estimated by two experimental devices： （i） a comparison of changes in the amount of assimilates in terms of carbohydrates and ^14C-labeled photosynthetic production that is left in the leaf blade of treated plants; and （ii） distribution patterns of ^14C-labeled leaf assimilates in the phloem transport system. The results indicate that CB and APM markedly inhibited the transfer of photosynthetic product from leaf to root via the leaf vein, while ACh enhanced the transfer of photosynthetic product in low concentrations （5.0×10^-4 mol/L） but inhibited it in higher concentrations （2.0×10^-3 mol/L） from leaf to root via the leaf vein. Autoradiograph imaging clearly reveals that ACh treatment is more effective than the control, and both CB and APM treatments effectively inhibit the passage of radioactive assimilates. All of the results support the postulation that the peripheral protoplasm in the sieve tube serves not only as a passive semi-permeable membrane, but is also directly involved in phloem transport.展开更多
In the phloem cap region o i Arabidopsis plants,sulfur-rich cells(S-cells)accumulate>100 mM glucosinolates(GLS),but are biosynthetically inactive.The source and route of S-cell-bound GLS remain elusive.In this stud...In the phloem cap region o i Arabidopsis plants,sulfur-rich cells(S-cells)accumulate>100 mM glucosinolates(GLS),but are biosynthetically inactive.The source and route of S-cell-bound GLS remain elusive.In this study,using single-cell sampling and scanning electron microscopy with energy-dispersive X-ray analysis we show that two GLS importers,NPF2.10/GTR1 and NPF2.11/GTR2,are critical for GLS accumulation in S-cells,although they are not localized in the S-cells.Comparison of GLS levels in S-cells in multiple combinations of homo-and heterografts o lg t r l gtr2,biosynthetic null mutant and wild-type plants indicate that S-cells accumulate GLS via symplasmic connections either directly from neighboring biosynthetic cells or indirectly to non-neighboring cells expressing GTR1/2.Distinct sources and transport routes exist for different types of GLS,and vary depending on the position of S-cells in the inflorescence stem.Based on these findings,we propose a model illustrating the GLS transport routes either directly from biosynthetic cells or via GTR-mediated import from apoplastic space radially into a symplasmic domain,wherein the S-cells are the ultimate sink.Similarly,we observed accumulation of the cyanogenic glucoside defensive compounds in high-turgor cells in the phloem cap of Lotus japonicus,suggesting that storage of defensive compounds in high-turgor cells may be a general mechanism for chemical protection of the phloem cap.展开更多
文摘Leaves from three_year_old solar greenhouse nectarine trees ( Prunus persica L. var. nectarina Ait. “Zao Hong Yan”) were used as materials in this study. It was the first time that the ultrastructural characteristics of phloem tissues of source leaves were observed and compared in normal and weak light intensities using the transmission electron microscopy. Results showed that the average diameters of companion cells (CC) and sieve elements (SE) of all kinds of veins were bigger in normal than that in weak light intensity, indicating that light could influence the cell development and growth. Dense cytoplasm with abundant mitochondria, endoplasmic reticulums, multivesicular bodies, vesicles and plastids were observed in normal light intensity. On the contrary, CC with small vacuolar structures and few mitochondrias, endoplasmic reticulums were shown in weak light. Misalignment of grana thylakoid margins of nectarine leaves also was seen in weak light. The sieve pores of SEs were obstructed in weak light. Chloroplasts with numerous starch grains and few mitochondrias were noticed in the mesophyll cell (MES) surrounding the bundle sheath in weak light. The storage of starch grains appeared to result from an unbalance between photosynthate production and export of photosynthates. This observation provided a strong support to the point that most leaves export the most of assimilates in the light time. Plasmodesmal densities between SE/CC, CC/PP (phloem parenchyma cell), PP/PP and PP/BSC (bundle_sheath cell) decreased in weak light. Plasmodesmata were observed between CC/SE (NS) (nacreous_walled sieve element), PP/BSC in branch veins in normal light intensity, but not in weak light. Thus apoplasmic pathway may be the main mode of transport of assimilates in weak light, however symplasmic pathway may be the main mode of transport of assimilates in normal light intensity. These results demonstrated that the solar greenhouse nectarine trees could be adapted to the weak light via the ultrastructure variation of phloem tissues of the source leaves.
基金InternationalFoundationforScience Sweden +1 种基金D/ 2 1 69_1 FoundationoftheEducationMinistryofChina .
文摘The development, cytological characters and ultrastructure of phloem ganglion in the nodal region of Phyllostachys edulis (Carr.) H. de Lehaie, a most economically important bamboo, were investigated and the possible physiological function of this special structure was proposed. The phloem ganglion derived directly from procambium is situated at the sites where the vascular bundle forks and is present in pairs. The phloem ganglion is spindle_like in appearance and usually consists of 4 to 6 layers. Two kinds of cells in the ganglion could be distinguished. In the middle, there are two layers of filiform cells with pointed ends so that there are no normal sieve plates. Nevertheless, there are many pits on the lateral wall of the filiform cells. The other type of cells located at both ends of the spindle which possess an intermediate form between the filiform cell and the normal sieve tube. The walls of these cells towards the filiform cells are strongly convex forming a special sieve plate. Ultrastructure study showed that cells in the ganglion are connected by enriched plasmodesma. During early differentiation, the paramural body and the ingrowth of cell wall could be observed. It indicates that the cells of phloem ganglion have the character of transfer cells. The organelles in the mature cells are mainly plastids with abundant accumulation of proteins of crystalline structure. The above_mentioned results suggest that the physiological function of the phloem ganglion is closely related with substance transport.
基金financially supported by the Youth Science and Technology Innovation Fund of NJFU(CXL2015018)the Project Funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions(PAPD)
文摘The fast growth of Tetracentron sinense is a potential valuable timber resource, but whether its anatomy and chemical components are suitable for timber is unknown. We used light microscopy and SEM to examine the anatomical structure and FITR to measure the chemical components of the phloem and xylem of this tree. Radial variations in growth ring width and tracheid dimensions were also evaluated. The sieve tube, phloem parenchyma cell and sclereids clusters were the main cells in phloem, and the tracheid was the fundamental cell in xylem. An unusual tracheid type, fiber-tracheids or vessel-liked elements was visible. Wood rays nonstoried, uniseriate and multiseriate, including heterogeneous II, occasionally I, and usually 3-6 cells wide. The mean growth-ring width was 2.53 +/- 0.46 mm, and the percentage of late wood was over 60%. For radial variation, growth-ring width increased at an early growth stage, and reached the largest increment during years 11-15, then decreased. The maximum growth-ring width was 5.313 mm. During late growth (60-85 years), trees also maintained a high radial growth increment. Radial variation in the percentage of late wood was uniform, about 50-70%, throughout the growth years. Growth patterns in the length and width of early and late wood were similar as the trees aged. From the FTIR results, the chemical components differed significantly between xylem and phloem, hemicellulose in particular was higher in the xylem than in the phloem, where it was apparently absent. All of these suggest that the composition of phloem in T. sinense is very similar to that of hardwood, and it has higher growth ratio and uniform wood properties.
基金supported by the Guizhou provincial scientific and technological program 20185261。
文摘Phloem is the woody tissue for the storage and long-distance transport of organic matter in vascular bundles.To reveal the process of secondary phloem development and differentiation in Pinus massoniana,the structure of the secondary phloem and the distribution of cell inclusions were observed by histochemical staining,spontaneous fluorescence of phenolic substances and cell segregation.Based on tissue development and differentiation characteristics of P.massoniana secondary phloem,the secondary phloem development was divided into seven stages:the functional phloem stage;the sieve cell lignification stage;the phloem ray bending stage;the parenchyma cell dedifferentiation and division stage;the dedifferentiated parenchyma cell population formation stage;the periderm alteration stage,and the rhytidome stage.An analysis of cell morphology and inclusion distribution characteristics showed that the sieve cells were deformed during lignification,the quantities of parenchyma and resin ducts increased with development and the crystal content in cells,as well as the levels of sugars and lipids in phloem parenchyma cells,increased with development.The results indicate that the P.massoniana phloem first lost longitudinal transport function and then increased its secretory,storage and mechanical functions.Ultimately,the parenchyma differentiated into the cortex and periderm,and the tissue outside the new periderm lignified to form the rhytidome,which fully developed into the protective tissue of the stem.
基金supported by grants from National Natural Science Foundation of China(grant number 32071798 to L.Y.Z)。
文摘Phloem loading and transport of sugar from leaves to sink tissues such as fruits are crucial for yield formation.Camellia oleifera is an evergreen horticultural crop with high value;however,its low production limits the development of the C.oleifera industry.In this study,using a combination of ultrastructural observation,fluorescence loss in photobleaching(FLIP)and inhibitor treatment,we revealed that C.oleifera leaves mainly adopt a symplastic loading route from mesophyll cells to the surrounding vascular bundle cells in minor veins.HPLC assays showed that sucrose is the main sugar transported and only a small amount of raffinose or stachyose was detected in petioles,supporting a passive symplastic loading route in C.oleifera leaves.Compared to leaves grown this year(LT),the carbohydrate synthesis capacity in leaves grown last year(LL)was decreased while LL retained more soluble sugar,suggesting a decrease in transport capacity with leaf ageing.TEM and tissue staining showed that a reduction in plasmodesmata density leads to a decline in the degree of cellular coupling and is responsible for the weakening transport capacity in older leaves.RNA-seq revealed several differentially expressed genes(DEGs)including CoPDCB1-1,CoSUT1 and CoSWEET12,which are likely involved in the regulation of phloem loading and sugar transport.An expression correlation network is constructed between PD-callose binding protein genes,sugar transporter genes and senescence-associated genes.Collectively,this study provides the evidence of the passive symplastic phloem loading pathway in C.oleifera leaves and constructs the correlation between sugar transport and leaf ageing.
基金supported by the Crop Breeding Special Project(XZ201901NB03)the Identification of experimental planting and ecological adaptability of rice in high-altitude areas of Tibet(XZ-2019-NK-NS-0010)。
文摘Salinity is a serious challenge for agriculture production by limiting the arable land.Rice is a major staple food crop but very sensitive to salt stress.In this study,we used Arabidopsis for the functional characterization of a rice F-box gene LOC_Os04g48270(OsPP12-A13)under salinity stress.OsPP12-A13 is a nuclear-localized protein that is strongly upregulated under salinity stress in rice and showed the highest expression in the stem,followed by roots and leaves.Two types of transgenic lines for OsPP12-A13 were generated,including constitutive tissue over-expression using the CaMV35S promoter and phloem specific over-expression using the pSUC2 promoter.Both types of transgenic plants showed salinity tolerance at the seedling stage through higher germination percentage and longer root length,as compared to control plants under salt stress in MS medium.Both the transgenic plants also exhibited salt tolerance at the reproductive stage through higher survival rate,plant dry biomass,and seed yield per plant as compared to control plants.Determination of Na+concentration in leaves,stem and roots of salt-stressed transgenic plants showed that Na^(+) concentration was less in leaf and stem as compared to roots.The opposite was observed in wild type stressed plants,suggesting that OsPP12-A13 may be involved in Na+transport from root to leaf.Transgenic plants also displayed less ROS levels and higher activities of peroxidase and glutathione S-transferase along with upregulation of their corresponding genes as compared to control plants which further indicated a role of OsPP12-A13 in maintaining ROS homeostasis under salt stress.Further,the non-significant difference between the transgenic lines obtained from the two vectors highlighted that OsPP12-A13 principally works in the phloem.Taken together,this study showed that OsPP12-A13 improves salt tolerance in rice,possibly by affecting Na^(+) transport and ROS homeostasis.
文摘Hyhrid rice has greatly contributed to rice production inChina. But concurrently a dramatic upsurge of rice plant-hopper occurred, particularly for the whitebacked plant-hopper (WBPH), Sogatella furcifera. It has become animportant economic insect pest of hybrid rice, although ithad only been a minor herbivore of rice before nation-wideexploitation of hybrid rice.
基金supported by the National Key Research and Development Program of China(2023YFD1400300)the Natural Science Foundation of Fujian Province(2021J01065 and 2022J01127)the National Natural Science Foundation of China(nos.61831920103014 and 32202270).
文摘Plant jasmonoyl-L-isoleucine(JA-Ile)is a major defense signal against insect feeding,but whether or how insect salivary effectors suppress JA-Ile synthesis and thus facilitate viral transmission in the plant phloem remains elusive.Insect carboxylesterases(CarEs)are the third major family of detoxification enzymes.Here,we identify a new leafhopper CarE,CarE10,that is specifically expressed in salivary glands and is secreted into the rice phloem as a saliva component.Leafhopper CarE10 directly binds to rice jasmonate resistant 1(JAR1)and promotes its degradation by the proteasome system.Moreover,the direct association of CarE10 with JAR1 clearly impairs JAR1 enzyme activity for conversion of JA to JA-Ile in an in vitro JAIle synthesis system.A devastating rice reovirus activates and promotes the co-secretion of virions and CarE10 via virus-induced vesicles into the saliva-storing salivary cavities of the leafhopper vector and ultimately into the rice phloem to establish initial infection.Furthermore,a virus-mediated increase in CarE10 secretion or overexpression of CarE10 in transgenic rice plants causes reduced levels of JAR1 and thus suppresses JA-Ile synthesis,promoting host attractiveness to insect vectors and facilitating initial viral transmission.Our findings provide insight into how the insect salivary protein CarE10 suppresses host JA-Ile synthesis to promote initial virus transmission in the rice phloem.
基金supported by Guangdong Basic and the Applied Basic Research Foundation(No.2022A1515011403)the Science and Technology Program of Guangdong Province(No.2022A0505090002)+1 种基金the National Natural Science Foundation of China(Nos.U23A2039 and 42007331)the Research Fund Program of Guangdong Provincial Key Laboratory of Environmental Pollution Control and Remediation Technology(No.2023B1212060016).
文摘The accumulation of Cd by rice poses significant health risks.Foliar fertilizationwith Zn can reduce grain Cd contents in rice grown in Cd-contaminated soils.However,atmospheric deposition on leaves is another vector of Cd contamination,and it remains unclear how Zn application affects the allocation of such Cd.We conducted an experiment where the flag leaves of rice plants were treated with solutions with various Zn concentrations and a constant Cd concentration.The 111Cd stable isotope was used to trace the flux of foliarapplied Cd.Higher levels of foliar-applied Zn enhanced Cd efflux and grain allocation.This is attributed to limited sequestration of foliar-applied Cd in the leaf cell symplasm and increased Cd desorption from leaf cell walls when a high Zn^(2+)concentration occurs in the apoplast.Nonionic Zn oxide nanoparticlesmitigated these effects.Additionally,the expressions of OsLCT1 and OsZIP7 in flag leaves and OsHMA2 and OsZIP7 in the uppermost nodes were upregulated under high-Zn^(2+)treatment,which may facilitate Cd phloem loading and grain allocation.Caution is advised in using foliar Zn in areas with high atmospheric Cd due to potential grain-contamination risks.
文摘Resistance of the melon line TGR-1551 to the aphid Aphis gossypii is based on preventing aphids from ingesting phloem sap. In electrical penetration graphs （EPGs）, this resistance has been characterized with A. gossypii showing unusually long phloem salivation periods （waveform El） mostly followed by pathway activities （waveform C） or if followed by phloem ingestion （waveform E2）, ingestion was not sustained for more than 10 min. Stylectomy with aphids on susceptible and resistant plants was performed during EPG recording while the stylet tips were phloem inserted. This was followed by dissection of the penetrated leaf section, plant tissue fixation, resin embedding, and ultrathin sectioning for transmission electron microscopic observation in order to study the resistance mechanism in the TGR. The most obvious aspect appeared to be the coagulation of phloem proteins inside the stylet canals and the punctured sieve elements. Stylets of 5 aphids per genotype were amputated during sieve element （SE） salivation （El） and SE ingestion （E2）. Cross-sections of stylet bundles in susceptible melon plants showed that the contents of the stylet canals were totally clear and also, no coagulated phloem proteins occurred in their punctured sieve elements. In contrast, electron-dense coagulations were found in both locations in the resistant plants. Due to calcium binding, aphid saliva has been hypothesized to play an essential role in preventing/suppressing such coagulations that cause occlusion of sieves plate and in the food canal of the aphid＇s stylets. Doubts about this role of E 1 salivation are discussed on the basis of our results.
基金supported by grants from the National Science Foundation(IOS-1339128 to W.J.L.)the National Natural Science Foundation of China(31770731to Z.Z.)+1 种基金Anhui Provincial the Department of Science and Technology(17030701049 to Z.Z.)the USDA National Institute of Food and Agriculture Specialty Crop Research Initiative(2015-51181-24285 to Z.F.)
文摘In response to phosphate(Pi) deficiency, it has been shown that micro-RNAs(miRNAs) and mRNAs are transported through the phloem for delivery to sink tissues. Growing evidence also indicates that long noncoding RNAs(lncRNAs) are critical regulators of Pi homeostasis in plants. However, whether lncRNAs are present in and move through the phloem, in response to Pi deficiency, remains to be established. Here, using cucumber as a model plant, we show that lncRNAs are enriched in the phloem translocation stream and respond,systemically, to an imposed Pi-stress. A well-known lncRNA, IPS1, the target mimic(TM) of miRNA399,accumulates to a high level in the phloem, but is not responsive to early Pi deficiency. An additional 24 miRNA TMs were also detected in the phloem translocation stream; among them miRNA171 TMs and miR166 TMs were induced in response to an imposed Pi stress.Grafting studies identified 22 lncRNAs which move systemically into developing leaves and root tips. A CU-rich PTB motif was further identified in these mobile lncRNAs. Our findings revealed that lncRNAs respond to Pi deficiency, non-cell-autonomously, and may act as systemic signaling agents to coordinate early Pi deficiency signaling, at the whole-plant level.
文摘The plant sucrose transporter SUT1 （from Solanum tuberosum, S. lycopersicum, or Zea mays） exhibits redoxdependent dimerization and targeting if heterologously expressed in S. cerevisiae （Krtigel et al., 2008）. It was also shown that SUT1 is present in motile vesicles when expressed in tobacco cells and that its targeting to the plasma membrane is reversible. StSUT1 is internalized in the presence of brefeldin A （BFA） in yeast, plant cells, and in mature sieve elements as confirmed by immunolocalization. These results were confirmed here and the dynamics of intracellular SUT1 localization were further elucidated. Inhibitor studies revealed that vesicle movement of SUT1 is actin-dependent. BFA-mediated effects might indicate that anterograde vesicle movement is possible even in mature sieve elements, and could involve components of the cytoskeleton that were previously thought to be absent in SEs. Our results are in contradiction to this old dogma of plant physiology and the potential of mature sieve elements should therefore be re-evaluated. In addition, SUT1 internalization was found to be dependent on the plasma membrane lipid composition. SUT1 belongs to the detergent-resistant membrane （DRM） fraction in planta and is targeted to membrane raft-like microdomains when expressed in yeast （Kr（igel et al,, 2008）, Here, SUT1-GFP expression in different yeast mutants, which were unable to perform en- docytosis and/or raft formation, revealed a strong link between SUT1 raft localization, the sterol composition and mem- brane potential of the yeast plasma membrane, and the capacity of the SUT1 protein to be internalized by endocytosis. The results provide new insight into the regulation of sucrose transport and the mechanism of endocytosis in plant cells.
基金supported by a grant from the United States-Israel Binational Science Foundation(BSF 2007052,to W.J.L.and S.W.)by a Postdoctoral Fellowship for Research Abroad from the Japanese Society for the Promotion of Science(awarded to Michitaka Notaguchi).
文摘In plants, the phloem is the component of the vascular system that delivers nutrients and transmits signals from mature leaves to developing sink tissues. Recent studies have identified proteins, mRNA, and small RNA within the phloem sap of several plant species. It is now of considerable interest to elucidate the biological functions of these potential long-distance signal agents, to further our understanding of how plants coordinate their developmental programs at the whole-plant level. In this study, we developed a strategy for the functional analysis of phloem-mobile mRNA by focusing on IAA transcripts, whose mobility has previously been reported in melon （Cucumis melo cv. Hale＇s Best Jumbo）. Indoleacetic acid （IAA） proteins are key transcriptional regulators of auxin signaling, and are involved in a broad range of developmental processes including root development. We used a combination of vasculature-enriched sampling and hetero-grafting techniques to identify IAA18 and IAA28 as phloemmobile transcripts in the model plant Arabidopsis thaliana. Micro-grafting experiments were used to confirm that these IAA transcripts, which are generated in vascular tissues of mature leaves, are then transported into the root system where they negatively regulate lateral root formation. Based on these findings, we present a model in which auxin distribution, in combination with phloem-mobile Aux/IAA transcripts, can determine the sites of auxin action.
基金Supported by the National Natural Science Foundation of China （39470432）.Acknowledgements We thank Cheng-Hou Lou and Richard Dawson （ChinaAgricultural University） for their writing assistance.
文摘We investigated the role of the ＂sieve tube-companion cell complex＂ lining the tube periphery, particularly the microfilament and microtubule, in assisting the pushing of phloem sap flow. We made a simple phloem transport system with a living radish plant, in which the conducting channel was exposed for local treatment with chemicals that are effective in modulating protoplasmic movement （acetylcholine, （ACh） a neurotransmitter in animals and insects; cytochalasin B, （CB） a specific inhibitor of many cellular responses that are mediated by microfilament systems and amiprophos-methyl, （APM） a specific inhibitor of many cellular responses that are mediated by microtubule systems）. Their effects on phloem transport were estimated by two experimental devices： （i） a comparison of changes in the amount of assimilates in terms of carbohydrates and ^14C-labeled photosynthetic production that is left in the leaf blade of treated plants; and （ii） distribution patterns of ^14C-labeled leaf assimilates in the phloem transport system. The results indicate that CB and APM markedly inhibited the transfer of photosynthetic product from leaf to root via the leaf vein, while ACh enhanced the transfer of photosynthetic product in low concentrations （5.0×10^-4 mol/L） but inhibited it in higher concentrations （2.0×10^-3 mol/L） from leaf to root via the leaf vein. Autoradiograph imaging clearly reveals that ACh treatment is more effective than the control, and both CB and APM treatments effectively inhibit the passage of radioactive assimilates. All of the results support the postulation that the peripheral protoplasm in the sieve tube serves not only as a passive semi-permeable membrane, but is also directly involved in phloem transport.
文摘In the phloem cap region o i Arabidopsis plants,sulfur-rich cells(S-cells)accumulate>100 mM glucosinolates(GLS),but are biosynthetically inactive.The source and route of S-cell-bound GLS remain elusive.In this study,using single-cell sampling and scanning electron microscopy with energy-dispersive X-ray analysis we show that two GLS importers,NPF2.10/GTR1 and NPF2.11/GTR2,are critical for GLS accumulation in S-cells,although they are not localized in the S-cells.Comparison of GLS levels in S-cells in multiple combinations of homo-and heterografts o lg t r l gtr2,biosynthetic null mutant and wild-type plants indicate that S-cells accumulate GLS via symplasmic connections either directly from neighboring biosynthetic cells or indirectly to non-neighboring cells expressing GTR1/2.Distinct sources and transport routes exist for different types of GLS,and vary depending on the position of S-cells in the inflorescence stem.Based on these findings,we propose a model illustrating the GLS transport routes either directly from biosynthetic cells or via GTR-mediated import from apoplastic space radially into a symplasmic domain,wherein the S-cells are the ultimate sink.Similarly,we observed accumulation of the cyanogenic glucoside defensive compounds in high-turgor cells in the phloem cap of Lotus japonicus,suggesting that storage of defensive compounds in high-turgor cells may be a general mechanism for chemical protection of the phloem cap.
