OPR3 is expressed in phloem cells and is vital for lateral root development in Arabidopsis

2013 ◽  
Vol 93 (2) ◽  
pp. 165-170 ◽  
Author(s):  
Shuaizhang Li ◽  
Jiajia Ma ◽  
Pei Liu

Li, S., Ma, J. and Liu, P. 2013. OPR3 is expressed in phloem cells and is vital for lateral root development in Arabidopsis. Can. J. Plant Sci. 93: 165–170. Jasmonates, a group of oxylipin phytohormones in angiosperms, play important roles in regulating plant growth and development and in responding to environmental stimuli. AtOPR3, a 12-oxo-phytodienoic acid (OPDA) reductase in Arabidopsis thaliana, has been proven to be vital in catalyzing jasmonate biosynthesis. Here, the temporal and spatial expression of AtOPR3 was investigated by promoter-GUS fusion in A. thaliana. In pOPR3::GUS transgenic plants, the GUS activity was detected in roots, leaves and all floral organs, and was highly induced by MeJA treatment. In addition, the GUS activity was principally detected in the phloem cells of the leaf veins. The sequence of the OPR3 promoter region was predicted to have 49 potential binding sites for transcription factors including the well-known Myc-like basic helix-loop-helix, GATA, MADS, MYB-like and Homeobox proteins. In consistent with an expression of OPR3 in lateral roots, there are more lateral roots in the opr3 mutant plants, in which OPR3 expression is knocking-out. In addition, the involvement of auxin biosynthesis in JA-regulated lateral root development is implied by our observation that the transcripts of ASA1, a gene involved in auxin biosynthesis, are decreased in opr3 plants.

2021 ◽  
Author(s):  
Pierre-Mathieu Pélissier ◽  
Hans Motte ◽  
Tom Beeckman

Abstract Lateral roots are important to forage for nutrients due to their ability to increase the uptake area of a root system. Hence, it comes as no surprise that lateral root formation is affected by nutrients or nutrient starvation, and as such contributes to the root system plasticity. Understanding the molecular mechanisms regulating root adaptation dynamics towards nutrient availability is useful to optimize plant nutrient use efficiency. There is at present a profound, though still evolving, knowledge on lateral root pathways. Here, we aimed to review the intersection with nutrient signaling pathways to give an update on the regulation of lateral root development by nutrients, with a particular focus on nitrogen. Remarkably, it is for most nutrients not clear how lateral root formation is controlled. Only for nitrogen, one of the most dominant nutrients in the control of lateral root formation, the crosstalk with multiple key signals determining lateral root development is clearly shown. In this update, we first present a general overview of the current knowledge of how nutrients affect lateral root formation, followed by a deeper discussion on how nitrogen signaling pathways act on different lateral root-mediating mechanisms for which multiple recent studies yield insights.


2020 ◽  
Vol 38 (4) ◽  
pp. 143-148
Author(s):  
G. W. Watson ◽  
A.M. Hewitt

Abstract The number and size of lateral roots of a tree seedling can be evaluated visually, and could potentially be used to select plants with better root systems early in nursery production. To evaluate how root architecture develops in young trees, root architecture of 37 species of trees was compared at two stages of development: as harvested seedlings, and then one year after replanting. The total number of lateral roots and the number of roots >2mm (0.08 in) diameter that were present on the portion of the taproot remaining on seedlings after standard root pruning were recorded. Neither could consistently predict the number of lateral roots on the root system one year after replanting. Development of roots (sum of diameters) regenerated from the cut end of the seedling taproot was equal or greater than lateral root development in 84 percent of evaluated species. Even when regenerated root development was significantly less than lateral root development, the regenerated roots still comprised up to 44 percent of the root system. Regenerated roots from the cut end of the taproot can become a major component of the architecture of the structural root system in nursery stock. Index words: structural roots, nursery production, root regeneration. Species used in this study: European black alder (Alnus glutinosa Gaertn.), green ash (Fraxinus pennsylvanica Marshall), quaking aspen (Populus tremuloides Michx.), European white birch. (Betula pendula Roth), river birch (Betula nigra L.), black locust (Robinia pseudoacacia L.), northern catalpa (Catalpa speciosa (Warder) Warder ex Engelm.), Mazzard cherry [Prunus avium [L.) L.], chokecherry (Prunus virginiana L.), American elm (Ulmus americana L.), Siberian elm (Ulmus pumilia L.), goldenchain tree (Laburnum anagyroides Medik.), northern hackberry (Celtis occidentalis L.), Cockspur hawthorn (Crateagus crus-galli L.), single seed hawthorn (Crateagus monogyna Jacq.), honeylocust (Gleditsia tricanthos L.), Japanese pagodatree [Sophora japonica (L.) Schott], Katsura tree (Cercidiphyllum japonicum Siebold & Zucc.), Kentucky coffee tree [Gymnocladus dioicus (L.) K. Koch], littleleaf linden (Tilia cordata Mill.), boxelder (Acer negundo L.), hedge maple (Acer campestre L.), Norway maple (Acer platanoides L.), red maple (Acer rubrum L.), silver maple (Acer saccharinum L.), sugar maple (Acer saccharum Marshall), sycamore maple (Acer pseudoplatanus L.), English Oak (Quercus robur L.), northern red oak (Quercus rubra L.), Siberian peashrub (Caragana arborescens Lam.), American plum (Prunus Americana Marshall ), Myrobalan plum (Prunus cerasifera Ehrh.), redbud (Cercis Canadensis L.), Russian olive (Elaeagnus angustifoliaI L.), tuliptree (Liriodendron tulipifera L.), black walnut (Juglans nigra L.), Japanese zelkova (Zelkova serrata (Thunb.) Makino).


2020 ◽  
Author(s):  
Hardik P. Gala ◽  
Amy Lanctot ◽  
Ken Jean-Baptiste ◽  
Sarah Guiziou ◽  
Jonah C. Chu ◽  
...  

AbstractRoot architecture is a major determinant of fitness, and is under constant modification in response to favorable and unfavorable environmental stimuli. Beyond impacts on the primary root, the environment can alter the position, spacing, density and length of secondary or lateral roots. Lateral root development is among the best-studied examples of plant organogenesis, yet there are still many unanswered questions about its earliest steps. Among the challenges faced in capturing these first molecular events is the fact that this process occurs in a small number of cells with unpredictable timing. Single-cell sequencing methods afford the opportunity to isolate the specific transcriptional changes occurring in cells undergoing this fate transition. Using this approach, we successfully captured the transcriptomes of initiating lateral root primordia, and discovered many previously unreported upregulated genes associated with this process. We developed a method to selectively repress target gene transcription in the xylem pole pericycle cells where lateral roots originate, and demonstrated that expression of several of these targets was required for normal root development. We also discovered novel subpopulations of cells in the pericycle and endodermal cell files that respond to lateral root initiation, highlighting the coordination across cell files required for this fate transition.One sentence summarySingle cell RNA sequencing reveals new molecular details about lateral root initiation, including the transcriptional impacts of the primordia on bordering cells.


Forests ◽  
2020 ◽  
Vol 11 (8) ◽  
pp. 798
Author(s):  
Shanon Hankin ◽  
Gary Watson

For urban trees with strong taproots, a shift in root growth towards increased lateral root development could improve tree performance in compacted, poorly drained urban soils. In effort to achieve this desired shift, various propagation and production practices exist within the nursery industry. However, the effectiveness of practices used to disrupt taproot development, as well as their impact on root architecture, has been largely undocumented. To determine how seedling root systems respond to taproot growth disruption, we pruned oak seedling taproots either mechanically at 5 and/or 15 cm, or via air pruning at 15 cm. Taproot regeneration and lateral root development were evaluated after two years. Taproot pruning resulted in multiple regenerated taproots. The location and number of times the taproot(s) was pruned did not appear to alter the ultimate number. Mechanical taproot pruning did not affect lateral root development above the first pruning cut location at 5 or 15 cm, but generally increased the density of lateral roots below the pruning cut, likely due to the multiple taproots present. Most lateral roots were fine roots less than 1 mm in diameter (fine roots), being unlikely to become long-lived components of the root system architecture. The average number of lateral roots on air pruned (AP) seedlings was generally greater than on the same taproot segment of control (C) seedlings. To determine how these seedling changes impact the root regeneration of liner stock, we planted both taproot pruned and taproot air pruned seedlings in in-ground fabric bags filled with field soil (B) or directly into the field without bags (F). Root regeneration potential (RRP) at the bottom and lateral surfaces of the root ball were evaluated. There was less RRP on the lateral surface of the root ball in taproot air pruned, container-grown (CG) compared to taproot pruned, bare root (BR) bur oak liners, and there was no difference in red oak liners. The multiple taproots of mechanically pruned BR seedlings did not result in excessive taproot development as liners. In contrast, CG seedling taproots restricted by air pruning produced more regenerated taproots after transplanting. While seedling taproot growth disruption does disrupt the growth of a dominant single taproot and alters the architecture toward increasing the number of lateral roots, these practices do not result in laterally dominated root architecture at the liner stage of nursery production. Future research should determine how these production methods effect lateral root growth after a tree is established in the landscape and determine appropriate combinations of production methods for different species.


Weed Science ◽  
1971 ◽  
Vol 19 (3) ◽  
pp. 265-268 ◽  
Author(s):  
Ghanem S. Hassawy ◽  
K. C. Hamilton

Trifluralin (α,α,α-trifluoro-2,6-dinitro-N,N-dipropyl-p-toluidine), IAA (indoleacetic acid), kinetin (6-furfurylamino purine), and their combinations in culture solutions did not affect cotton (Gossypium hirsutumL., var. Deltapine Smooth Leaf) germination but reduced primary root and shoot lengths of seedlings. Trifluralin alone and in combination with IAA or kinetin inhibited lateral root development. When IAA and kinetin were both applied with 5 ppmw trifluralin, lateral roots developed.


2020 ◽  
pp. jbc.RA120.014543
Author(s):  
Jordan M. Chapman ◽  
Gloria K. Muday

Flavonoids are a class of specialized metabolites with subclasses including flavonols and anthocyanins, which have unique properties as antioxidants. Flavonoids modulate plant development, but whether and how they impact lateral root development is unclear. We examined potential roles for flavonols in this process using Arabidopsis thaliana mutants with defects in genes encoding key enzymes in flavonoid biosynthesis. We observed the tt4 and fls1 mutants, which produce no flavonols, have increased lateral root emergence. The tt4 root phenotype was reversed by genetic and chemical complementation. To more specifically define the flavonoids involved, we tested an array of flavonoid biosynthetic mutants, eliminating roles for anthocyanins and the flavonols quercetin and isorhamnetin in modulating root development. Instead, two tt7 mutant alleles, with defects in a branchpoint enzyme blocking quercetin biosynthesis, formed reduced numbers of lateral roots, and tt7-2 had elevated levels of kaempferol. Using a flavonol-specific dye, we observed that in the tt7-2 mutant, kaempferol accumulated within lateral root primordia at higher levels than wild-type. These data are consistent with kaempferol, or downstream derivatives, acting as a negative regulator of lateral root emergence. We examined ROS accumulation using ROS-responsive probes and found reduced fluorescence of a superoxide-selective probe within the primordia of tt7-2 compared to wild type, but not in the tt4 mutant, consistent with opposite effects of these mutants on lateral root emergence. These results support a model in which increased level of kaempferol in the lateral root primordia of tt7-2 reduces superoxide concentration and ROS-stimulated lateral root emergence.


Author(s):  
Kaushal K. Bhati ◽  
Anil Kumar ◽  
Ajay Kumar Pandey

TaABCC13 is member of wheat ABCC subclass of transporters. The RNAi mediated silencing of this transporter in wheat results in lowering of seed phytic acid level and other developmental defects. In addition to that, wheat ABCC13 was involved in cadmium detoxification as evident by the complementation assays in yeast. The appearance of early lateral roots in these transgenic seedlings speculated the possibility for studying the role of localized auxin-mediated effects. In the current study, firstly, the expression of auxin related genes was studied in the transgenic roots. Enhanced expression of genes pertaining to either auxin biosynthesis or its transport was observed in transgenic wheat seedling roots suggesting the direct effect of the hormone. Further, the early emergence of lateral roots in transgenic wheat seedlings was affected due to the presence of auxin-transport inhibitor suggesting the direct effect of hormones in root development. In conclusion, herein we provide the novel evidence for the auxin mediated regulation of lateral root emergence in TaABCC13:RNAi seedlings.


Weed Science ◽  
1970 ◽  
Vol 18 (4) ◽  
pp. 520-522 ◽  
Author(s):  
J. A. Norton ◽  
J. P. Walter ◽  
J. B. Storey

Trifluralina,a,a-trifluoro-2,6-dinitro-N,N-dipropyl-p-toluidine) applied at 1.12 kg/ha inhibited lateral root development on field-grown pecan(Carya illinoensis(Wang.) K. Koch) seedlings. In a greenhouse study, inhibition of lateral roots, club-shaped radicles, and restricted penetration of tap roots resulted when pecans were planted in soil treated with 1.0 ppm trifluralin. When pecans were planted above soil treated with trifluralin, normal root development occurred only in the soil which had not been treated. Lateral roots were inhibited in the trifluralin-treated soil. Pecan nuts from trifluralin plots were smaller than those collected from controls, but other factors of quality were statistically equal or superior to nuts harvested in plots which had been treated with 2-chloro-4,6-bis-(ethylamino)-s-triazine (simazine) and 3-(3,4-dichlorophenyl)-1,1-dimethylurea (diuron). The smaller nut size was attributed to lateral root inhibition by trifluralin early during nut development.


2019 ◽  
Vol 39 (11) ◽  
pp. 1907-1921
Author(s):  
Dongdong Tian ◽  
Yueyuan Liu ◽  
Lidan Tian ◽  
Mengjie Wan ◽  
Bo Zheng ◽  
...  

Abstract As one of the major groups of small post-translationally modified peptides, the CLV3/EMBRYO SURROUNDING REGION-RELATED (CLE)-like (CLEL) peptide family has been reported to regulate root growth, lateral root development and plant gravitropic responses in Arabidopsis thaliana. In this study, we identified 12 CLEL genes in Populus trichocarpa and performed a comprehensive bioinformatics analysis on these genes. Among them, five P. trichocarpa CLELs (PtrCLELs) were revised with new gene models. All of these PtrCLEL proteins were structurally similar to the A. thaliana CLELs (AtCLELs), including an N-terminal signal peptide, a conserved C-terminal 13-amino-acid CLEL motif and a variable intermediate region. In silico and quantitative real-time PCR analyses showed that PtrCLELs were widely expressed in various tissues, including roots, leaves, buds and stems. Exogenous application of chemically synthesized PtrCLEL peptides resulted in wavy or curly roots and reduced lateral root formation in A. thaliana. Moreover, germinating Populus deltoides seedlings on a growth medium containing these peptides caused the roots to thicken and to form abnormal lateral roots, in many cases in clusters. Anatomical and histological changes in thickened roots were further investigated by treating Populus 717 cuttings with the PtrCLEL10 peptide. We observed that root thickening was mainly due to an increased number of cells in the epidermis, hypodermis and cortex. The results of our study suggested that PtrCLEL and AtCLEL genes encode proteins with similar protein structures, sequences of peptide motif and peptide activities on developing roots. The activities of PtrCLEL peptides in root development were species-dependent.


2019 ◽  
Author(s):  
Feng Zhang ◽  
Wenqing Tao ◽  
Ruiqi Sun ◽  
Junxia Wang ◽  
Cuiling Li ◽  
...  

AbstractThe development of lateral roots in Arabidopsis thaliana is strongly dependent on signaling directed by the AUXIN RESPONSE FACTOR7 (ARF7), which in turn activates LATERAL ORGAN BOUNDARIES DOMAIN (LBD) transcription factors (LBD16, 18, 29 and 33). Here, the product of PRH1, a PR-1 homolog annotated previously as encoding a pathogen-responsive protein, was identified as a target of ARF7-mediated auxin signaling and also as participating in the development of lateral roots. PRH1 was shown to be strongly induced by auxin treatment, and plants lacking a functional copy of PRH1 formed fewer lateral roots. The transcription of PRH1 was controlled by the binding of both ARF7 and LBDs to its promoter region. An interaction was detected between PRH1 and GATA23, a protein which regulates cell identity in lateral root founder cells.Author SummaryIn Arabidopsis thaliana AUXIN RESPONSE FACTOR7 (ARF7)-mediated auxin signaling plays a key role in lateral roots (LRs) development. The LATERAL ORGAN BOUNDARIES DOMAIN (LBD) transcription factors (LBD16, 18, 29 and 33) act downstream of ARF7-mediated auxin signaling to control LRs formation. Here, the PR-1 homolog PRH1 was identified as a novel target of both ARF7 and LBDs (especially the LBD29) during auxin induced LRs formation, as both ARF7 and LBDs were able to bind to the PRH1 promoter. More interestingly, PRH1 has a physical interaction with GATA23, which has been also reported to be up-regulated by auxin and influences LR formation through its regulation of LR founder cell identity. Whether the interaction between GATA23 and PRH1 affects the stability and/or the activity of either (or both) of these proteins remains an issue to be explored. This study provides improves new insights about how auxin regulates lateral root development.


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