hypocotyl elongation
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2022 ◽  
Vol 8 (2) ◽  
Author(s):  
Minmin Du ◽  
Firas Bou Daher ◽  
Yuanyuan Liu ◽  
Andrew Steward ◽  
Molly Tillmann ◽  
...  

Auxin concentration–dependent cell expansion coordinates hypocotyl elongation and apical hook development for soil emergence.


2021 ◽  
Author(s):  
Francois Jobert ◽  
Stephanie Guenin ◽  
Aline Voxeur ◽  
Kieran JD Lee ◽  
Sophie Bouton ◽  
...  

Pectins occur in primary cell walls and consist of multiblock co‐polymers among which homogalacturonan (HG) is the simplest and most abundant form. Methylesterification patterns of HG are tuned by pectin methylesterases (PMEs), the activities of which are controlled by specific inhibitors (PMEIs). By impacting cell wall mechanical properties, PME‐mediated regulation of HG methylesterification plays a major role in several developmental processes, including seed germination and dark-grown hypocotyl elongation. Arabidopsis PME36 is preferentially expressed during the late stage of seed development and, using the knock‐out mutant pme36-1, we show here that PME36 is required to implement the characteristic pattern of de-methylesterified pectin in the mature seed. Surprisingly, while this pattern is strongly impaired in pme36-1 mature seed, no phenotypical effect is observed in the mutant during seed germination and dark-grown hypocotyl elongation, suggesting the existence of a compensatory mechanism overcoming the defect in pectin de-methylesterification. By analyzing hormone contents and gene expression, a strong, dynamic, and long-lasting physiological disorder is revealed in the mutant. These results suggest the existence of complex connections between pectin remodeling, transcriptomic regulations and hormonal homeostasis, modulating several physiological parameters to ensure the maintenance of a normal seed-to-seedling developmental program in pme36-1. Considered for a long time as an end-point passive effector mainly involved in modification of cell wall mechanics, the role of pectin methylesterification needs to be reconsidered as a modulator acting upstream of diverse regulatory pathways involved in plant development.


2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Gilor Kelly ◽  
Danja Brandsma ◽  
Aiman Egbaria ◽  
Ofer Stein ◽  
Adi Doron-Faigenboim ◽  
...  

AbstractThe hypocotyls of germinating seedlings elongate in a search for light to enable autotrophic sugar production. Upon exposure to light, photoreceptors that are activated by blue and red light halt elongation by preventing the degradation of the hypocotyl-elongation inhibitor HY5 and by inhibiting the activity of the elongation-promoting transcription factors PIFs. The question of how sugar affects hypocotyl elongation and which cell types stimulate and stop that elongation remains unresolved. We found that overexpression of a sugar sensor, Arabidopsis hexokinase 1 (HXK1), in guard cells promotes hypocotyl elongation under white and blue light through PIF4. Furthermore, expression of PIF4 in guard cells is sufficient to promote hypocotyl elongation in the light, while expression of HY5 in guard cells is sufficient to inhibit the elongation of the hy5 mutant and the elongation stimulated by HXK1. HY5 exits the guard cells and inhibits hypocotyl elongation, but is degraded in the dark. We also show that the inhibition of hypocotyl elongation by guard cells’ HY5 involves auto-activation of HY5 expression in other tissues. It appears that guard cells are capable of coordinating hypocotyl elongation and that sugar and HXK1 have the opposite effect of light on hypocotyl elongation, converging at PIF4.


2021 ◽  
Vol 1 (1) ◽  
Author(s):  
Bin Liu ◽  
Jinyang Weng ◽  
Dailu Guan ◽  
Yan Zhang ◽  
Qingliang Niu ◽  
...  

2021 ◽  
Author(s):  
Daniele Rosado ◽  
Amanda Ackermann ◽  
Olya Spassibojko ◽  
Magdalena Rossi ◽  
Ullas V Pedmale

Shade-intolerant plants rapidly elongate their stems, branches, and leaf stalks to compete with their neighboring vegetation to maximize sunlight capture for photosynthesis. This rapid growth adaptation, known as the shade avoidance response (SAR), comes at a cost; reduced biomass, crop yield, and root growth. Significant progress has been made on the mechanistic understanding of hypocotyl elongation during SAR; however, the molecular account of how root growth is repressed is not well understood. Here, we explore the mechanisms by which low red:far-red induced SAR restrict the primary and lateral root (LR) growth. By analyzing whole-genome transcriptome, we identified a core set of shade-induced genes in the roots of Arabidopsis and tomato seedlings grown in the shade. Abiotic and biotic stressors also induce many of these shade-induced genes and are predominantly regulated by the WRKY transcription factors. Correspondingly, a majority of the WRKYs were also among the shade-induced genes. Functional analysis using transgenics of these shade-induced WRKYs revealed their role is essentially to restrict primary root and LR growth in the shade, and captivatingly, they did not affect hypocotyl elongation. Similarly, we also show that ethylene hormone signaling is necessary to limit root growth in the shade. Our study proposes that during SAR, shade-induced WRKY26, 45, and 75, and ethylene reprogram gene expression in the root to restrict its growth and development. The reduced growth of root organs helps the plant divert its critical resources to the elongating organs in the shoot to ensure competitiveness under limiting photosynthetic radiation


2021 ◽  
Vol 12 ◽  
Author(s):  
Saddam Hussain ◽  
Wei Wang ◽  
Sajjad Ahmed ◽  
Xutong Wang ◽  
Adnan ◽  
...  

Auxin is one of the traditional plant hormones, whereas peptide hormones are peptides with hormone activities. Both auxin and plant peptide hormones regulate multiple aspects of plant growth and development, and there are cross-talks between auxin and plant peptide hormones. PAMP-INDUCED SECRETED PEPTIDES (PIPs) and PIP-LIKEs (PIPLs) are a new family of plant peptide hormone, and PIPL3/TARGET OF LBD SIXTEEN 2 (TOLS2) has been shown to regulate lateral root formation in Arabidopsis. We report here the identification of PIP2 as an auxin response gene, and we found it plays a role in regulating root and hypocotyl development in Arabidopsis. By using quantitative RT-PCR, we found that the expression of PIP2 but not PIP1 and PIP3 was induced by auxin, and auxin induced expression of PIP2 was reduced in nph4-1 and arf19-4, the lost-of-function mutants of Auxin Response Factor 7 (ARF7) and ARF19, respectively. By generating and characterizing overexpressing transgenic lines and gene edited mutants for PIP2, we found that root length in the PIP2 overexpression plant seedlings was slightly shorter when compared with that in the Col wild type plants, but root length of the pip2 mutant seedlings remained largely unchanged. For comparison, we also generated overexpressing transgenic lines and gene edited mutants for PIP3, as well as pip2 pip3 double mutants. Surprisingly, we found that root length in the PIP3 overexpression plant seedlings is shorter than that of the PIP2 overexpression plant seedlings, and the pip3 mutant seedlings also produced short roots. However, root length in the pip2 pip3 double mutant seedlings is largely similar to that in the pip3 single mutant seedlings. On the other hand, hypocotyl elongation assays indicate that only the 35S:PIP2 transgenic plant seedlings produced longer hypocotyls when compared with the Col wild type seedlings. Further analysis indicates that PIP2 promotes cell division as well as cell elongation in hypocotyls. Taken together, our results suggest that PIP2 is an auxin response gene, and PIP2 plays a role in regulating root and hypocotyl elongation in Arabidopsis likely via regulating cell division and cell elongation.


Author(s):  
Yun Kong ◽  
Youbin Zheng

Microgreens growing under electric (aka artificial) lighting in controlled environments often have short hypocotyls, which can be difficult for machine harvest. To investigate whether early-stage dark treatment can promote hypocotyl elongation without compromising microgreen yield and quality, two different seed-size species, sunflower (Helianthus annuus ‘Black oil’) and arugula (Eruca sativa ‘Rocket’), were tested. Seeds of sunflower and arugula were sown in pots, and the pots were placed inside support trays. During the first 5 days after seeding, half of the pots per species within each tray were covered with an upside-down black tray as dark treatment, and another half were kept under light. The light treatment was provided by continuous (24-h) lighting with a combination of red (85%) and blue (15%) light-emitting diodes at a photosynthetic photo flux density of around 100 µmol m−2 s−1. After 5 days of dark treatment, the black covers were removed and the plants were grown under the above lighting treatment till harvesting. The microgreens were harvested at 7 d and 12 d after seeding for sunflower and arugula, respectively. Early-stage dark treatment promoted hypocotyl elongation by 26% and 28% for sunflower and arugula, respectively. Microgreen yield was increased by 13% for sunflower and reduced by 24% for arugula under dark treatment. Dark treatment increased cotyledon succulence by 14% for sunflower, but reduced cotyledon size by about 25% for arugula despite increases in red color and succulence of arugula hypocotyls. For both species, cotyledon color and soluble solids content were not affected by dark treatment.


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