scholarly journals Cell wall hydrolases act in concert during aerenchyma development in sugarcane roots

2019 ◽  
Vol 124 (6) ◽  
pp. 1067-1089 ◽  
Author(s):  
Adriana Grandis ◽  
Débora C C Leite ◽  
Eveline Q P Tavares ◽  
Bruna C Arenque-Musa ◽  
Jonas W Gaiarsa ◽  
...  
Keyword(s):  
Cell Wall ◽  
Root Tip ◽  
Partial Hydrolysis ◽  
Glycosyl Hydrolases ◽  
Aerenchyma Formation ◽  
Protein Levels ◽  
Composite Formation ◽  
Hydrolysis Of Cellulose ◽  
Cell Wall Hydrolases ◽  
Cell Wall Disassembly

Abstract Background and Aims Cell wall disassembly occurs naturally in plants by the action of several glycosyl-hydrolases during different developmental processes such as lysigenous and constitutive aerenchyma formation in sugarcane roots. Wall degradation has been reported in aerenchyma development in different species, but little is known about the action of glycosyl-hydrolases in this process. Methods In this work, gene expression, protein levels and enzymatic activity of cell wall hydrolases were assessed. Since aerenchyma formation is constitutive in sugarcane roots, they were assessed in segments corresponding to the first 5 cm from the root tip where aerenchyma develops. Key Results Our results indicate that the wall degradation starts with a partial attack on pectins (by acetyl esterases, endopolygalacturonases, β-galactosidases and α-arabinofuranosidases) followed by the action of β-glucan-/callose-hydrolysing enzymes. At the same time, there are modifications in arabinoxylan (by α-arabinofuranosidases), xyloglucan (by XTH), xyloglucan–cellulose interactions (by expansins) and partial hydrolysis of cellulose. Saccharification revealed that access to the cell wall varies among segments, consistent with an increase in recalcitrance and composite formation during aerenchyma development. Conclusion Our findings corroborate the hypothesis that hydrolases are synchronically synthesized, leading to cell wall modifications that are modulated by the fine structure of cell wall polymers during aerenchyma formation in the cortex of sugarcane roots.

scholarly journals The Arabidopsis Root Tip (Phospho)Proteomes at Growth-Promoting versus Growth-Repressing Conditions Reveal Novel Root Growth Regulators

Cells ◽  
2021 ◽  
Vol 10 (7) ◽  
pp. 1665
Author(s):  
Natalia Nikonorova ◽  
Evan Murphy ◽  
Cassio Flavio Fonseca de Lima ◽  
Shanshuo Zhu ◽  
Brigitte van de Cotte ◽  
...  
Keyword(s):  
Cell Wall ◽  
Root Growth ◽  
Growth Regulators ◽  
Growth Regulation ◽  
Phosphorylation Site ◽  
Primary Root ◽  
Root Tip ◽  
Arabidopsis Root ◽  
Growth Promoting ◽  
The Impact

Auxin plays a dual role in growth regulation and, depending on the tissue and concentration of the hormone, it can either promote or inhibit division and expansion processes in plants. Recent studies have revealed that, beyond transcriptional reprogramming, alternative auxin-controlled mechanisms regulate root growth. Here, we explored the impact of different concentrations of the synthetic auxin NAA that establish growth-promoting and -repressing conditions on the root tip proteome and phosphoproteome, generating a unique resource. From the phosphoproteome data, we pinpointed (novel) growth regulators, such as the RALF34-THE1 module. Our results, together with previously published studies, suggest that auxin, H+-ATPases, cell wall modifications and cell wall sensing receptor-like kinases are tightly embedded in a pathway regulating cell elongation. Furthermore, our study assigned a novel role to MKK2 as a regulator of primary root growth and a (potential) regulator of auxin biosynthesis and signalling, and suggests the importance of the MKK2 Thr31 phosphorylation site for growth regulation in the Arabidopsis root tip.

Ultrastructure of Medicago sativa rhizodermis cells over their early development

Biologia ◽  
2008 ◽  
Vol 63 (2) ◽  
Author(s):  
Lucia Mikolajová ◽  
Halina Vargová ◽  
Zora Hanáčková ◽  
Milada Čiamporová
Keyword(s):  
Cell Wall ◽  
Medicago Sativa ◽  
Root Hair ◽  
Phosphotungstic Acid ◽  
Root Tip ◽  
Cell Wall Polysaccharides ◽  
Golgi Bodies ◽  
Internalization Process ◽  
Subcellular Level ◽  
Root Hair Initiation

AbstractUltrastructure was investigated along the files of developing epidermal cells in the root tip of a model plant Medicago sativa, in which all rhizodermal cells are potential hair-forming trichoblasts. Differentiation at subcellular level was observed up to the stage of bulge initiation in the trichoblasts. Root hair initiation indicated by the emergence of bulges from trichoblasts was detected at various distances from the root tip and, it was independent of the trichoblast size.During rhizodermal cell differentiation, starch grains accumulated in the plastids. Nuclei located in the central part of the young, meristematic cells moved towards the inner periclinal wall as the central vacuole enlarged. The bulging region of the trichoblasts located opposite the nucleus and was rich in mitochondria, ER, ribosomes, and Golgi bodies, and contained also vesicles enclosing fibrillar material. This material responded positively to phosphotungstic acid, which was used for detection of cell wall polysaccharides. The cell wall thickness within the bulging domain was significantly lower than in other parts of trichoblasts. We suggest that internalization of cell wall polysaccharides occurs within the bulging area, contributing to local thinning of the cell wall and providing a source of osmotically active compounds for maintaining turgor in the trichoblast. Thus, the internalization process might be necessary for root hair outgrowth.

scholarly journals Conserved Processes and Lineage-Specific Proteins in Fungal Cell Wall Evolution

2007 ◽  
Vol 6 (12) ◽  
pp. 2269-2277 ◽  
Author(s):  
Juan E. Coronado ◽  
Saad Mneimneh ◽  
Susan L. Epstein ◽  
Wei-Gang Qiu ◽  
Peter N. Lipke
Keyword(s):  
Cell Wall ◽  
Protein Function ◽  
Phosphatidyl Inositol ◽  
Low Complexity ◽  
Open Reading Frames ◽  
Specific Cell ◽  
Glycosyl Hydrolases ◽  
Fungal Cell ◽  
Structural Wall ◽  
Lineage Specificity

ABSTRACT The cell wall is a defining organelle that differentiates fungi from its sister clades in the opisthokont superkingdom. With a sensitive technique to align low-complexity protein sequences, we have identified 187 cell wall-related proteins in Saccharomyces cerevisiae and determined the presence or absence of homologs in 17 other fungal genomes. There were both conserved and lineage-specific cell wall proteins, and the degree of conservation was strongly correlated with protein function. Some functional classes were poorly conserved and lineage specific: adhesins, structural wall glycoprotein components, and unannotated open reading frames. These proteins are primarily those that are constituents of the walls themselves. On the other hand, glycosyl hydrolases and transferases, proteases, lipases, proteins in the glycosyl phosphatidyl-inositol-protein synthesis pathway, and chaperones were strongly conserved. Many of these proteins are also conserved in other eukaryotes and are associated with wall synthesis in plants. This gene conservation, along with known similarities in wall architecture, implies that the basic architecture of fungal walls is ancestral to the divergence of the ascomycetes and basidiomycetes. The contrasting lineage specificity of wall resident proteins implies diversification. Therefore, fungal cell walls consist of rapidly diversifying proteins that are assembled by the products of an ancestral and conserved set of genes.

scholarly journals The Jacalin-Related Lectin HvHorcH Is Involved in the Physiological Response of Barley Roots to Salt Stress

2021 ◽  
Vol 22 (19) ◽  
pp. 10248
Author(s):  
Katja Witzel ◽  
Andrea Matros ◽  
Uwe Bertsch ◽  
Tariq Aftab ◽  
Twan Rutten ◽  
...  
Keyword(s):  
Salt Stress ◽  
Salt Tolerance ◽  
Extracellular Fluid ◽  
Root Tip ◽  
Salinity Treatment ◽  
Root Tips ◽  
Salt Stress Response ◽  
Cdna Sequences ◽  
Barley Cultivars ◽  
Protein Levels

Salt stress tolerance of crop plants is a trait with increasing value for future food production. In an attempt to identify proteins that participate in the salt stress response of barley, we have used a cDNA library from salt-stressed seedling roots of the relatively salt-stress-tolerant cv. Morex for the transfection of a salt-stress-sensitive yeast strain (Saccharomyces cerevisiae YSH818 Δhog1 mutant). From the retrieved cDNA sequences conferring salt tolerance to the yeast mutant, eleven contained the coding sequence of a jacalin-related lectin (JRL) that shows homology to the previously identified JRL horcolin from barley coleoptiles that we therefore named the gene HvHorcH. The detection of HvHorcH protein in root extracellular fluid suggests a secretion under stress conditions. Furthermore, HvHorcH exhibited specificity towards mannose. Protein abundance of HvHorcH in roots of salt-sensitive or salt-tolerant barley cultivars were not trait-specific to salinity treatment, but protein levels increased in response to the treatment, particularly in the root tip. Expression of HvHorcH in Arabidopsis thaliana root tips increased salt tolerance. Hence, we conclude that this protein is involved in the adaptation of plants to salinity.

scholarly journals Histological Observation of Primary and Secondary Aerenchyma Formation in Adventitious Roots of Syzygium kunstleri (King) Bahadur and R.C.Gaur Grown in Hypoxic Medium

Forests ◽  
2019 ◽  
Vol 10 (2) ◽  
pp. 137 ◽  
Author(s):  
Hong-Duck Sou ◽  
Masaya Masumori ◽  
Hiroyuki Kurokochi ◽  
Takeshi Tange
Keyword(s):  
Formation Process ◽  
Rainy Season ◽  
Adventitious Roots ◽  
Root Tip ◽  
Histological Observation ◽  
Root Tips ◽  
Aerenchyma Formation

Trees growing in wetlands develop adventitious roots from the trunk during the rainy season and adapt to the flooded environment by forming primary (schizogenous or lysigenous) and secondary aerenchyma in the roots. Therefore, it is necessary to clarify the formation process of each type of aerenchyma in these adventitious roots. In this study, saplings of Syzygium kunstleri (King) Bahadur and R.C.Gaur were grown under four different treatments, and a total of 12 adventitious roots generated from trunks were used to clarify the distribution of each aerenchyma type in the roots using light or epi-florescence microscopy. Schizogenous aerenchyma was observed in the root tips where the root color was white or light brown, whereas lysigenous aerenchyma was found at some distance from the root tip where the root color gradually changed from light to dark brown. The secondary aerenchyma and periderm were observed in dark brown parts near the root base. None or only one layer of phellem cells was detected in the white roots near the root tip, but dark brown roots near the root base had at least three layers of phellem cells. Considering these results, oxygen transportation may occur between primary and secondary aerenchyma at the point where two or more layers of phellem cells are formed.

scholarly journals Domain-specific and cell type-specific localization of two types of cell wall matrix polysaccharides in the clover root tip.

1992 ◽  
Vol 118 (2) ◽  
pp. 467-479 ◽  
Author(s):  
M A Lynch ◽  
L A Staehelin
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Cellular Differentiation ◽  
Cortical Cell ◽  
Middle Lamella ◽  
Root Cap ◽  
Root Tip ◽  
Cortical Cells ◽  
Peripheral Cell ◽  
Clover Root

Using immunocytochemical techniques and antibodies that specifically recognize xyloglucan (anti-XG), polygalacturonic acid/rhamnogalacturonan I (anti-PGA/RG-I), and methylesterified pectins (JIM 7), we have shown that these polysaccharides are differentially synthesized and localized during cell development and differentiation in the clover root tip. In cortical cells XG epitopes are present at a threefold greater density in the newly formed cross walls than in the older longitudinal walls, and PGA/RG-I epitopes are detected solely in the expanded middle lamella of cortical cell corners, even after pretreatment of sections with pectinmethylesterase to uncover masked epitopes. These results suggest that in cortical cells XG and PGA/RG-I are differentially localized not only to particular wall domains, but also to particular cell walls. In contrast to their nonoverlapping distribution in cortical cells, XG epitopes and PGA/RG-I epitopes largely colocalize in the epidermal cell walls. The results also demonstrate that the middle lamella of the longitudinal walls shared by epidermal cells and by epidermal and cortical cells constitutes a barrier to the diffusion of cell wall and mucilage molecules. Synthesis of XG and PGA/RG-I epitope-containing polysaccharides also varies during cellular differentiation in the root cap. The differentiation of gravitropic columella cells into mucilage-secreting peripheral cells is marked by a dramatic increase in the synthesis and secretion of molecules containing XG and PGA/RG-I epitopes. In contrast, JIM 7 epitopes are present at abundant levels in columella cell walls, but are not detectable in peripheral cell walls or in secreted mucilage. There were also changes in the cisternal labeling of the Golgi stacks during cellular differentiation in the root tip. Whereas PGA/RG-I epitopes are detected primarily in cis- and medial Golgi cisternae in cortical cells (Moore, P. J., K. M. M. Swords, M. A. Lynch, and L. A. Staehelin. 1991. J. Cell Biol. 112:589-602), they are localized predominantly in the trans-Golgi cisternae and the trans-Golgi network in epidermal and peripheral root cap cells. These observations suggest that during cellular differentiation the plant Golgi apparatus can be both structurally and functionally reorganized.

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