Root cap–derived cells and mucilage: a protective network at the root tip

PROTOPLASMA ◽  
2021 ◽  
Author(s):  
Azeddine Driouich ◽  
Alexia Gaudry ◽  
Barbara Pawlak ◽  
John P. Moore
Keyword(s):  
Root Cap ◽  
1992 ◽  
Vol 118 (2) ◽  
pp. 467-479 ◽  
Author(s):  
M A Lynch ◽  
L A Staehelin

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.


1983 ◽  
Vol 61 (5) ◽  
pp. 1491-1505 ◽  
Author(s):  
Jonathan A. Arias ◽  
Larry D. Dunkle ◽  
Charles E. Bracker

Cytological and developmental effects induced by Periconia circinata toxin were examined to better understand the mechanism of action for this toxin. Roots of sorghum seedlings susceptible and resistant to P. circinata were incubated in 500 ng toxin/mL (treated) or water (controls). Root cap cells of resistant seedlings treated with the toxin were cytologically similar to those of controls, although the toxin caused a transient inhibition of mitosis in cells of the primary root tip. In outer root cap cells of susceptible seedlings treated for 0.25 h, hypersecretory activity was lost, secretory vesicles were fewer, and secretory product accumulated between the plasma membrane and cell wall. Also, inner root cap cells showed increased vacuolation. Longer treatments caused increased vacuolation, loss of starch, increased numbers of lipid bodies, pleomorphic amyloplasts, regularly stacked endoplasmic reticulum, apparent changes in the amounts of cytomembranes, dispersion of heterochromatin, and autolysis. Mitochondrial morphology was normal, but lesions in the tonoplast occurred before autolysis. The toxin also inhibited expansion and sloughing off of root cap cells and mitotic activity in the root tip. Stacked endoplasmic reticulum, nonhypersecretory dictyosomes, fewer secretory vesicles, increased vacuolation, reorganization of heterochromatin, and increased secretory product outside the protoplast were induced by P. circinata toxin and by cyanide. These data suggested that a cyanogenic compound is biologically active in cells treated with P. circinata toxin. Our results suggest that the toxin transiently affects resistant seedlings and in susceptible seedlings alters vacuolar expansion, secretory activity, and endomembrane flow, although other processes may also be affected.


1974 ◽  
Vol 139 (3) ◽  
pp. 525-534 ◽  
Author(s):  
Kenneth Wright ◽  
D. H. Northcote

1. The patterns of incorporation of radioactivity from d-[U-14C]glucose into the pectic components of sections of sycamore roots changed so that sections nearer the tip incorporated relatively more label into arabinose and galactose compared with uronic acid. 2. Radioactive maize root-cap slime was prepared and found to contain three water-soluble component polymers which were electrophoretically (i) neutral, (ii) weakly acidic and (iii) strongly acidic at pH6.5. The neutral component was a glucan. The other components, which could be degraded by trans-elimination, consisted of an acidic backbone chain composed of galacturonic acid and glucose, attached to which were different proportions of neutral sugars. Arabinose, galactose and fucose, the main neutral sugars of the weakly and strongly acidic materials, were absent from the neutral fraction. 3. Fucose was a major sugar in maize-root slime and in a slime of similar composition synthesized by a maize callus of shoot origin. Only trace amounts were found in sycamore, pea and wheat root tips, and in pectin prepared from maize roots and coleoptiles. A high proportion of fucose is therefore a chemical characteristic of maize slime, and slime synthesis indicated a state of differentiation of the tissue. 4. The similarity between the slime and pectin is discussed; slime is a form of pectin modified in such a way as to provide a hydrated protective coating around the root tip.


Plants ◽  
2021 ◽  
Vol 10 (3) ◽  
pp. 605
Author(s):  
Yiting Ruan ◽  
Ke Chen ◽  
Yangyang Su ◽  
Suyu Jiang ◽  
Ping Xu ◽  
...  

The Agrobacterium rhizogenes hairy root transformation system is widely used in symbiotic studies of model legumes. It typically relies on fluorescent reporters, such as DsRed, for identification of transgenic roots. The MtLAP1 transcription factor has been utilized as a reporter system in Medicago truncatula based on production of anthocyanin pigment. Here, we describe a version of this reporter driven by a root-cap specific promoter for direct observation of anthocyanin accumulation in root tips, which allows the identification of transgenic hairy roots by the naked eye. Results from our analysis suggest that the reporter had no significant effects on nodulation of M. truncatula. This approach, by virtue of its strong and specific expression in root cap cells, greatly reduces false positives and false negatives, and its use of an easily scored visible pigment should allow greater versatility and efficiency in root biology studies.


Author(s):  
Peter B. Tinker ◽  
Peter Nye

The uptake of nutrient and other ions into the root from the surrounding soil is the main topic of this book. To understand it, we need to know how the nutrient uptake and demand of the plant is expressed at the root surface. The main interest is on how the demand at the root surface can be quantitatively defined in terms of its uptake characteristics. For this reason, our explanation of the ion uptake mechanism of the root itself is brief, and is intended mainly for readers who have not studied the subject deeply. The subject has become considerably more complex since 1977, but this detailed knowledge has not yet coalesced into a full model of how ions are absorbed, such as ultimately will allow root uptake properties to be predicted. There have been many good reviews in the recent past, and the following may be consulted: Clarkson & Hanson 1980; Glass 1983; Luttge 1983; Clarkson 1985; Sanders 1990; Clarkson & Luttge 1991; Marschner 1995. We will describe the structure of a single root only briefly here, since this information can be found in standard texts (Troughton 1957; Esau 1965; Cutter 1978; Fahn 1982). Figures 5.1-5.5 show the general structure, but here we stress points that have a special bearing on the process of ion uptake or root behaviour in soil. Byrne (1974) noted that the anatomy of soil-grown roots may differ somewhat from that of solution-grown roots. The architecture of whole root systems in soil is dealt with in chapter 9.The root tip is a highly important part of the root. The apical meristem (the ‘quiescent centre’) is a fraction of a millimetre behind the visible root tip; cells that form behind the centre of this develop into the root, whereas those in front of the centre form the root cap. These cells gradually reach the surface of the cap, and there are rubbed off and lost into the soil at a rate of several thousand per day in maize. Often, these cells are visible in the mucigel that forms from the base of the root cap and covers the young root (section 8.1.3), and can remain alive in the gel for a period.


Author(s):  
Ganesh Alagarasan ◽  
Vishnu Shukla ◽  
Ankita Mohapatra ◽  
Abin George ◽  
Durga Prasad Bhukya ◽  
...  

Land plants harbour robust roots to grow in diverse soil ecosystems. The distal end of the primary root tip has specialized tissue, called “root cap.” The evolution of root cap-like structures in early plants rudimentary roots and well-developed root caps in vascular plants hints towards developing an adaptive trait for a localized plant habitat. Root cap interacts with soil and assists roots in penetrating the below ground, avoid/adsorb metals, uptake water, minerals, and regulates rhizosphere microbiota that drives plant-soil feedback. Besides, the root cap governs lateral root patterning and directs root growth in varying conditions. This review article presents the retrospective and our perspective on root cap characters for root-soil interaction. We discussed the anatomy of root cap among the different taxa of land plants and their relevance in diverse habitats and elucidated the root cap functions under various growth conditions. We took advantage of recently published single-cell RNAseq data and shed light on biological relevance of root cap cell-type enriched genes from arabidopsis, rice, maize, and tomato. Additionally, analyzed the transcription factor binding site enrichment in root cap enriched genes and constructed gene-regulatory networks operating in root cap to contribute its multi-faceted role in plant growth and adaptation.


1978 ◽  
Vol 170 (3) ◽  
pp. 599-608 ◽  
Author(s):  
J R Green ◽  
D H Northcote

The synthesis of the maize root slime polysaccharides was investigated by using [1-3H]-fucose as a marker for slime production. Three fractions were separated by centrifugation in a CsCl density gradient. Two of these were glycoproteins and occurred within the membranes of the cells of the root tip; the third was the slime polysaccharides. Radioactive pulse-chase experiments showed that the glycoproteins were precursors of the slime polysaccharides, and the carbohydrate portion of the glycoproteins had a similar composition to that of the free slime. The linkage between the protein and the carbohydrate of one of the glycoproteins was shown to be a xylose-threonine bond. It is postulated that the slime polysaccharides are synthesized and transported on proteins within the membrane system of the root tip.


Author(s):  
Y. R. Chen ◽  
Y. F. Huang ◽  
W. S. Chen

Acid phosphatases are widely distributed in different tisssues of various plants. Studies on subcellular localization of acid phosphatases show they might be present in cell wall, plasma lemma, mitochondria, plastid, vacuole and nucleus. However, their localization in rice cell varies with developmental stages of cells and plant tissues. In present study, acid phosphatases occurring in root cap are examined.Sliced root tips of ten-day-old rice(Oryza sativa) seedlings were fixed in 0.1M cacodylate buffer containing 2.5% glutaraldehyde for 2h, washed overnight in same buffer solution, incubated in Gomori's solution at 37° C for 90min, post-fixed in OsO4, dehydrated in ethanol series and finally embeded in Spurr's resin. Sections were doubly stained with uranyl acetate and lead citrate, and observed under Hitachi H-600 at 75 KV.


Author(s):  
James Cronshaw ◽  
Jamison E. Gilder

Adenosine triphosphatase (ATPase) activity has been shown to be associated with numerous physiological processes in both plants and animal cells. Biochemical studies have shown that in higher plants ATPase activity is high in cell wall preparations and is associated with the plasma membrane, nuclei, mitochondria, chloroplasts and lysosomes. However, there have been only a few ATPase localization studies of higher plants at the electron microscope level. Poux (1967) demonstrated ATPase activity associated with most cellular organelles in the protoderm cells of Cucumis roots. Hall (1971) has demonstrated ATPase activity in root tip cells of Zea mays. There was high surface activity largely associated with the plasma membrane and plasmodesmata. ATPase activity was also demonstrated in mitochondria, dictyosomes, endoplasmic reticulum and plastids.


1996 ◽  
Author(s):  
Michael P. Amaranthus ◽  
Debbie Page-Dumroese ◽  
Al Harvey ◽  
Efren Cazares ◽  
Larry F. Bednar

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