Ultrastructural and developmental alterations induced by Periconia circinata toxin in the root tip of sorghum

1983 ◽  
Vol 61 (5) ◽  
pp. 1491-1505 ◽  
Author(s):  
Jonathan A. Arias ◽  
Larry D. Dunkle ◽  
Charles E. Bracker
Keyword(s):  
Endoplasmic Reticulum ◽  
Primary Root ◽  
Root Cap ◽  
Biologically Active ◽  
Root Tip ◽  
Mitochondrial Morphology ◽  
Secretory Vesicles ◽  
Secretory Product ◽  
Periconia Circinata ◽  
In Cells

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.

Morphometric analysis of ultrastructural changes induced by Periconia circinata toxin in the outer root cap of sorghum

1983 ◽  
Vol 61 (5) ◽  
pp. 1506-1509
Author(s):  
Jonathan A. Arias ◽  
Larry D. Dunkle ◽  
Charles E. Bracker
Keyword(s):  
Endoplasmic Reticulum ◽  
Plasma Membrane ◽  
Morphometric Analysis ◽  
Secretory Vesicle ◽  
Root Cap ◽  
Toxic Effects ◽  
Ultrastructural Changes ◽  
Vesicle Membrane ◽  
Periconia Circinata ◽  
Resistant Genotypes

Outer root cap cells of sorghum seedlings treated with the host-specific toxin produced by Periconia circinata were analyzed morphometrically to detect changes in the quantities of cytomembranes and numbers of organelles and thus extend our observations of qualitative cytological responses to the toxin. In seedlings susceptible to the pathogen, brief (0.25 h) treatment with the toxin resulted in a marked and permanent decrease in the amounts of secretory vesicle membrane. By 2 h treatment, only secretory vesicle membrane was decreased, but longer treatments led to an increased amount of endoplasmic reticulum (4 h), which later decreased together with the amount of dictyosome membrane, while the amount of tonoplast increased (8 h). In resistant seedlings treated with the toxin, early but transient increases were detected in the quantities of plasma membrane, secretory vesicle membrane, dictyosome membrane, and endoplasmic reticulum and in the number of dictyosomes. Insensitivity to the toxin may involve the ability of resistant genotypes to recover from the toxic effects.

scholarly journals Root cap at soil interface: a driving force towards plant adaptation and development

2021 ◽  
Author(s):  
Ganesh Alagarasan ◽  
Vishnu Shukla ◽  
Ankita Mohapatra ◽  
Abin George ◽  
Durga Prasad Bhukya ◽  
...  
Keyword(s):  
Regulatory Networks ◽  
Primary Root ◽  
Growth Conditions ◽  
Root Cap ◽  
Land Plants ◽  
Root Tip ◽  
Plant Soil ◽  
Soil Ecosystems ◽  
Specialized Tissue ◽  
Plant Habitat

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.

Analysis of the Anterior Secretory Cells of Onchidohs Muricata (Nudibranchia)

1981 ◽  
Vol 39 ◽  
pp. 614-615
Author(s):  
Roy Skidmore
Keyword(s):  
Endoplasmic Reticulum ◽  
Secretory Granules ◽  
Golgi Body ◽  
The Body ◽  
Secretory Cells ◽  
Secretory Vesicles ◽  
High Magnification ◽  
Large Numbers ◽  
Membrane Bound ◽  
Sole Of The Foot

The long-necked secretory cells in Onchidoris muricata are distributed in the anterior sole of the foot. These cells are interspersed among ciliated columnar and conical cells as well as short-necked secretory gland cells. The long-necked cells contribute a significant amount of mucoid materials to the slime on which the nudibranch travels. The body of these cells is found in the subepidermal tissues. A long process extends across the basal lamina and in between cells of the epidermis to the surface of the foot. The secretory granules travel along the process and their contents are expelled by exocytosis at the foot surface.The contents of the cell body include the nucleus, some endoplasmic reticulum, and an extensive Golgi body with large numbers of secretory vesicles (Fig. 1). The secretory vesicles are membrane bound and contain a fibrillar matrix. At high magnification the similarity of the contents in the Golgi saccules and the secretory vesicles becomes apparent (Fig. 2).

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.

scholarly journals Nodal Endoplasmic Reticulum, a Specialized Form of Endoplasmic Reticulum Found in Gravity-Sensing Root Tip Columella Cells

2001 ◽  
Vol 125 (1) ◽  
pp. 252-265 ◽  
Author(s):  
Hui Qiong Zheng ◽  
L. Andrew Staehelin
Keyword(s):  
Endoplasmic Reticulum ◽  
Root Tip ◽  
Specialized Form ◽  
Columella Cells

scholarly journals MITOCHONDRIAL LOCALIZATION OF OXIDATIVE ENZYMES: STAINING RESULTS WITH TWO TETRAZOLIUM SALTS

1961 ◽  
Vol 9 (1) ◽  
pp. 47-61 ◽  
Author(s):  
Alex B. Novikoff ◽  
Woo-Yung Shin ◽  
Joan Drucker
Keyword(s):  
Rat Kidney ◽  
Intracellular Localization ◽  
Oxidative Enzymes ◽  
Mitochondrial Morphology ◽  
Mitochondrial Localization ◽  
Enzyme Localization ◽  
Aqueous Interfaces ◽  
Physicochemical Factors ◽  
Lipofuscin Granules ◽  
In Cells

A comparison is made of the staining results obtained with Nitro-BT and MTT-Co++ as acceptors when DPNH is the substrate in frozen sections of cold formol-calcium-fixed rat kidney (normal and following ligation of the blood vessels) and human liver containing lipofuscin granules. The kidney results are evaluated in terms of mitochondrial morphology seen after classical mitochondrial stains and in electron micrographs. It is concluded that, except for formazan deposition on lipid-aqueous interfaces, Nitro-BT staining indicates the intracellular localization of oxidative enzymes, at least at the level of light microscopy. In contrast, the use of MTT-Co++ is not reliable for such intracellular localizations. The deposition of the formazan of MTT-Co++ is determined in large part by physicochemical factors other than enzyme localization. Despite marked abnormalities of the mitochondria in cells of the ligated kidney, MTT-Co++ formazan is generally deposited in the same dotlike fashion as in cells of normal kidney.

Identification and characterization of novel QTL conferring internal detoxification of aluminum in soybean

2021 ◽  
Author(s):  
Yang Li ◽  
Heng Ye ◽  
Li Song ◽  
Tri D Vuong ◽  
Qijian Song ◽  
...  
Keyword(s):  
Root Length ◽  
Root Elongation ◽  
Primary Root ◽  
Pedigree Analysis ◽  
Length Ratio ◽  
Root Tip ◽  
Root Initiation ◽  
Al Tolerance ◽  
Al Stress ◽  
Root Length Ratio

Abstract Aluminum (Al) toxicity inhibits soybean root growth, leading to insufficient water and nutrient uptake. In this research, two soybean lines (Magellan and PI 567731) were identified differing in Al tolerance as determined by primary root length ratio (PRL_Ratio), total root length ratio (TRL_Ratio), and root tip number ratio (RTN_Ratio) under Al stress compared to unstressed controlled conditions. Serious root necrosis was observed in PI 567731, but not in Magellan under Al stress. An F8 recombinant inbred line population derived from a cross between Magellan and PI 567731 was used to map the quantitative trait loci (QTL) for Al-tolerance. Three QTL on chromosomes 3, 13, and 20, with tolerant-alleles from Magellan, were identified. qAl_Gm13 and qAl_Gm20, explained large phenotypic variations (13-27%) and played roles in maintaining root elongation. qAl_Gm03 was involved in maintaining root initiation under Al stress. These results suggested the importance of using the parameters of root elongation and root initiation in Al tolerance studies. In addition, qAl_Gm13 and qAl_Gm20 were confirmed in near-isogenic backgrounds and were identified to epistatically regulate Al tolerance in internal detoxification instead of Al 3+ exclusion. The candidate genes for qAl_Gm13 and qAl_Gm20 were suggested by analyzing a previous RNA-seq study. Phylogenetic and pedigree analysis identified the tolerant alleles of both loci derived from the US ancestor line, A.K.[FC30761], originally from China. Our results provide novel genetic resources for breeding Al-tolerant soybeans and suggest that the internal detoxification contributes to soybean tolerance to excessive soil Al.

Localization and quantification of endoplasmic reticulum Ca(2+)-ATPase isoform transcripts

1995 ◽  
Vol 269 (3) ◽  
pp. C775-C784 ◽  
Author(s):  
K. D. Wu ◽  
W. S. Lee ◽  
J. Wey ◽  
D. Bungard ◽  
J. Lytton
Keyword(s):  
Endoplasmic Reticulum ◽  
Critical Role ◽  
Qualitative Assessment ◽  
Cell Physiology ◽  
Striated Muscles ◽  
Physiological Processes ◽  
Alternatively Spliced ◽  
Spleen Lymphocytes ◽  
Fast Twitch ◽  
In Cells

The Ca(2+)-adenosinetriphosphatase pump of the sarcoplasmic or endoplasmic reticulum (SERCA) plays a critical role in Ca2+ signaling and homeostasis in all cells and is encoded by a family of homologous and alternatively spliced genes. To understand more clearly the role the different isoforms play in cell physiology, we have undertaken a quantitative and qualitative assessment of the tissue distribution of transcripts encoding each SERCA isoform. SERCA1 expression is restricted to fast-twitch striated muscles, SERCA2a to cardiac and slow-twitch striated muscles, whereas SERCA2b is ubiquitously expressed. SERCA3 is expressed most abundantly in large and small intestine, thymus, and cerebellum and at lower levels in spleen, lymph node, and lung. In situ hybridization analyses revealed SERCA3 transcripts in cells of the intestinal crypt, the thymic cortex, and Purkinje cells in cerebellum. In addition, SERCA3 was expressed abundantly in isolated rat spleen lymphocytes, in various murine lymphoid cell lines, and in primary cultured microvascular endothelial cells. This analysis demonstrates that SERCA3 is expressed selectively in cells in which Ca2+ signaling plays a critical and sensitive role in regulating physiological processes.

scholarly journals Novel role of the ER/SR Ca2+ sensor STIM1 in the regulation of cardiac metabolism

2019 ◽  
Vol 316 (5) ◽  
pp. H1014-H1026 ◽  
Author(s):  
Helen E. Collins ◽  
Betty M. Pat ◽  
Luyun Zou ◽  
Silvio H. Litovsky ◽  
Adam R. Wende ◽  
...  
Keyword(s):  
Endoplasmic Reticulum ◽  
Fatty Acid ◽  
Pyruvate Dehydrogenase ◽  
Glucose Utilization ◽  
Cardiac Metabolism ◽  
Mitochondrial Morphology ◽  
Acid Uptake ◽  
Stromal Interaction Molecule 1 ◽  
First Time

The endoplasmic reticulum/sarcoplasmic reticulum Ca2+ sensor stromal interaction molecule 1 (STIM1), a key mediator of store-operated Ca2+ entry, is expressed in cardiomyocytes and has been implicated in regulating multiple cardiac processes, including hypertrophic signaling. Interestingly, cardiomyocyte-restricted deletion of STIM1 (crSTIM1-KO) results in age-dependent endoplasmic reticulum stress, altered mitochondrial morphology, and dilated cardiomyopathy in mice. Here, we tested the hypothesis that STIM1 deficiency may also impact cardiac metabolism. Hearts isolated from 20-wk-old crSTIM1-KO mice exhibited a significant reduction in both oxidative and nonoxidative glucose utilization. Consistent with the reduction in glucose utilization, expression of glucose transporter 4 and AMP-activated protein kinase phosphorylation were all reduced, whereas pyruvate dehydrogenase kinase 4 and pyruvate dehydrogenase phosphorylation were increased, in crSTIM1-KO hearts. Despite similar rates of fatty acid oxidation in control and crSTIM1-KO hearts ex vivo, crSTIM1-KO hearts contained increased lipid/triglyceride content as well as increased fatty acid-binding protein 4, fatty acid synthase, acyl-CoA thioesterase 1, hormone-sensitive lipase, and adipose triglyceride lipase expression compared with control hearts, suggestive of a possible imbalance between fatty acid uptake and oxidation. Insulin-mediated alterations in AKT phosphorylation were observed in crSTIM1-KO hearts, consistent with cardiac insulin resistance. Interestingly, we observed abnormal mitochondria and increased lipid accumulation in 12-wk crSTIM1-KO hearts, suggesting that these changes may initiate the subsequent metabolic dysfunction. These results demonstrate, for the first time, that cardiomyocyte STIM1 may play a key role in regulating cardiac metabolism. NEW & NOTEWORTHY Little is known of the physiological role of stromal interaction molecule 1 (STIM1) in the heart. Here, we demonstrate, for the first time, that hearts lacking cardiomyocyte STIM1 exhibit dysregulation of both cardiac glucose and lipid metabolism. Consequently, these results suggest a potentially novel role for STIM1 in regulating cardiac metabolism.

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