scholarly journals De novo Cortical Cell Division Triggered by the Phytopathogen Rhodococcus fascians in Tobacco

2001 ◽  
Vol 14 (2) ◽  
pp. 189-195 ◽  
Author(s):  
Carmem-Lara de O. Manes ◽  
Marc Van Montagu ◽  
Els Prinsen ◽  
Koen Goethals ◽  
Marcelle Holsters
Keyword(s):  
Cell Division ◽  
Host Plants ◽  
De Novo ◽  
Cortical Cell ◽  
Multiple Shoot ◽  
Infection Process ◽  
Cortical Cells ◽  
Shoot Primordia ◽  
Gene Coding ◽  
Rhodococcus Fascians

Plant growth, development, and morphology can be affected by several environmental stimuli and by specific interactions with phytopathogens. In many cases, plants respond to pathogenic stimuli by adapting their hormone levels. Here, the interaction between the phytopathogen Rhodococcus fascians and one of its host plants, tobacco, was analyzed phenotypically and molecularly. To elucidate the basis of the cell division modulation and shoot primordia initiation caused by R. fascians, tobacco plants were infected at leaf axils and shoot apices. Adventitious meristems that gave rise to multiple-shoot primordia (leafy galls) were formed. The use of a transgenic line carrying the mitotic CycB1 promoter fused to the reporter gene coding for β-glucuronidase from Escherichia coli (uidA), revealed that stem cortical cells were stimulated to divide in an initial phase of the leafy gall ontogenesis. Local cytokinin and auxin levels throughout the infection process as well as modulation of expression of the cell cycle regulator gene Nicta;CycD3;2 are discussed.

scholarly journals SHORT-ROOT paralogs mediate feedforward regulation of D-type cyclin to promote nodule formation in soybean

2022 ◽  
Vol 119 (3) ◽  
pp. e2108641119
Author(s):  
Chunhua Wang ◽  
Meng Li ◽  
Yang Zhao ◽  
Nengsong Liang ◽  
Haiyang Li ◽  
...  
Keyword(s):  
Cell Division ◽  
Vascular Tissue ◽  
De Novo ◽  
Cortical Cell ◽  
Nodule Formation ◽  
Cytokinin Signaling ◽  
Short Root ◽  
Cell Divisions ◽  
Early Nodulin ◽  
Nodulin Genes

Nitrogen fixation in soybean takes place in root nodules that arise from de novo cell divisions in the root cortex. Although several early nodulin genes have been identified, the mechanism behind the stimulation of cortical cell division during nodulation has not been fully resolved. Here we provide evidence that two paralogs of soybean SHORT-ROOT (GmSHR) play vital roles in soybean nodulation. Expression of GmSHR4 and GmSHR5 (GmSHR4/5) is induced in cortical cells at the beginning of nodulation, when the first cell divisions occur. The expression level of GmSHR4/5 is positively associated with cortical cell division and nodulation. Knockdown of GmSHR5 inhibits cell division in outer cortical layers during nodulation. Knockdown of both paralogs disrupts the cell division throughout the cortex, resulting in poorly organized nodule primordia with delayed vascular tissue formation. GmSHR4/5 function by enhancing cytokinin signaling and activating early nodulin genes. Interestingly, D-type cyclins act downstream of GmSHR4/5, and GmSHR4/5 form a feedforward loop regulating D-type cyclins. Overexpression of D-type cyclins in soybean roots also enhanced nodulation. Collectively, we conclude that the GmSHR4/5-mediated pathway represents a vital module that triggers cytokinin signaling and activates D-type cyclins during nodulation in soybean.

Anatomical comparison of wild-type and non-nodulating mutant chickpea (Cicer arietinum)

1990 ◽  
Vol 68 (6) ◽  
pp. 1201-1207 ◽  
Author(s):  
Leslie J. Matthews ◽  
Thomas M. Davis
Keyword(s):  
Cell Division ◽  
Cicer Arietinum ◽  
Root Hair ◽  
Root Nodule ◽  
Cortical Cell ◽  
Infection Process ◽  
Nodule Formation ◽  
Cell Infection ◽  
Infection Threads ◽  
Nodule Symbiosis

Non-nodulating chickpea (Cicer arietinum L.) mutant PM233B was characterized anatomically via comparison with its normally nodulating parent line ICC 640. Root hair and cortical cell infection threads, cortical cell division centers, and nodule formation were observed by light microscopy in serial root sections of ICC 640, but were absent in PM233B. Scanning electron microscope observations of inoculated root sections showed that ICC 640 and PM233B were indistinguishable in adsorption of chickpea Rhizobium strain CC1192. Thus, the rhizobial infection process was blocked in PM233B at a stage subsequent to root hair adsorption of bacteria, but prior to initiation of infection threads and root cortical cell division. Reciprocal shoot grafts between ICC 640 and PM233B demonstrated that the non-nodulation phenotype of PM233B was controlled by the root, and not the shoot, genotype. Key words: chickpea, Cicer arietinum, root nodule, symbiosis, non-nodulating mutant.

Computing with Self-Excitatory Cliques: A Model and an Application to Hyperacuity-Scale Computation in Visual Cortex

1999 ◽  
Vol 11 (1) ◽  
pp. 21-66 ◽  
Author(s):  
Douglas A. Miller ◽  
Steven W. Zucker
Keyword(s):  
Visual Processing ◽  
Network Architecture ◽  
Early Stage ◽  
Cortical Cell ◽  
Pyramidal Cells ◽  
Direct Calculation ◽  
Formal Theory ◽  
Cortical Cells ◽  
Cell Counts ◽  
Spatiotemporal Response

We present a model of visual computation based on tightly inter-connected cliques of pyramidal cells. It leads to a formal theory of cell assemblies, a specific relationship between correlated firing patterns and abstract functionality, and a direct calculation relating estimates of cortical cell counts to orientation hyperacuity. Our network architecture is unique in that (1) it supports a mode of computation that is both reliable and efficent; (2) the current-spike relations are modeled as an analog dynamical system in which the requisite computations can take place on the time scale required for an early stage of visual processing; and (3) the dynamics are triggered by the spatiotemporal response of cortical cells. This final point could explain why moving stimuli improve vernier sensitivity.

Early Periderm Ontogeny in Fraxinuspennsylvanica, Ailanthusaltissima, Robiniapseudoacacia, and Pinusresinosa, Seedlings

1972 ◽  
Vol 2 (2) ◽  
pp. 135-143 ◽  
Author(s):  
G. A. Borger ◽  
T. T. Kozlowski
Keyword(s):  
Cell Layer ◽  
Cortical Cell ◽  
Cortical Cells ◽  
Mother Cells

The subepidermal cell layer was the site of origin of the first periderm in the hypocotyl and internodes of Fraxinuspennsylvanica and Ailanthusaltissima. In the hypocotyl of Robiniapsendoacacia, the first periderm arose in cortical cells near the phloem; in the internodes it originated in the subepidermal, second, or third cortical cell layer. The outermost cell layer of the pericycle gave rise to the first periderm in the hypocotyl of Pinusresinosa. In all four species, periderm appeared first near the base of the hypocotyl and developed acropetally. In A. altissima and R. pseudoaeacia, phellem mother cells were cut off by the phellogen. These subsequently divided to produce phellem cells. In F. pennsylvanica and P. resinosa, phellem cells were produced directly from the phellogen.

scholarly journals The 3D architecture and molecular foundations of de novo centriole assembly via bicentrioles

2020 ◽  
Author(s):  
Sónia Gomes Pereira ◽  
Ana Laura Sousa ◽  
Catarina Nabais ◽  
Tiago Paixão ◽  
Alexander. J. Holmes ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Cell Division ◽  
De Novo ◽  
Cellular Functions ◽  
Spindle Poles ◽  
3D Architecture ◽  
Centriole Assembly ◽  
Work Supports ◽  
Wall Components

Abstract/SummaryCentrioles are structurally conserved organelles, composing both centrosomes and cilia. In animal cycling cells, centrioles often form through a highly characterized process termed canonical duplication. However, a large diversity of eukaryotes form centrioles de novo through uncharacterized pathways. This unexplored diversity is key to understanding centriole assembly mechanisms and how they evolved to assist specific cellular functions. Here, combining electron microscopy and tomography, we show that during spermatogenesis of the moss Physcomitrium patens, centrioles are born as a co-axially oriented centriole pair united by a cartwheel. We observe that microtubules emanate from those bicentrioles, which localize to the spindle poles during cell division. Thereafter, each bicentriole breaks apart, and the two resulting sister centrioles mature asymmetrically, elongating specific microtubule triplets and a naked cartwheel. Subsequently, two cilia are assembled which are capable of beating asynchronously. We further show that conserved cartwheel and centriole wall components, SAS6, BLD10 and POC1 are expressed during spermatogenesis and are required for this de novo biogenesis pathway. Our work supports a scenario where centriole biogenesis is more diverse than previously thought and that conserved molecular modules underlie diversification of this essential pathway.

Anatomy of Wild Garlic Bulbs During and Subsequent to After-Ripening

Weed Science ◽  
1972 ◽  
Vol 20 (3) ◽  
pp. 233-237 ◽  
Author(s):  
J. F. Stritzke ◽  
E. J. Peters
Keyword(s):  
Cell Division ◽  
Microscopic Examination ◽  
Cell Elongation ◽  
Leaf Primordia ◽  
Root Primordia ◽  
Ripening Period ◽  
Shoot Primordia ◽  
Division Cell ◽  
Wild Garlic

Microscopic examination of central and soft offset bulbs of wild garlic(Allium vinealeL.) at senescence of the parent plants in May and June revealed embryonic plants with numerous root primordia and four or five shoot primordia. Hardshell bulbs and aerial bulblets contained only one or two root primordia and three leaf primordia. The embryonic plants of central, soft offset, and hardshell bulbs elongated slowly during the after-ripening period. Rapid cell division, cell elongation, and initiation of new leaves took place after termination of the after-ripening period in all but the dormant hardshell bulbs. In November, new hardshell bulbs could be seen at the base of plants developed from central and soft offset bulbs.

Refining the Life Cycle of Plasmodiophora brassicae

2020 ◽  
Vol 110 (10) ◽  
pp. 1704-1712 ◽  
Author(s):  
Lijiang Liu ◽  
Li Qin ◽  
Zhuqing Zhou ◽  
Wilhelmina G. H. M. Hendriks ◽  
Shengyi Liu ◽  
...  
Keyword(s):  
Life Cycle ◽  
Plasmodiophora Brassicae ◽  
Secondary Infection ◽  
Life Stage ◽  
Infection Process ◽  
Epidermal Cells ◽  
Sexual Life ◽  
Cortical Cells ◽  
Susceptible Host ◽  
Clubroot Disease

As a soilborne protist pathogen, Plasmodiophora brassicae causes the devastating clubroot disease on Brassicaceae crops worldwide. Due to its intracellular obligate biotrophic nature, the life cycle of P. brassicae is still not fully understood. Here, we used fluorescent probe-based confocal microscopy and transmission electron microscopy (TEM) to investigate the infection process of P. brassicae on the susceptible host Arabidopsis under controlled conditions. We found that P. brassicae can initiate the primary infection in both root hairs and epidermal cells, producing the uninucleate primary plasmodium at 1 day postinoculation (dpi). After that, the developed multinucleate primary plasmodium underwent condensing and cytoplasm cleavage into uninucleate zoosporangia from 1 to 4 dpi. This was subsequently followed by the formation of multinucleate zoosporangia and the production of secondary zoospores within zoosporangium. Importantly, the secondary zoospores performed a conjugation in the root epidermal cells after their release. TEM revealed extensive uninucleate secondary plasmodium in cortical cells at 8 dpi, indicating the establishment of the secondary infection. The P. brassicae subsequently developed into binucleate, quadrinucleate, and multinucleate secondary plasmodia from 10 to 15 dpi, during which the clubroot symptoms appeared. The uninucleate resting spores were first observed in the cortical cells at 24 dpi, marking the completion of a life cycle. We also provided evidence that the secondary infection of P. brassicae may represent the diploid sexual life stage. From these findings, we propose a refined life cycle of P. brassicae which will contribute to understanding of the complicated infection biology of P. brassicae.

NHE3 activity and trafficking depend on the state of actin organization in proximal tubule

2001 ◽  
Vol 280 (2) ◽  
pp. F283-F290 ◽  
Author(s):  
C. Chalumeau ◽  
D. Du Cheyron ◽  
N. Defontaine ◽  
O. Kellermann ◽  
M. Paillard ◽  
...  
Keyword(s):  
Proximal Tubule ◽  
Cortical Cell ◽  
Membrane Vesicles ◽  
Cytochalasin D ◽  
The State ◽  
Protein Abundance ◽  
Transport Activity ◽  
Cortical Cells ◽  
Actin Organization ◽  
Luminal Membrane

The present study was addressed to define the contribution of cytoskeleton elements in the kidney proximal tubule Na+/H+ exchanger 3 (NHE3) activity under basal conditions. We used luminal membrane vesicles (LMV) isolated from suspensions of rat cortical tubules pretreated with either colchicine (Colch) or cytochalasin D (Cyto D). Colch pretreatment of suspensions (200 μM for 60 min) moderately decreased LMV NHE3 activity. Cyto D pretreatment (1 μM for 60 min) elicited an increase in LMV NHE3 transport activity but did not increase Na-glucose cotransport activity. Cyto D pretreatment of suspensions did not change the apparent affinity of NHE3 for internal H+. In contrast, after Cyto D pretreatment of the suspensions, NHE3 protein abundance was increased in LMV and remained unchanged in cortical cell homogenates. The effect of Cyto D on NHE3 was further assessed with cultures of murine cortical cells. The amount of surface biotinylated NHE3 increased on Cyto D treatment, whereas NHE3 protein abundance was unchanged in cell homogenates. In conclusion, under basal conditions NHE3 activity depends on the state of actin organization possibly involved in trafficking processes between luminal membrane and intracellular compartment.

A shared gene drives lateral root development and root nodule symbiosis pathways in Lotus

Science ◽  
2019 ◽  
Vol 366 (6468) ◽  
pp. 1021-1023 ◽  
Author(s):  
Takashi Soyano ◽  
Yoshikazu Shimoda ◽  
Masayoshi Kawaguchi ◽  
Makoto Hayashi
Keyword(s):  
Root Development ◽  
Lateral Root ◽  
Root Nodule ◽  
Root Nodules ◽  
Lotus Japonicus ◽  
Cortical Cell ◽  
Cortical Cells ◽  
Lateral Root Development ◽  
Lateral Organ ◽  
Nodule Symbiosis

Legumes develop root nodules in symbiosis with nitrogen-fixing rhizobial bacteria. Rhizobia evoke cell division of differentiated cortical cells into root nodule primordia for accommodating bacterial symbionts. In this study, we show that NODULE INCEPTION (NIN), a transcription factor in Lotus japonicus that is essential for initiating cortical cell divisions during nodulation, regulates the gene ASYMMETRIC LEAVES 2-LIKE18/LATERAL ORGAN BOUNDARIES DOMAIN16a (ASL18/LBD16a). Orthologs of ASL18/LBD16a in nonlegume plants are required for lateral root development. Coexpression of ASL18a and the CCAAT box–binding protein Nuclear Factor-Y (NF-Y) subunits, which are also directly targeted by NIN, partially suppressed the nodulation-defective phenotype of L. japonicusdaphne mutants, in which cortical expression of NIN was attenuated. Our results demonstrate that ASL18a and NF-Y together regulate nodule organogenesis. Thus, a lateral root developmental pathway is incorporated downstream of NIN to drive nodule symbiosis.

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