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      Spatiotemporal Pattern of Ectopic Cell Divisions Contribute to Mis-Shaped Phenotype of Primary and Lateral Roots of katanin1 Mutant

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          Abstract

          Pattern formation, cell proliferation, and directional cell growth, are driving factors of plant organ shape, size, and overall vegetative development. The establishment of vegetative morphogenesis strongly depends on spatiotemporal control and synchronization of formative and proliferative cell division patterns. In this context, the progression of cell division and the regulation of cell division plane orientation are defined by molecular mechanisms converging to the proper positioning and temporal reorganization of microtubule arrays such as the preprophase microtubule band, the mitotic spindle and the cytokinetic phragmoplast. By focusing on the tractable example of primary root development and lateral root emergence in Arabidopsis thaliana, genetic studies have highlighted the importance of mechanisms underlying microtubule reorganization in the establishment of the root system. In this regard, severe alterations of root growth, and development found in extensively studied katanin1 mutants of A. thaliana ( fra2, lue1, and ktn1-2), were previously attributed to defective rearrangements of cortical microtubules and aberrant cell division plane reorientation. How KATANIN1-mediated microtubule severing contributes to tissue patterning and organ morphogenesis, ultimately leading to anisotropy in microtubule organization is a trending topic under vigorous investigation. Here we addressed this issue during root development, using advanced light-sheet fluorescence microscopy (LSFM) and long-term imaging of ktn1-2 mutant expressing the GFP-TUA6 microtubule marker. This method allowed spatial and temporal monitoring of cell division patterns in growing roots. Analysis of acquired multidimensional data sets revealed the occurrence of ectopic cell divisions in various tissues including the calyptrogen and the protoxylem of the main root, as well as in lateral root primordia. Notably the ktn1-2 mutant exhibited excessive longitudinal cell divisions (parallel to the root axis) at ectopic positions. This suggested that changes in the cell division pattern and the occurrence of ectopic cell divisions contributed significantly to pleiotropic root phenotypes of ktn1-2 mutant. LSFM provided evidence that KATANIN1 is required for the spatiotemporal control of cell divisions and establishment of tissue patterns in living A. thaliana roots.

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          Most cited references75

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          Transcriptional regulation of ROS controls transition from proliferation to differentiation in the root.

          The balance between cellular proliferation and differentiation is a key aspect of development in multicellular organisms. Using high-resolution expression data from the Arabidopsis root, we identified a transcription factor, UPBEAT1 (UPB1), that regulates this balance. Genomewide expression profiling coupled with ChIP-chip analysis revealed that UPB1 directly regulates the expression of a set of peroxidases that modulate the balance of reactive oxygen species (ROS) between the zones of cell proliferation and the zone of cell elongation where differentiation begins. Disruption of UPB1 activity alters this ROS balance, leading to a delay in the onset of differentiation. Modulation of either ROS balance or peroxidase activity through chemical reagents affects the onset of differentiation in a manner consistent with the postulated UPB1 function. This pathway functions independently of auxin and cytokinin plant hormonal signaling. Comparison to ROS-regulated growth control in animals suggests that a similar mechanism is used in plants and animals. Copyright © 2010 Elsevier Inc. All rights reserved.
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            Cellular organisation of the Arabidopsis thaliana root.

            The anatomy of the developing root of Arabidopsis is described using conventional histological techniques, scanning and transmission electron microscopy. The root meristem is derived from cells of the hypophysis and adjacent cells of the embryo proper. The postembryonic organization of the root is apparent in the mature embryo and is maintained in the growing primary root after germination. Cell number and location is relatively invariant in the primary root, with 8 cortical and endodermal cell files but more variable numbers of pericycle and epidermal cells. The organisation of cells in lateral roots is similar to that of the primary root but with more variability in the numbers of cell files in each layer. [3H]thymidine labeling of actively growing roots indicates that a quiescent centre of four central cells (derived from the hypophysis) is located between the root cap columella and the stele. This plate of four cells is surrounded by three groups of cells in, proximal, distal and lateral positions. The labeling patterns of these cells suggest that they are the initials for the files of cells that comprise the root. They give rise to four sets of cell files: the stele, the cortex and endodermis, the epidermis and lateral root-cap and the columella. A model of meristem activity is proposed based on these data. This description of Arabidopsis root structure underpins future work on the developmental genetics of root morphogenesis.
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              Organization and cell differentiation in lateral roots of Arabidopsis thaliana.

              Lateral root formation in plants involves the stimulation of mature pericycle cells to proliferate and redifferentiate to create a new organ. The simple organization of the root of Arabidopsis thaliana allows the development of lateral root primordia to be characterized histologically. We have divided the process of lateral root development into 8 stages defined by specific anatomical characteristics and cell divisions. To identify the cell types in the developing primordium we have generated a collection of marker lines that express beta-glucuronidase in a tissue- or cell type-specific manner in the root. Using these tools we have constructed a model describing the lineage of each cell type in the lateral root. These studies show that organization and cell differentiation in the lateral root primordia precede the appearance of a lateral root meristem, with differential gene expression apparent after the first set of divisions of the pericycle.
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                Author and article information

                Contributors
                Journal
                Front Plant Sci
                Front Plant Sci
                Front. Plant Sci.
                Frontiers in Plant Science
                Frontiers Media S.A.
                1664-462X
                09 June 2020
                2020
                : 11
                : 734
                Affiliations
                Department of Cell Biology, Centre of the Region Haná for Biotechnological and Agricultural Research, Faculty of Science, Palacký University Olomouc , Olomouc, Czechia
                Author notes

                Edited by: Peter Nick, Karlsruhe Institute of Technology (KIT), Germany

                Reviewed by: Takashi Hashimoto, Nara Institute of Science and Technology (NAIST), Japan; Olivier Hamant, Université de Lyon, France

                *Correspondence: Miroslav Ovečka miroslav.ovecka@ 123456upol.cz

                This article was submitted to Plant Cell Biology, a section of the journal Frontiers in Plant Science

                Article
                10.3389/fpls.2020.00734
                7296145
                32582258
                4cc91638-9b1c-4e0e-92fe-269521ab3ff9
                Copyright © 2020 Ovečka, Luptovčiak, Komis, Šamajová, Samakovli and Šamaj.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 13 March 2020
                : 07 May 2020
                Page count
                Figures: 9, Tables: 0, Equations: 0, References: 86, Pages: 18, Words: 11294
                Categories
                Plant Science
                Original Research

                Plant science & Botany
                arabidopsis,ectopic cell division,light-sheet fluorescence microscopy,live cell imaging,katanin,microtubules,root development

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