scholarly journals Homologs of SCAR/WAVE complex components are required for epidermal cell morphogenesis in rice

2016 ◽  
Vol 67 (14) ◽  
pp. 4311-4323 ◽  
Author(s):  
Wenqi Zhou ◽  
Yuchuan Wang ◽  
Zhongliang Wu ◽  
Liang Luo ◽  
Ping Liu ◽  
...  
2008 ◽  
Vol 53 (1) ◽  
pp. 157-171 ◽  
Author(s):  
Tatsuya Sakai ◽  
Hannie van der Honing ◽  
Miki Nishioka ◽  
Yukiko Uehara ◽  
Mihoko Takahashi ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Kotomi Kikukawa ◽  
Kazuki Yoshimura ◽  
Akira Watanabe ◽  
Takumi Higaki

During cotyledon growth, the pavement cells, which make up most of the epidermal layer, undergo dynamic morphological changes from simple to jigsaw puzzle-like shapes in most dicotyledonous plants. Morphological analysis of cell shapes generally involves the segmentation of cells from input images followed by the extraction of shape descriptors that can be used to assess cell shape. Traditionally, replica and fluorescent labeling methods have been used for time-lapse observation of cotyledon epidermal cell morphogenesis, but these methods require expensive microscopes and can be technically demanding. Here, we propose a silver-nano-ink coating method for time-lapse imaging and quantification of morphological changes in the epidermal cells of growing Arabidopsis thaliana cotyledons. To obtain high-resolution and wide-area cotyledon surface images, we placed the seedlings on a biaxial goniometer and adjusted the cotyledons, which were coated by dropping silver ink onto them, to be as horizontal to the focal plane as possible. The omnifocal images that had the most epidermal cell shapes in the observation area were taken at multiple points to cover the whole surface area of the cotyledon. The multi-point omnifocal images were automatically stitched, and the epidermal cells were automatically and accurately segmented by machine learning. Quantification of cell morphological features based on the segmented images demonstrated that the proposed method could quantitatively evaluate jigsaw puzzle-shaped cell growth and morphogenesis. The method was successfully applied to phenotyping of the bpp125 triple mutant, which has defective pavement cell morphogenesis. The proposed method will be useful for time-lapse non-destructive phenotyping of plant surface structures and is easier to use than the conversional methods that require fluorescent dye labeling or transformation with marker gene constructs and expensive microscopes such as the confocal laser microscope.


2020 ◽  
Vol 11 ◽  
Author(s):  
Petra Cifrová ◽  
Denisa Oulehlová ◽  
Eva Kollárová ◽  
Jan Martinek ◽  
Amparo Rosero ◽  
...  

2021 ◽  
Vol 220 (8) ◽  
Author(s):  
Anne Pipathsouk ◽  
Rachel M. Brunetti ◽  
Jason P. Town ◽  
Brian R. Graziano ◽  
Artù Breuer ◽  
...  

How local interactions of actin regulators yield large-scale organization of cell shape and movement is not well understood. Here we investigate how the WAVE complex organizes sheet-like lamellipodia. Using super-resolution microscopy, we find that the WAVE complex forms actin-independent 230-nm-wide rings that localize to regions of saddle membrane curvature. This pattern of enrichment could explain several emergent cell behaviors, such as expanding and self-straightening lamellipodia and the ability of endothelial cells to recognize and seal transcellular holes. The WAVE complex recruits IRSp53 to sites of saddle curvature but does not depend on IRSp53 for its own localization. Although the WAVE complex stimulates actin nucleation via the Arp2/3 complex, sheet-like protrusions are still observed in ARP2-null, but not WAVE complex-null, cells. Therefore, the WAVE complex has additional roles in cell morphogenesis beyond Arp2/3 complex activation. Our work defines organizing principles of the WAVE complex lamellipodial template and suggests how feedback between cell shape and actin regulators instructs cell morphogenesis.


Author(s):  
N.C. Lyon ◽  
W. C. Mueller

Schumacher and Halbsguth first demonstrated ectodesmata as pores or channels in the epidermal cell walls in haustoria of Cuscuta odorata L. by light microscopy in tissues fixed in a sublimate fixative (30% ethyl alcohol, 30 ml:glacial acetic acid, 10 ml: 65% nitric acid, 1 ml: 40% formaldehyde, 5 ml: oxalic acid, 2 g: mecuric chloride to saturation 2-3 g). Other workers have published electron micrographs of structures transversing the outer epidermal cell in thin sections of plant leaves that have been interpreted as ectodesmata. Such structures are evident following treatment with Hg++ or Ag+ salts and are only rarely observed by electron microscopy. If ectodesmata exist without such treatment, and are not artefacts, they would afford natural pathways of entry for applied foliar solutions and plant viruses.


1991 ◽  
Vol 53 (1) ◽  
pp. 3-6
Author(s):  
SHIN'ICHI INOHARA
Keyword(s):  

2020 ◽  
Vol 40 (10) ◽  
pp. 870-872
Author(s):  
T. R. Ablyaz ◽  
E. S. Shlykov ◽  
K. R. Muratov

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