Armadillo repeat-containing kinesins and a NIMA-related kinase are required for epidermal-cell morphogenesis in Arabidopsis

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.


2016 ◽  
Vol 67 (14) ◽  
pp. 4311-4323 ◽  
Author(s):  
Wenqi Zhou ◽  
Yuchuan Wang ◽  
Zhongliang Wu ◽  
Liang Luo ◽  
Ping Liu ◽  
...  

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

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.


2018 ◽  
Author(s):  
Isadora Cavalcante ◽  
Eric Clauser ◽  
Anna Vaczlavik ◽  
Ludivine Drougat ◽  
Claudimara Lotfi ◽  
...  

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

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