scholarly journals Plant cell divisions: variations from the shortest symmetric path

2020 ◽  
Vol 48 (6) ◽  
pp. 2743-2752
Author(s):  
Léo Serra ◽  
Sarah Robinson
Keyword(s):  
Cell Division ◽  
Cell Polarity ◽  
Plant Cell ◽  
Cell Walls ◽  
Direct Consequence ◽  
Spatial Arrangement ◽  
Subcellular Structure ◽  
Cell Divisions ◽  
Developmental Contexts ◽  
Hormonal Signalling

In plants, the spatial arrangement of cells within tissues and organs is a direct consequence of the positioning of the new cell walls during cell division. Since the nineteenth century, scientists have proposed rules to explain the orientation of plant cell divisions. Most of these rules predict the new wall will follow the shortest path passing through the cell centroid halving the cell into two equal volumes. However, in some developmental contexts, divisions deviate significantly from this rule. In these situations, mechanical stress, hormonal signalling, or cell polarity have been described to influence the division path. Here we discuss the mechanism and subcellular structure required to define the cell division placement then we provide an overview of the situations where division deviates from the shortest symmetric path.

scholarly journals Cells tile a flat plane by controlling geometries during morphogenesis of Pyropia thalli

PeerJ ◽  
2017 ◽  
Vol 5 ◽  
pp. e3314 ◽  
Author(s):  
Kai Xu ◽  
Yan Xu ◽  
Dehua Ji ◽  
Ting Chen ◽  
Changsheng Chen ◽  
...  
Keyword(s):  
Cell Proliferation ◽  
Cell Division ◽  
Light Microscope ◽  
Cell Walls ◽  
Single Layer ◽  
Two Dimensional ◽  
Regular Polygons ◽  
Cell Divisions ◽  
Stages Of Growth ◽  
Perfect Model

Background Pyropia haitanensis thalli, which are made of a single layer of polygonal cells, are a perfect model for studying the morphogenesis of multi-celled organisms because their cell proliferation process is an excellent example of the manner in which cells control their geometry to create a two-dimensional plane. Methods Cellular geometries of thalli at different stages of growth revealed by light microscope analysis. Results This study showed the cell division transect the middle of the selected paired-sides to divide the cell into two equal portions, thus resulting in cell sides ≥4 and keeping the average number of cell sides at approximately six even as the thallus continued to grow, such that more than 90% of the cells in thalli longer than 0.08 cm had 5–7 sides. However, cell division could not fully explain the distributions of intracellular angles. Results showed that cell-division-associated fast reorientation of cell sides and cell divisions together caused 60% of the inner angles of cells from longer thalli to range from 100–140°. These results indicate that cells prefer to form regular polygons. Conclusions This study suggests that appropriate cell-packing geometries maintained by cell division and reorientation of cell walls can keep the cells bordering each other closely, without gaps.

scholarly journals A Plant-Specific Polarity Module Establishes Cell Fate Asymmetry in the Arabidopsis Stomatal Lineage

2019 ◽  
Author(s):  
Matthew H. Rowe ◽  
Juan Dong ◽  
Annika K. Weimer ◽  
Dominique C. Bergmann
Keyword(s):  
Genetic Diversity ◽  
Cell Fate ◽  
Cell Polarity ◽  
Asymmetric Cell Division ◽  
Diverse Range ◽  
Asymmetric Cell Divisions ◽  
Cell Divisions ◽  
Collective Activity ◽  
Developmental Contexts ◽  
Stomatal Lineage

SUMMARYGenerating cell polarity in anticipation of asymmetric cell division is required in many developmental contexts across a diverse range of species. Physical and genetic diversity among major multicellular taxa, however, demand different molecular solutions to this problem. The Arabidopsis stomatal lineage displays asymmetric, stem cell-like and oriented cell divisions, which require the activity of the polarly localized protein, BASL. Here we identify the plant-specific BREVIS RADIX (BRX) family as localization and activity partners of BASL. We show that members of the BRX family are polarly localized to peripheral domains in stomatal lineage cells and that their collective activity is required for asymmetric cell divisions. We further demonstrate a mechanism for these behaviors by uncovering mutual, yet unequal dependencies of BASL and the BRX family for each other’s localization and segregation at the periphery of stomatal lineage cells.

scholarly journals Cycling in a crowd: coordination of plant cell division, growth, and cell fate

2021 ◽  
Author(s):  
Robert Sablowski ◽  
Crisanto Gutierrez
Keyword(s):  
Cell Cycle ◽  
Cell Division ◽  
Cell Fate ◽  
Plant Cell ◽  
Cell Cycle Progression ◽  
Specific Cell ◽  
Cell Fates ◽  
Cycle Progression ◽  
Cell Divisions ◽  
Major Player

Abstract The reiterative organogenesis that drives plant growth relies on the constant production of new cells, which remain encased by interconnected cell walls. For these reasons, plant morphogenesis strictly depends on the rate and orientation of both cell division and cell growth. Important progress has been made in recent years in understanding how cell cycle progression and the orientation of cell divisions are coordinated with cell and organ growth and with the acquisition of specialized cell fates. We review basic concepts and players in plant cell cycle and division, and then focus on their links to growth-related cues, such as metabolic state, cell size, cell geometry, and cell mechanics, and on how cell cycle progression and cell division are linked to specific cell fates. The retinoblastoma pathway has emerged as a major player in the coordination of the cell cycle with both growth and cell identity, while microtubule dynamics are central in the coordination of oriented cell divisions. Future challenges include clarifying feedbacks between growth and cell cycle progression, revealing the molecular basis of cell division orientation in response to mechanical and chemical signals, and probing the links between cell fate changes and chromatin dynamics during the cell cycle.

scholarly journals How Does a Plant Cell Build a New Cell Wall When Dividing?

2021 ◽  
Vol 9 ◽  
Author(s):  
Mingqin Chang ◽  
Georgia Drakakaki
Keyword(s):  
Cell Wall ◽  
Cell Division ◽  
Plant Cell ◽  
Cell Walls ◽  
Building Materials ◽  
Plant Cells ◽  
Construction Workers ◽  
Animal Cells

If you live in an apartment or a house, you will notice that your home has different rooms separated by walls. A plant is just like your home, except there are many small rooms, called cells. Plant cells, like rooms, are also separated by cell walls. Cell walls are unique and are not found in animal cells. In a building, if you want to turn one large room into two small rooms, you build a new wall to divide it. This is similar to how a plant cell divides into two cells during cell division. To build a wall in a building, you need to employ construction workers, design the building plan, buy building materials, and finally assembly the wall. How does the plant cell take care of these different jobs? This article explains how the cell wall is built in a plant cell during cell division.

scholarly journals A microtubule-based mechanism predicts cell division orientation in plant embryogenesis

2018 ◽  
Author(s):  
Bandan Chakrabortty ◽  
Viola Willemsen ◽  
Thijs de Zeeuw ◽  
Che-Yang Liao ◽  
Dolf Weijers ◽  
...  
Keyword(s):  
Cell Division ◽  
Cell Walls ◽  
Cell Shape ◽  
Cortical Microtubule ◽  
Minimal Set ◽  
Division Plane ◽  
Plant Morphogenesis ◽  
Cell Divisions ◽  
Microtubule Stability ◽  
Underlying Mechanisms

AbstractOriented cell divisions are significant in plant morphogenesis because plant cells are embedded in cell walls and cannot relocate. Cell divisions follow various regular orientations, but the underlying mechanisms have not been clarified. We show that cell-shape dependent self-organisation of cortical microtubule arrays is crucial for determining planes of early tissue-generating divisions and forms the basis for robust control of cell division orientation in the embryo. To achieve this, we simulate microtubules on actual cell surface shapes from which we derive a minimal set of three rules for proper array orientation. The first rule captures the effects of cell shape alone on microtubule organisation, the second rule describes the regulation of microtubule stability at cell edges and the third rule includes the differential effect of auxin on local microtubule stability. These rules explain early embryonic division plane orientations and offer a framework for understanding patterned cell divisions in plant morphogenesis.

Stimulated Virus Production in Vinblastine and Cytochalasin-Induced Multinucleate Cells

1970 ◽  
Vol 28 ◽  
pp. 186-187
Author(s):  
Krishan Awtar
Keyword(s):  
Cell Division ◽  
Normal Cell ◽  
Virus Production ◽  
Multinucleate Cells ◽  
Daughter Cells ◽  
Cell Divisions ◽  
Nuclear Membranes ◽  
Division 2 ◽  
Vinblastine Sulfate

Exposure of cells to low sublethal but mitosis-arresting doses of vinblastine sulfate (Velban) results in the initial arrest of cells in mitosis followed by their subsequent return to an “interphase“-like stage. A large number of these cells reform their nuclear membranes and form large multimicronucleated cells, some containing as many as 25 or more micronuclei (1). Formation of large multinucleate cells is also caused by cytochalasin, by causing the fusion of daughter cells at the end of an otherwise .normal cell division (2). By the repetition of this process through subsequent cell divisions, large cells with 6 or more nuclei are formed.

Exploration of cell wall architecture with the rapid-freeze deep-etch technique

1993 ◽  
Vol 51 ◽  
pp. 128-129
Author(s):  
Béatrice Satiat-Jeunemaitre ◽  
Chris Hawes
Keyword(s):  
Plant Cell ◽  
Cell Walls ◽  
Cell Biology ◽  
Molecular Model ◽  
Three Dimensional ◽  
Secretory Activity ◽  
Wall Structure ◽  
Specimen Preparation ◽  
Molecular Architecture ◽  
Plant Cell Walls

The comprehension of the molecular architecture of plant cell walls is one of the best examples in cell biology which illustrates how developments in microscopy have extended the frontiers of a topic. Indeed from the first electron microscope observation of cell walls it has become apparent that our understanding of wall structure has advanced hand in hand with improvements in the technology of specimen preparation for electron microscopy. Cell walls are sub-cellular compartments outside the peripheral plasma membrane, the construction of which depends on a complex cellular biosynthetic and secretory activity (1). They are composed of interwoven polymers, synthesised independently, which together perform a number of varied functions. Biochemical studies have provided us with much data on the varied molecular composition of plant cell walls. However, the detailed intermolecular relationships and the three dimensional arrangement of the polymers in situ remains a mystery. The difficulty in establishing a general molecular model for plant cell walls is also complicated by the vast diversity in wall composition among plant species.

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