scholarly journals Alignment between PIN1 Polarity and Microtubule Orientation in the Shoot Apical Meristem Reveals a Tight Coupling between Morphogenesis and Auxin Transport

PLoS Biology ◽  
2010 ◽  
Vol 8 (10) ◽  
pp. e1000516 ◽  
Author(s):  
Marcus G. Heisler ◽  
Olivier Hamant ◽  
Pawel Krupinski ◽  
Magalie Uyttewaal ◽  
Carolyn Ohno ◽  
...  
Keyword(s):  
Shoot Apical Meristem ◽  
Apical Meristem ◽  
Auxin Transport ◽  
Tight Coupling ◽  
Microtubule Orientation

scholarly journals Ontogenetic Changes in Auxin Biosynthesis and Distribution Determine the Organogenic Activity of the Shoot Apical Meristem in pin1 Mutants

2019 ◽  
Vol 20 (1) ◽  
pp. 180 ◽  
Author(s):  
Alicja Banasiak ◽  
Magdalena Biedroń ◽  
Alicja Dolzblasz ◽  
Mateusz Adam Berezowski
Keyword(s):  
Shoot Apical Meristem ◽  
Apical Meristem ◽  
Auxin Transport ◽  
Vascular System ◽  
Auxin Biosynthesis ◽  
Wild Type ◽  
Ontogenetic Changes ◽  
Auxin Distribution ◽  
Stem Development ◽  
Knockout Mutation

In the shoot apical meristem (SAM) of Arabidopsis, PIN1-dependent polar auxin transport (PAT) regulates two crucial developmental processes: organogenesis and vascular system formation. However, the knockout mutation in the PIN1 gene does not fully inhibit these two processes. Therefore, we investigated a potential source of auxin for organogenesis and vascularization during inflorescence stem development. We analyzed auxin distribution in wild-type (WT) and pin1 mutant plants using a refined protocol of auxin immunolocalization; auxin activity, with the response reporter pDR5:GFP; and expression of auxin biosynthesis genes YUC1 and YUC4. Our results revealed that regardless of the functionality of PIN1-mediated PAT, auxin is present in the SAM and vascular strands. In WT plants, auxin always accumulates in all cells of the SAM, whereas in pin1 mutants, its localization within the SAM changes ontogenetically and is related to changes in the structure of the vascular system, organogenic activity of SAM, and expression levels of YUC1 and YUC4 genes. Our findings indicate that the presence of auxin in the meristem of pin1 mutants is an outcome of at least two PIN1-independent mechanisms: acropetal auxin transport from differentiated tissues with the use of vascular strands and auxin biosynthesis within the SAM.

scholarly journals Feedback from Lateral Organs Controls Shoot Apical Meristem Growth by Modulating Auxin Transport

2018 ◽  
Vol 44 (2) ◽  
pp. 204-216.e6 ◽  
Author(s):  
Bihai Shi ◽  
Xiaolu Guo ◽  
Ying Wang ◽  
Yuanyuan Xiong ◽  
Jin Wang ◽  
...  
Keyword(s):  
Shoot Apical Meristem ◽  
Apical Meristem ◽  
Auxin Transport ◽  
Lateral Organs

scholarly journals Toward a 3D model of phyllotaxis based on a biochemically plausible auxin-transport mechanism

2018 ◽  
Author(s):  
Félix P. Hartmann ◽  
Pierre Barbier de Reuille ◽  
Cris Kuhlemeier
Keyword(s):  
Shoot Apical Meristem ◽  
Apical Meristem ◽  
Auxin Transport ◽  
Vascular System ◽  
Three Dimensional ◽  
Integrative Approach ◽  
Dimensional Model ◽  
Three Dimensional Model ◽  
Leaf Formation ◽  
Cell Layers

AbstractPolar auxin transport lies at the core of many self-organizing phenomena sustaining continuous plant organogenesis. In angiosperms, the shoot apical meristem is a potentially unique system in which the two main modes of auxin-driven patterning— convergence and canalization—co-occur in a coordinated manner and in a fully three-dimensional geometry. In the epidermal layer, convergence points form, from which auxin is canalized towards inner tissue. Each of these two patterning processes has been extensively investigated separately, but the integration of both in the shoot apical meristem remains poorly understood. We present here a first attempt of a three-dimensional model of auxin-driven patterning during phyllotaxis. We base our simulations on a biochemically plausible mechanism of auxin transport proposed by Cieslak et al. (2015) which generates both convergence and canalization patterns. We are able to reproduce most of the dynamics of PIN1 polarization in the meristem, and we explore how the epidermal and inner cell layers act in concert during phyllotaxis. In addition, we discuss the mechanism by which initiating veins connect to the already existing vascular system.Author summaryThe regularity of leaf arrangement around stems has long puzzled scientists. The key role played by the plant hormone auxin is now well established. On the surface of the tissue responsible for leaf formation, auxin accumulates at several points, from which new leaves eventually emerge. Auxin also guides the progression of new veins from the nascent leaves to the vascular system of the plant. Models of auxin transport have been developed to explain either auxin accumulation or auxin-driven venation. We propose the first three-dimensional model embracing both phenomena using a unifying mechanism of auxin transport. This integrative approach allows an assessment of our present knowledge on how auxin contributes to the early development of leaves. Our model reproduces many observations of auxin dynamics. It highlights how the inner and epidermal tissues act together to position new leaves. We also show that an additional, yet unknown, mechanism is required to attract new developing veins towards the main vasculature of the plant.

scholarly journals ERECTA Family Genes Regulate Auxin Transport in the Shoot Apical Meristem and Forming Leaf Primordia

2013 ◽  
Vol 162 (4) ◽  
pp. 1978-1991 ◽  
Author(s):  
Ming-Kun Chen ◽  
Rebecca L. Wilson ◽  
Klaus Palme ◽  
Franck Anicet Ditengou ◽  
Elena D. Shpak
Keyword(s):  
Shoot Apical Meristem ◽  
Apical Meristem ◽  
Auxin Transport ◽  
Leaf Primordia

scholarly journals Sample preparation for laser-microdissection of soybean shoot apical meristem

2012 ◽  
Vol 3 (1) ◽  
pp. 3 ◽  
Author(s):  
Chui E. Wong ◽  
Mohan B. Singh ◽  
Prem L. Bhalla
Keyword(s):  
Sample Preparation ◽  
Shoot Apical Meristem ◽  
Apical Meristem ◽  
Laser Microdissection ◽  
Specific Cell ◽  
Legume Crop ◽  
Continuous Formation ◽  
Molecular Events ◽  
Depth Analysis ◽  
Specialized Equipment

The shoot apical meristem houses stem cells responsible for the continuous formation of aerial plant organs including leaves and stems throughout the life of plants. Laser-microdissection in combination with high-throughput technology such as next generation sequencing permits an in-depth analysis of molecular events associated with specific cell type of interest. Sample preparation is the most critical step in ensuring good quality RNA to be extracted from samples following laser-microdissection. Here, we optimized the sample preparation for a major legume crop, soybean. We used Farmer’s solution as a fixative and paraffin as the embedding medium for soybean shoot apical meristem tissue without the use of any specialized equipment. Shorter time for tissue fixation (two days) was found to be critical for the preservation of RNA in soybean shoot apical meristem. We further demonstrated the utility of this method for different tissues derived from soybean and rice. The method outlined here shall facilitate studies on crop plants involving laser-microdissection.

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