Faculty Opinions recommendation of Transcriptional control of a plant stem cell niche.

Author(s):  
Miltos Tsiantis
2010 ◽  
Vol 18 (5) ◽  
pp. 841-853 ◽  
Author(s):  
Wolfgang Busch ◽  
Andrej Miotk ◽  
Federico D. Ariel ◽  
Zhong Zhao ◽  
Joachim Forner ◽  
...  

2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Ting Li ◽  
An Yan ◽  
Neha Bhatia ◽  
Alphan Altinok ◽  
Eldad Afik ◽  
...  

Nature ◽  
2005 ◽  
Vol 436 (7053) ◽  
pp. 1030-1034 ◽  
Author(s):  
Chen Chen ◽  
Wenjun Ouyang ◽  
Vadim Grigura ◽  
Qing Zhou ◽  
Kay Carnes ◽  
...  

2017 ◽  
Author(s):  
Jérémy Gruel ◽  
Julia Deichmann ◽  
Benoit Landrein ◽  
Thomas Hitchcock ◽  
Henrik Jönsson

AbstractThe plant shoot apical meristem holds a stem cell niche from which all aerial organs originate. Using a computational approach we show that a mixture of monomers and heterodimers of the transcription factors WUSCHEL and HAIRY MERISTEM is sufficient to pattern the stem cell niche, and predict that immobile heterodimers form a regulatory ‘pocket’ surrounding the stem cells. The model achieves to reproduce an array of perturbations, including mutants and tissue size modifications. We also show its ability to reproduce the recently observed dynamical shift of the stem cell niche during the development of an axillary meristem. The work integrates recent experimental results to answer the longstanding question of how the asymmetry of expression between the stem cell marker CLAVATA3 and its activator WUSCHEL is achieved, and recent findings of plasticity in the system.


2016 ◽  
Vol 2 (1) ◽  
pp. e1500989 ◽  
Author(s):  
Jérémy Gruel ◽  
Benoit Landrein ◽  
Paul Tarr ◽  
Christoph Schuster ◽  
Yassin Refahi ◽  
...  

How molecular patterning scales to organ size is highly debated in developmental biology. We explore this question for the characteristic gene expression domains of the plant stem cell niche residing in the shoot apical meristem. We show that a combination of signals originating from the epidermal cell layer can correctly pattern the key gene expression domains and notably leads to adaptive scaling of these domains to the size of the tissue. Using live imaging, we experimentally confirm this prediction. The identified mechanism is also sufficient to explain de novo stem cell niches in emerging flowers. Our findings suggest that the deformation of the tissue transposes meristem geometry into an instructive scaling and positional input for the apical plant stem cell niche.


2020 ◽  
Vol 71 (2) ◽  
pp. 211-213
Author(s):  
K. Sato ◽  
S. Chitose ◽  
K. Sato ◽  
F. Sato ◽  
T. Kurita ◽  
...  

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