scholarly journals Six2 and Wnt Regulate Self-Renewal and Commitment of Nephron Progenitors through Shared Gene Regulatory Networks

2012 ◽  
Vol 23 (3) ◽  
pp. 637-651 ◽  
Author(s):  
Joo-Seop Park ◽  
Wenxiu Ma ◽  
Lori L. O'Brien ◽  
Eunah Chung ◽  
Jin-Jin Guo ◽  
...  
Keyword(s):  
Gene Regulatory Networks ◽  
Regulatory Networks ◽  
Self Renewal ◽  
Nephron Progenitors ◽  
Gene Regulatory ◽  
Shared Gene

scholarly journals PCL2 modulates gene regulatory networks controlling self-renewal and commitment in embryonic stem cells

Cell Cycle ◽  
2011 ◽  
Vol 10 (1) ◽  
pp. 45-51 ◽  
Author(s):  
Emily Walker ◽  
Janet L. Manias ◽  
Wing Y. Chang ◽  
William L. Stanford
Keyword(s):  
Stem Cells ◽  
Embryonic Stem Cells ◽  
Gene Regulatory Networks ◽  
Regulatory Networks ◽  
Embryonic Stem ◽  
Self Renewal ◽  
Gene Regulatory

scholarly journals Evo-engineering and the Cellular and Molecular Origins of the Vertebrate Spinal Cord

2016 ◽  
Author(s):  
Ben Steventon ◽  
Alfonso Martinez Arias
Keyword(s):  
Spinal Cord ◽  
Gene Regulatory Networks ◽  
Regulatory Networks ◽  
Systems Approach ◽  
Continuous Process ◽  
Neural Plate ◽  
Model Organisms ◽  
Self Renewal ◽  
Gene Regulatory ◽  
Vertebrate Embryos

AbstractThe formation of the spinal cord during early embryonic development in vertebrate embryos is a continuous process that begins at gastrulation and continues through to the completion of somitogenesis. Despite the conserved usage of patterning mechanisms and gene regulatory networks that act to generate specify spinal cord progenitors, there now exists two seemingly disparate models to account for their action. In the first, a posterior localized signalling source transforms previously anterior-specified neural plate into the spinal cord. In the second, a population of bipotent stem cells undergo continuous self-renewal and differentiation to progressively lay down the spinal cord and axial mesoderm by posterior growth. Whether this represents fundamental differences between the experimental model organisms utilised in the generation of these models remains to be addressed. Here we review lineage studies across four key vertebrate models: mouse, chicken, Xenopus and zebrafish and relate this to the underlying gene regulatory networks that are known to be required for spinal cord formation. We propose that by applying a dynamical systems approach to understanding how distinct neural and mesodermal fates arise from a bipotent progenitor pool, it is possible to begin to understand how differences in the dynamical cell behaviours such as proliferation rates and cell movements can map onto conserved regulatory networks to generate diversity in the timing of tissue generation and patterning during development.

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