scholarly journals A Unified Genomic Mechanism of Cell-Fate Change

2021 ◽  
Author(s):  
Masa Tsuchiya ◽  
Alessandro Giuliani ◽  
Giovanna Zimatore ◽  
Jekaterina Erenpreisa ◽  
Kenichi Yoshikawa

The purpose of our studies is to elucidate the nature of massive control of whole genome expression with a particular emphasis on cell-fate change. Whole genome expression is coordinated by the emergence of a critical point (CP: a peculiar set of bi-phasic genes) through the genome-engine. In response to stimuli, the genome expression self-organizes three critical states, each exhibiting distinct collective behaviors with its center of mass acting as a local attractor, coexisting with whole genome attractor (GA). Genome-engine mechanism accounts for local attractors interaction in phase space. The CP acts as the organizing center of cell-fate change, and its activation makes local perturbation spread over the genome affecting GA. The activation of CP is in turn elicited by hot-spots genes with elevated temporal variance, normally in charge to keep genome expression at pace with microenvironment fluctuations. When hot-spots oscillation exceeds a given threshold, the CP synchronizes with the GA driving genome expression state transition. The expression synchronization wave invading the entire genome depends on the power law fusion-bursting dynamics of silencing pericentromere-associated heterochromatin domains and the consequent folding-unfolding status of transcribing euchromatin domains. The proposed mechanism is a unified step toward a time-evolutional transition theory of biological regulation.

2018 ◽  
Author(s):  
Masa Tsuchiya ◽  
Alessandro Giuliani ◽  
Kenichi Yoshikawa

AbstractIn our current studies on whole genome expression in several biological processes, we have demonstrated the actual existence of self-organized critical control (SOC) of gene expression at both population and single cell level. SOC allows for cell-fate change by critical transition encompassing the entire genome expression that, in turn, is partitioned into distinct response domains (critical states).In this paper, we go more in depth into the elucidation of SOC control of genome expression focusing on the determination of critical point (CP) and associated distinct critical states in single-cell genome expression. This leads us to the proposal of a potential universal model with genome-engine mechanism for cell-fate change. Our findings suggest that the CP is fixed point in terms of temporal expression variance, where the CP (set of critical genes) becomes active (ON) for cell-fate change (‘super-critical’ in genome-state) or else inactive (OFF) state (‘sub-critical’ in genome-state); this may lead to a novel scenario of the cell-fate control through activating or inactivating CP.


2002 ◽  
Vol 278 (5) ◽  
pp. 3339-3346 ◽  
Author(s):  
Beena Pillai ◽  
Jiyoti Verma ◽  
Anju Abraham ◽  
Princy Francis ◽  
Yadunanda Kumar ◽  
...  

BMC Genomics ◽  
2013 ◽  
Vol 14 (1) ◽  
pp. 662 ◽  
Author(s):  
Yanjie Xu ◽  
Shan Gao ◽  
Yingjie Yang ◽  
Mingyun Huang ◽  
Lina Cheng ◽  
...  

2012 ◽  
Vol 47 (2) ◽  
pp. 303-307 ◽  
Author(s):  
Atif Saeed ◽  
Lenka Barreto ◽  
Sudhesna Guha Neogii ◽  
Andrea Loos ◽  
Ian Mcfarlane ◽  
...  

BMC Genomics ◽  
2007 ◽  
Vol 8 (1) ◽  
pp. 237 ◽  
Author(s):  
Guy M Lenk ◽  
Gerard Tromp ◽  
Shantel Weinsheimer ◽  
Zoran Gatalica ◽  
Ramon Berguer ◽  
...  

Neurogenetics ◽  
2007 ◽  
Vol 8 (2) ◽  
pp. 71-81 ◽  
Author(s):  
Melanie Kuhn ◽  
Karina Haebig ◽  
Michael Bonin ◽  
Natalia Ninkina ◽  
Vladimir L. Buchman ◽  
...  

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