Regulatory feedback loops bridge the human gene regulatory network and regulate carcinogenesis

2017 ◽  
Vol 20 (3) ◽  
pp. 976-984 ◽  
Author(s):  
Yun-Ru Chen ◽  
Hsuan-Cheng Huang ◽  
Chen-Ching Lin
2011 ◽  
Vol 8 (12) ◽  
pp. 1050-1052 ◽  
Author(s):  
John S Reece-Hoyes ◽  
A Rasim Barutcu ◽  
Rachel Patton McCord ◽  
Jun Seop Jeong ◽  
Lizhi Jiang ◽  
...  

Author(s):  
Gianvito Pio ◽  
Paolo Mignone ◽  
Giuseppe Magazzù ◽  
Guido Zampieri ◽  
Michelangelo Ceci ◽  
...  

Abstract Motivation Gene regulation is responsible for controlling numerous physiological functions and dynamically responding to environmental fluctuations. Reconstructing the human network of gene regulatory interactions is thus paramount to understanding the cell functional organisation across cell types, as well as to elucidating pathogenic processes and identifying molecular drug targets. Although significant effort has been devoted towards this direction, existing computational methods mainly rely on gene expression levels, possibly ignoring the information conveyed by mechanistic biochemical knowledge. Moreover, except for a few recent attempts, most of the existing approaches only consider the information of the organism under analysis, without exploiting the information of related model organisms. Results We propose a novel method for the reconstruction of the human gene regulatory network, based on a transfer learning strategy that synergically exploits information from human and mouse, conveyed by gene-related metabolic features generated in-silico from gene expression data. Specifically, we learn a predictive model from metabolic activity inferred via tissue-specific metabolic modelling of artificial gene knockouts. Our experiments show that the combination of our transfer learning approach with the constructed metabolic features provides a significant advantage in terms of reconstruction accuracy, as well as additional clues on the contribution of each constructed metabolic feature. Availability The system, the datasets and all the results obtained in this study are available at: https://doi.org/10.6084/m9.figshare.c.5237687 Supplementary information Supplementary data are available at Bioinformatics online.


2015 ◽  
Vol 9 (4) ◽  
pp. 128-134 ◽  
Author(s):  
Matthew B. Carson ◽  
Jianlei Gu ◽  
Guangjun Yu ◽  
Hui Lu

2016 ◽  
Vol 27 (05) ◽  
pp. 1650056 ◽  
Author(s):  
Rajesh Karmakar

We study the oscillatory behavior of a gene regulatory network with interlinked positive and negative feedback loop. The frequency and amplitude are two important properties of oscillation. The studied network produces two different modes of oscillation. In one mode (mode-I), frequency of oscillation remains constant over a wide range of amplitude and in the other mode (mode-II) the amplitude of oscillation remains constant over a wide range of frequency. Our study reproduces both features of oscillations in a single gene regulatory network and shows that the negative plus positive feedback loops in gene regulatory network offer additional advantage. We identified the key parameters/variables responsible for different modes of oscillation. The network is flexible in switching between different modes by choosing appropriately the required parameters/variables.


2012 ◽  
Vol 40 (18) ◽  
pp. 8849-8861 ◽  
Author(s):  
Junil Kim ◽  
Minsoo Choi ◽  
Jeong-Rae Kim ◽  
Hua Jin ◽  
V. Narry Kim ◽  
...  

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