Computational neurogenetic modelling: A pathway to new discoveries in genetic neuroscience

被引:15
作者
Benuskova, Lubica [1 ]
Jain, Vishal [1 ]
Wysoski, Simei G. [1 ]
Kasabov, Nikola K. [1 ]
机构
[1] Auckland Univ Technol, Knowledge Engn & Discovery Res Inst, Auckland, New Zealand
关键词
computational neurogenetic modelling; protein sequence analysis; gene-brain relationship; pattern discovery; AMPAR; GABRA; NMDAR;
D O I
10.1142/S0129065706000627
中图分类号
TP18 [人工智能理论];
学科分类号
081104 ; 0812 ; 0835 ; 1405 ;
摘要
The paper presents a methodology for using computational neurogenetic modelling (CNGM) to bring new original insights into how genes influence the dynamics of brain neural networks. CNGM is a novel computational approach to brain neural network modelling that integrates dynamic gene networks with artificial neural network model (ANN). Interaction of genes in neurons affects the dynamics of the whole ANN model through neuronal parameters, which are no longer constant but change as a function of gene expression. Through optimization of interactions within the internal gene regulatory network (GRN), initial gene/protein expression values and ANN parameters, particular target states of the neural network behaviour can be achieved, and statistics about gene interactions can be extracted. In such a way, we have obtained an abstract CRN that contains predictions about particular gene interactions in neurons for subunit genes of AMPA, GABA(A) and NMDA neuro-receptors. The extent of sequence conservation for 20 subunit proteins of all these receptors was analysed using standard bioinformatics multiple alignment procedures. We have observed abundance of conserved residues but the most interesting observation has been the consistent conservation of phenylalanine (F at position 269) and leucine (L at position 353) in all 20 proteins with no mutations. We hypothesise that these regions can be the basis for mutual interactions. Existing knowledge on evolutionary linkage of their protein families and analysis at molecular level indicate that the expression of these individual subunits should be coordinated, which provides the biological justification for our optimized GRN.
引用
收藏
页码:215 / 226
页数:12
相关论文
共 35 条
[1]  
[Anonymous], 2004, The Birth of the Mind: How a Tiny Number of Genes Creates the Complexities of Human Thought
[2]   Genomic control of receptor function [J].
Burnashev, N ;
Rozov, A .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2000, 57 (11) :1499-1507
[3]   Neuronal oscillations in cortical networks [J].
Buzsáki, G ;
Draguhn, A .
SCIENCE, 2004, 304 (5679) :1926-1929
[4]   Insulin-like growth factor 1 regulates developing brain glucose metabolism [J].
Cheng, CM ;
Reinhardt, RR ;
Lee, WH ;
Joncas, G ;
Patel, SC ;
Bondy, CA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (18) :10236-10241
[5]   Multiple sequence alignment with the Clustal series of programs [J].
Chenna, R ;
Sugawara, H ;
Koike, T ;
Lopez, R ;
Gibson, TJ ;
Higgins, DG ;
Thompson, JD .
NUCLEIC ACIDS RESEARCH, 2003, 31 (13) :3497-3500
[6]  
D'haeseleer P, 1999, Pac Symp Biocomput, P41
[7]   GABAB receptor-mediated effects in human and rat neocortical neurones in vitro [J].
Deisz, RA .
NEUROPHARMACOLOGY, 1999, 38 (11) :1755-1766
[8]   Spatiotemporal analysis of local field potentials and unit discharges in cat cerebral cortex during natural wake and sleep states [J].
Destexhe, A ;
Contreras, D ;
Steriade, M .
JOURNAL OF NEUROSCIENCE, 1999, 19 (11) :4595-4608
[9]  
Destexhe A, 1998, J NEUROSCI, V18, P9099
[10]  
Gerstner W., 2002, SPIKING NEURON MODEL