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Reconstructing Generalized Logical Networks of Transcriptional Regulation in Mouse Brain from Temporal Gene Expression Data
被引:14
作者:
Song, Mingzhou
[1
]
Lewis, Chris K.
[1
]
Lance, Eric R.
[1
]
Chesler, Elissa J.
[2
]
Yordanova, Roumyana Kirova
[3
]
Langston, Michael A.
[4
]
Lodowski, Kerrie H.
[5
]
Bergeson, Susan E.
[6
]
机构:
[1] New Mexico State Univ, Dept Comp Sci, Las Cruces, NM 88003 USA
[2] Oak Ridge Natl Lab, Biosci Div, Syst Genet Grp, Oak Ridge, TN 37831 USA
[3] Bristol Myers Squibb R&D, Dept Appl Genom, Princeton, NJ 08543 USA
[4] Univ Tennessee, Dept Comp Sci, Knoxville, TN 37996 USA
[5] Case Western Reserve Univ, Sch Med, Dept Pharmacol, Cleveland, OH 44106 USA
[6] Texas Tech Univ, Dept Pharmacol & Neurosci, Lubbock, TX 79430 USA
基金:
澳大利亚研究理事会;
美国国家卫生研究院;
美国国家科学基金会;
关键词:
D O I:
10.1155/2009/545176
中图分类号:
Q [生物科学];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Gene expression time course data can be used not only to detect differentially expressed genes but also to find temporal associations among genes. The problem of reconstructing generalized logical networks to account for temporal dependencies among genes and environmental stimuli from transcriptomic data is addressed. A network reconstruction algorithm was developed that uses statistical significance as a criterion for network selection to avoid false-positive interactions arising from pure chance. The multinomial hypothesis testing-based network reconstruction allows for explicit specification of the false-positive rate, unique from all extant network inference algorithms. The method is superior to dynamic Bayesian network modeling in a simulation study. Temporal gene expression data from the brains of alcohol-treated mice in an analysis of the molecular response to alcohol are used for modeling. Genes from major neuronal pathways are identified as putative components of the alcohol response mechanism. Nine of these genes have associations with alcohol reported in literature. Several other potentially relevant genes, compatible with independent results from literature mining, may play a role in the response to alcohol. Additional, previously unknown gene interactions were discovered that, subject to biological verification, may offer new clues in the search for the elusive molecular mechanisms of alcoholism. Copyright (C) 2009 Mingzhou (Joe) Song et al.
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页数:13
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