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Yin and Yang of disease genes and death genes between reciprocally scale-free biological networks
- Source :
- Nucleic Acids Research, NUCLEIC ACIDS RESEARCH(41): 20
- Publication Year :
- 2013
- Publisher :
- Oxford University Press (OUP), 2013.
-
Abstract
- Biological networks often show a scale-free topology with node degree following a power-law distribution. Lethal genes tend to form functional hubs, whereas non-lethal disease genes are located at the periphery. Uni-dimensional analyses, however, are flawed. We created and investigated two distinct scale-free networks; a protein-protein interaction (PPI) and a perturbation sensitivity network (PSN). The hubs of both networks exhibit a low molecular evolutionary rate (P < 8 x 10(-12), P < 2 x 10(-4)) and a high codon adaptation index (P < 2 x 10(-16), P < 2 x 10(-8)), indicating that both hubs have been shaped under high evolutionary selective pressure. Moreover, the topologies of PPI and PSN are inversely proportional: hubs of PPI tend to be located at the periphery of PSN and vice versa. PPI hubs are highly enriched with lethal genes but not with disease genes, whereas PSN hubs are highly enriched with disease genes and drug targets but not with lethal genes. PPI hub genes are enriched with essential cellular processes, but PSN hub genes are enriched with environmental interaction processes, having more TATA boxes and transcription factor binding sites. It is concluded that biological systems may balance internal growth signaling and external stress signaling by unifying the two opposite scale-free networks that are seemingly opposite to each other but work in concert between death and disease.
- Subjects :
- Genetics
Codon Adaptation Index
Binding Sites
TATA box
Saccharomyces cerevisiae
Computational Biology
Molecular Sequence Annotation
Biology
biology.organism_classification
Models, Biological
TATA Box
Evolution, Molecular
DNA binding site
Genes
Protein Interaction Mapping
Lethal allele
Disease
Genes, Lethal
Transcription factor
Gene
Biological network
Transcription Factors
Subjects
Details
- ISSN :
- 13624962 and 03051048
- Volume :
- 41
- Database :
- OpenAIRE
- Journal :
- Nucleic Acids Research
- Accession number :
- edsair.doi.dedup.....12055b81cb003580406af06d0c329383