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<p>Genetic interaction and protein-protein interaction networks have proved among the most important tools for inference of gene function and genotype-phenotype relationship. It remains unclear, however, how these two networks are related to each other. Here we demonstrate that the strengths of epistatic genetic interactions between two genes strongly correlate with the binding free energies of interactions between their cognate proteins, for both yeast and human genomes. Consequently, we show that genetic interaction and protein-protein interaction networks can reciprocally predict each other. Further, we observe that functional divergence and redundancy in duplicated genes (paralogs) are reflected in the binding affinity of their interactions with other proteins and in their genetic interaction strengths. Finally, we demonstrate that the overall topologies of genetic interaction and protein-protein interaction networks significantly overlap in two topological features: modules, in which genes/proteins are organized by common function, and connectors, which link modules to each other. This opens avenues for integrated network approaches in understanding cellular processes and flow of genomic information.</p>

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Protein-protein interactions are a major source of epistasis in genetic interaction networks

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年2月5日

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  • Xavier Castellanos-Girouard,
  • Adrian W. R. Serohijos,
  • Stephen W. Michnick

摘要

Genetic interaction and protein-protein interaction networks have proved among the most important tools for inference of gene function and genotype-phenotype relationship. It remains unclear, however, how these two networks are related to each other. Here we demonstrate that the strengths of epistatic genetic interactions between two genes strongly correlate with the binding free energies of interactions between their cognate proteins, for both yeast and human genomes. Consequently, we show that genetic interaction and protein-protein interaction networks can reciprocally predict each other. Further, we observe that functional divergence and redundancy in duplicated genes (paralogs) are reflected in the binding affinity of their interactions with other proteins and in their genetic interaction strengths. Finally, we demonstrate that the overall topologies of genetic interaction and protein-protein interaction networks significantly overlap in two topological features: modules, in which genes/proteins are organized by common function, and connectors, which link modules to each other. This opens avenues for integrated network approaches in understanding cellular processes and flow of genomic information.