Email updates

Keep up to date with the latest news and content from BMC Systems Biology and BioMed Central.

Open Access Highly Accessed Research article

Crosstalk between transcription factors and microRNAs in human protein interaction network

Chen-Ching Lin1, Ya-Jen Chen1, Cho-Yi Chen23, Yen-Jen Oyang1, Hsueh-Fen Juan14* and Hsuan-Cheng Huang5*

Author affiliations

1 Graduate Institute of Biomedical Electronics and Bioinformatics, National Taiwan University, Taipei 106, Taiwan

2 Genome and Systems Biology Degree Program, National Taiwan University, Taipei 106, Taiwan

3 Institute of Biological Chemistry, Academia Sinica, Taipei 115, Taiwan

4 Department of Life Science and Institute of Molecular and Cellular Biology, National Taiwan University, Taipei 106, Taiwan

5 Institute of Biomedical Informatics, Center for Systems and Synthetic Biology, National Yang-Ming University, Taipei 112, Taiwan

For all author emails, please log on.

Citation and License

BMC Systems Biology 2012, 6:18  doi:10.1186/1752-0509-6-18

Published: 13 March 2012

Abstract

Background

Gene regulatory networks control the global gene expression and the dynamics of protein output in living cells. In multicellular organisms, transcription factors and microRNAs are the major families of gene regulators. Recent studies have suggested that these two kinds of regulators share similar regulatory logics and participate in cooperative activities in the gene regulatory network; however, their combinational regulatory effects and preferences on the protein interaction network remain unclear.

Methods

In this study, we constructed a global human gene regulatory network comprising both transcriptional and post-transcriptional regulatory relationships, and integrated the protein interactome into this network. We then screened the integrated network for four types of regulatory motifs: single-regulation, co-regulation, crosstalk, and independent, and investigated their topological properties in the protein interaction network.

Results

Among the four types of network motifs, the crosstalk was found to have the most enriched protein-protein interactions in their downstream regulatory targets. The topological properties of these motifs also revealed that they target crucial proteins in the protein interaction network and may serve important roles of biological functions.

Conclusions

Altogether, these results reveal the combinatorial regulatory patterns of transcription factors and microRNAs on the protein interactome, and provide further evidence to suggest the connection between gene regulatory network and protein interaction network.