Understanding Tissue-Specific Gene Regulation

Abhijeet R. Sonawane(Brigham and Women's Hospital), John Platig(Harvard University), Maud Fagny(Harvard University), Cho-Yi Chen(Harvard University), Joseph N. Paulson(Harvard University), Camila M. Lopes‐Ramos(Harvard University), Dawn L. DeMeo(Brigham and Women's Hospital), John Quackenbush(Brigham and Women's Hospital), Kimberly Glass(Brigham and Women's Hospital), Marieke L. Kuijjer(Harvard University)
Cell Reports
October 1, 2017
Cited by 460Open Access
Full Text

Abstract

Although all human tissues carry out common processes, tissues are distinguished by gene expression patterns, implying that distinct regulatory programs control tissue specificity. In this study, we investigate gene expression and regulation across 38 tissues profiled in the Genotype-Tissue Expression project. We find that network edges (transcription factor to target gene connections) have higher tissue specificity than network nodes (genes) and that regulating nodes (transcription factors) are less likely to be expressed in a tissue-specific manner as compared to their targets (genes). Gene set enrichment analysis of network targeting also indicates that the regulation of tissue-specific function is largely independent of transcription factor expression. In addition, tissue-specific genes are not highly targeted in their corresponding tissue network. However, they do assume bottleneck positions due to variability in transcription factor targeting and the influence of non-canonical regulatory interactions. These results suggest that tissue specificity is driven by context-dependent regulatory paths, providing transcriptional control of tissue-specific processes.


Related Papers

No related papers found

Powered by citation graph analysis