Abstract

BackgroundThe ability of a transcription factor to regulate its targets is modulated by a variety of genetic and epigenetic mechanisms. Alternative splicing can modulate gene function by adding or removing certain protein domains, and therefore affect the activity of protein. Reverse engineering of gene regulatory networks using gene expression profiles has proven valuable in dissecting the logical relationships among multiple proteins during the transcriptional regulation. However, it is unclear whether alternative splicing of certain proteins affects the activity of other transcription factors.ResultsIn order to investigate the roles of alternative splicing during transcriptional regulation, we constructed a statistical model to infer whether the alternative splicing events of modulator proteins can affect the ability of key transcription factors in regulating the expression levels of their transcriptional targets. We tested our strategy in KIRC (Kidney Renal Clear Cell Carcinoma) using the RNA-seq data downloaded from TCGA (the Cancer Genomic Atlas). We identified 828of modulation relationships between the splicing levels of modulator proteins and activity levels of transcription factors. For instance, we found that the activity levels of GR (glucocorticoid receptor) protein, a key transcription factor in kidney, can be influenced by the splicing status of multiple proteins, including TP53, MDM2 (mouse double minute 2 homolog), RBM14 (RNA-binding protein 14) and SLK (STE20 like kinase). The influenced GR-targets are enriched by key cancer-related pathways, including p53 signaling pathway, TR/RXR activation, CAR/RXR activation, G1/S checkpoint regulation pathway, and G2/M DNA damage checkpoint regulation pathway.ConclusionsOur analysis suggests, for the first time, that exon inclusion levels of certain regulatory proteins can affect the activities of many transcription factors. Such analysis can potentially unravel a novel mechanism of how splicing variation influences the cellular function and provide important insights for how dysregulation of splicing outcome can lead to various diseases.

Highlights

  • The ability of a transcription factor to regulate its targets is modulated by a variety of genetic and epigenetic mechanisms

  • We develop a simple regression-based statistical model for evaluating whether the interactions of the percentage of inclusion level of a putative modulator protein and the expression levels of transcription factors jointly contribute to the expression levels of the target genes

  • Model framework In this study, we construct a regression-based linear model to infer the interactions between the activity of transcription factor (TF), evaluated by correlation between the expression levels of the TF and its targets (T), and the percentage of inclusion of a putative exon in a modulator protein (M)

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Summary

Introduction

The ability of a transcription factor to regulate its targets is modulated by a variety of genetic and epigenetic mechanisms. Reverse engineering of gene regulatory networks using gene expression profiles has proven valuable in dissecting the logical relationships among multiple proteins during the transcriptional regulation. It is unclear whether alternative splicing of certain proteins affects the activity of other transcription factors. Differences in the gene expression levels of splicing regulatory factor have been observed in many cancers, and these proteins often affect the splicing patterns of many genes that function in certain cancer-specific biological pathways, including cell cycle progression, cellular proliferation and migration, and RNA processing [8,9,10]. One example is that when the PSI value of a specific exon in M is high, the expression levels of the putative transcription factor correlates with its targets, while such correlation relation is lost when the PSI value is low

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