Abstract

BackgroundThe regenerative response of Schwann cells after peripheral nerve injury is a critical process directly related to the pathophysiology of a number of neurodegenerative diseases. This SC injury response is dependent on an intricate gene regulatory program coordinated by a number of transcription factors and microRNAs, but the interactions among them remain largely unknown. Uncovering the transcriptional and post-transcriptional regulatory networks governing the Schwann cell injury response is a key step towards a better understanding of Schwann cell biology and may help develop novel therapies for related diseases. Performing such comprehensive network analysis requires systematic bioinformatics methods to integrate multiple genomic datasets.ResultsIn this study we present a computational pipeline to infer transcription factor and microRNA regulatory networks. Our approach combined mRNA and microRNA expression profiling data, ChIP-Seq data of transcription factors, and computational transcription factor and microRNA target prediction. Using mRNA and microRNA expression data collected in a Schwann cell injury model, we constructed a regulatory network and studied regulatory pathways involved in Schwann cell response to injury. Furthermore, we analyzed network motifs and obtained insights on cooperative regulation of transcription factors and microRNAs in Schwann cell injury recovery.ConclusionsThis work demonstrates a systematic method for gene regulatory network inference that may be used to gain new information on gene regulation by transcription factors and microRNAs.

Highlights

  • The regenerative response of Schwann cells after peripheral nerve injury is a critical process directly related to the pathophysiology of a number of neurodegenerative diseases

  • Overview of Transcription factor (TF) and miRNA regulatory network inference We developed a systematic approach, termed InteGRaNet, for inferring TF and miRNA regulatory networks involved in Schwann cells (SC) injury response

  • Comparing miRNA expression profiles with mRNA expression profiles, we found that, of the 87 miRNAs expressed in peripheral nerve, 17, 26, 6, and 6 miRNAs were correlated with the expression profile of the four Injury response gene cluster (IRGC), respectively (Additional file 3: Table S3). 5 and 8 miRNAs were anticorrelated with the expression profile of Cluster 3 and Cluster 4 (Additional file 4: Table S4)

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Summary

Introduction

The regenerative response of Schwann cells after peripheral nerve injury is a critical process directly related to the pathophysiology of a number of neurodegenerative diseases. This SC injury response is dependent on an intricate gene regulatory program coordinated by a number of transcription factors and microRNAs, but the interactions among them remain largely unknown. A comprehensive delineation of the TF and miRNA regulatory network underlying the SC injury response may shed light on fundamental aspects of SC biology This information could help fulfill the therapeutic potential of modulating the SC injury response in a number of neurodegenerative diseases characterized by peripheral axonopathy

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