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  4. Elucidating MicroRNA Regulatory Networks Using Transcriptional, Post-transcriptional, and Histone Modification Measurements

Elucidating MicroRNA Regulatory Networks Using Transcriptional, Post-transcriptional, and Histone Modification Measurements

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Author(s)
Gurtan, Allan M.
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JnBaptiste, Courtney K.
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Bosson, Andrew
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Milani, Pamela
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Matthews, Bryan J.
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Yap, Yoon S.
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Sharp, Phillip A.
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Fraenkel, Ernest
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Gosline, Sara Jane Calafell
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Gurtan, Allan M.
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Date Issued
December 2015
Journal
Cell Reports
Publisher
Elsevier
Citation
Gosline, Sara J.C., Allan M. Gurtan, Courtney K. JnBaptiste, Andrew Bosson, Pamela Milani, Simona Dalin, Bryan J. Matthews, Yoon S. Yap, Phillip A. Sharp, and Ernest Fraenkel. “Elucidating MicroRNA Regulatory Networks Using Transcriptional, Post-Transcriptional, and Histone Modification Measurements.” Cell Reports 14, no. 2 (January 2016): 310–19.
Version
Final published version
Abstract
MicroRNAs (miRNAs) regulate diverse biological processes by repressing mRNAs, but their modest effects on direct targets, together with their participation in larger regulatory networks, make it challenging to delineate miRNA-mediated effects. Here, we describe an approach to characterizing miRNA-regulatory networks by systematically profiling transcriptional, post-transcriptional and epigenetic activity in a pair of isogenic murine fibroblast cell lines with and without Dicer expression. By RNA sequencing (RNA-seq) and CLIP (crosslinking followed by immunoprecipitation) sequencing (CLIP-seq), we found that most of the changes induced by global miRNA loss occur at the level of transcription. We then introduced a network modeling approach that integrated these data with epigenetic data to identify specific miRNA-regulated transcription factors that explain the impact of miRNA perturbation on gene expression. In total, we demonstrate that combining multiple genome-wide datasets spanning diverse regulatory modes enables accurate delineation of the downstream miRNA-regulated transcriptional network and establishes a model for studying similar networks in other systems.
MIT Department
Massachusetts Institute of Technology. Department of Biological Engineering
Massachusetts Institute of Technology. Department of Biology
Koch Institute for Integrative Cancer Research at MIT
Terms of Use
Creative Commons Attribution
http://creativecommons.org/licenses/by-nc-nd/4.0/
Persistent DSpace Link
http://hdl.handle.net/1721.1/101699
DOI of Published Version
https://doi.org/10.1016/j.celrep.2015.12.031
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