Toward the human cellular microRNAome

Matthew N. McCall, Min Sik Kim, Mohammed Adil, Arun H. Patil, Yin Lu, Christopher J. Mitchell, Pamela Leal-Rojas, Jinchong Xu, Manoj Kumar, Valina L. Dawson, Ted M. Dawson, Alexander S. Baras, Avi Z. Rosenberg, Dan E. Arking, Kathleen H. Burns, Akhilesh Pandey, Marc K. Halushka

Research output: Contribution to journalArticlepeer-review

58 Scopus citations

Abstract

MicroRNAs are short RNAs that serve as regulators of gene expression and are essential components of normal development as well as modulators of disease. MicroRNAs generally act cell-autonomously, and thus their localization to specific cell types is needed to guide our understanding of microRNA activity. Current tissue-level data have caused considerable confusion, and comprehensive cell-level data do not yet exist. Here, we establish the landscape of human cell-specific microRNA expression. This project evaluated 8 billion small RNA-seq reads from 46 primary cell types, 42 cancer or immortalized cell lines, and 26 tissues. It identified both specific and ubiquitous patterns of expression that strongly correlate with adjacent superenhancer activity. Analysis of unaligned RNA reads uncovered 207 unknown minor strand (passenger) microRNAs of known microRNA loci and 495 novel putative microRNA loci. Although cancer cell lines generally recapitulated the expression patterns of matched primary cells, their isomiR sequence families exhibited increased disorder, suggesting DROSHA- and DICER1-dependent microRNA processing variability. Cell-specific patterns of microRNA expression were used to de-convolute variable cellular composition of colon and adipose tissue samples, highlighting one use of these cell-specific microRNA expression data. Characterization of cellular microRNA expression across a wide variety of cell types provides a new understanding of this critical regulatory RNA species.

Original languageEnglish (US)
Pages (from-to)1769-1781
Number of pages13
JournalGenome Research
Volume27
Issue number10
DOIs
StatePublished - Oct 2017

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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