Toward the human cellular microRNAome

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 act...

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Published in:Genome research Vol. 27; no. 10; pp. 1769 - 1781
Main Authors: McCall, Matthew N, Kim, Min-Sik, Adil, Mohammed, Patil, Arun H, Lu, Yin, Mitchell, Christopher J, Leal-Rojas, Pamela, Xu, Jinchong, Kumar, Manoj, Dawson, Valina L, Dawson, Ted M, Baras, Alexander S, Rosenberg, Avi Z, Arking, Dan E, Burns, Kathleen H, Pandey, Akhilesh, Halushka, Marc K
Format: Journal Article
Language:English
Published: United States Cold Spring Harbor Laboratory Press 01-10-2017
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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.
AbstractList 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.
Author Kim, Min-Sik
Adil, Mohammed
Dawson, Ted M
Pandey, Akhilesh
Mitchell, Christopher J
Dawson, Valina L
Xu, Jinchong
Patil, Arun H
Baras, Alexander S
Arking, Dan E
McCall, Matthew N
Halushka, Marc K
Kumar, Manoj
Burns, Kathleen H
Rosenberg, Avi Z
Leal-Rojas, Pamela
Lu, Yin
AuthorAffiliation 8 Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA
11 Neuroregeneration and Stem Cell Programs, Institute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA
14 Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA
4 Department School of Life Sciences, B.S. Abdur Rahman University, Chennai, 600048, India
2 Department of Applied Chemistry, Kyung Hee University, Yongin, Gyeonggi 17104, South Korea 3
3 McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA
15 Department of Pharmacology and Molecular Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA
5 School of Biotechnology, KIIT University, Bhubaneswar, Odisha, 751024, India
10 Center of Excellence in Translational Medicine (CEMT) & Scientific and Technological Bioresource Nucleus (BIOREN), Universi
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(2021111811163697000_27.10.1769.52) 2017; 168
(2021111811163697000_27.10.1769.34) 2016; 5
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(2021111811163697000_27.10.1769.6) 2015; 10
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(2021111811163697000_27.10.1769.56) 2008; 9
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(2021111811163697000_27.10.1769.19) 2016; 35
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(2021111811163697000_27.10.1769.42) 2016; 99
(2021111811163697000_27.10.1769.58) 2016; 13
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Snippet MicroRNAs are short RNAs that serve as regulators of gene expression and are essential components of normal development as well as modulators of disease....
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SubjectTerms Adult
Cell Line, Transformed
Cell Line, Tumor
Humans
Male
MicroRNAs - biosynthesis
MicroRNAs - genetics
Organ Specificity
Resource
RNA Processing, Post-Transcriptional - physiology
Title Toward the human cellular microRNAome
URI https://www.ncbi.nlm.nih.gov/pubmed/28877962
https://www.proquest.com/docview/1936622919
https://pubmed.ncbi.nlm.nih.gov/PMC5630040
Volume 27
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