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Discovery, Annotation, and Functional Analysis of Long Noncoding RNAs Controlling Cell-Cycle Gene Expression and Proliferation in Breast Cancer Cells

We describe a computational approach that integrates GRO-seq and RNA-seq data to annotate long noncoding RNAs (lncRNAs), with increased sensitivity for low-abundance lncRNAs. We used this approach to characterize the lncRNA transcriptome in MCF-7 human breast cancer cells, including >700 previous...

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Published in:Molecular cell 2015-08, Vol.59 (4), p.698-711
Main Authors: Sun, Miao, Gadad, Shrikanth S., Kim, Dae-Seok, Kraus, W. Lee
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cited_by cdi_FETCH-LOGICAL-c632t-440d1e6fa6d126bb0c2e2415dea5b2f0d85a4fa8c8fc01218ff41de0a39020b13
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container_title Molecular cell
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creator Sun, Miao
Gadad, Shrikanth S.
Kim, Dae-Seok
Kraus, W. Lee
description We describe a computational approach that integrates GRO-seq and RNA-seq data to annotate long noncoding RNAs (lncRNAs), with increased sensitivity for low-abundance lncRNAs. We used this approach to characterize the lncRNA transcriptome in MCF-7 human breast cancer cells, including >700 previously unannotated lncRNAs. We then used information about the (1) transcription of lncRNA genes from GRO-seq, (2) steady-state levels of lncRNA transcripts in cell lines and patient samples from RNA-seq, and (3) histone modifications and factor binding at lncRNA gene promoters from ChIP-seq to explore lncRNA gene structure and regulation, as well as lncRNA transcript stability, regulation, and function. Functional analysis of selected lncRNAs with altered expression in breast cancers revealed roles in cell proliferation, regulation of an E2F-dependent cell-cycle gene expression program, and estrogen-dependent mitogenic growth. Collectively, our studies demonstrate the use of an integrated genomic and molecular approach to identify and characterize growth-regulating lncRNAs in cancers. •A sensitive approach for annotating lncRNAs that integrates GRO-seq and RNA-seq data•Identification of lncRNAs in breast cancer cells, including >700 not yet annotated•Differences between lncRNA and mRNA gene promoters; similarities with enhancers•LncRNAs 152 and 67 control the cell cycle and gene expression in breast cancer cells Sun et al. use a computational genomics pipeline with GRO-seq and RNA-seq data to identify ∼1,900 lncRNAs in breast cancer cells, including >700 lncRNAs not previously annotated. Functional analyses of lncRNA152 and lncRNA67 indicate roles in cell proliferation and the regulation of an E2F-dependent cell-cycle gene expression program.
doi_str_mv 10.1016/j.molcel.2015.06.023
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Collectively, our studies demonstrate the use of an integrated genomic and molecular approach to identify and characterize growth-regulating lncRNAs in cancers. •A sensitive approach for annotating lncRNAs that integrates GRO-seq and RNA-seq data•Identification of lncRNAs in breast cancer cells, including &gt;700 not yet annotated•Differences between lncRNA and mRNA gene promoters; similarities with enhancers•LncRNAs 152 and 67 control the cell cycle and gene expression in breast cancer cells Sun et al. use a computational genomics pipeline with GRO-seq and RNA-seq data to identify ∼1,900 lncRNAs in breast cancer cells, including &gt;700 lncRNAs not previously annotated. 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subjects Base Sequence
breast neoplasms
Breast Neoplasms - genetics
Breast Neoplasms - metabolism
Breast Neoplasms - pathology
cell cycle
Cell Cycle Proteins - genetics
Cell Cycle Proteins - metabolism
Cell Proliferation
Female
gene expression
Gene Expression Regulation, Neoplastic
genes
histones
Humans
MCF-7 Cells
Molecular Sequence Annotation
neoplasm cells
non-coding RNA
patients
RNA, Long Noncoding - physiology
sequence analysis
Transcriptome
title Discovery, Annotation, and Functional Analysis of Long Noncoding RNAs Controlling Cell-Cycle Gene Expression and Proliferation in Breast Cancer Cells
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