Local regulation of gene expression by lncRNA promoters, transcription, and splicing
Abstract
Mammalian genomes are pervasively transcribed to produce thousands of long non-coding RNAs (lncRNAs). A few of these lncRNAs have been shown to recruit regulatory complexes through RNA–protein interactions to influence the expression of nearby genes, and it has been suggested that many other lncRNAs can also act as local regulators. Such local functions could explain the observation that lncRNA expression is often correlated with the expression of nearby genes. However, these correlations have been challenging to dissect and could alternatively result from processes that are not mediated by the lncRNA transcripts themselves. For example, some gene promoters have been proposed to have dual functions as enhancers, and the process of transcription itself may contribute to gene regulation by recruiting activating factors or remodelling nucleosomes. Here we use genetic manipulation in mouse cell lines to dissect 12 genomic loci that produce lncRNAs and find that 5 of these loci influence the expression of a neighbouring gene in cis. Notably, none of these effects requires the specific lncRNA transcripts themselves and instead involves general processes associated with their production, including enhancer-like activity of gene promoters, the process of transcription, and the splicing of the transcript. Furthermore, such effects are not limited to lncRNA loci: we find that four out of six protein-coding loci also influence the expression of a neighbour. These results demonstrate that cross-talk among neighbouring genes is a prevalent phenomenon that can involve multiple mechanisms and cis-regulatory signals, including a role for RNA splice sites. These mechanisms may explain the function and evolution of some genomic loci that produce lncRNAs and broadly contribute to the regulation of both coding and non-coding genes.
Additional Information
© 2016 Macmillan Publishers. Received 16 April; accepted 10 October 2016. Published online 26 October 2016. We thank S. Grossman, J. Rinn, M. Yassour, P. Sharp, L. Boyer, M. Ray, C. Fulco, M. Munschauer, T. Wang and N. Friedman for discussions; A. Goren and Broad Technology Labs for ChIP; J. Lis, D. Mahat and A. Shishkin for technical advice and reagents; and J. Flannick for computational tools. J.M.E. is supported by the Fannie and John Hertz Foundation and the National Defense Science and Engineering Graduate Fellowship. M.G. is supported the NIH Director's Early Independence Award (DP5OD012190), the Edward Mallinckrodt Foundation, the Sontag Foundation, and the Searle Scholars Program. Work in the Lander Laboratory is supported by the Broad Institute. Author Contributions: J.M.E., M.G. and E.S.L. conceived and designed the study. J.M.E., J.E.H., G.M., M.K. and P.E.M. developed knockout protocols and performed genetic manipulations. E.M.P. and J.M.E. performed all other experiments. J.M.E. developed computational tools and analysed data. J.M.E. and J.C. performed evolutionary analysis. J.M.E. and E.S.L. wrote the manuscript with input from all authors. E.S.L. supervised the work and obtained funding. Data availability. Sequencing data for this study is available at the Gene Expression Omnibus (GSE80262 and GSE85798), and additional visualizations of the data are available at http://pubs.broadinstitute.org/neighboring-genes/. Code availability. Code for the analyses described in this paper is available from the authors upon request. Competing financial interests: The Broad Institute holds patents and has filed patent applications on technologies related to other aspects of CRISPR.Attached Files
Accepted Version - nihms-1056089.pdf
Supplemental Material - nature20149-s1.pdf
Supplemental Material - nature20149-s2.xlsx
Supplemental Material - nature20149-s3.xlsx
Supplemental Material - nature20149-s4.xlsx
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Additional details
- PMCID
- PMC6853796
- Eprint ID
- 71034
- Resolver ID
- CaltechAUTHORS:20161012-162725499
- Fannie and John Hertz Foundation
- National Defense Science and Engineering Graduate (NDSEG) Fellowship
- NIH
- DP5OD012190
- Edward Mallinckrodt, Jr. Foundation
- Sontag Foundation
- Searle Scholars Program
- Broad Institute of MIT and Harvard
- Created
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2016-10-27Created from EPrint's datestamp field
- Updated
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2022-02-16Created from EPrint's last_modified field