Systematic perturbation of retroviral LTRs reveals widespread long-range effects on human gene regulation

  1. Daniel R Fuentes
  2. Tomek Swigut
  3. Joanna Wysocka  Is a corresponding author
  1. Stanford University School of Medicine, United States

Abstract

Recent work suggests extensive adaptation of transposable elements (TEs) for host gene regulation. However, high numbers of integrations typical of TEs, coupled with sequence divergence within families, have made systematic interrogation of the regulatory contributions of TEs challenging. Here, we employ CARGO, our recent method for CRISPR gRNA multiplexing, to facilitate targeting of LTR5HS, an ape-specific class of HERVK (HML-2) LTRs that is active during early development and present in ~700 copies throughout the human genome. We combine CARGO with CRISPR activation or interference to, respectively, induce or silence LTR5HS en masse, and demonstrate that this system robustly targets the vast majority of LTR5HS insertions. Remarkably, activation/silencing of LTR5HS is associated with reciprocal up- and down-regulation of hundreds of human genes. These effects require presence of retroviral sequences, but occur over long genomic distances, consistent with a pervasive function of LTR5HS elements as early embryonic enhancers in apes.

Data availability

Sequencing data have been deposited in GEO under accession codes GSE111331, GSE111332 and GSE111337.

The following data sets were generated
The following previously published data sets were used

Article and author information

Author details

  1. Daniel R Fuentes

    Cancer Biology Program, Stanford University School of Medicine, Stanford, United States
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-0412-6933
  2. Tomek Swigut

    Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, United States
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-7649-6781
  3. Joanna Wysocka

    Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, United States
    For correspondence
    wysocka@stanford.edu
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-6909-6544

Funding

National Science Foundation (Graduate Research Fellowship Program)

  • Daniel R Fuentes

Howard Hughes Medical Institute

  • Joanna Wysocka

National Institute of General Medical Sciences (R01GM112720)

  • Joanna Wysocka

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Reviewing Editor

  1. Edith Heard, Institut Curie, France

Version history

  1. Received: February 26, 2018
  2. Accepted: August 1, 2018
  3. Accepted Manuscript published: August 2, 2018 (version 1)
  4. Version of Record published: September 26, 2018 (version 2)

Copyright

© 2018, Fuentes et al.

This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.

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  1. Daniel R Fuentes
  2. Tomek Swigut
  3. Joanna Wysocka
(2018)
Systematic perturbation of retroviral LTRs reveals widespread long-range effects on human gene regulation
eLife 7:e35989.
https://doi.org/10.7554/eLife.35989

Share this article

https://doi.org/10.7554/eLife.35989

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