Transposable elements as a potent source of diverse <i>cis</i> -regulatory sequences in mammalian genomes

  • Vasavi Sundaram
    European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK
  • Joanna Wysocka
    Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, USA

説明

<jats:p> Eukaryotic gene regulation is mediated by <jats:italic>cis</jats:italic> -regulatory elements, which are embedded within the vast non-coding genomic space and recognized by the transcription factors in a sequence- and context-dependent manner. A large proportion of eukaryotic genomes, including at least half of the human genome, are composed of transposable elements (TEs), which in their ancestral form carried their own <jats:italic>cis</jats:italic> -regulatory sequences able to exploit the host <jats:italic>trans</jats:italic> environment to promote TE transcription and facilitate transposition. Although not all present-day TE copies have retained this regulatory function, the preexisting regulatory potential of TEs can provide a rich source of <jats:italic>cis</jats:italic> -regulatory innovation for the host. Here, we review recent evidence documenting diverse contributions of TE sequences to gene regulation by functioning as enhancers, promoters, silencers and boundary elements. We discuss how TE-derived enhancer sequences can rapidly facilitate changes in existing gene regulatory networks and mediate species- and cell-type-specific regulatory innovations, and we postulate a unique contribution of TEs to species-specific gene expression divergence in pluripotency and early embryogenesis. With advances in genome-wide technologies and analyses, systematic investigation of TEs' <jats:italic>cis</jats:italic> -regulatory potential is now possible and our understanding of the biological impact of genomic TEs is increasing. </jats:p> <jats:p>This article is part of a discussion meeting issue ‘Crossroads between transposons and gene regulation’.</jats:p>

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