4.7 Article

Integrated analysis sheds light on evolutionary trajectories of young transcription start sites in the human genome

Journal

GENOME RESEARCH
Volume 28, Issue 5, Pages 676-688

Publisher

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1101/gr.231449.117

Keywords

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Funding

  1. Francis Crick Institute from Cancer Research UK [FC010110]
  2. UK Medical Research Council [FC010110]
  3. Wellcome Trust [FC010110]
  4. Winton Charitable Foundation's
  5. Wellcome Trust Joint Investigator Award [103760/Z/14/Z]
  6. MRC eMedLab Medical Bioinformatics Infrastructure Award [MR/L016311/1]
  7. Okinawa Institute of Science & Technology Graduate University
  8. EMBO long-term postdoctoral fellowship [ALTF 1499-2016]
  9. MRC [MC_UP_1102/1, MR/L016311/1] Funding Source: UKRI
  10. Wellcome Trust [103760/Z/14/Z] Funding Source: Wellcome Trust

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Understanding the molecular mechanisms and evolution of the gene regulatory system remains a major challenge in biology. Transcription start sites (TSSs) are especially interesting because they are central to initiating gene expression. Previous studies revealed widespread transcription initiation and fast turnover of TSSs in mammalian genomes. Yet, how new TSSs originate and how they evolve over time remain poorly understood. To address these questions, we analyzed similar to 200,000 human TSSs by integrating evolutionary (inter-and intra-species) and functional genomic data, particularly focusing on evolutionarily young TSSs that emerged in the primate lineage. TSSs were grouped according to their evolutionary age using sequence alignment information as a proxy. Comparisons of young and old TSSs revealed that (1) new TSSs emerge through a combination of intrinsic factors, like the sequence properties of transposable elements and tandem repeats, and extrinsic factors such as their proximity to existing regulatory modules; (2) new TSSs undergo rapid evolution that reduces the inherent instability of repeat sequences associated with a high propensity of TSS emergence; and (3) once established, the transcriptional competence of surviving TSSs is gradually enhanced, with evolutionary changes subject to temporal (fewer regulatory changes in younger TSSs) and spatial constraints (fewer regulatory changes in more isolated TSSs). These findings advance our understanding of how regulatory innovations arise in the genome throughout evolution and highlight the genomic robustness and evolvability in these processes.

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