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Exploring the structural landscape of DNA maintenance proteins

Author

Listed:
  • Kenneth Bødkter Schou

    (Danish Cancer Society
    University of Southern Denmark
    Karolinska Institute)

  • Samuel Mandacaru

    (University of Southern Denmark)

  • Muhammad Tahir

    (University of Southern Denmark)

  • Nikola Tom

    (Danish Cancer Institute (DCI))

  • Ann-Sofie Nilsson

    (Karolinska Institute)

  • Jens S. Andersen

    (University of Southern Denmark)

  • Matteo Tiberti

    (Danish Cancer Society Research Center)

  • Elena Papaleo

    (Danish Cancer Society Research Center
    Technical University of Denmark)

  • Jiri Bartek

    (Danish Cancer Society
    Karolinska Institute)

Abstract

Evolutionary annotation of genome maintenance (GM) proteins has conventionally been established by remote relationships within protein sequence databases. However, often no significant relationship can be established. Highly sensitive approaches to attain remote homologies based on iterative profile-to-profile methods have been developed. Still, these methods have not been systematically applied in the evolutionary annotation of GM proteins. Here, by applying profile-to-profile models, we systematically survey the repertoire of GM proteins from bacteria to man. We identify multiple GM protein candidates and annotate domains in numerous established GM proteins, among other PARP, OB-fold, Macro, TUDOR, SAP, BRCT, KU, MYB (SANT), and nuclease domains. We experimentally validate OB-fold and MIS18 (Yippee) domains in SPIDR and FAM72 protein families, respectively. Our results indicate that, surprisingly, despite the immense interest and long-term research efforts, the repertoire of genome stability caretakers is still not fully appreciated.

Suggested Citation

  • Kenneth Bødkter Schou & Samuel Mandacaru & Muhammad Tahir & Nikola Tom & Ann-Sofie Nilsson & Jens S. Andersen & Matteo Tiberti & Elena Papaleo & Jiri Bartek, 2024. "Exploring the structural landscape of DNA maintenance proteins," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-49983-7
    DOI: 10.1038/s41467-024-49983-7
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