Exploring the structural landscape of DNA maintenance proteins

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.

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Publication Details

Journal
Nature Communications
Published
2024-09-05
DOI
https://doi.org/10.1038/s41467-024-49983-7
Citations
6
Primary Topic
DNA Repair Mechanisms
Type
article
Field-Weighted Citation Impact
1.40

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article

Exploring the structural landscape of DNA maintenance proteins

Kenneth B. Schou, Nikola Tom, Matteo Tiberti, Jens Andersen et al.
6 citations
Nature Communications
DNA Repair Mechanisms
1.40
article

Exploring the structural landscape of DNA maintenance proteins

Kenneth B. Schou, Nikola Tom, Matteo Tiberti, Jens Andersen, Samuel Coelho Mandacaru, Ann-Sofie Nilsson, Elena Papaleo, Jiří Bártek, Muhammad Tahir
article en
6 citations

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.

Nature CommunicationsVol. 15(1)
University of Southern Denmark (DK), Science for Life Laboratory (SE), Danish Cancer Society (DK), Technical University of Denmark (DK)
National Research Foundation, Danmarks Grundforskningsfond, Cancerfonden, Carlsbergfondet, Karolinska Institutet, Novo Nordisk, Vetenskapsrådet, Novo Nordisk Fonden
Openalex Percentile: Top 19%
DNA Repair Mechanisms
1.40
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