Structural and biochemical basis for DNA and RNA catalysis by human Topoisomerase 3β
Xi Yang,
Sourav Saha,
Wei Yang,
Keir C. Neuman and
Yves Pommier ()
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Xi Yang: National Cancer Institute, NIH
Sourav Saha: National Cancer Institute, NIH
Wei Yang: National Institute of Diabetes and Digestive and Kidney Diseases, NIH
Keir C. Neuman: National Institutes of Health
Yves Pommier: National Cancer Institute, NIH
Nature Communications, 2022, vol. 13, issue 1, 1-14
Abstract:
Abstract In metazoans, topoisomerase 3β (TOP3B) regulates R-loop dynamics and mRNA translation, which are critical for genome stability, neurodevelopment and normal aging. As a Type IA topoisomerase, TOP3B acts by general acid-base catalysis to break and rejoin single-stranded DNA. Passage of a second DNA strand through the transient break permits dissipation of hypernegative DNA supercoiling and catenation/knotting. Additionally, hsTOP3B was recently demonstrated as the human RNA topoisomerase, required for normal neurodevelopment and proposed to be a potential anti-viral target upon RNA virus infection. Here we elucidate the biochemical mechanisms of human TOP3B. We delineate the roles of divalent metal ions, and of a conserved Lysine residue (K10) in the differential catalysis of DNA and RNA. We also demonstrate that three regulatory factors fine-tune the catalytic performance of TOP3B: the TOP3B C-terminal tail, its protein partner TDRD3, and the sequence of its DNA/RNA substrates.
Date: 2022
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-32221-3
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DOI: 10.1038/s41467-022-32221-3
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