Yang Xi, Chen Xuemin, Yang Wei, Pommier Yves
Developmental Therapeutics Branch & Laboratory of Molecular Pharmacology, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, USA.
Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, NIH, Bethesda, MD, USA.
Nat Commun. 2025 Jan 19;16(1):834. doi: 10.1038/s41467-025-55959-y.
Type IA topoisomerases (TopoIAs) are present in all living organisms. They resolve DNA/RNA catenanes, knots and supercoils by breaking and rejoining single-stranded DNA/RNA segments and allowing the passage of another nucleic acid segment through the break. Topoisomerase III-β (TOP3B), the only RNA topoisomerase in metazoans, promotes R-loop disassembly and translation of mRNAs. Defects in TOP3B lead to severe neurological diseases. We present a series of cryo-EM structures of human TOP3B with its cofactor TDRD3 during cleavage and rejoining of DNA or RNA, thus elucidating the roles of divalent metal ions and key enzyme residues in each step of the catalytic cycle. We also obtained the structure of an open-gate configuration that addresses the long-standing question of the strand-passage mechanism. Our studies reveal how TOP3B catalyzes both DNA and RNA relaxation, while TOP3A acts only on DNA.
IA型拓扑异构酶(TopoIAs)存在于所有生物中。它们通过断裂和重新连接单链DNA/RNA片段,并允许另一个核酸片段通过断裂处,来解开DNA/RNA连环体、结和超螺旋。拓扑异构酶III-β(TOP3B)是后生动物中唯一的RNA拓扑异构酶,它促进R环的拆解和mRNA的翻译。TOP3B缺陷会导致严重的神经疾病。我们展示了一系列人TOP3B与其辅因子TDRD3在DNA或RNA切割和重新连接过程中的冷冻电镜结构,从而阐明了二价金属离子和关键酶残基在催化循环各步骤中的作用。我们还获得了一种开放门构象的结构,解决了长期存在的链通过机制问题。我们的研究揭示了TOP3B如何催化DNA和RNA松弛,而TOP3A仅作用于DNA。