{"title":"IA型拓扑异构酶的构象改变促进了链的通过。","authors":"Deepesh Sigdel, Dillon Balthrop, Maria Mills","doi":"10.1016/j.jmb.2025.169402","DOIUrl":null,"url":null,"abstract":"<p><p>Type IA topoisomerases are present in all kingdoms of life and are responsible for simplifying torsionally strained DNA structures during fundamental cellular processes. The common model for this simplification is based upon the concept of passage of an intact DNA strand through a transient cut in another single DNA strand. This process requires the protein to undergo several conformational changes. In this review, we discuss these conformational changes across the strand passage cycle from DNA binding through opening and closing of a protein mediated DNA gate. We also examine the involvement of the diverse C-terminal domains of these enzymes during strand-passage and current open questions in the field.</p>","PeriodicalId":369,"journal":{"name":"Journal of Molecular Biology","volume":" ","pages":"169402"},"PeriodicalIF":4.5000,"publicationDate":"2025-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Conformational Changes in Type IA Topoisomerases Facilitate Strand Passage.\",\"authors\":\"Deepesh Sigdel, Dillon Balthrop, Maria Mills\",\"doi\":\"10.1016/j.jmb.2025.169402\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Type IA topoisomerases are present in all kingdoms of life and are responsible for simplifying torsionally strained DNA structures during fundamental cellular processes. The common model for this simplification is based upon the concept of passage of an intact DNA strand through a transient cut in another single DNA strand. This process requires the protein to undergo several conformational changes. In this review, we discuss these conformational changes across the strand passage cycle from DNA binding through opening and closing of a protein mediated DNA gate. We also examine the involvement of the diverse C-terminal domains of these enzymes during strand-passage and current open questions in the field.</p>\",\"PeriodicalId\":369,\"journal\":{\"name\":\"Journal of Molecular Biology\",\"volume\":\" \",\"pages\":\"169402\"},\"PeriodicalIF\":4.5000,\"publicationDate\":\"2025-08-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Molecular Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1016/j.jmb.2025.169402\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Molecular Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.jmb.2025.169402","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Conformational Changes in Type IA Topoisomerases Facilitate Strand Passage.
Type IA topoisomerases are present in all kingdoms of life and are responsible for simplifying torsionally strained DNA structures during fundamental cellular processes. The common model for this simplification is based upon the concept of passage of an intact DNA strand through a transient cut in another single DNA strand. This process requires the protein to undergo several conformational changes. In this review, we discuss these conformational changes across the strand passage cycle from DNA binding through opening and closing of a protein mediated DNA gate. We also examine the involvement of the diverse C-terminal domains of these enzymes during strand-passage and current open questions in the field.
期刊介绍:
Journal of Molecular Biology (JMB) provides high quality, comprehensive and broad coverage in all areas of molecular biology. The journal publishes original scientific research papers that provide mechanistic and functional insights and report a significant advance to the field. The journal encourages the submission of multidisciplinary studies that use complementary experimental and computational approaches to address challenging biological questions.
Research areas include but are not limited to: Biomolecular interactions, signaling networks, systems biology; Cell cycle, cell growth, cell differentiation; Cell death, autophagy; Cell signaling and regulation; Chemical biology; Computational biology, in combination with experimental studies; DNA replication, repair, and recombination; Development, regenerative biology, mechanistic and functional studies of stem cells; Epigenetics, chromatin structure and function; Gene expression; Membrane processes, cell surface proteins and cell-cell interactions; Methodological advances, both experimental and theoretical, including databases; Microbiology, virology, and interactions with the host or environment; Microbiota mechanistic and functional studies; Nuclear organization; Post-translational modifications, proteomics; Processing and function of biologically important macromolecules and complexes; Molecular basis of disease; RNA processing, structure and functions of non-coding RNAs, transcription; Sorting, spatiotemporal organization, trafficking; Structural biology; Synthetic biology; Translation, protein folding, chaperones, protein degradation and quality control.