{"title":"Mitotic signalling in progenitor cells: Integrating cell division with cell specification","authors":"Torcato Martins , Yuu Kimata","doi":"10.1016/j.ceb.2025.102542","DOIUrl":null,"url":null,"abstract":"<div><div>Mitotic signalling mediated by cell cycle regulators (CCRs) is pivotal for coordinating cell division and fate specification across metazoans. CCRs, including cyclin-dependent kinases and ubiquitin ligases, use post-translational modifications for rapid, dynamic regulation of the cell cycle, ensuring its unidirectionality and integration with fate determination. This review explores recent findings that further elucidate CCRs’ noncanonical functions, particularly in progenitor cells. Advancements in quantitative <em>in vivo</em> imaging, precise genome editing, and single-cell omics have provided unprecedented spatiotemporal resolution into the mechanisms through which CCRs regulate asymmetric cell division, epigenetic regulation, and cell cycle variations. The evolution of CCRs underscores their crucial role in integrating cellular and developmental signals in multicellular organisms, with implications for disease and therapeutic strategies.</div></div>","PeriodicalId":50608,"journal":{"name":"Current Opinion in Cell Biology","volume":"95 ","pages":"Article 102542"},"PeriodicalIF":6.0000,"publicationDate":"2025-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Opinion in Cell Biology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0955067425000808","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Mitotic signalling mediated by cell cycle regulators (CCRs) is pivotal for coordinating cell division and fate specification across metazoans. CCRs, including cyclin-dependent kinases and ubiquitin ligases, use post-translational modifications for rapid, dynamic regulation of the cell cycle, ensuring its unidirectionality and integration with fate determination. This review explores recent findings that further elucidate CCRs’ noncanonical functions, particularly in progenitor cells. Advancements in quantitative in vivo imaging, precise genome editing, and single-cell omics have provided unprecedented spatiotemporal resolution into the mechanisms through which CCRs regulate asymmetric cell division, epigenetic regulation, and cell cycle variations. The evolution of CCRs underscores their crucial role in integrating cellular and developmental signals in multicellular organisms, with implications for disease and therapeutic strategies.
期刊介绍:
Current Opinion in Cell Biology (COCEBI) is a highly respected journal that specializes in publishing authoritative, comprehensive, and systematic reviews in the field of cell biology. The journal's primary aim is to provide a clear and readable synthesis of the latest advances in cell biology, helping specialists stay current with the rapidly evolving field. Expert authors contribute to the journal by annotating and highlighting the most significant papers from the extensive body of research published annually, offering valuable insights and saving time for readers by distilling key findings.
COCEBI is part of the Current Opinion and Research (CO+RE) suite of journals, which leverages the legacy of editorial excellence, high impact, and global reach to ensure that the journal is a widely read resource integral to scientists' workflow. It is published by Elsevier, a publisher known for its commitment to excellence in scientific publishing and the communication of reproducible biomedical research aimed at improving human health. The journal's content is designed to be an invaluable resource for a diverse audience, including researchers, lecturers, teachers, professionals, policymakers, and students.