Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/118246
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dc.contributorSchool of Optometryen_US
dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.contributorResearch Centre for SHARP Visionen_US
dc.creatorYuan, Fen_US
dc.creatorTan, YSen_US
dc.creatorWang, Hen_US
dc.creatorAli, ANen_US
dc.creatorYuan, Qen_US
dc.creatorChou, SMen_US
dc.creatorYen, YHen_US
dc.creatorNarayanan, Gen_US
dc.creatorZhou, Len_US
dc.creatorShboul, Men_US
dc.creatorBonnard, Cen_US
dc.creatorReversade, Ben_US
dc.creatorZhang, SCen_US
dc.date.accessioned2026-03-26T01:22:24Z-
dc.date.available2026-03-26T01:22:24Z-
dc.identifier.urihttp://hdl.handle.net/10397/118246-
dc.language.isoenen_US
dc.publisherNature Publishing Groupen_US
dc.rights© The Author(s) 2026.en_US
dc.rightsOpen Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.en_US
dc.rightsThe following publication Yuan, F., Tan, Y.S., Wang, H. et al. IVNS1ABP mutation drives cellular senescence in newly identified progeroid neuropathy. Nat Commun (2026) is available at https://doi.org/10.1038/s41467-026-70756-x.en_US
dc.titleIVNS1ABP mutation drives cellular senescence in newly identified progeroid neuropathyen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.doi10.1038/s41467-026-70756-xen_US
dcterms.abstractWe identified a new progeroid syndrome with severe neuropathy and intellectual deficits but its underlying cellular and molecular mechanism is unknown. Exome sequencing revealed a homozygous mutation in the IVNS1ABP gene, which encodes IVNS1ABP, an influenza virus non-structural protein-1 binding protein. To investigate disease mechanisms, we generated isogenic induced pluripotent stem cells (iPSCs) from patient fibroblasts and differentiated them into neural progenitor cells (NPCs). Mutant IVNS1ABP fibroblasts, iPSCs, and NPCs exhibited defective cytokinesis, increased DNA damage, and premature cellular senescence. Consistent with these findings, cerebral organoids showed early differentiation of NPCs into neurons. Molecular profiling as well as biochemical and cellular analysis revealed altered binding of mutant IVNS1ABP to actin / actin-associated proteins and dysregulated actin dynamics during cytokinesis. Taken together, we propose that mutant IVNS1ABP dysregulates actin polymerization and organization which is at least partly responsible for the cellular senescence phenotypes in this progeroid neuropathy.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationNature communications, Published: 19 March 2026, Latest Research articles, https://doi.org/10.1038/s41467-026-70756-xen_US
dcterms.isPartOfNature communicationsen_US
dcterms.issued2026-
dc.identifier.eissn2041-1723en_US
dc.description.validate202603 bcchen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera4353-
dc.identifier.SubFormID52629-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextWe would like to thank all members of Su-Chun’s laboratories for their discussions and suggestions. We thank Andrew Petersen for technical help on CRISPR editing. F.Y. was supported by Duke-NUS Medical School Khoo Postdoctoral Fellowship (KPFA/2020/0038) and a National Medical Research Council Open Fund (OFYIRG22jul-0021). C.B. was supported by an NMRC Open Fund—Young Individual Research Grant (OF-YIRG/0048/2017). B.R is a fellow of the National Research Foundation (NRF, Singapore) and Branco Weiss Foundation (Switzerland) and an EMBO Young Investigator. This work was also funded by a Strategic Positioning Fund for Genetic Orphan Diseases (SPF2012/005) and an inaugural A*STAR Investigatorship from the Agency for Science, Technology and Research in Singapore to B.R.; S.-C.Z. was supported by Singapore Ministry of Education Research Fund (MOE2018-T2-2-103); Singapore Ministry of Health Research Fund (MOH-000207 and MOH-000212).en_US
dc.description.pubStatusEarly releaseen_US
dc.description.oaCategoryCCen_US
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