Distinct roles of septins in cytokinesis: SEPT9 mediates midbody abscission
Open accessAbstract
Septins are a family of GTP-binding proteins implicated in mammalian cell division. Most studies examining the role of septins in this process have treated the family as a whole, thus neglecting the possibility that individual members may have diverse functions. To address this, we individually depleted each septin family member expressed in HeLa cells by siRNA and assayed for defects in cell division by immunofluorescence and time-lapse microscopy. Depletion of SEPT2, SEPT7, and SEPT11 causes defects in the early stages of cytokinesis, ultimately resulting in binucleation. In sharp contrast, SEPT9 is dispensable for the early stages of cell division, but is critical for the final separation of daughter cells. Rescue experiments indicate that SEPT9 isoforms containing the N-terminal region are sufficient to drive cytokinesis. We demonstrate that SEPT9 mediates the localization of the vesicle-tethering exocyst complex to the midbody, providing mechanistic insight into the role of SEPT9 during abscission.
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Knockdown of Septin 2, 6 or 7 results in similar violent membrane blebbing and abnormal mitotic exit.
“Indeed, knockdown of Septin 2, 6 or 7 has been shown to result in similar violent membrane blebbing and abnormal mitotic exit [28, 29]”
From Tumor Treating Fields Perturb the Localization of Septins and Cause Aberrant Mitotic Exit (2015) · cites this paper as [29]
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Tumor Treating Fields Perturb the Localization of Septins and Cause Aberrant Mitotic Exit
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- Authors
- Estey, M. P., Di Ciano-Oliveira, C., Froese, C. D., Bejide, M. T., & Trimble, W. S.
- Affiliations
- University of Toronto (CA)
- Program in Cell Biology, Hospital for Sick Children, Toronto, Ontario M5G 1X8, Canada 1
- Hospital for Sick Children (CA)
- Corresponding author
- Trimble, William S.
- ORCID
- Trimble, William S.
- Venue
- Journal of Cell Biology
- Publisher
- Rockefeller University Press
- Published
- 2010-11-08
- Volume
- 191
- Issue
- 4
- Pages
- 741-749
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- PMC
- PMC2983063
- OpenAlex
- W2163000142
- Cited by
- 231
- References
- 45
- Citations by year
- 2026: 8 · 2025: 6 · 2024: 9 · 2023: 13 · 2022: 17 · 2021: 17 · 2020: 14 · 2019: 18 · 2018: 20 · 2017: 17 · 2016: 9 · 2015: 13 · 2014: 17 · 2013: 19 · 2012: 18
- FWCI
- 7.28
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- The Journal of Cell Biology (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion, cc-by-nc-sa)
- PubMed (publishedVersion)
- Funders
- Natural Sciences and Engineering Research Council of Canada
- Ontario Ministry of Research and Innovation
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Keywords
- septins, SEPT9, cytokinesis, SEPT2, SEPT7, binucleation, exocyst complex, vesicle tethering, cell division, HeLa cells
- MeSH terms
- Cell Line, Humans, Protein Isoforms, RNA, Small Interfering, Cytokinesis, Septins, Time-Lapse Imaging
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