Dr Sharron Vass S.Vass@napier.ac.uk
Lecturer
Dr Sharron Vass S.Vass@napier.ac.uk
Lecturer
Sue Cotterill
Ana M. Valdeolmillos
Jos� L. Barbero
Enmoore Lin
William D. Warren
Margarete M.S. Heck
Background: The coordination of cell cycle events is necessary to ensure the proper duplication and dissemination of the genome. In this study, we examine the consequences of depleting Drad21 and SA, two non-SMC subunits of the cohesin complex, by dsRNA-mediated interference in Drosophila cultured cells.
Results: We have shown that a bona fide cohesin complex exists in Drosophila embryos. Strikingly, the Drad21/Scc1 and SA/Scc3 non-SMC subunits associate more intimately with one another than they do with the SMCs. We have observed defects in mitotic progression in cells from which Drad21 has been depleted: cells delay in prometaphase with normally condensed, but prematurely separated, sister chromatids and with abnormal spindle morphology. Much milder defects are observed when SA is depleted from cells. The dynamics of the chromosome passenger protein, INCENP, are affected after Drad21 depletion. We have also made the surprising observation that SA is unstable in the absence of Drad21; however, we have shown that the converse is not true. Interference with Drad21 in living Drosophila embryos also has deleterious effects on mitotic progression.
Conclusions: We conclude that Drad21, as a member of a cohesin complex, is required in Drosophila cultured cells and embryos for proper mitotic progression. The protein is required in cultured cells for chromosome cohesion, spindle morphology, dynamics of a chromosome passenger protein, and stability of the cohesin complex, but apparently not for normal chromosome condensation. The observation of SA instability in the absence of Drad21 implies that the expression of cohesin subunits and assembly of the cohesin complex will be tightly regulated.
Vass, S., Cotterill, S., Valdeolmillos, A. M., Barbero, J. L., Lin, E., Warren, W. D., & Heck, M. M. (2003). Depletion of Drad21/Scc1 in Drosophila Cells Leads to Instability of the Cohesin Complex and Disruption of Mitotic Progression. Current Biology, 13(3), 208-218. https://doi.org/10.1016/S0960-9822%2803%2900047-2
Journal Article Type | Article |
---|---|
Acceptance Date | Dec 5, 2002 |
Online Publication Date | Feb 6, 2003 |
Publication Date | Feb 4, 2003 |
Deposit Date | Sep 21, 2016 |
Publicly Available Date | Sep 22, 2016 |
Journal | Current Biology |
Print ISSN | 0960-9822 |
Electronic ISSN | 1879-0445 |
Publisher | Elsevier |
Peer Reviewed | Peer Reviewed |
Volume | 13 |
Issue | 3 |
Pages | 208-218 |
DOI | https://doi.org/10.1016/S0960-9822%2803%2900047-2 |
Keywords | cell cycle events, Drosophila, cultured cells, cohesin complex, mitotic progression, |
Public URL | http://researchrepository.napier.ac.uk/Output/369828 |
Contract Date | Sep 21, 2016 |
Vass Et Al. 2003
(717 Kb)
PDF
Margarete Heck (1959–2023): Cell biologist, geneticist, and incandescent social spark
(2023)
Journal Article
A role for the metalloprotease invadolysin in insulin signaling and adipogenesis
(2016)
Journal Article
Impact of Glucocorticoid Induced Reprogramming on Functional, Histological and Molecular Signalling in the Adult Zebrafish Heart
(2015)
Presentation / Conference Contribution
Invadolysin acts genetically via the SAGA complex to modulate chromosome structure
(2015)
Journal Article
About Edinburgh Napier Research Repository
Administrator e-mail: repository@napier.ac.uk
This application uses the following open-source libraries:
Apache License Version 2.0 (http://www.apache.org/licenses/)
Apache License Version 2.0 (http://www.apache.org/licenses/)
SIL OFL 1.1 (http://scripts.sil.org/OFL)
MIT License (http://opensource.org/licenses/mit-license.html)
CC BY 3.0 ( http://creativecommons.org/licenses/by/3.0/)
Powered by Worktribe © 2025
Advanced Search