New regulators of mitosis
New regulators of mitosis
Mitosis is essential for accurate chromosome segregation into daughter cells, and defects in this process can lead to aneuploidy and cancer. The M-Cdk complex (Cyclin-Dependent Kinase 1-Cyclin B) is a key regulator of mitosis, phosphorylating substrates to drive mitotic stages such as prophase and anaphase. While several M-Cdk substrates have been characterised, many remain unexplored.
This thesis focuses on KIAA1671 and KIAA1143, identified from a phosphoproteomic screen of MCdk substrates. KIAA1671 showed a distinct mitotic phenotype and was found to influence spindle stability and actin filament organisation during mitosis and interphase. Its role in actin dynamics and spindle assembly, crucial for spindle positioning and chromosome alignment, was investigated. Loss of KIAA1671 causes spindle elongation and delayed mitosis, emphasising its role in mitotic integrity. Phosphorylation of KIAA1671 in prophase and metaphase suggests a regulatory mechanism controlling its spindle interactions.
KIAA1143 localises to RNA-processing foci and plays a role in cell cycle regulation. Its depletion disrupts mitotic timing, implicating it in the control of cell cycle progression.
Cell cycle, Mitosis, KIAA1671, KIAA1143, Actin, Cell division, RNA processing, proteomics
University of Southampton
Adenekan, Fiyinfoluwa Olufemi
7b100e84-4d04-40da-b969-e7f186ee3da0
2025
Adenekan, Fiyinfoluwa Olufemi
7b100e84-4d04-40da-b969-e7f186ee3da0
Przewloka, Marcin
9b25e73c-ec15-43df-a5a4-ac9574bb20ab
Hochegger, Helfrid
fda7b8b7-3352-4561-a6d1-4191e95fe716
Adenekan, Fiyinfoluwa Olufemi
(2025)
New regulators of mitosis.
University of Southampton, Doctoral Thesis, 235pp.
Record type:
Thesis
(Doctoral)
Abstract
Mitosis is essential for accurate chromosome segregation into daughter cells, and defects in this process can lead to aneuploidy and cancer. The M-Cdk complex (Cyclin-Dependent Kinase 1-Cyclin B) is a key regulator of mitosis, phosphorylating substrates to drive mitotic stages such as prophase and anaphase. While several M-Cdk substrates have been characterised, many remain unexplored.
This thesis focuses on KIAA1671 and KIAA1143, identified from a phosphoproteomic screen of MCdk substrates. KIAA1671 showed a distinct mitotic phenotype and was found to influence spindle stability and actin filament organisation during mitosis and interphase. Its role in actin dynamics and spindle assembly, crucial for spindle positioning and chromosome alignment, was investigated. Loss of KIAA1671 causes spindle elongation and delayed mitosis, emphasising its role in mitotic integrity. Phosphorylation of KIAA1671 in prophase and metaphase suggests a regulatory mechanism controlling its spindle interactions.
KIAA1143 localises to RNA-processing foci and plays a role in cell cycle regulation. Its depletion disrupts mitotic timing, implicating it in the control of cell cycle progression.
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New Cell Regulators of Mitosis
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Published date: 2025
Keywords:
Cell cycle, Mitosis, KIAA1671, KIAA1143, Actin, Cell division, RNA processing, proteomics
Identifiers
Local EPrints ID: 505496
URI: http://eprints.soton.ac.uk/id/eprint/505496
PURE UUID: a91d25ae-b0f2-4641-8a9f-2d0ce763a594
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Date deposited: 10 Oct 2025 16:36
Last modified: 11 Oct 2025 02:10
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Contributors
Thesis advisor:
Helfrid Hochegger
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