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New regulators of mitosis

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
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 - Version of Record
Restricted to Repository staff only until 27 February 2026.
Available under License University of Southampton Thesis Licence.
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Final-thesis-submission-Examination-Mr-Fiyin-Adenekan
Restricted to Repository staff only

More information

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
ORCID for Fiyinfoluwa Olufemi Adenekan: ORCID iD orcid.org/0009-0003-7654-3044
ORCID for Marcin Przewloka: ORCID iD orcid.org/0000-0002-0329-9162

Catalogue record

Date deposited: 10 Oct 2025 16:36
Last modified: 11 Oct 2025 02:10

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Contributors

Thesis advisor: Marcin Przewloka ORCID iD
Thesis advisor: Helfrid Hochegger

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