Javascript must be enabled to continue!
Abstract 1638: Regulation of spindle pole integrity by the MASTL-ENSA-aurora a pathway during mitosis
View through CrossRef
Abstract
The preservation of spindle pole integrity is crucial for proper spindle assembly and chromosome segregation in mitosis, yet the precise mechanisms governing spindle pole integrity remain elusive. During mitosis, phosphorylated Ensa (p-ENSA) localizes to spindle poles, and the inhibition of ENSA leads to a range of mitotic defects, including misaligned chromosomes, multipolar spindles, asymmetric bipolar spindles, and centrosome aberrations, resulting in a delayed mitotic progression. Remarkably, the mitotic delay induced by ENSA inhibition is alleviated upon depletion of PP2A-B55α, but spindle pole defects persist. Significantly, we have observed an interaction between ENSA and Aurora A during mitosis, and the inhibition of ENSA diminishes Aurora A expression at the mitotic spindle poles. Intriguingly, the injection of MKI-2-sensitized tumors is associated with heightened chromosomal instability and downregulation of the MASTL-ENSA-Aurora A pathway in an orthotopic breast cancer mouse model. These findings offer new insights into the regulation of spindle pole integrity through the MASTL-ENSA-Aurora A pathway during mitosis, emphasizing the pivotal role of ENSA in recruiting Aurora A to the spindle pole, independently of PP2A-B55α.
Citation Format: Seul Kim, Kyoungho Jun, Ye-Hyun Kim, Jae Sung Kim. Regulation of spindle pole integrity by the MASTL-ENSA-aurora a pathway during mitosis [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2024; Part 1 (Regular Abstracts); 2024 Apr 5-10; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2024;84(6_Suppl):Abstract nr 1638.
American Association for Cancer Research (AACR)
Title: Abstract 1638: Regulation of spindle pole integrity by the MASTL-ENSA-aurora a pathway during mitosis
Description:
Abstract
The preservation of spindle pole integrity is crucial for proper spindle assembly and chromosome segregation in mitosis, yet the precise mechanisms governing spindle pole integrity remain elusive.
During mitosis, phosphorylated Ensa (p-ENSA) localizes to spindle poles, and the inhibition of ENSA leads to a range of mitotic defects, including misaligned chromosomes, multipolar spindles, asymmetric bipolar spindles, and centrosome aberrations, resulting in a delayed mitotic progression.
Remarkably, the mitotic delay induced by ENSA inhibition is alleviated upon depletion of PP2A-B55α, but spindle pole defects persist.
Significantly, we have observed an interaction between ENSA and Aurora A during mitosis, and the inhibition of ENSA diminishes Aurora A expression at the mitotic spindle poles.
Intriguingly, the injection of MKI-2-sensitized tumors is associated with heightened chromosomal instability and downregulation of the MASTL-ENSA-Aurora A pathway in an orthotopic breast cancer mouse model.
These findings offer new insights into the regulation of spindle pole integrity through the MASTL-ENSA-Aurora A pathway during mitosis, emphasizing the pivotal role of ENSA in recruiting Aurora A to the spindle pole, independently of PP2A-B55α.
Citation Format: Seul Kim, Kyoungho Jun, Ye-Hyun Kim, Jae Sung Kim.
Regulation of spindle pole integrity by the MASTL-ENSA-aurora a pathway during mitosis [abstract].
In: Proceedings of the American Association for Cancer Research Annual Meeting 2024; Part 1 (Regular Abstracts); 2024 Apr 5-10; San Diego, CA.
Philadelphia (PA): AACR; Cancer Res 2024;84(6_Suppl):Abstract nr 1638.
Related Results
In Cellulo Kinase Screen Identifies Potential MASTL Substrates
In Cellulo Kinase Screen Identifies Potential MASTL Substrates
Abstract
MASTL (microtubule-associated serine/threonine kinase-like) has emerged as a critical regulator of mitosis and as a potential oncogene in a variety of cancer types...
SILAC kinase screen identifies potential MASTL substrates
SILAC kinase screen identifies potential MASTL substrates
AbstractMicrotubule-associated serine/threonine kinase-like (MASTL) has emerged as a critical regulator of mitosis and as a potential oncogene in a variety of cancer types. To date...
Aurora-A Kinase: A Novel Target for the Immunotherapy Against Human Leukemias.
Aurora-A Kinase: A Novel Target for the Immunotherapy Against Human Leukemias.
Abstract
Aurora-A kinase (Aurora-A) is one of the serine/threonine kinase families, which is located on the long arm of chromosome 20q13, is mainly expressed in G2/M...
Chromosome biorientation requires Aurora B’s spatial separation from its outer kinetochore substrates but not its turnover at kinetochores
Chromosome biorientation requires Aurora B’s spatial separation from its outer kinetochore substrates but not its turnover at kinetochores
SummaryFor correct chromosome segregation in mitosis, sister kinetochores must interact with microtubules from opposite spindle poles (biorientation). For this, aberrant kinetochor...
NuSAP1 promotes bipolar spindle assembly in
Trypanosoma brucei
by bundling spindle microtubules
NuSAP1 promotes bipolar spindle assembly in
Trypanosoma brucei
by bundling spindle microtubules
Abstract
The parasitic protozoan
Trypanosoma brucei
assembles a bipolar mitotic spindle and undergoes a close...
Experimental analysis of the reproduction of spindle poles
Experimental analysis of the reproduction of spindle poles
ABSTRACT
We have investigated the functional properties of the mechanisms that control the reproduction of spindle poles in fertilized sea-urchin eggs. By prolonging...
Abstract 1619: Discovering a new physiological substrate of Aurora-A kinase
Abstract 1619: Discovering a new physiological substrate of Aurora-A kinase
Abstract
Aurora-A is a serine/threonine kinase that has oncogenic properties in vivo. The expression and kinase activity of Aurora-A are up-regulated in many cancers...
Microtubule pivoting driven by spindle elongation rescues polar chromosomes to ensure faithful mitosis
Microtubule pivoting driven by spindle elongation rescues polar chromosomes to ensure faithful mitosis
Abstract
Polar chromosomes represent a subset of ~7 chromosomes in human cells that initially attach to the mitotic spindle behind the spindle pole. These chromosom...

