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Updated: Jun 3, 2026

Associated Chromosome Trap for Identifying Long-range DNA Interactions
Published on: April 23, 2011
DDA3 associates with MCAK and controls chromosome congression
Chang-Young Jang1, Guowei Fang
1School of Pharmacy, Sookmyung Women's University, Seoul 140-742, Republic of Korea. cyjang@sookmyung.ac.kr
Abstract:
DDA3 regulates spindle microtubule (MT) dynamics and chromosome movement in mitosis through its interaction with and subsequent recruitment of Kif2a, a minus end-MT depolymerase. Depletion of DDA3 causes a hyper-stabilization of spindle MT, a loss of inter-kinetochore tension, and a defect in chromosome congression, leading to unaligned chromosomes at metaphase. We report here that DDA3 is also localized at kinetochores and interacts with MCAK. Furthermore, CENP-E, a plus end-motor protein, accumulates at kinetochores in unaligned chromosomes in mitotic cells depleted of DDA3. On the other hand, the localization of chromosomal passenger complex (CPC) and the kinase activity of Aurora B are normal in DDA3-depleted cells. We conclude that MCAK and CENP-E are involved in DDA3-mediated chromosome congression.
Insights
DDA3 protein is crucial for proper chromosome movement during cell division by regulating microtubule dynamics. Its depletion leads to chromosome misalignment, involving MCAK and CENP-E in this process.
Area of Science:
- Cell Biology
- Molecular Biology
- Genetics
Background:
- DDA3 protein regulates spindle microtubule (MT) dynamics and chromosome movement in mitosis.
- Depletion of DDA3 results in hyper-stabilized spindle MT, loss of inter-kinetochore tension, and defective chromosome congression, leading to metaphase chromosome misalignment.
Purpose of the Study:
- To investigate the role of DDA3 in kinetochore function and chromosome congression.
- To identify other proteins involved in DDA3-mediated chromosome alignment.
Main Methods:
- Depletion of DDA3 protein in mitotic cells.
- Immunofluorescence microscopy to assess protein localization.
- Analysis of spindle MT dynamics and chromosome alignment.
Main Results:
- DDA3 is localized at kinetochores and interacts with MCAK.
- CENP-E accumulates at kinetochores in DDA3-depleted cells with unaligned chromosomes.
- Localization and activity of the chromosomal passenger complex (CPC) and Aurora B kinase remain normal in DDA3-depleted cells.
Conclusions:
- DDA3 plays a role in kinetochore-MT attachments and chromosome congression.
- MCAK and CENP-E are identified as key players in DDA3-mediated chromosome alignment during mitosis.
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