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세포분열 과정에서의 Mis18α 인산화에 대한 기능 연구 : Functional studies on the phosphorylation of Mis18α in the regulation of cell division
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- Authors
- Advisor
- 백성희
- Major
- 자연과학대학 생명과학부
- Issue Date
- 2018-02
- Publisher
- 서울대학교 대학원
- Keywords
- Mis18α ; Aurora B kinase ; PLK1 ; Mitosis-specific phosphorylation ; Polo Box Domain ; kinetochore
- Description
- 학위논문 (박사)-- 서울대학교 대학원 : 자연과학대학 생명과학부, 2018. 2. 백성희.
- Abstract
- Mis18α, a component of Mis18 complex comprising of Mis18α, Mis18β, and M18BP1, is known to localize at the centromere from late telophase to early G1 phase and plays a priming role in CENP-A deposition. Although its role in CENP-A deposition is well established, the other function of Mis18α remains unknown. Here, I elucidate a new function of Mis18α that is critical for the proper progression of cell cycle independent of its role in CENP-A deposition. I find that Aurora B kinase phosphorylates Mis18α during mitosis not affecting neither centromere localization of Mis18 complex nor centromere loading of CENP-A. However, the replacement of endogenous Mis18α by phosphorylation-defective mutant causes mitotic defects including micronuclei formation, chromosome misalignment, and the chromatin bridges or lagging chromatids. Interestingly, PLK1, another mitotic kinase, shows decreased recruitment in Mis18α phosphorylation-defective cell lines. PBD of PLK1 recognizes Mis18α phosphorylation so that its kinetochore recruitment can be enhanced. Together, my data demonstrate that Aurora B kinase-mediated mitotic phosphorylation of Mis18α is a crucial event for faithful cell cycle progression through the enhanced recruitment of PLK1 to the kinetochore.
- Language
- Korean
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