| Literature DB >> 28834753 |
Marco R Cosenza1, Anna Cazzola1, Annik Rossberg1, Nicole L Schieber2, Gleb Konotop3, Elena Bausch1, Alla Slynko4, Tim Holland-Letz4, Marc S Raab5, Taronish Dubash6, Hanno Glimm6, Sven Poppelreuther7, Christel Herold-Mende8, Yannick Schwab2, Alwin Krämer9.
Abstract
Chromosomal instability is a hallmark of cancer and correlates with the presence of extra centrosomes, which originate from centriole overduplication. Overduplicated centrioles lead to the formation of centriole rosettes, which mature into supernumerary centrosomes in the subsequent cell cycle. While extra centrosomes promote chromosome missegregation by clustering into pseudo-bipolar spindles, the contribution of centriole rosettes to chromosome missegregation is unknown. We used multi-modal imaging of cells with conditional centriole overduplication to show that mitotic rosettes in bipolar spindles frequently harbor unequal centriole numbers, leading to biased chromosome capture that favors binding to the prominent pole. This results in chromosome missegregation and aneuploidy. Rosette mitoses lead to viable offspring and significantly contribute to progeny production. We further show that centrosome abnormalities in primary human malignancies frequently consist of centriole rosettes. As asymmetric centriole rosettes generate mitotic errors that can be propagated, rosette mitoses are sufficient to cause chromosome missegregation in cancer.Entities:
Keywords: PLK4; STIL; cancer; centriole; centrosome; chromosomal instability; chromosome missegregation; merotely; microtubule; mitosis
Mesh:
Year: 2017 PMID: 28834753 DOI: 10.1016/j.celrep.2017.08.005
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423