Loading and Unloading: Orchestrating Centrosome Duplication and Spindle Assembly by Ran/Crm1

• Published in: Cell cycle (Georgetown, Tex.) Tex.), 2005-11, Vol.4 (11), p.1510-1514
• Main Authors: Budhu, Anuradha S., Wang, Xin W.
• Format: Article
• Language: English
• Subjects: Animals; Binding; Biology; Bioscience; Calcium; Cancer; Cell; Cell Cycle Proteins - chemistry; Cell Cycle Proteins - metabolism; Cell Cycle Proteins - physiology; Centrosome - chemistry; Centrosome - metabolism; Centrosome - physiology; Cycle; Exportin 1 Protein; Humans; Karyopherins - chemistry; Karyopherins - metabolism; Karyopherins - physiology; Landes; Organogenesis; Protein Transport - physiology; Proteins; ran GTP-Binding Protein - chemistry; ran GTP-Binding Protein - metabolism; ran GTP-Binding Protein - physiology; Receptors, Cytoplasmic and Nuclear - chemistry; Receptors, Cytoplasmic and Nuclear - metabolism; Receptors, Cytoplasmic and Nuclear - physiology; Spindle Apparatus - chemistry; Spindle Apparatus - metabolism; Spindle Apparatus - physiology
• ISSN: 1538-4101; 1551-4005
• DOI: 10.4161/cc.4.11.2187

The cell cycle is an intricate process of DNA replication and cell division thatconcludes with the formation of two genetically equivalent daughter cells. In thisprogression, the centrosome is duplicated once and only once during the G1/S transitionto produce the bipolar spindle and ensure proper chromosome segregation. The presenceof multiple centrosomes in cancer cells suggests that this process is mis-regulated duringcarcinogenesis. This suggests that certain factors exist that license the progression ofcentrosome duplication and serve to inhibit further duplications during a single cell cycle.Recent studies suggest that the Ran/Crm1 complex not only regulates nucleocytoplasmictransport but is also independently involved in mitotic spindle assembly. Factors that arecapable of interacting with Ran/Crm1 through their nuclear export sequences, such ascyclins/cdks, p53 and Brca1/2, may potentially function as centrosome checkpoints akinto the G1/S and G2/M checkpoints of the cell cycle. Our recent findings indicate thatnucleophosmin, a protein whose trafficking is mediated by the Ran/Crm1 network, is oneof such checkpoint factors for maintaining proper centrosome duplication. We proposethat Ran/Crm1 may act as a 'loading dock' to coordinate various checkpoint factors inregulating the fidelity of centrosome duplication during cell cycle progression, and thedisruption of these processes may lead to genomic instability and an acceleration ofoncogenesis.