The spindle checkpoint: structural insights into dynamic signalling
Abstract
Chromosome segregation is a complex and astonishingly accurate process whose inner working is beginning to be understood at the molecular level. The spindle checkpoint plays a key role in ensuring the fidelity of this process. It monitors the interactions between chromosomes and microtubules, and delays mitotic progression to allow extra time to correct defects. Here, we review and integrate findings on the dynamics of checkpoint proteins at kinetochores with structural information about signalling complexes.
References
The Saccharomyces cerevisiae spindle pole body duplication gene MPS1 is part of a mitotic checkpoint
Human T cell leukemia virus type 1 oncoprotein Tax targets the human mitotic checkpoint protein MAD1
Cytoplasmic dynein is required for poleward chromosome movement during mitosis in Drosophila embryos
Modes of spindle pole body inheritance and segregation of the Bfa1p-Bub2p checkpoint protein complex
Human Mps1 kinase is required for the spindle assembly checkpoint but not for centrosome duplication
Citations
Dynamics of centromere and kinetochore proteins; implications for checkpoint signaling and silencing
WD repeat-containing mitotic checkpoint proteins act as transcriptional repressors during interphase
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