Distinct roles of spindle checkpoint proteins in meiosis Current Biology Biology Diagrams The spindle assembly checkpoint (SAC) is critical for sensing defective microtubule-kinetochore attachments and tension across the kinetochore and functions to arrest cells in prometaphase to allow time to repair any errors before proceeding into anaphase. Dysregulation of the SAC leads to chromosome segregation errors that have been linked to human diseases like cancer. Although much has During mitosis and meiosis, the spindle assembly checkpoint acts to maintain genome stability by delaying cell division until accurate chromosome segregation can be guaranteed. Accuracy requires that chromosomes become correctly attached to the microtubule spindle apparatus via their kinetochores. When not correctly attached to the spindle, kinetochores activate the spindle assembly checkpoint The spindle assembly checkpoint controls cell cycle progression during mitosis, synchronizing it with the attachment of chromosomes to spindle microtubules. PRP4 is a spindle assembly checkpoint protein required for MPS1, MAD1, and MAD2 localization to the kinetochores. J. Cell Biol. 179, 601-609 10.1083/jcb.200703133 (doi:10.1083/jcb
The spindle assembly checkpoint (SAC) is a pivotal regulatory mechanism during mitosis that ensures accurate chromosome segregation. It functions by monitoring the attachment of chromosomes to the spindle apparatus via the kinetochore, a protein structure that forms on each chromosome [20], [21].
Principles and dynamics of spindle assembly checkpoint signalling Biology Diagrams
Howell, B. J. et al. Cytoplasmic dynein/dynactin drives kinetochore protein transport to the spindle poles and has a role in mitotic spindle checkpoint inactivation. J. Cell Biol. 155 , 1159
They provide a landing platform for the spindle-assembly checkpoint (SAC) proteins 56. The Ndc80/HEC1 complex seems to be directly involved in microtubule binding 80 , 81 . a, Domain organization of key spindle assembly checkpoint (SAC) proteins, where proteins and protein domains are depicted to scale.Binding partners of key domains are indicated and amino acids Abstract. In cells containing disrupted spindles, the spindle assembly checkpoint arrests the cell cycle in metaphase. The budding uninhibited by benzimidazole (Bub) 1, mitotic arrest-deficient (Mad) 1, and Mad2 proteins promote this checkpoint through sustained inhibition of the anaphase-promoting complex/cyclosome.
