A mathematical model of Aurora B activity in prophase and metaphase

Doherty, Kevin; Meere, Martin; Piiroinen, Petri T.

doi:10.1016/j.mbs.2016.04.013

Cited by 1 publication

(1 citation statement)

References 107 publications

(167 reference statements)

Supporting

Mentioning

Contrasting

Order By: Relevance

“…Such mechanisms may involve dynamic regulation of CPC (including Aurora B). For example, the following mechanisms are suggested: First, CPC may be released from its localization sites and reach the substrates of Aurora B kinase at the outer kinetochores [65,89]. If the localization sites are closer to the substrates, CPC would reach substrates more frequently.…”

Section: Other Mechanisms Regulating the Kinetochore-mt Interactions ...mentioning

confidence: 99%

SWAP, SWITCH, and STABILIZE: Mechanisms of Kinetochore–Microtubule Error Correction

Tanaka

Zhang

2022

Cells

View full text Add to dashboard Cite

For correct chromosome segregation in mitosis, eukaryotic cells must establish chromosome biorientation where sister kinetochores attach to microtubules extending from opposite spindle poles. To establish biorientation, any aberrant kinetochore–microtubule interactions must be resolved in the process called error correction. For resolution of the aberrant interactions in error correction, kinetochore–microtubule interactions must be exchanged until biorientation is formed (the SWAP process). At initiation of biorientation, the state of weak kinetochore–microtubule interactions should be converted to the state of stable interactions (the SWITCH process)—the conundrum of this conversion is called the initiation problem of biorientation. Once biorientation is established, tension is applied on kinetochore–microtubule interactions, which stabilizes the interactions (the STABILIZE process). Aurora B kinase plays central roles in promoting error correction, and Mps1 kinase and Stu2 microtubule polymerase also play important roles. In this article, we review mechanisms of error correction by considering the SWAP, SWITCH, and STABILIZE processes. We mainly focus on mechanisms found in budding yeast, where only one microtubule attaches to a single kinetochore at biorientation, making the error correction mechanisms relatively simpler.

show abstract

Section: Other Mechanisms Regulating the Kinetochore-mt Interactions ...mentioning

confidence: 99%