Chromosome biorientation and APC activity remain uncoupled in oocytes with reduced volume
Chromosome biorientation and APC activity remain uncoupled in oocytes with reduced volume
The spindle assembly checkpoint (SAC) prevents chromosome mis-segregation by coupling anaphase-onset with correct chromosome attachment and tension to microtubules. It does this by generating a diffusible signal from free kinetochores into the cytoplasm, inhibiting the anaphase-promoting complex (APC). The volume in which this signal remains effective is unknown. This raises the possibility that cell volume may be the reason why the SAC is weak, and chromosome segregation error-prone, in mammalian oocytes. Here, by a process of serial bisection, we analyzed the influence of oocyte volume on the ability of the SAC to inhibit bivalent segregation in meiosis I. We were able to generate oocytes with cytoplasmic volumes reduced by 86% and observed changes in APC activity consistent with increased SAC control. However, bivalent biorientation remained uncoupled from APC activity, leading to error-prone chromosome segregation. We conclude that volume is one factor contributing to SAC weakness in oocytes. However additional factors likely uncouple chromosome biorientation with APC activity.
3949-3957
Lane, Simon I.R.
8e80111f-5012-4950-a228-dfb8fb9df52d
Jones, Keith T.
73e8e2b5-cd67-4691-b1a9-4e7bc9066af4
4 December 2017
Lane, Simon I.R.
8e80111f-5012-4950-a228-dfb8fb9df52d
Jones, Keith T.
73e8e2b5-cd67-4691-b1a9-4e7bc9066af4
Lane, Simon I.R. and Jones, Keith T.
(2017)
Chromosome biorientation and APC activity remain uncoupled in oocytes with reduced volume.
Journal of Cell Biology, 216 (12), .
(doi:10.1083/jcb.201606134).
Abstract
The spindle assembly checkpoint (SAC) prevents chromosome mis-segregation by coupling anaphase-onset with correct chromosome attachment and tension to microtubules. It does this by generating a diffusible signal from free kinetochores into the cytoplasm, inhibiting the anaphase-promoting complex (APC). The volume in which this signal remains effective is unknown. This raises the possibility that cell volume may be the reason why the SAC is weak, and chromosome segregation error-prone, in mammalian oocytes. Here, by a process of serial bisection, we analyzed the influence of oocyte volume on the ability of the SAC to inhibit bivalent segregation in meiosis I. We were able to generate oocytes with cytoplasmic volumes reduced by 86% and observed changes in APC activity consistent with increased SAC control. However, bivalent biorientation remained uncoupled from APC activity, leading to error-prone chromosome segregation. We conclude that volume is one factor contributing to SAC weakness in oocytes. However additional factors likely uncouple chromosome biorientation with APC activity.
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Lane and Jones 2017_JCB
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jcb.201606134.full
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Accepted/In Press date: 7 September 2017
e-pub ahead of print date: 4 October 2017
Published date: 4 December 2017
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Local EPrints ID: 414765
URI: http://eprints.soton.ac.uk/id/eprint/414765
ISSN: 1540-8140
PURE UUID: d914d6e8-75b1-4d87-9da0-1e8124eaae44
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Date deposited: 10 Oct 2017 16:31
Last modified: 16 Mar 2024 04:15
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Author:
Simon I.R. Lane
Author:
Keith T. Jones
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