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Chromosome biorientation and APC activity remain uncoupled in oocytes with reduced volume

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.
1540-8140
3949-3957
Lane, Simon I.R.
8e80111f-5012-4950-a228-dfb8fb9df52d
Jones, Keith T.
73e8e2b5-cd67-4691-b1a9-4e7bc9066af4
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), 3949-3957. (doi:10.1083/jcb.201606134).

Record type: Article

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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More information

Accepted/In Press date: 7 September 2017
e-pub ahead of print date: 4 October 2017
Published date: 4 December 2017

Identifiers

Local EPrints ID: 414765
URI: http://eprints.soton.ac.uk/id/eprint/414765
ISSN: 1540-8140
PURE UUID: d914d6e8-75b1-4d87-9da0-1e8124eaae44
ORCID for Simon I.R. Lane: ORCID iD orcid.org/0000-0002-8155-0981
ORCID for Keith T. Jones: ORCID iD orcid.org/0000-0002-0294-0851

Catalogue record

Date deposited: 10 Oct 2017 16:31
Last modified: 16 Mar 2024 04:15

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Contributors

Author: Simon I.R. Lane ORCID iD
Author: Keith T. Jones ORCID iD

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