-
Something wrong with this record ?
Lack of response to unaligned chromosomes in mammalian female gametes
J. Sebestova, A. Danylevska, L. Novakova, M. Kubelka, M. Anger,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Free Medical Journals
from 2002 to 1 year ago
PubMed Central
from 2009 to 1 year ago
Europe PubMed Central
from 2009 to 1 year ago
PubMed
22871737
DOI
10.4161/cc.21398
Knihovny.cz E-resources
- MeSH
- Anaphase MeSH
- Aneuploidy MeSH
- Time-Lapse Imaging methods MeSH
- Histones genetics metabolism MeSH
- Kinetochores metabolism MeSH
- Ubiquitin-Protein Ligase Complexes genetics metabolism MeSH
- Microscopy, Confocal methods MeSH
- M Phase Cell Cycle Checkpoints MeSH
- Metaphase MeSH
- Microinjections MeSH
- Mice, Inbred C57BL MeSH
- Mice MeSH
- Oocytes cytology metabolism MeSH
- Chromosome Pairing * MeSH
- Proteolysis MeSH
- Chromosomes, Mammalian genetics metabolism MeSH
- Mammals MeSH
- Chromosome Segregation * MeSH
- Carrier Proteins genetics metabolism MeSH
- Tubulin genetics metabolism MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Chromosome segregation errors are highly frequent in mammalian female meiosis, and their incidence gradually increases with maternal age. The fate of aneuploid eggs is obviously dependent on the stringency of mechanisms for detecting unattached or repairing incorrectly attached kinetochores. In case of their failure, the newly formed embryo will inherit the impaired set of chromosomes, which will have severe consequences for its further development. Whether spindle assembly checkpoint (SAC) in oocytes is capable of arresting cell cycle progression in response to unaligned kinetochores was discussed for a long time. It is known that abolishing SAC increases frequency of chromosome segregation errors and causes precocious entry into anaphase; SAC, therefore, seems to be essential for normal chromosome segregation in meiosis I. However, it was also reported that for anaphase-promoting complex (APC) activation, which is a prerequisite for entering anaphase; alignment of only a critical mass of kinetochores on equatorial plane is sufficient. This indicates that the function of SAC and of cooperating chromosome attachment correction mechanisms in oocytes is different from somatic cells. To analyze this phenomenon, we used live cell confocal microscopy to monitor chromosome movements, spindle formation, APC activation and polar body extrusion (PBE) simultaneously in individual oocytes at various time points during first meiotic division. Our results, using oocytes from aged animals and interspecific crosses, demonstrate that multiple unaligned kinetochores and severe congression defects are tolerated at the metaphase to anaphase transition, although such cells retain sensitivity to nocodazole. This indicates that checkpoint mechanisms, operating in oocytes at this point, are essential for accurate timing of APC activation in meiosis I, but they are insufficient in detection or correction of unaligned chromosomes, preparing thus conditions for propagation of the aneuploidy to the embryo.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc13012556
- 003
- CZ-PrNML
- 005
- 20240326132931.0
- 007
- ta
- 008
- 130404s2012 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.4161/cc.21398 $2 doi
- 035 __
- $a (PubMed)22871737
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Sebestova, Jaroslava $u Institute of Animal Physiology and Genetics, Libechov, Czech Republic.
- 245 10
- $a Lack of response to unaligned chromosomes in mammalian female gametes / $c J. Sebestova, A. Danylevska, L. Novakova, M. Kubelka, M. Anger,
- 520 9_
- $a Chromosome segregation errors are highly frequent in mammalian female meiosis, and their incidence gradually increases with maternal age. The fate of aneuploid eggs is obviously dependent on the stringency of mechanisms for detecting unattached or repairing incorrectly attached kinetochores. In case of their failure, the newly formed embryo will inherit the impaired set of chromosomes, which will have severe consequences for its further development. Whether spindle assembly checkpoint (SAC) in oocytes is capable of arresting cell cycle progression in response to unaligned kinetochores was discussed for a long time. It is known that abolishing SAC increases frequency of chromosome segregation errors and causes precocious entry into anaphase; SAC, therefore, seems to be essential for normal chromosome segregation in meiosis I. However, it was also reported that for anaphase-promoting complex (APC) activation, which is a prerequisite for entering anaphase; alignment of only a critical mass of kinetochores on equatorial plane is sufficient. This indicates that the function of SAC and of cooperating chromosome attachment correction mechanisms in oocytes is different from somatic cells. To analyze this phenomenon, we used live cell confocal microscopy to monitor chromosome movements, spindle formation, APC activation and polar body extrusion (PBE) simultaneously in individual oocytes at various time points during first meiotic division. Our results, using oocytes from aged animals and interspecific crosses, demonstrate that multiple unaligned kinetochores and severe congression defects are tolerated at the metaphase to anaphase transition, although such cells retain sensitivity to nocodazole. This indicates that checkpoint mechanisms, operating in oocytes at this point, are essential for accurate timing of APC activation in meiosis I, but they are insufficient in detection or correction of unaligned chromosomes, preparing thus conditions for propagation of the aneuploidy to the embryo.
- 650 _2
- $a anafáze $7 D000705
- 650 _2
- $a aneuploidie $7 D000782
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a transportní proteiny $x genetika $x metabolismus $7 D002352
- 650 12
- $a párování chromozomů $7 D023902
- 650 12
- $a segregace chromozomů $7 D020090
- 650 _2
- $a savčí chromozomy $x genetika $x metabolismus $7 D033481
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a histony $x genetika $x metabolismus $7 D006657
- 650 _2
- $a kinetochory $x metabolismus $7 D018386
- 650 _2
- $a kontrolní body M fáze buněčného cyklu $7 D059566
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a savci $7 D008322
- 650 _2
- $a metafáze $7 D008677
- 650 _2
- $a myši $7 D051379
- 650 _2
- $a myši inbrední C57BL $7 D008810
- 650 _2
- $a mikroinjekce $7 D008845
- 650 _2
- $a konfokální mikroskopie $x metody $7 D018613
- 650 _2
- $a oocyty $x cytologie $x metabolismus $7 D009865
- 650 _2
- $a proteolýza $7 D059748
- 650 _2
- $a časosběrné zobrazování $x metody $7 D059008
- 650 _2
- $a tubulin $x genetika $x metabolismus $7 D014404
- 650 _2
- $a komplexy ubikvitinligas $x genetika $x metabolismus $7 D043743
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Mac Gillavry Danylevska, Anna, $d 1983- $7 xx0315558
- 700 1_
- $a Novakova, Lucia
- 700 1_
- $a Kubelka, Michal
- 700 1_
- $a Anger, Martin $7 gn_A_00006952
- 773 0_
- $w MED00173232 $t Cell Cycle $x 1551-4005 $g Roč. 11, č. 16 (2012), s. 3011-8
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/22871737 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20130404 $b ABA008
- 991 __
- $a 20240326132928 $b ABA008
- 999 __
- $a ok $b bmc $g 975754 $s 810837
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2012 $b 11 $c 16 $d 3011-8 $i 1551-4005 $m Cell Cycle $n Cell Cycle $x MED00173232
- LZP __
- $a Pubmed-20130404