Detail
Article
Online article
FT
Medvik - BMC
  • 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,

. 2012 ; 11 (16) : 3011-8.

Language English Country United States

Document type Journal Article, Research Support, Non-U.S. Gov't

E-resources Online Full text

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

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

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...