• Je něco špatně v tomto záznamu ?

Genetic Interactions between the Aurora Kinases Reveal New Requirements for AURKB and AURKC during Oocyte Meiosis

AL. Nguyen, D. Drutovic, BN. Vazquez, W. El Yakoubi, AS. Gentilello, M. Malumbres, P. Solc, K. Schindler,

. 2018 ; 28 (21) : 3458-3468.e5. [pub] 20181025

Jazyk angličtina Země Velká Británie

Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc19045147

Grantová podpora
F31 HD089597 NICHD NIH HHS - United States
R01 GM112801 NIGMS NIH HHS - United States

Errors in chromosome segregation during female meiosis I occur frequently, and aneuploid embryos account for 1/3 of all miscarriages in humans [1]. Unlike mitotic cells that require two Aurora kinase (AURK) homologs to help prevent aneuploidy (AURKA and AURKB), mammalian germ cells also require a third (AURKC) [2, 3]. AURKA is the spindle-pole-associated homolog, and AURKB/C are the chromosome-localized homologs. In mitosis, AURKB has essential roles as the catalytic subunit of the chromosomal passenger complex (CPC), regulating chromosome alignment, kinetochore-microtubule attachments, cohesion, the spindle assembly checkpoint, and cytokinesis [4, 5]. In mouse oocyte meiosis, AURKC takes over as the predominant CPC kinase [6], although the requirement for AURKB remains elusive [7]. In the absence of AURKC, AURKB compensates, making defining potential non-overlapping functions difficult [6, 8]. To investigate the role(s) of AURKB and AURKC in oocytes, we analyzed oocyte-specific Aurkb and Aurkc single- and double-knockout (KO) mice. Surprisingly, we find that double KO female mice are fertile. We demonstrate that, in the absence of AURKC, AURKA localizes to chromosomes in a CPC-dependent manner. These data suggest that AURKC prevents AURKA from localizing to chromosomes by competing for CPC binding. This competition is important for adequate spindle length to support meiosis I. We also describe a unique requirement for AURKB to negatively regulate AURKC to prevent aneuploidy. Together, our work reveals oocyte-specific roles for the AURKs in regulating each other's localization and activity. This inter-kinase regulation is critical to support wild-type levels of fecundity in female mice.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc19045147
003      
CZ-PrNML
005      
20200113081807.0
007      
ta
008      
200109s2018 xxk f 000 0|eng||
009      
AR
024    7_
$a 10.1016/j.cub.2018.08.052 $2 doi
035    __
$a (PubMed)30415701
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxk
100    1_
$a Nguyen, Alexandra L $u Department of Genetics, Rutgers University, 145 Bevier Road, Piscataway, NJ 08854, USA.
245    10
$a Genetic Interactions between the Aurora Kinases Reveal New Requirements for AURKB and AURKC during Oocyte Meiosis / $c AL. Nguyen, D. Drutovic, BN. Vazquez, W. El Yakoubi, AS. Gentilello, M. Malumbres, P. Solc, K. Schindler,
520    9_
$a Errors in chromosome segregation during female meiosis I occur frequently, and aneuploid embryos account for 1/3 of all miscarriages in humans [1]. Unlike mitotic cells that require two Aurora kinase (AURK) homologs to help prevent aneuploidy (AURKA and AURKB), mammalian germ cells also require a third (AURKC) [2, 3]. AURKA is the spindle-pole-associated homolog, and AURKB/C are the chromosome-localized homologs. In mitosis, AURKB has essential roles as the catalytic subunit of the chromosomal passenger complex (CPC), regulating chromosome alignment, kinetochore-microtubule attachments, cohesion, the spindle assembly checkpoint, and cytokinesis [4, 5]. In mouse oocyte meiosis, AURKC takes over as the predominant CPC kinase [6], although the requirement for AURKB remains elusive [7]. In the absence of AURKC, AURKB compensates, making defining potential non-overlapping functions difficult [6, 8]. To investigate the role(s) of AURKB and AURKC in oocytes, we analyzed oocyte-specific Aurkb and Aurkc single- and double-knockout (KO) mice. Surprisingly, we find that double KO female mice are fertile. We demonstrate that, in the absence of AURKC, AURKA localizes to chromosomes in a CPC-dependent manner. These data suggest that AURKC prevents AURKA from localizing to chromosomes by competing for CPC binding. This competition is important for adequate spindle length to support meiosis I. We also describe a unique requirement for AURKB to negatively regulate AURKC to prevent aneuploidy. Together, our work reveals oocyte-specific roles for the AURKs in regulating each other's localization and activity. This inter-kinase regulation is critical to support wild-type levels of fecundity in female mice.
650    _2
$a aneuploidie $7 D000782
650    _2
$a zvířata $7 D000818
650    _2
$a aurora kinasa A $x genetika $x metabolismus $7 D064096
650    _2
$a aurora kinasa B $x genetika $x metabolismus $7 D064107
650    _2
$a aurora kinasa C $x genetika $x metabolismus $7 D064108
650    _2
$a segregace chromozomů $x genetika $7 D020090
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a fertilita $x genetika $7 D005298
650    12
$a meióza $7 D008540
650    _2
$a myši $7 D051379
650    _2
$a oocyty $x metabolismus $7 D009865
655    _2
$a časopisecké články $7 D016428
655    _2
$a Research Support, N.I.H., Extramural $7 D052061
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Drutovic, David $u Institute of Animal Physiology and Genetics, Academy of Sciences of the Czech Republic, Rumburská 89, Libechov 277 21, Czech Republic.
700    1_
$a Vazquez, Berta N $u Department of Genetics, Rutgers University, 145 Bevier Road, Piscataway, NJ 08854, USA.
700    1_
$a El Yakoubi, Warif $u Department of Genetics, Rutgers University, 145 Bevier Road, Piscataway, NJ 08854, USA.
700    1_
$a Gentilello, Amanda S $u Department of Genetics, Rutgers University, 145 Bevier Road, Piscataway, NJ 08854, USA.
700    1_
$a Malumbres, Marcos $u Cell Division and Cancer Group, Spanish National Cancer Research Centre (CNIO), Calle de Melchor Fernández Almagro, 3, Madrid 28029, Spain.
700    1_
$a Solc, Petr $u Institute of Animal Physiology and Genetics, Academy of Sciences of the Czech Republic, Rumburská 89, Libechov 277 21, Czech Republic.
700    1_
$a Schindler, Karen $u Department of Genetics, Rutgers University, 145 Bevier Road, Piscataway, NJ 08854, USA. Electronic address: schindler@dls.rutgers.edu.
773    0_
$w MED00006482 $t Current biology : CB $x 1879-0445 $g Roč. 28, č. 21 (2018), s. 3458-3468.e5
856    41
$u https://pubmed.ncbi.nlm.nih.gov/30415701 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20200109 $b ABA008
991    __
$a 20200113082139 $b ABA008
999    __
$a ok $b bmc $g 1483416 $s 1083820
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2018 $b 28 $c 21 $d 3458-3468.e5 $e 20181025 $i 1879-0445 $m Current biology $n Curr Biol $x MED00006482
GRA    __
$a F31 HD089597 $p NICHD NIH HHS $2 United States
GRA    __
$a R01 GM112801 $p NIGMS NIH HHS $2 United States
LZP    __
$a Pubmed-20200109

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...