• Je něco špatně v tomto záznamu ?

Regulation of 4E-BP1 activity in the mammalian oocyte

D. Jansova, M. Koncicka, A. Tetkova, R. Cerna, R. Malik, E. Del Llano, M. Kubelka, A. Susor,

. 2017 ; 16 (10) : 927-939. [pub] 20170308

Jazyk angličtina Země Spojené státy americké

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc18010762
E-zdroje Online Plný text

NLK Free Medical Journals od 2002 do Před 1 rokem
PubMed Central od 2009 do Před 1 rokem
Europe PubMed Central od 2009 do Před 1 rokem

Fully grown mammalian oocytes utilize transcripts synthetized and stored during earlier development. RNA localization followed by a local translation is a mechanism responsible for the regulation of spatial and temporal gene expression. Here we show that the mouse oocyte contains 3 forms of cap-dependent translational repressor expressed on the mRNA level: 4E-BP1, 4E-BP2 and 4E-BP3. However, only 4E-BP1 is present as a protein in oocytes, it becomes inactivated by phosphorylation after nuclear envelope breakdown and as such it promotes cap-dependent translation after NEBD. Phosphorylation of 4E-BP1 can be seen in the oocytes after resumption of meiosis but it is not detected in the surrounding cumulus cells, indicating that 4E-BP1 promotes translation at a specific cell cycle stage. Our immunofluorescence analyses of 4E-BP1 in oocytes during meiosis I showed an even localization of global 4E-BP1, as well as of its 4E-BP1 (Thr37/46) phosphorylated form. On the other hand, 4E-BP1 phosphorylated on Ser65 is localized at the spindle poles, and 4E-BP1 phosphorylated on Thr70 localizes on the spindle. We further show that the main positive regulators of 4E-BP1 phosphorylation after NEBD are mTOR and CDK1 kinases, but not PLK1 kinase. CDK1 exerts its activity toward 4E-BP1 phosphorylation via phosphorylation and activation of mTOR. Moreover, both CDK1 and phosphorylated mTOR co-localize with 4E-BP1 phosphorylated on Thr70 on the spindle at the onset of meiotic resumption. Expression of the dominant negative 4E-BP1 mutant adversely affects translation and results in spindle abnormality. Taken together, our results show that the phosphorylation of 4E-BP1 promotes translation at the onset of meiosis to support the spindle assembly and suggest an important role of CDK1 and mTOR kinases in this process. We also show that the mTOR regulatory pathway is present in human oocytes and is likely to function in a similar way as in mouse oocytes.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc18010762
003      
CZ-PrNML
005      
20180419085104.0
007      
ta
008      
180404s2017 xxu f 000 0|eng||
009      
AR
024    7_
$a 10.1080/15384101.2017.1295178 $2 doi
035    __
$a (PubMed)28272965
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxu
100    1_
$a Jansova, Denisa $u a Institute of Animal Physiology and Genetics, ASC , Libechov , Czech Republic.
245    10
$a Regulation of 4E-BP1 activity in the mammalian oocyte / $c D. Jansova, M. Koncicka, A. Tetkova, R. Cerna, R. Malik, E. Del Llano, M. Kubelka, A. Susor,
520    9_
$a Fully grown mammalian oocytes utilize transcripts synthetized and stored during earlier development. RNA localization followed by a local translation is a mechanism responsible for the regulation of spatial and temporal gene expression. Here we show that the mouse oocyte contains 3 forms of cap-dependent translational repressor expressed on the mRNA level: 4E-BP1, 4E-BP2 and 4E-BP3. However, only 4E-BP1 is present as a protein in oocytes, it becomes inactivated by phosphorylation after nuclear envelope breakdown and as such it promotes cap-dependent translation after NEBD. Phosphorylation of 4E-BP1 can be seen in the oocytes after resumption of meiosis but it is not detected in the surrounding cumulus cells, indicating that 4E-BP1 promotes translation at a specific cell cycle stage. Our immunofluorescence analyses of 4E-BP1 in oocytes during meiosis I showed an even localization of global 4E-BP1, as well as of its 4E-BP1 (Thr37/46) phosphorylated form. On the other hand, 4E-BP1 phosphorylated on Ser65 is localized at the spindle poles, and 4E-BP1 phosphorylated on Thr70 localizes on the spindle. We further show that the main positive regulators of 4E-BP1 phosphorylation after NEBD are mTOR and CDK1 kinases, but not PLK1 kinase. CDK1 exerts its activity toward 4E-BP1 phosphorylation via phosphorylation and activation of mTOR. Moreover, both CDK1 and phosphorylated mTOR co-localize with 4E-BP1 phosphorylated on Thr70 on the spindle at the onset of meiotic resumption. Expression of the dominant negative 4E-BP1 mutant adversely affects translation and results in spindle abnormality. Taken together, our results show that the phosphorylation of 4E-BP1 promotes translation at the onset of meiosis to support the spindle assembly and suggest an important role of CDK1 and mTOR kinases in this process. We also show that the mTOR regulatory pathway is present in human oocytes and is likely to function in a similar way as in mouse oocytes.
650    _2
$a zvířata $7 D000818
650    _2
$a proteinkinasa CDC2 $x genetika $7 D016203
650    _2
$a transportní proteiny $x genetika $x metabolismus $7 D002352
650    _2
$a buněčný cyklus $x genetika $7 D002453
650    _2
$a vývojová regulace genové exprese $7 D018507
650    _2
$a lidé $7 D006801
650    _2
$a myši $7 D051379
650    _2
$a oocyty $x růst a vývoj $x metabolismus $7 D009865
650    _2
$a fosfoproteiny $x genetika $x metabolismus $7 D010750
650    _2
$a fosforylace $7 D010766
650    _2
$a proteosyntéza $7 D014176
650    _2
$a aparát dělícího vřeténka $x genetika $7 D008941
650    _2
$a TOR serin-threoninkinasy $x genetika $7 D058570
655    _2
$a časopisecké články $7 D016428
700    1_
$a Koncicka, Marketa $u a Institute of Animal Physiology and Genetics, ASC , Libechov , Czech Republic.
700    1_
$a Tetkova, Anna $u a Institute of Animal Physiology and Genetics, ASC , Libechov , Czech Republic.
700    1_
$a Cerna, Renata $u a Institute of Animal Physiology and Genetics, ASC , Libechov , Czech Republic.
700    1_
$a Malik, Radek $u b Institute of Molecular Genetics, ASCR , Prague , Czech Republic.
700    1_
$a Del Llano, Edgar $u a Institute of Animal Physiology and Genetics, ASC , Libechov , Czech Republic.
700    1_
$a Kubelka, Michal $u a Institute of Animal Physiology and Genetics, ASC , Libechov , Czech Republic.
700    1_
$a Susor, Andrej $u a Institute of Animal Physiology and Genetics, ASC , Libechov , Czech Republic.
773    0_
$w MED00173232 $t Cell cycle $x 1551-4005 $g Roč. 16, č. 10 (2017), s. 927-939
856    41
$u https://pubmed.ncbi.nlm.nih.gov/28272965 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20180404 $b ABA008
991    __
$a 20180419085204 $b ABA008
999    __
$a ok $b bmc $g 1288247 $s 1007574
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2017 $b 16 $c 10 $d 927-939 $e 20170308 $i 1551-4005 $m Cell Cycle $n Cell Cycle $x MED00173232
LZP    __
$a Pubmed-20180404

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...