-
Je něco špatně v tomto záznamu ?
Inhibition of Skp1-Cullin-F-box complexes during bovine oocyte maturation and preimplantation development leads to delayed development of embryos†
V. Kinterova, J. Kanka, V. Petruskova, T. Toralova,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Free Medical Journals
od 1969
ProQuest Central
od 2017-01-01 do Před 1 rokem
Open Access Digital Library
od 1969-04-01
Health & Medicine (ProQuest)
od 2017-01-01 do Před 1 rokem
PubMed
30535233
DOI
10.1093/biolre/ioy254
Knihovny.cz E-zdroje
- MeSH
- blastocysta cytologie účinky léků fyziologie MeSH
- časové faktory MeSH
- cyklopentany farmakologie MeSH
- embryo savčí MeSH
- embryonální vývoj účinky léků MeSH
- IVM techniky metody veterinární MeSH
- kultivované buňky MeSH
- multiproteinové komplexy antagonisté a inhibitory metabolismus MeSH
- oocyty cytologie účinky léků fyziologie MeSH
- oogeneze účinky léků MeSH
- proteinligasy komplexu SCF antagonisté a inhibitory metabolismus fyziologie MeSH
- pyrimidiny farmakologie MeSH
- skot MeSH
- zvířata MeSH
- Check Tag
- skot MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
The mechanism of maternal protein degradation during preimplantation development has not been clarified yet. It is thought that a lot of maternal proteins are degraded by the ubiquitin-proteasome system. In this study, we focused on the role of the SCF (Skp1-Cullin-F-box) complexes during early bovine embryogenesis. We inhibited them using MLN4924, an inhibitor of SCF complex ligases controlled by neddylation. Oocytes maturated in MLN4924 could be fertilized, but we found no cumulus cell expansion and a high number of polyspermy after in vitro fertilization. We also found a statistically significant deterioration of development after MLN4924 treatment. After treatment with MLN4924 from the four-cell to late eight-cell stage, we found a statistically significant delay in their development; some of the treated embryos were, however, able to reach the blastocyst stage later. We found reduced levels of mRNA of EGA markers PAPOLA and U2AF1A, which can be related to this developmental delay. The cultivation with MLN4924 caused a significant increase in protein levels in MLN4924-treated oocytes and embryos; no such change was found in cumulus cells. To detect the proteins affected by MLN4924 treatment, we performed a Western blot analysis of selected proteins (SMAD4, ribosomal protein S6, centromeric protein E, P27, NFKB inhibitor alpha, RNA-binding motif protein 19). No statistically significant increase in protein levels was detected in either treated embryos or oocytes. In summary, our study shows that SCF ligases are necessary for the correct maturation of oocytes, cumulus cell expansion, fertilization, and early preimplantation development of cattle.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc20022792
- 003
- CZ-PrNML
- 005
- 20201214124819.0
- 007
- ta
- 008
- 201125s2019 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1093/biolre/ioy254 $2 doi
- 035 __
- $a (PubMed)30535233
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Kinterova, Veronika $u Laboratory of Developmental Biology, Institute of Animal Physiology and Genetics Academy of Science of Czech Republic, v.v.i., Libechov, Czech Republic. Department of Veterinary Sciences, Czech University of Life Sciences in Prague, Prague, Czech Republic.
- 245 10
- $a Inhibition of Skp1-Cullin-F-box complexes during bovine oocyte maturation and preimplantation development leads to delayed development of embryos† / $c V. Kinterova, J. Kanka, V. Petruskova, T. Toralova,
- 520 9_
- $a The mechanism of maternal protein degradation during preimplantation development has not been clarified yet. It is thought that a lot of maternal proteins are degraded by the ubiquitin-proteasome system. In this study, we focused on the role of the SCF (Skp1-Cullin-F-box) complexes during early bovine embryogenesis. We inhibited them using MLN4924, an inhibitor of SCF complex ligases controlled by neddylation. Oocytes maturated in MLN4924 could be fertilized, but we found no cumulus cell expansion and a high number of polyspermy after in vitro fertilization. We also found a statistically significant deterioration of development after MLN4924 treatment. After treatment with MLN4924 from the four-cell to late eight-cell stage, we found a statistically significant delay in their development; some of the treated embryos were, however, able to reach the blastocyst stage later. We found reduced levels of mRNA of EGA markers PAPOLA and U2AF1A, which can be related to this developmental delay. The cultivation with MLN4924 caused a significant increase in protein levels in MLN4924-treated oocytes and embryos; no such change was found in cumulus cells. To detect the proteins affected by MLN4924 treatment, we performed a Western blot analysis of selected proteins (SMAD4, ribosomal protein S6, centromeric protein E, P27, NFKB inhibitor alpha, RNA-binding motif protein 19). No statistically significant increase in protein levels was detected in either treated embryos or oocytes. In summary, our study shows that SCF ligases are necessary for the correct maturation of oocytes, cumulus cell expansion, fertilization, and early preimplantation development of cattle.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a blastocysta $x cytologie $x účinky léků $x fyziologie $7 D001755
- 650 _2
- $a skot $7 D002417
- 650 _2
- $a kultivované buňky $7 D002478
- 650 _2
- $a cyklopentany $x farmakologie $7 D003517
- 650 _2
- $a embryo savčí $7 D004622
- 650 _2
- $a embryonální vývoj $x účinky léků $7 D047108
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a IVM techniky $x metody $x veterinární $7 D059471
- 650 _2
- $a multiproteinové komplexy $x antagonisté a inhibitory $x metabolismus $7 D046912
- 650 _2
- $a oocyty $x cytologie $x účinky léků $x fyziologie $7 D009865
- 650 _2
- $a oogeneze $x účinky léků $7 D009866
- 650 _2
- $a pyrimidiny $x farmakologie $7 D011743
- 650 _2
- $a proteinligasy komplexu SCF $x antagonisté a inhibitory $x metabolismus $x fyziologie $7 D044843
- 650 _2
- $a časové faktory $7 D013997
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Kanka, Jiri $u Laboratory of Developmental Biology, Institute of Animal Physiology and Genetics Academy of Science of Czech Republic, v.v.i., Libechov, Czech Republic.
- 700 1_
- $a Petruskova, Veronika $u Laboratory of Developmental Biology, Institute of Animal Physiology and Genetics Academy of Science of Czech Republic, v.v.i., Libechov, Czech Republic. Faculty of Science, Charles University in Prague, Prague, Czech Republic.
- 700 1_
- $a Toralova, Tereza $u Laboratory of Developmental Biology, Institute of Animal Physiology and Genetics Academy of Science of Czech Republic, v.v.i., Libechov, Czech Republic.
- 773 0_
- $w MED00000747 $t Biology of reproduction $x 1529-7268 $g Roč. 100, č. 4 (2019), s. 896-906
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/30535233 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20201125 $b ABA008
- 991 __
- $a 20201214124819 $b ABA008
- 999 __
- $a ok $b bmc $g 1595111 $s 1113468
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 100 $c 4 $d 896-906 $e 20190401 $i 1529-7268 $m Biology of reproduction $n Biol Reprod $x MED00000747
- LZP __
- $a Pubmed-20201125