Nuclear Remodeling in Bovine Somatic Cell Nuclear Transfer Embryos Using MG132-Treated Recipient Oocytes

Autor: Ribeiro-Mason, Karlla, Boulesteix, Claire, Fleurot, Renaud, Aguirre-Lavin, Tiphaine, Adenot, Pierre, Debey, Pascale, Le Bourhis, Daniel, Beaujean, Nathalie, Ruffini, Sylvie, Vignon, Xavier, Gall, Laurence
Přispěvatelé: Biologie du Développement et Reproduction (BDR), Institut National de la Recherche Agronomique (INRA), Biologie du développement et reproduction (BDR), École nationale vétérinaire d'Alfort (ENVA)-Institut National de la Recherche Agronomique (INRA)-Centre National de la Recherche Scientifique (CNRS), Centre National de la Recherche Scientifique (CNRS)-École nationale vétérinaire d'Alfort (ENVA)-Institut National de la Recherche Agronomique (INRA)
Rok vydání: 2010
Předmět:
Nuclear Transfer Techniques
Leupeptins
Cloning
Organism

[SDV]Life Sciences [q-bio]
Maturation-Promoting Factor
Cyclin B
Embryonic Development
macromolecular substances
[SDV.BC]Life Sciences [q-bio]/Cellular Biology
Cysteine Proteinase Inhibitors
03 medical and health sciences
0302 clinical medicine
medicine
Animals
BIOLOGIE DU DEVELOPPEMENT
Blastocyst
immunofluorescence
Kinase activity
SOMATIC CELL NUCLEAR TRANSFER
[SDV.BDD]Life Sciences [q-bio]/Development Biology
Cells
Cultured

ComputingMilieux_MISCELLANEOUS
030304 developmental biology
Cell Nucleus
0303 health sciences
030219 obstetrics & reproductive medicine
biology
EMBRYO
[SDV.BDLR]Life Sciences [q-bio]/Reproductive Biology
Embryo
Cell Biology
Fibroblasts
Cellular Reprogramming
Embryo
Mammalian

Oocyte
Molecular biology
Chromatin
Embryo transfer
Cell biology
medicine.anatomical_structure
Premature chromosome condensation
Oocytes
biology.protein
Somatic cell nuclear transfer
Cattle
Developmental Biology
Biotechnology
Zdroj: CELLULAR REPROGRAMMING
CELLULAR REPROGRAMMING, 2010, 12 (6), pp.729-738. ⟨10.1089/cell.2010.0035⟩
ISSN: 2152-4998
2152-4971
DOI: 10.1089/cell.2010.0035
Popis: International audience; The early events in the nuclear reprogramming process during somatic cell nuclear transfer (SCNT) consist of morphological remodeling of the donor nucleus including premature chromosome condensation (PCC). In the present study, the objective was to increase oocyte M-Phase Promoting Factor (MPF) kinase activity and to examine the fate of the donor nucleus and the development of SCNT embryos thereafter. Indeed, in controls, recipient oocytes activated upon nuclear transfer, undergo a decrease in MPF activity, responsible for the inability to promote PCC in 77.8% of reconstituted embryos. Here we showed that exposure of the recipient oocyte to the proteasome inhibitor MG132 prior to fusion inhibited the degradation of cyclin B, which normally occurred immediately after activation by electro stimulation, and therefore sustained a high level of MPF. Treatment with MG132 also significantly increased the percentage of SCNT embryos with PCC when compared to the nontreated SCNT control embryos (94.1 vs. 22.2%, respectively, p
Databáze: OpenAIRE