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Effects of Activation Methods on DNA Synthesis and Development of Parthenogenetic Porcine Embryos

Authors
Ock, S. A.Kwack, D. O.Kumar, B. MohanaHan, J.Kim, S. W.Rho, G. J.
Issue Date
Dec-2011
Publisher
WILEY-BLACKWELL
Citation
REPRODUCTION IN DOMESTIC ANIMALS, v.46, no.6, pp 1082 - 1089
Pages
8
Indexed
SCI
SCIE
SCOPUS
Journal Title
REPRODUCTION IN DOMESTIC ANIMALS
Volume
46
Number
6
Start Page
1082
End Page
1089
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/23459
DOI
10.1111/j.1439-0531.2011.01790.x
ISSN
0936-6768
1439-0531
Abstract
This study investigated the timing of DNA synthesis and patterns of pronuclear (PN) formation during the first cell cycle, and its influence on developmental competence, velocity and proliferation index of porcine parthenote blastocysts produced by different activation treatments. Oocytes were activated as follows: electrical stimulation (EST), EST combined with 7.5 mu g/ml cytochalasin B (EST + CCB), 10 mu g/ml cycloheximide (EST + CHX) and 1.9 mM 6-dimethylaminopurine (EST + 6-DMAP) for 3 h. DNA synthesis and PN formation were evaluated using 1 mM 5'bromo-2'deoxy-uridne (BrdU) at 2 h intervals from 1 to 13 h or 5 to 13 h of post-activation (hpa), respectively. In EST, DNA synthesis started at 3 hpa, reached the peak at 11 hpa and decreased at 13 hpa. Treatment with 6-DMAP resulted in an early increase of DNA synthesis at 3 hpa, whereas CCB delayed DNA synthesis for 2 h. In EST and EST + 6-DMAP, most of the eggs showed 1PN, whereas, incidence of 2PN in EST + CCB was higher than 1PN. EST + CHX was observed with 1PN, 2PN and multiple PN. Blastocyst rate in EST + CCB and EST + 6-DMAP were significantly (p < 0.05) higher than EST + CHX. But, the developmental velocity was not different among groups. Proliferation index of blastocysts, as indicated the number of blastomere at S-phase of the cell cycle was low in all groups. In conclusion, CCB, CHX and 6-DMAP used for producing porcine parthenogenetic embryos induced different onset of DNA synthesis and PN, but they did not affect the subsequent embryo development.
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