Biol Reprod 2009 SSR Annual Meeting Abstracts
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Biology of Reproduction 65, 253-259 (2001)
© 2001 Society for the Study of Reproduction, Inc.


Regular Article

Parthenogenetic Activation of Rhesus Monkey Oocytes and Reconstructed Embryos1

Shoukhrat M. Mitalipova, Kevin D. Nussera, and Don P. Wolf2,a,b

a Oregon Regional Primate Research Center, Beaverton, Oregon 97006 b Departments of Obstetrics and Gynecology, and Physiology and Pharmacology, Oregon Health Sciences University, Portland, Oregon 97201

ABSTRACT

This study determines the efficiency of sequential calcium treatments (electroporation or ionomycin) combined with protein synthesis (cycloheximide) or phosphorylation inhibitors (6-dimethylaminopurine) or the specific maturation promoting factor (MPF) inhibitor, roscovitine, in inducing artificial activation and development of rhesus macaque parthenotes or nuclear transfer embryos. Exposure of oocytes arrested at metaphase II (MII) to ionomycin followed by 6-dimethylaminopurine or to electroporation followed by cycloheximide and cytochalasin B induced pronuclear formation and development to the blastocyst stage at a rate similar to control embryos produced by intracytoplasmic sperm injection. Parthenotes did not complete meiosis or extrude a second polar body, consistent with their presumed diploid status. In contrast, oocytes treated sequentially with ionomycin and roscovitine extruded the second polar body and formed a pronucleus at a rate higher than that observed in controls. Following reconstruction by nuclear transfer, activation with ionomycin/6-dimethylaminopurine resulted in embryos that contained a single pronucleus and no polar bodies. All nuclear transfer embryos activated with ionomycin/roscovitine contained one large pronucleus. However, a third of these embryos emitted one or two polar bodies, clearly containing chromatin material. In summary, we have identified simple yet effective methods of oocyte or cytoplast activation in the monkey, ionomycin/6-dimethylaminopurine, electroporation/cycloheximide/cytochalasin B, and ionomycin/roscovitine, which are applicable to parthenote or nuclear transfer embryo production.

FOOTNOTES

First decision: 9 January 2001.

1 Supported by National Institutes of Health grant RR12804 to D.P.W. and by grant RR00163.

2 Correspondence: Don Wolf, Oregon Regional Primate Research Center, 505 NW 185th Ave., Beaverton, OR 97006. FAX: 503 690 5384; wolfd{at}ohsu.edu




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