초록 ▼

An optimum time has been discovered for obtaining porcine oocytes with improved developmental competence. Harvested oocytes are matured by culturing in vitro, and then activated ＿42-46 hours after beginning of the culture period. Alternatively, ovulation is induced in a donor female using a gonadotr

An optimum time has been discovered for obtaining porcine oocytes with improved developmental competence. Harvested oocytes are matured by culturing in vitro, and then activated ＿42-46 hours after beginning of the culture period. Alternatively, ovulation is induced in a donor female using a gonadotrophic hormone (optionally monitored by ultrasonography), maturation is allowed to proceed in vivo, and then the harvested oocyte is activated ＿44-48 hours after inducing ovulation. Outside the optimal time frame, the ability of the oocytes to undergo parthenogenetic activation declines markedly. These methods overcome problems encountered with previous protocols for nuclear transfer and assisted reproduction in the pig.

대표청구항 ▼

1. An improvement in the nuclear transfer method for cloning a pig, in which a pig oocyte is harvested from a donor animal and enucleated, the nucleus of a pig somatic cell is transferred into the enucleated oocyte to produce a combined cell, the combined cell is activated to produce an embryo, and

1. An improvement in the nuclear transfer method for cloning a pig, in which a pig oocyte is harvested from a donor animal and enucleated, the nucleus of a pig somatic cell is transferred into the enucleated oocyte to produce a combined cell, the combined cell is activated to produce an embryo, and the embryo is developed in a recipient animal of the same species to produce the cloned pig; wherein the improvement comprises: maturing the harvested oocyte by in vitro culture before enucleation and transfer of the pig somatic cell nucleus into the enucleated oocyte, and activating the combined cell, wherein the time from beginning maturation to activation is about 42-46 hours; thereby producing an embryo with an improved probability of developing into a cloned pig in the recipient animal. 2. The method of claim 1, wherein the oocyte is matured by culturing in a medium containing gonadotropic hormone and follicle stimulating hormone. 3. The method of claim 1, wherein the combined cell is activated by electrical stimulation. 4. The method of claim 1, wherein the nucleus is transferred from a quiescent cell. 5. The method of claim 1, in which the oocyte is cultured for about 42-46 hours as a cumulus oocyte complex. 6. An improvement in the nuclear transfer method for producing a non-human mammal, in which an oocyte is harvested from a donor mammal and enucleated, the nucleus of a somatic cell of the same species is transferred into the enucleated oocyte to produce a combined cell, the combined cell is activated to produce an embryo, and the embryo is developed in a recipient mammal of the same species to produce the mammal; wherein the non-human mammal is a pig, and the improvement comprises: maturing the harvested oocyte by in vitro culture before enucleation and transfer of the mammalian somatic cell nucleus into the enucleated oocyte, and activating the combined cell, wherein the time from beginning maturation to activation is about 43-45 hours; thereby producing an embryo with an improved probability of developing into a pig in the recipient mammal. 7. The method of claim 6, wherein the oocyte is matured by culturing in a medium containing gonadotropic hormone and follicle stimulating hormone. 8. The method of claim 6, which the cacyte is cultured for about 43-45 hours as a cumulus oocyte complex. 9. The method of claim 6, wherein the nucleus is transferred from a quiescent cell. 10. The method of claim 6, wherein the combined cell is activated by electrical stimulation.