Methods for correcting mitotic spindle defects and optimizing preimplantation embryonic developmental rates associated with somatic cell nuclear transfer in animals

• US 20060037086A1
• Filed: 12/03/2004
• Published: 02/16/2006
• Est. Priority Date: 04/09/2003
• Status: Abandoned Application

• Current Assignee: Magee-Womens Health Corporation
• Original Assignee: Magee-Womens Health Corporation
• Inventors: Simerly, Calvin R., Schatten, Gerald P., Navara, Christopher S.
• Application Number:
  US11/003,006
• Publication Number:
  US 20060037086A1
• Time in Patent Office: Days
• US Class Current: 800/9
• CPC Class Codes: A01K 2227/106 Primate
• CPC Class Codes: A01K 67/0273 Cloned vertebrates
• CPC Class Codes: A61P 15/00 Drugs for genital or sexual disorders for disorders of sex hormones A61P5/24; Contraceptives
• CPC Class Codes: A61P 25/00 Drugs for disorders of the nervous system
• CPC Class Codes: A61P 3/00 Drugs for disorders of the metabolism of the blood or the extracellular fluid A61P7/00
• CPC Class Codes: A61P 35/00 Antineoplastic agents
• CPC Class Codes: A61P 37/00 Drugs for immunological or allergic disorders
• CPC Class Codes: A61P 5/00 Drugs for disorders of the endocrine system
• CPC Class Codes: A61P 9/00 Drugs for disorders of the cardiovascular system
• CPC Class Codes: C12N 15/877 Techniques for producing new mammalian cloned embryos
• CPC Class Codes: C12N 15/8776 Primate embryos
• CPC Class Codes: C12N 2517/04 Cells produced using nuclear transfer
• CPC Class Codes: C12N 5/0604 Whole embryos; Culture medium therefor
• CPC Class Codes: C12N 5/0609 Oocytes, oogonia fertilised oocytes C12N5/0604

Abstract

The present invention is directed to various methodologies to make NT a practical procedure for animals, specifically, primates including human and non-human primates. Furthermore, the methods and molecular components provided by the present invention provide a practical means for producing embryos with desired characteristics. In a specific embodiment, the methodology of the present invention comprises introducing nuclei having desired characteristics along with one or more molecular components into an enucleated egg, thus creating a nuclear transfer construct, culturing the egg to produce a viable embryo, transferring the embryo to the oviducts of a female, and producing a cloned animal.

Claims

1. A method comprising the steps of:

introducing nuclei along with one or more molecular components into an extrusion-enucleated egg, thus creating a nuclear transfer construct;

culturing said nuclear transfer construct to produce a viable embryo;

transferring said embryo to the oviducts of a female; and

producing a cloned animal.

2. The method of claim 1, wherein said enucleated egg is a cumulus-free oocyte.

3. The method of claim 1, wherein said enucleated egg is enucleated pre-metaphase II.

4. The method of claim 1, wherein said enucleated egg is enucleated just prior to metaphase II arrest.

5. The method of claim 1, wherein said extrusion comprises:

holding said egg with a holding micropipette;

partially dissecting the zonal pellucida of said egg with a needle by making a slit near the first polar body of said egg;

extruding the first polar body and adjacent cytoplasm containing the meiotic spindle, ranging from about telophase-I to about pro-metaphase-II, by squeezing said needle.

6. The method of claim 5, wherein said holding micropipette has an about 110 μ

m inner diameter.

7. The method of claim 5, wherein said needle is a glass needle.

8. The method of claim 1, wherein said egg is enucleated in Hepes-buffered TALP supplemented with BSA and cytochalasin B.

9. The method of claim 1, wherein said egg is enucleated in Hepes-buffered TALP supplemented with about 0.3% BSA and about 7.5 μ

g/ml cytochalasin B.

10. The method of claim 1, wherein said nuclei are derived from a somatic cell nuclear donor source.

11. The method of claim 10, wherein said nuclei derived from said somatic cell nuclear donor source include dissociated cumulus cells.

12. The method of claim 11, wherein said dissociated cumulus cells are autologous.

13. The method of claim 11, wherein said dissociated cumulus cells are heterologous.

14. The method of claim 11, wherein said dissociated cumulus cells are autologous and heterologous.

15. The method of claim 1, wherein said nuclei are derived from primary rhesus fibroblast cell lines.

16. The method of claim 1, wherein said nuclei are derived from donor blastomeres.

17. The method of claim 1, wherein said nuclei are transferred into the perivitelline space of said enucleated egg.

18. The method of claim 1, wherein said nuclear transfer constructs are equilibrated with mannitol solution.

19. The method of claim 18, wherein said mannitol solution comprises about 0.3 M mannitol solution containing about 0.5 mM Hepes, about 0.1 mM CaCl₂, and about 0.1 mM MgCl₂.

20. The method of claim 18, wherein said nuclear transfer constructs are equilibrated with said mannitol solution for about 4 minutes.

21. The method of claim 18, wherein after said equilibration with said mannitol solution, said nuclear transfer constructs are transferred to a chamber containing an electrode overlaid with said mannitol solution.

22. The method of claim 18, wherein after said equilibration with said mannitol solution, said nuclear transfer constructs are transferred to a chamber containing electrodes overlaid with said mannitol solution.

23. The method of claim 22, wherein said chamber contains two electrodes overlaid with said mannitol solution.

24. The method of claim 1, wherein said nuclei and said egg are fused with two DC pulses.

25. The method of claim 24, wherein said DC pulses constitute about 2.7 kK/cm.

26. The method of claim 24, wherein the duration of said DC pulses is about 15 μ

s.

27. The method of claim 1, wherein said nuclear transfer construct is developed in culture media.

28. The method of claim 27, wherein said culture media includes G1, G2, and modified synthetic oviductal fluid (mSOF).

29. The method of claim 27, wherein said nuclear transfer construct is developed in said culture media sequentially.

30. The method of claim 27, wherein said nuclear transfer construct is developed in G1 for about 48 hours after nuclear transfer.

31. The method of claim 27, wherein said nuclear transfer construct is developed in G1 media for about 48 hours after nuclear transfer and then developed in G2 media for an about another 48 hours.

32. The method of claim 27, wherein said nuclear transfer construct is developed in G1 media for about 48 hours after nuclear transfer and then developed in G2 media for an about another 48 hours and transferred to mSOF around the morula stage until said nuclear transfer construct reaches the blastocyst stage.

33. The method of claim 27, wherein said mSOF media further comprises fructose.

34. The method of claim 1, wherein said nuclei have desired characteristics.

35. The method of claim 34, wherein said desired characteristics are linked to a specific disease or disorder.

36. The method of claim 35, wherein said specific disease or disorder is selected from the group consisting of cardiovascular disease, neurological disease, reproductive disorder, cancer, eye disease, endocrine disorder, pulmonary disease, metabolic disorder, autoimmune disorder, and aging.

37. The method of claim 1, wherein said introducing step comprises performing SCNT.

38. The method of claim 37, further comprising the step of performing pronuclear removal after SCNT.

39. The method of claim 37, further comprising the step of performing a second nuclear transfer following said SCNT.

40. The method of claim 1, wherein said introducing step further comprises performing meiotic spindle collapse.

41. The method of claim 1, further comprising the step of performing ooplasmic supplementation following said introducing step.

42. The method of claim 41, wherein said ooplamsic supplementation is performed by ooplast electrofusion.

43. The method of claim 41, wherein said ooplasmic supplementation is performed by microinjection.

44. The method of claim 1, wherein said one or more molecular components comprise centrosomal components normally present in sperm centrosomes.

45. The method of claim 1, wherein said one or more molecular components comprise mitotic motor proteins and centrosome proteins.

46. The method of claim 45, wherein said mitotic motor proteins comprise kinesins.

47. The method of claim 46, wherein said kinesins comprise HSET kinesin.

48. The method of claim 45, wherein said centrosome proteins comprise NuMA.

49. The method of claim 1, wherein said animal is a primate.

50. The method of claim 49, wherein said animal is a non-human primate.

51. The method of claim 50, wherein said non-human primate is a monkey.

52. The method of claim 49, wherein said primate is a human.

53. The method of claim 1, wherein said viable embryo is transgenic.

54. The method of claim 1, further comprising the step of producing embryonic stem cells from said viable embryo.

55. The method of claim 54, wherein said embryonic stem cells are human and said viable embryo is human.

56-214. -214. (canceled)