Methods for cloning mammals using reprogrammed donor chromatin or donor cells

a technology of chromatin or donor cells, applied in the field of mammals cloning, can solve the problems of low efficiency of cloning mammals using donor somatic cells, loss of mid to late term pregnancies, and loss of nuclear transplant embryos, so as to increase the extent of reprogramming, improve the viability of cloned fetuses, and restore the membrane integrity of cells

Inactive Publication Date: 2006-09-21
KYOWA HAKKO KIRIN CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0004] The purpose of the present invention is to provide improved methods for cloning mammals. In particular, these methods involve the condensation of a donor nucleus into a chromatin mass to allow the release of nuclear components such as transcription factors that may promote the transcription of genes that are undesirable for the development of the nuclear transplant embryo into a viable offspring. In a related method, a permeabilized cell is incubated with a reprogramming media (e.g., a cell extract) to allow the addition or removal of factors from the cell, and then the plasma membrane of the permeabilized cell is resealed to enclose the desired factors and restore the membrane integrity of the cell. If de

Problems solved by technology

Unfortunately, the efficiency of cloning mammals using donor somatic cells is generally low, resulting in only about 1-2% of nuclear transplant embryos developing to

Method used

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  • Methods for cloning mammals using reprogrammed donor chromatin or donor cells
  • Methods for cloning mammals using reprogrammed donor chromatin or donor cells
  • Methods for cloning mammals using reprogrammed donor chromatin or donor cells

Examples

Experimental program
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Effect test

example 1

Evidence For Nuclear Reprogramming Deficiencies in Traditional Bovine Nuclear Transplant Embryos

Distribution of Nuclear Envelope, Nuclear Matrix, and Chromatin-Matrix Interface Components During Bovine Preimplantation Development

[0073] To determine the distribution of nuclear envelope (B-type and A / C-type lamins), nuclear matrix (NuMA), and chromatin-matrix interface (AKAP95) components in preimplantation embryos, bovine embryos were produced by in vitro fertilization (IVF) and examined by immunofluorescence analysis. Bovine in vitro fertilization was performed as described previously (Collas et al., Mol. Reprod. Devel. 34:212-223, 1993). Briefly, frozen-thawed bovine sperm from a single bull was layered on top of a 45-90% Percoll gradient and centrifuged for 30 minutes at 700×g. The concentration of sperm in the pellet was determined, and the sperm was diluted such that the final concentration at fertilization was 106 sperm / ml. At 22 hours post maturation, oocytes were washed th...

example 2

Use of Reprogrammed Donor Chromatin Masses to Clone Mammals

[0088] To overcome the problem of incomplete reprogramming in traditional nuclear transfer embryos that was demonstrated in Example 1, new methods were developed to more efficiently reprogram donor chromatin prior to nuclear transfer. These methods involve incubating a nucleus from a donor cell in a reprogramming media (e.g., a cell extract) that results in nuclear envelope dissolution and possibly chromatin condensation. This nuclear envelope breakdown and chromatin condensation allows the release of transcription regulatory proteins that were attached to the chromosomes and that would otherwise promote the transcription of genes undesirable for oocyte, embryo, or fetus development. Additionally, regulatory proteins from the reprogramming media may bind the chromatin mass and promote the transcription of genes desirable for development.

Bulk Preparation of Donor Nuclei for Use in Cloning

[0089] As many as several million ...

example 3

Use of Reprogrammed Permeabilized Cells to Clone Mammals

[0115] Cells may also be reprogrammed without requiring the isolation of nuclei or chromatin masses from the cells. In this method, cells are permeabilized and then incubated in an interphase or mitotic reprogramming media under conditions that allow the exchange of factors between the media (e.g., a cell extract) and the cells. If an interphase media is used, the nuclei in the cells remain membrane-bounded; if a mitotic media is used, nuclear envelope breakdown and chromatin condensation may occur. After the nuclei are reprogrammed by incubation in this media, the plasma membrane is preferably resealed, forming an intact reprogrammed cell that contains desired factors from the media. If desired, the media can be enriched with additional nuclear factors as described in Example 2. The reprogrammed cells are then fused with recipient oocytes, and embryos formed from the reconstituted oocytes are inserted into maternal recipient ...

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Abstract

The invention provides methods for cloning mammals that allow the donor chromosomes or donor cells to be reprogrammed prior to insertion into an enucleated oocyte. The invention also features methods of inserting chromosomes or nuclei into recipient cells.

Description

CROSS-REFERENCE TO RELATED APPLICATION [0001] This application is a divisional application of and claims priority from U.S. patent application Ser. No. 10 / 032,191, filed Dec. 21, 2001, which claims benefit of the filing date of U.S. Provisional Application No. 60 / 258,151, filed Dec. 22, 2000, hereby incorporated by reference.BACKGROUND OF THE INVENTION [0002] In general, the invention features improved methods for cloning mammals and methods for inserting chromosomes, nuclei, or chromatin masses into recipient cells. [0003] The cloning of mammals allows the production of multiple mammals with an identical DNA content. The donor genetic material used to generate these mammals may be selected or engineered such that the cloned mammals have desirable properties, such as increased resistance to disease. Unfortunately, the efficiency of cloning mammals using donor somatic cells is generally low, resulting in only about 1-2% of nuclear transplant embryos developing to term (Polejaeva et a...

Claims

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Application Information

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IPC IPC(8): A01K67/027A01K67/02A01K67/00C12N15/09C12N15/873C12N15/877
CPCA01K2227/103A01K2227/105A01K2227/107A01K2227/108A01K2267/02C12N15/873C12N15/8771C12N2501/999C12N2517/10A01K67/0273A01K2227/101A01K2227/102C12N15/00
Inventor COLLAS, PHILIPPEROBL, JAMES M.SULLIVAN, EDDIEKASINATHAN, P.
Owner KYOWA HAKKO KIRIN CO LTD
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