Impeding Xist Expression from the Active X Chromosome Improves Mouse Somatic Cell Nuclear Transfer

Author:

Inoue Kimiko12,Kohda Takashi3,Sugimoto Michihiko1,Sado Takashi4,Ogonuki Narumi1,Matoba Shogo1,Shiura Hirosuke1,Ikeda Rieko1,Mochida Keiji1,Fujii Takashi5,Sawai Ken5,Otte Arie P.6,Tian X. Cindy7,Yang Xiangzhong7,Ishino Fumitoshi3,Abe Kuniya12,Ogura Atsuo128

Affiliation:

1. BioResource Center, RIKEN, 305-0024 Tsukuba, Japan.

2. Graduate School of Life and Environmental Science, University of Tsukuba, 305-8572 Tsukuba, Japan.

3. Medical Research Institute, Tokyo Medical and Dental University, 113-8510 Tokyo, Japan.

4. Medical Institute of Bioregulation, Kyushu University, 812-8582 Fukuoka, Japan.

5. Faculty of Agriculture, Iwate University, 020-8550 Iwate, Japan.

6. Swammerdam Institute for Life Sciences, University of Amsterdam, 1018 TV Amsterdam, Netherlands.

7. Center for Regenerative Biology and Department of Animal Science, University of Connecticut, Storrs, CT 06269, USA.

8. The Center for Disease Biology and Integrative Medicine, Faculty of Medicine, University of Tokyo, 113-0033 Tokyo, Japan.

Abstract

Cloning Futures Cloning mammals by somatic cell nuclear transfer is a technique with many potential applications in regenerative medicine, agriculture, and pharmaceutics; however, it is inefficient because of the incidence of aberrant genomic reprogramming. Inoue et al. (p. 496 , published online 16 September) found that the gene product of Xist , which normally inactivates one of the two X chromosomes in females, was unexpectedly expressed ectopically from active X chromosomes in cloned mice. When Xist was deleted from the mice, gene expression returned to normal and the efficiency of somatic cell nuclear transfer increased about ninefold, offering promise for future nuclear transfer technology.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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