Successful mouse cloning of an outbred strain by trichostatin A treatment after somatic nuclear transfer.

Although the somatic cloning technique has been used for numerous applications and basic research of reprogramming in various species, extremely low success rates have plagued this technique for a decade. Further in mice, the "clonable" strains have been limited to mainly hybrid F1 strains such as B6D2F1. Recently, we established a new efficient cloning technique using trichostatin A (TSA) which leads to a 2-5 fold increase in success rates for mouse cloning of B6D2F1 cumulus cells. To further test the validity of this TSA cloning technique, we tried to clone the adult ICR mouse, an outbred strain, which has never been directly cloned before. Only when TSA was used did we obtain both male and female cloned mice from cumulus and fibroblast cells of adult ICR mice with 4-5% success rates, which is comparable to 5-7% of B6D2F1. Thus, the TSA treatment is the first cloning technique to allow us to successfully clone outbred mice, demonstrating that this technique not only improves the success rates of cloning from hybrid strains, but also enables mouse cloning from normally "unclonable" strains.

[1]  E. Selker Trichostatin A causes selective loss of DNA methylation in Neurospora. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[2]  H. Ohta,et al.  Establishment of Male and Female Nuclear Transfer Embryonic Stem Cell Lines from Different Mouse Strains and Tissues1 , 2005, Biology of reproduction.

[3]  Hiroshi Ohta,et al.  Significant improvement of mouse cloning technique by treatment with trichostatin A after somatic nuclear transfer. , 2006, Biochemical and biophysical research communications.

[4]  K. Mochida,et al.  Effects of Donor Cell Type and Genotype on the Efficiency of Mouse Somatic Cell Cloning1 , 2003, Biology of reproduction.

[5]  Y. Ono,et al.  Cloned Mice from Fetal Fibroblast Cells Arrested at Metaphase by a Serial Nuclear Transfer1 , 2001, Biology of reproduction.

[6]  V. Tabar,et al.  Differentiation of Embryonic Stem Cell Lines Generated from Adult Somatic Cells by Nuclear Transfer , 2001, Science.

[7]  Ben S. Wittner,et al.  Association of valproate‐induced teratogenesis with histone deacetylase inhibition in vivo , 2005, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[8]  R. Yanagimachi,et al.  Cloning of male mice from adult tail-tip cells , 1999, Nature Genetics.

[9]  H. Ohta,et al.  Propagation of an infertile hermaphrodite mouse lacking germ cells by using nuclear transfer and embryonic stem cell technology. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[10]  Y. Tsunoda,et al.  Role of Histone Acetylation in Reprogramming of Somatic Nuclei Following Nuclear Transfer1 , 2006, Biology of reproduction.

[11]  T. Wakayama,et al.  Effect of timing of the removal of oocyte chromosomes before or after injection of somatic nucleus on development of NT embryos. , 2003, Cloning and stem cells.

[12]  M. Ziman,et al.  Variation in the methylation profile and structure of Pax3 and Pax7 among different mouse strains and during expression. , 1997, Gene.

[13]  R. Yanagimachi,et al.  Mouse cloning with nucleus donor cells of different age and type , 2001, Molecular reproduction and development.

[14]  R. Yanagimachi,et al.  Comparison of oocyte-activating agents for mouse cloning. , 1999, Cloning.

[15]  M. Surani,et al.  Adult phenotype in the mouse can be affected by epigenetic events in the early embryo. , 1993, Development.

[16]  R. Yanagimachi,et al.  Effect of cytokinesis inhibitors, DMSO and the timing of oocyte activation on mouse cloning using cumulus cell nuclei. , 2001, Reproduction.

[17]  H. Matsuoka,et al.  Production of a cloned mouse by nuclear transfer from a fetal fibroblast cell of a mouse closed colony strain. , 2004, Experimental animals.

[18]  H. Ohta,et al.  Harmful or Not: Trichostatin A treatment of embryos generated by ICSI or ROSI , 2006, Central European Journal of Biology.

[19]  M. Boiani,et al.  Production of cloned mice by somatic cellnuclear transfer , 2006, Nature Protocols.

[20]  D. Solter,et al.  Effect of egg composition on the developmental capacity of androgenetic mouse embryos. , 1991, Development.

[21]  Satoshi Tanaka,et al.  Epigenetic Control of Mouse Oct-4 Gene Expression in Embryonic Stem Cells and Trophoblast Stem Cells* , 2004, Journal of Biological Chemistry.

[22]  H. Ohta,et al.  Mice cloned by nuclear transfer from somatic and ntES cells derived from the same individuals. , 2005, The Journal of reproduction and development.

[23]  Jun Ma,et al.  Regulation of Zygotic Gene Activation in the Preimplantation Mouse Embryo: Global Activation and Repression of Gene Expression1 , 2001, Biology of reproduction.

[24]  Maurizio Zuccotti,et al.  Full-term development of mice from enucleated oocytes injected with cumulus cell nuclei , 1998, Nature.

[25]  H. Ohta,et al.  Epigenetic abnormalities of the mouse paternal zygotic genome associated with microinsemination of round spermatids. , 2006, Developmental biology.

[26]  S. Simonsson,et al.  DNA demethylation is necessary for the epigenetic reprogramming of somatic cell nuclei , 2004, Nature Cell Biology.

[27]  R. Ohlsson,et al.  The paternal allele of the H19 gene is progressively silenced during early mouse development: the acetylation status of histones may be involved in the generation of variegated expression patterns. , 1998, Development.