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Development of Reversing the Usual Order of Somatic Cell Nuclear Transfer in Mice  

Kang, Ho-In (Cellular Reprogramming and Embryo Biotechnology Lab, Dental Research Institute and CLS21, Seoul National University School of Dentistry)
Sung, Ji-Hye (Cellular Reprogramming and Embryo Biotechnology Lab, Dental Research Institute and CLS21, Seoul National University School of Dentistry)
Roh, Sang-Ho (Cellular Reprogramming and Embryo Biotechnology Lab, Dental Research Institute and CLS21, Seoul National University School of Dentistry)
Publication Information
Journal of Embryo Transfer / v.26, no.1, 2011 , pp. 85-89 More about this Journal
Abstract
Somatic cell nuclear transfer (SCNT) is a useful tool for reproducing genetically identical animals or producing transgenic animals. Many reports have demonstrated that the efficiency of animal cloning by SCNT requires reprogramming of the somatic nucleus to a totipotent like-state. The SCNT-related reprogramming might mimic the natural reprogramming process that occurs during normal mammalian development. However, recent evidence indicates that the reprogramming event by SCNT is incomplete. In this study, the traditional SCNT procedure (TNT) was modified by injecting donor nuclei into recipient cytoplasm prior to the enucleation process to expose the donor nucleus before removing the karyoplast containing the chromosomes of the oocytes which might possess additional reprogramming factors, and this modified technique was named as reversing the usual order of SCNT (RONT). Other procedures including activation and in vitro culture were the same as TNT. Contrary to expectations, the rate of blastocyst development was not different significantly between RONT and TNT (8.6% and 7.9%, respectively). However, duration of micromanipulation performed by the same technician and equipments was remarkably reduced because the ruptured oocytes after nuclear injection were excluded from the enucleation process. This study suggests that RONT, a simplified SCNT protocol, shortens the duration of SCNT procedure and this less time-costing protocol may enable the researchers to perform murine SCNT easier.
Keywords
mouse; somatic cell nuclear transfer; maternal chromosome associated factor;
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1 Wakayama T, Perry AC, Zuccotti M, Johnson KR and Yanagimachi R. 1998. Full-term development of mice from enucleated oocytes injected with cumulus cell nuclei. Nature 394:369-374.   DOI   ScienceOn
2 Wakayama T, Tabar V, Rodriguez I, Perry AC, Studer L and Mombaerts P. 2001. Differentiation of embryonic stem cell lines generated from adult somatic cells by nuclear transfer. Science 292:740-743.   DOI
3 Wilmut I, Schnieke AE, McWhir J, Kind AJ and Campbell K H. 1997. Viable offspring derived from fetal and adult mammalian cells. Nature 385:810-813.   DOI   ScienceOn
4 Ohgane J, Wakayama T, Senda S, Yamazaki Y, Inoue K, Ogura A, Marh J, Tanaka S, Yanagimachi R and Shiota K. 2004. The Sall3 locus is an epigenetic hotspot of aberrant DNA methylation associated with placentomegaly of cloned mice. Genes. Cells. 9:253-260.   DOI   ScienceOn
5 Rybouchkin A, Kato Y and Tsunoda Y. 2006. Role of histone acetylation in reprogramming of somatic nuclei following nuclear transfer. Biol. Reprod. 74:1083-1089.   DOI   ScienceOn
6 Wakayama S, Cibelli JB and Wakayama T. 2003. Effect of timing of the removal of oocyte chromosomes before or after injection of somatic nucleus on development of NT embryos. Cloning Stem Cells 5:181-189.   DOI   ScienceOn
7 Shin T, Kraemer D, Pryor J, Liu L, Rugila J, Howe L, Buck S, Murphy K, Lyons L and Westhusin M. 2002. A cat cloned by nuclear transplantation. Nature 415:859.   DOI   ScienceOn
8 Szollosi D, Czolowska R, Soltynska MS and Tarkowski AK. 1986. Remodelling of thymocyte nuclei in activated mouse oocytes: An ultrastructural study. Eur. J. Cell. Biol. 42:140-151.
9 Wade PA and Kikyo N. 2002. Chromatin remodeling in nuclear cloning. Eur. J. Biochem. 269:2284-2287.   DOI   ScienceOn
10 Wakayama S, Kishigami S, Thuan NV, Ohta H, Hikichi T, Mizutani E, Bui HT, Miyake M and Wakayama T. 2008. Effect of volume of oocyte cytoplasm on embryo development after parthenogenetic activation, intracytoplasmic sperm injection, or somatic cell nuclear transfer. Zygote 16:211-222.   DOI
11 Erbach GT, Lawitts JA, Papaioannou VE and Biggers JD. 1994. Differential growth of the mouse preimplantation embryo in chemically defined media. Biol. Reprod. 50:1027-1033.   DOI   ScienceOn
12 Kishigami S, Mizutani E, Ohta H, Hikichi T, Thuan NV, Wakayama S, Bui HT and Wakayama T. 2006. Significant improvement of mouse cloning technique by treatment with trichostatin A after somatic nuclear transfer. Biochem. Biophys. Res. Commun. 340:183-189.   DOI   ScienceOn
13 Kato Y, Tani T and Tsunoda Y. 2000. Cloning of calves from various somatic cell types of male and female adult, newborn and fetal cows. J. Reprod. Fertil. 120:231-237.
14 Kim JM, Ogura A, Nagata M and Aoki F. 2002. Analysis of the mechanism for chromatin remodeling in embryos reconstructed by somatic nuclear transfer. Biol. Reprod. 67:760-766.   DOI   ScienceOn
15 Kim MK, Jang G, Oh HJ, Yuda F, Kim HJ, Hwang WS, Hossein MS , Kim JJ, Shin NS, Kang SK and Lee BC. 2007. Endangered wolves cloned from adult somatic cells. Cloning Stem Cells 9:130-137.   DOI   ScienceOn
16 Kishikawa H, Wakayama T and Yanagimachi R. 1999. Comparison of oocyte-activating agents for mouse cloning. Cloning 1:153-159.   DOI   ScienceOn
17 Latham KE. 1999. Mechanisms and control of embryonic genome activation in mammalian embryos. Int. Rev. Cytol. 193:71-124.
18 Collas P, Le Guellec K and Tasken K. 1999. The A-kinase-anchoring protein AKAP95 is a multivalent protein with a key role in chromatin condensation at mitosis. J. Cell. Biol. 147:1167-1180.   DOI   ScienceOn
19 Casas A, Valiente-Banuet A, Rojas-Martinez A and Davila P. 1999. Reproductive biology and the process of domestication of the columnar cactus Stenocereus Stellatus in Central Mexico. Am. J. Bot. 86:534.   DOI   ScienceOn
20 Chatot CL, Ziomek CA, Bavister BD, Lewis JL and Torres I. 1989. An improved culture medium supports development of random-bred 1-cell mouse embryos in vitro. J. Reprod. Fertil. 86:679-688.   DOI
21 Enright BP, Kubota C, Yang X and Tian XC. 2003. Epigenetic characteristics and development of embryos cloned from donor cells treated by trichostatin A or 5-aza-2'-deoxycytidine. Biol. Reprod. 69:896-901.   DOI   ScienceOn