skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Somatic cell nuclear transfer: Infinite reproduction of a unique diploid genome

Journal Article · · Experimental Cell Research
 [1];  [1]; ;  [2];  [1]
  1. Laboratory for Genomic Reprogramming, Center for Developmental Biology, RIKEN Kobe, 2-2-3 Minatojima-minamimachi, Kobe 650-0047 (Japan)
  2. Kinki University, 930 Nishimitani, Kinokawa 599-5993 (Japan)

In mammals, a diploid genome of an individual following fertilization of an egg and a spermatozoon is unique and irreproducible. This implies that the generated unique diploid genome is doomed with the individual ending. Even as cultured cells from the individual, they cannot normally proliferate in perpetuity because of the 'Hayflick limit'. However, Dolly, the sheep cloned from an adult mammary gland cell, changes this scenario. Somatic cell nuclear transfer (SCNT) enables us to produce offspring without germ cells, that is, to 'passage' a unique diploid genome. Animal cloning has also proven to be a powerful research tool for reprogramming in many mammals, notably mouse and cow. The mechanism underlying reprogramming, however, remains largely unknown and, animal cloning has been inefficient as a result. More momentously, in addition to abortion and fetal mortality, some cloned animals display possible premature aging phenotypes including early death and short telomere lengths. Under these inauspicious conditions, is it really possible for SCNT to preserve a diploid genome? Delightfully, in mouse and recently in primate, using SCNT we can produce nuclear transfer ES cells (ntES) more efficiently, which can preserve the eternal lifespan for the 'passage' of a unique diploid genome. Further, new somatic cloning technique using histone-deacetylase inhibitors has been developed which can significantly increase the previous cloning rates two to six times. Here, we introduce SCNT and its value as a preservation tool for a diploid genome while reviewing aging of cloned animals on cellular and individual levels.

OSTI ID:
21128187
Journal Information:
Experimental Cell Research, Vol. 314, Issue 9; Other Information: DOI: 10.1016/j.yexcr.2008.01.027; PII: S0014-4827(08)00065-7; Copyright (c) 2008 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0014-4827
Country of Publication:
United States
Language:
English

Similar Records

Significant improvement of mouse cloning technique by treatment with trichostatin A after somatic nuclear transfer
Journal Article · Fri Feb 03 00:00:00 EST 2006 · Biochemical and Biophysical Research Communications · OSTI ID:21128187

Production of rhesus monkey cloned embryos expressing monomeric red fluorescent protein by interspecies somatic cell nuclear transfer
Journal Article · Fri Feb 21 00:00:00 EST 2014 · Biochemical and Biophysical Research Communications · OSTI ID:21128187

HSPC117 deficiency in cloned embryos causes placental abnormality and fetal death
Journal Article · Fri Jul 02 00:00:00 EDT 2010 · Biochemical and Biophysical Research Communications · OSTI ID:21128187