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Epigenetically unstable

Jonathan B Weitzman

Genome Biology 2001, 2:spotlight-20010709-01  doi:10.1186/gb-spotlight-20010709-01

The electronic version of this article is the complete one and can be found online at:

Published:9 July 2001

© 2001 BioMed Central Ltd

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In the July 6 Science, Humpherys et al. describe extensive analysis of the expression of imprinted genes in mice derived from cloning by nuclear transfer (NT) (Science 2001, 293:95-97). They examined mRNA levels for several imprinted genes including H19 and Igf2, Peg1/Mest, Mest/Grb10, Peg3 and Snrpn. They found that the expression of imprinted genes varied widely between the placentas of cloned embryos and in the organs of newborn cloned mice. H19 expression was often silenced and Igf2 expression was increased compared to controls. These abnormalities correlated with hypermethylation of the H19 differentially methylated region (DMR). Analysis of NT ES-cell clones and subclones revealed similar variations in H19 and Peg1 expression, differences in methylation and epigenetic heterogeneity. Humpherys et al. used tetraploid complementation and nuclear transfer experiments to show that the expression of imprinted genes varied widely even in mice derived from cells of the same ES-cell subclone. They conclude that the epigenetic state of ES cells is extremely unstable and that mammalian development appears surprisingly tolerant to epigenetic abnormalities.


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  2. Hybrid vigor, fetal overgrowth, and viability of mice derived by nuclear cloning and tetraploid embryo complementation.

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