First published online January 13, 2009
Development 136, 303e (2009)
© The Company of Biologists Limited
ES cells make an imprint
Genomic imprinting - parental-specific gene expression in which either the
maternal or paternal copy of a gene is expressed - is important in early
development and can contribute to disease. To date, imprinting has been mostly
studied in mammalian embryos, which often entails long experimental time
frames. Now, on p. 437,
Denise Barlow and colleagues demonstrate that differentiating embryonic stem
(ES) cells provide a much-needed in vitro system for studying this phenomenon.
The authors show that imprinted expression of the Igf2r gene is
established when ES cells differentiate, and that this coincides with the
onset of the paternal-specific expression of Airn, a non-coding RNA
that, in the mouse, silences the paternal allele of Igf2r. These
events mimic aspects of imprinting that occur in the mouse embryo during and
after implantation. Surprisingly, during ES cell differentiation, expression
from the paternal Igf2r promoter remains constant instead of being
silenced, while expression from the maternal Igf2r promoter increases
up to tenfold, revealing a novel mechanism for Airn-mediated
imprinting - through an expression bias rather than silencing.

CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati
Twitter What's this?
Related articles in Development:
- An in vitro ES cell imprinting model shows that imprinted expression of the Igf2r gene arises from an allele-specific expression bias
- Paulina A. Latos, Stefan H. Stricker, Laura Steenpass, Florian M. Pauler, Ru Huang, Basak H. Senergin, Kakkad Regha, Martha V. Koerner, Katarzyna E. Warczok, Christine Unger, and Denise P. Barlow
Development 2009 136: 437-448.
[Abstract]
[Full Text]