Published in: Science vol. 286, no. 5441, pp. 955-958 (October 29, 1999):



"Epigenetic Inheritance of Active Chromatin After Removal of the Main Transactivator".

Giacomo Cavalli 1,2 and Renato Paro 1

1 Center for Molecular Biology (ZMBH), University of Heidelberg, Im Neuenheimer Feld 282,
69120 Heidelberg, Germany.

2 Insitute of Human Genetics, 141, rue de la Cardonille, 34396 Montpellier, France.



Abstract:

The Drosophila Polycomb and trithorax group proteins act through chromosomal elements such as Fab-7 to maintain repressed or active gene expression, respectively. A Fab-7 element is switched from a silenced to a mitotically heritable active state by an embryonic pulse of transcription. Here, histone H4 hyperacetylation was found to be associated with Fab-7 after activation, suggesting that H4 hyperacetylation may be a heritable epigenetic tag of the activated element. Activated Fab-7 enables transcription of a gene even after withdrawal of the primary transcription factor. This feature may allow epigenetic maintenance of active states of developmental genes after decay of their embryonic regulators.



Top of Page - Euchromatin Network - Current Research - Forums - Other Sites - Future Events -

For Further Information and Feedback:
E-mail: frenster@euchromatin.net
John H. Frenster, M.D.
Physicians' Educational Series
247 Stockbridge Avenue
Atherton, CA 94027-5446
Phone: 650/367-6483
Fax: 650/364-1773
WebSite: http://www.frenster.com/

euchromatin: "the most active portion of the genome within the cell nucleus".