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First published online August 29, 2005

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Histone code written on nuclear envelope

The positioning of chromatin within the nucleus plays an important role in gene regulation. The underlying mechanisms are poorly understood, but recent evidence indicates that architectural features such as the nuclear envelope (NE) can control gene expression by defining specific repressive environments. On p. 4017, Gideon Rechavi and co-workers define the role of a key NE protein, LAP2ß, in this process. They find that LAP-2 ß acts as a general repressor that can inhibit various transcription factors (e.g. NF-ßB, p53 and E2F proteins) in luciferase reporter assays. They also observe that it interacts and colocalizes at the NE with HDAC-3, one of a group of histone deacetylases known to repress transcription by modifying histones. By contrast, LAP-2 ß does not interact with the related enzyme HDAC1. The authors go on to demonstrate that the HDAC inhibitor trichostatin A blocks the repressive effect of LAP-2 ß and that LAP2 ß can induce deacetylation of histone H4 both in vitro and in vivo. Their findings provide valuable insight into the role of the NE in epigenetics and could be particularly significant given the various severe laminopathies that arise from disruption of NE protein function.

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The nuclear-envelope protein and transcriptional repressor LAP2ß interacts with HDAC3 at the nuclear periphery, and induces histone H4 deacetylation

Raz Somech, Sigal Shaklai, Orit Geller, Ninette Amariglio, Amos J. Simon, Gideon Rechavi, and Einav Nili Gal-Yam
JCS 2005 118: 4017-4025. [Abstract] [Full Text]  

This Article Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Email this article to a friend Related articles in JCS Similar articles in this journal Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via Google Scholar Google Scholar Search for Related Content Social Bookmarking                         What's this?