Regulating large chromatin domains
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Correspondence: Jonathan B Weitzman jonathanweitzman@hotmail.com
Genome Biology 2002, 3:spotlight-20021015-01 doi:10.1186/gb-spotlight-20021015-01
The electronic version of this article is the complete one and can be found online at:
| Published: | 15 October 2002 |
© 2002 BioMed Central Ltd
Research news
The thymocyte-specific SATB1 (special AT-rich sequence binding 1) protein binds to base-unpairing regions (BURs) of chromosomal DNA within matrix-attachment regions (MARs) and assembles a SATB1 network structure that can regulate gene expression over relatively large distances. In the October 10 Nature, Yasui et al. describe biochemical analysis of SATB1 within BUR-binding complexes (Nature 2002, 419:641-645). They analysed extracts from the thymi of normal and knockout (SATB1-/-) mice and found that components of the NURD, CHRAC and ACF chromatin-remodelling complexes co-purified with SATB1. Immunoprecipitation analysis showed that SATB1 recruits histone deacetylases and remodelling complexes, and represses the IL-2Ralpha (inteleukin-2 receptor alpha gene) locus. Changes in nucleosome positioning in the absence of SATB1 could be observed as much as 8 kilobases away, suggesting that mechanisms of this sort play a general a role in global gene regulation.
References
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A tissue-specific MAR/SAR DNA-binding protein with unusual binding site recognition.
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