Regulation of ISW2 by Concerted Action of Histone H4 Tail and Extranucleosomal DNA
- 1 October 2006
- journal article
- Published by Taylor & Francis in Molecular and Cellular Biology
- Vol. 26 (20) , 7388-7396
- https://doi.org/10.1128/mcb.01159-06
Abstract
The stable contact of ISW2 with nucleosomal DNA approximately 20 bp from the dyad was shown by DNA footprinting and photoaffinity labeling using recombinant histone octamers to require the histone H4 N-terminal tail. Efficient ISW2 remodeling also required the H4 N-terminal tail, although the lack of the H4 tail can be mostly compensated for by increasing the incubation time or concentration of ISW2. Similarly, the length of extranucleosomal DNA affected the stable contact of ISW2 with this same internal nucleosomal site, with the optimal length being 70 to 85 bp. These data indicate the histone H4 tail, in concert with a favorable length of extranucleosomal DNA, recruits and properly orients ISW2 onto the nucleosome for efficient nucleosome remodeling. One consequence of this property of ISW2 is likely its previously observed nucleosome spacing activity.Keywords
This publication has 42 references indexed in Scilit:
- Two Distinct Mechanisms of Chromatin Interaction by the Isw2 Chromatin Remodeling Complex In VivoMolecular and Cellular Biology, 2005
- Salt-dependent Intra- and Internucleosomal Interactions of the H3 Tail Domain in a Model Oligonucleosomal ArrayPublished by Elsevier ,2005
- Functional Role of Extranucleosomal DNA and the Entry Site of the Nucleosome in Chromatin Remodeling by ISW2Molecular and Cellular Biology, 2004
- Chromatin Remodeling In VivoMolecular Cell, 2003
- Structures and interactions of the core histone tail domainsBiopolymers, 2003
- Modulation of ISWI function by site‐specific histone acetylationEMBO Reports, 2002
- What does ‘chromatin remodeling’ mean?Trends in Biochemical Sciences, 2000
- New DNA sequence rules for high affinity binding to histone octamer and sequence-directed nucleosome positioningJournal of Molecular Biology, 1998
- The N tails of histones H3 and H4 adopt a highly structured conformation in the nucleosome 1 1Edited by T. RichmondJournal of Molecular Biology, 1997
- A highly basic histone H4 domain bound to the sharply bent region of nucleosomal DNANature, 1988