Click here to close
Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly.
We suggest using a current version of Chrome,
FireFox, or Safari.
J Biol Chem
2010 Nov 05;28545:34597-607. doi: 10.1074/jbc.M110.140061.
Show Gene links
Show Anatomy links
Nucleosome interactions and stability in an ordered nucleosome array model system.
Blacketer MJ
,
Feely SJ
,
Shogren-Knaak MA
.
???displayArticle.abstract???
Although it is well established that the majority of eukaryotic DNA is sequestered as nucleosomes, the higher-order structure resulting from nucleosome interactions as well as the dynamics of nucleosome stability are not as well understood. To characterize the structural and functional contribution of individual nucleosomal sites, we have developed a chromatin model system containing up to four nucleosomes, where the array composition, saturation, and length can be varied via the ordered ligation of distinct mononucleosomes. Using this system we find that the ligated tetranucleosomal arrays undergo intra-array compaction. However, this compaction is less extensive than for longer arrays and is histone H4tail-independent, suggesting that well ordered stretches of four or fewer nucleosomes do not fully compact to the 30-nm fiber. Like longer arrays, the tetranucleosomal arrays exhibit cooperative self-association to form species composed of many copies of the array. This propensity for self-association decreases when the fraction of nucleosomes lacking H4 tails is systematically increased. However, even tetranucleosomal arrays with only two octamers possessing H4 tails recapitulate most of the inter-array self-association. Varying array length shows that systems as short as dinucleosomes demonstrate significant self-association, confirming that relatively few determinants are required for inter-array interactions and suggesting that in vivo multiple interactions of short runs of nucleosomes might contribute to complex fiber-fiber interactions. Additionally, we find that the stability of nucleosomes toward octamer loss increases with array length and saturation, suggesting that in vivo stretches of ordered, saturated nucleosomes could serve to protect these regions from histone ejection.
Adkins,
Chromatin disassembly from the PHO5 promoter is essential for the recruitment of the general transcription machinery and coactivators.
2007, Pubmed
Adkins,
Chromatin disassembly from the PHO5 promoter is essential for the recruitment of the general transcription machinery and coactivators.
2007,
Pubmed
Boeger,
Nucleosomes unfold completely at a transcriptionally active promoter.
2003,
Pubmed
Carruthers,
Assembly of defined nucleosomal and chromatin arrays from pure components.
1999,
Pubmed
Dialynas,
Linking Heterochromatin Protein 1 (HP1) to cancer progression.
2008,
Pubmed
Dorigo,
Chromatin fiber folding: requirement for the histone H4 N-terminal tail.
2003,
Pubmed
,
Xenbase
Dorigo,
Nucleosome arrays reveal the two-start organization of the chromatin fiber.
2004,
Pubmed
,
Xenbase
Eltsov,
Analysis of cryo-electron microscopy images does not support the existence of 30-nm chromatin fibers in mitotic chromosomes in situ.
2008,
Pubmed
Fan,
H2A.Z alters the nucleosome surface to promote HP1alpha-mediated chromatin fiber folding.
2004,
Pubmed
Francis,
Chromatin compaction by a polycomb group protein complex.
2004,
Pubmed
Georgel,
Chromatin compaction by human MeCP2. Assembly of novel secondary chromatin structures in the absence of DNA methylation.
2003,
Pubmed
Gordon,
The core histone N-terminal tail domains function independently and additively during salt-dependent oligomerization of nucleosomal arrays.
2005,
Pubmed
,
Xenbase
Grigoryev,
MENT, a heterochromatin protein that mediates higher order chromatin folding, is a new serpin family member.
1999,
Pubmed
Hediger,
Heterochromatin protein 1: don't judge the book by its cover!
2006,
Pubmed
Jessen,
Active PHO5 chromatin encompasses variable numbers of nucleosomes at individual promoters.
2006,
Pubmed
Kan,
The H4 tail domain participates in intra- and internucleosome interactions with protein and DNA during folding and oligomerization of nucleosome arrays.
2009,
Pubmed
Köhler,
Programming of gene expression by Polycomb group proteins.
2008,
Pubmed
Kwon,
The heterochromatin protein 1 (HP1) family: put away a bias toward HP1.
2008,
Pubmed
Lam,
Chromatin decouples promoter threshold from dynamic range.
2008,
Pubmed
Li,
Cross-talk between histone H3 tails produces cooperative nucleosome acetylation.
2008,
Pubmed
Lowary,
New DNA sequence rules for high affinity binding to histone octamer and sequence-directed nucleosome positioning.
1998,
Pubmed
Luger,
Preparation of nucleosome core particle from recombinant histones.
1999,
Pubmed
,
Xenbase
Luger,
Crystal structure of the nucleosome core particle at 2.8 A resolution.
1997,
Pubmed
Nikitina,
MeCP2-chromatin interactions include the formation of chromatosome-like structures and are altered in mutations causing Rett syndrome.
2007,
Pubmed
Noll,
Sucrose gradient techniques and applications to nucleosome structure.
1989,
Pubmed
Reinke,
Histones are first hyperacetylated and then lose contact with the activated PHO5 promoter.
2003,
Pubmed
Richmond,
The structure of DNA in the nucleosome core.
2003,
Pubmed
Robinson,
EM measurements define the dimensions of the "30-nm" chromatin fiber: evidence for a compact, interdigitated structure.
2006,
Pubmed
Routh,
Nucleosome repeat length and linker histone stoichiometry determine chromatin fiber structure.
2008,
Pubmed
Schalch,
X-ray structure of a tetranucleosome and its implications for the chromatin fibre.
2005,
Pubmed
,
Xenbase
Schwarz,
Formation and stability of higher order chromatin structures. Contributions of the histone octamer.
1994,
Pubmed
Schwarz,
Reversible oligonucleosome self-association: dependence on divalent cations and core histone tail domains.
1996,
Pubmed
Segal,
A genomic code for nucleosome positioning.
2006,
Pubmed
Shogren-Knaak,
Histone H4-K16 acetylation controls chromatin structure and protein interactions.
2006,
Pubmed
Sinha,
Role of direct interactions between the histone H4 Tail and the H2A core in long range nucleosome contacts.
2010,
Pubmed
,
Xenbase
Springhetti,
Role of the M-loop and reactive center loop domains in the folding and bridging of nucleosome arrays by MENT.
2003,
Pubmed
Strick,
Cation-chromatin binding as shown by ion microscopy is essential for the structural integrity of chromosomes.
2001,
Pubmed
Thåström,
Histone-DNA binding free energy cannot be measured in dilution-driven dissociation experiments.
2004,
Pubmed
,
Xenbase
Thoma,
Involvement of histone H1 in the organization of the nucleosome and of the salt-dependent superstructures of chromatin.
1979,
Pubmed
Tse,
Hybrid trypsinized nucleosomal arrays: identification of multiple functional roles of the H2A/H2B and H3/H4 N-termini in chromatin fiber compaction.
1997,
Pubmed
van Holde,
Chromatin fiber structure: Where is the problem now?
2007,
Pubmed
Widlund,
Identification and characterization of genomic nucleosome-positioning sequences.
1997,
Pubmed
Workman,
Nucleosome displacement in transcription.
2006,
Pubmed
Yang,
The chromatin-remodeling enzyme ACF is an ATP-dependent DNA length sensor that regulates nucleosome spacing.
2006,
Pubmed
Yuan,
Genome-scale identification of nucleosome positions in S. cerevisiae.
2005,
Pubmed
Zheng,
Salt-dependent intra- and internucleosomal interactions of the H3 tail domain in a model oligonucleosomal array.
2005,
Pubmed
,
Xenbase
Zofall,
Chromatin remodeling by ISW2 and SWI/SNF requires DNA translocation inside the nucleosome.
2006,
Pubmed