Literature DB >> 9169189

In vitro reconstitution and analysis of mononucleosomes containing defined DNAs and proteins.

J J Hayes1, K M Lee.   

Abstract

Increasingly, biochemical analyses of processes that occur within eukaryotic nuclei such as transcription and replication require the construction of specific chromatin substrates. Nucleosome complexes reconstituted in vitro have been key elements in a variety of recent studies of polymerase progression and trans-acting factor binding activities. Reconstituted complexes can be easily constructed from purified components in quantities suitable for biochemical and biophysical studies. In addition, reconstituted mononucleosome complexes exhibit native biochemical and biophysical properties but necessarily contain much less heterogeneity with regard to both protein and DNA components than bulk complexes isolated from natural sources. This review details the protocols for reconstitution of model mononucleosome complexes that contain unique DNA sequences and specifically tailored core histone proteins and describes common pitfalls associated with these procedures.

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Year:  1997        PMID: 9169189     DOI: 10.1006/meth.1997.0441

Source DB:  PubMed          Journal:  Methods        ISSN: 1046-2023            Impact factor:   3.608


  33 in total

1.  A novel labeling technique reveals a function for histone H2A/H2B dimer tail domains in chromatin assembly in vivo.

Authors:  C Thiriet; J J Hayes
Journal:  Genes Dev       Date:  2001-08-15       Impact factor: 11.361

2.  R2 retrotransposition on assembled nucleosomes depends on the translational position of the target site.

Authors:  Junqiang Ye; Zungyoon Yang; Jeffrey J Hayes; Thomas H Eickbush
Journal:  EMBO J       Date:  2002-12-16       Impact factor: 11.598

3.  Structural features of transcription factor IIIA bound to a nucleosome in solution.

Authors:  Joseph M Vitolo; Zungyoon Yang; Ravi Basavappa; Jeffrey J Hayes
Journal:  Mol Cell Biol       Date:  2004-01       Impact factor: 4.272

4.  SWI/SNF remodeling and p300-dependent transcription of histone variant H2ABbd nucleosomal arrays.

Authors:  Dimitar Angelov; André Verdel; Woojin An; Vladimir Bondarenko; Fabienne Hans; Cécile-Marie Doyen; Vassily M Studitsky; Ali Hamiche; Robert G Roeder; Philippe Bouvet; Stefan Dimitrov
Journal:  EMBO J       Date:  2004-09-16       Impact factor: 11.598

5.  The divalent cations Ca2+ and Mg2+ play specific roles in stabilizing histone-DNA interactions within nucleosomes that are partially redundant with the core histone tail domains.

Authors:  Zungyoon Yang; Jeffrey J Hayes
Journal:  Biochemistry       Date:  2011-10-31       Impact factor: 3.162

6.  The core histone N-terminal tail domains negatively regulate binding of transcription factor IIIA to a nucleosome containing a 5S RNA gene via a novel mechanism.

Authors:  Zungyoon Yang; Chunyang Zheng; Christophe Thiriet; Jeffrey J Hayes
Journal:  Mol Cell Biol       Date:  2005-01       Impact factor: 4.272

7.  Mechanism of polymerase II transcription repression by the histone variant macroH2A.

Authors:  Cécile-Marie Doyen; Woojin An; Dimitar Angelov; Vladimir Bondarenko; Flore Mietton; Vassily M Studitsky; Ali Hamiche; Robert G Roeder; Philippe Bouvet; Stefan Dimitrov
Journal:  Mol Cell Biol       Date:  2006-02       Impact factor: 4.272

8.  The NH2 tail of the novel histone variant H2BFWT exhibits properties distinct from conventional H2B with respect to the assembly of mitotic chromosomes.

Authors:  Mathieu Boulard; Thierry Gautier; Gaelh Ouengue Mbele; Véronique Gerson; Ali Hamiche; Dimitar Angelov; Philippe Bouvet; Stefan Dimitrov
Journal:  Mol Cell Biol       Date:  2006-02       Impact factor: 4.272

9.  The H3 tail domain participates in multiple interactions during folding and self-association of nucleosome arrays.

Authors:  Pu-Yeh Kan; Xu Lu; Jeffrey C Hansen; Jeffrey J Hayes
Journal:  Mol Cell Biol       Date:  2007-01-22       Impact factor: 4.272

10.  Acetylation-modulated communication between the H3 N-terminal tail domain and the intrinsically disordered H1 C-terminal domain.

Authors:  Fanfan Hao; Kevin J Murphy; Tomoya Kujirai; Naoki Kamo; Junko Kato; Masako Koyama; Akimitsu Okamato; Gosuke Hayashi; Hitoshi Kurumizaka; Jeffrey J Hayes
Journal:  Nucleic Acids Res       Date:  2020-11-18       Impact factor: 16.971

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