Literature DB >> 3656450

Spectroscopic studies on histone-DNA interactions. I. The interaction of histone (H2A, H2B) dimer with DNA: DNA sequence dependence.

I Oohara1, A Wada.   

Abstract

Binding of the histone (H2A, H2B) dimer with chicken erythrocyte DNA has been studied by salt-titration spectroscopy in equilibrium conditions. The circular dichroism of DNA near 275 nm is depressed by the interaction with (H2A, H2B) at low concentrations of salt. The depression increases with increasing amounts of (H2A, H2B), and reaches a plateau at an (H2A, H2B) to DNA ratio of 1.5 (w/w), at which one (H2A, H2B) dimer occupies 28 base-pairs of DNA. The fluorescence emission intensity of the tyrosine residues in (H2A, H2B) is depressed by the H2A, H2B)-DNA interaction. When the DNA-(H2A, H2B) complex is titrated with NaCl, these two signals show transitions with increasing ionic strength of the buffer, whose normalized transition curves agree well. The midpoint of the transition is about 0.42 M-NaCl for a sample with a DNA concentration of 0.05 mg/ml and an (H2A, H2B) to DNA ratio of 0.4 (w/w). The fluorescence titration curves have been analyzed to obtain the binding constant for the (H2A, H2B) dimer with DNA. The sample concentration dependence of the titration profiles is consistent with the model of non-cooperative binding of (H2A, H2B) dimer to DNA. The titration profiles are reversible. The obtained binding constant for the (H2A, H2B) dimer with chicken erythrocyte DNA at 20 degrees C (pH 7.6), as a function of the ionic strength, I, is as follows: log10K = -14.9 log10(I)-1.2. The change of enthalpy delta H accompanied by the binding of the (H2A, H2B) dimer is nearly equal to zero, within an error of +/- 1.4 kcal/mol (1 cal = 4.184 J). DNA sequence dependence of the stability of DNA-(H2A, H2B) interactions is observed using reconstituted materials of synthetic DNAs. A decreasing stability of the interaction is observed following the order: the duplex of poly[(dA)-(dT)] greater than chicken erythrocyte DNA or the copolymer duplex of poly(dA).poly(dT) greater than the duplex of poly[(dG)-(dC)]. The difference in free energy of the association of the (H2A,H2B) dimer between the two copolymers is 0.8 kcal/mol.

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Year:  1987        PMID: 3656450     DOI: 10.1016/0022-2836(87)90699-1

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  12 in total

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2.  Drug-induced anti-histone autoantibodies display two patterns of reactivity with substructures of chromatin.

Authors:  R W Burlingame; R L Rubin
Journal:  J Clin Invest       Date:  1991-08       Impact factor: 14.808

3.  Nucleosomal regulation of chromatin composition and nuclear assembly revealed by histone depletion.

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Journal:  Nat Struct Mol Biol       Date:  2014-06-22       Impact factor: 15.369

4.  Asymmetric unwrapping of nucleosomal DNA propagates asymmetric opening and dissociation of the histone core.

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Journal:  Proc Natl Acad Sci U S A       Date:  2016-12-27       Impact factor: 11.205

5.  Genetic dissection of SLE pathogenesis. Sle1 on murine chromosome 1 leads to a selective loss of tolerance to H2A/H2B/DNA subnucleosomes.

Authors:  C Mohan; E Alas; L Morel; P Yang; E K Wakeland
Journal:  J Clin Invest       Date:  1998-03-15       Impact factor: 14.808

6.  The histone chaperone Nap1 promotes nucleosome assembly by eliminating nonnucleosomal histone DNA interactions.

Authors:  Andrew J Andrews; Xu Chen; Alexander Zevin; Laurie A Stargell; Karolin Luger
Journal:  Mol Cell       Date:  2010-03-26       Impact factor: 17.970

7.  Genesis and evolution of antichromatin autoantibodies in murine lupus implicates T-dependent immunization with self antigen.

Authors:  R W Burlingame; R L Rubin; R S Balderas; A N Theofilopoulos
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8.  The central role of chromatin in autoimmune responses to histones and DNA in systemic lupus erythematosus.

Authors:  R W Burlingame; M L Boey; G Starkebaum; R L Rubin
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9.  The mechanics behind DNA sequence-dependent properties of the nucleosome.

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Journal:  Nucleic Acids Res       Date:  2012-03-26       Impact factor: 16.971

10.  Selective requirement of H2B N-Terminal tail for p14ARF-induced chromatin silencing.

Authors:  Jongkyu Choi; Hyunjung Kim; Kyunghwan Kim; Bomi Lee; Wange Lu; Woojin An
Journal:  Nucleic Acids Res       Date:  2011-08-16       Impact factor: 16.971

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