Literature DB >> 6641700

Differential promotion and suppression of Z leads to B transitions in poly[d(G-C)] by histone subclasses, polyamino acids and polyamines.

W C Russell, B Precious, S R Martin, P M Bayley.   

Abstract

The right-handed (B) conformation of poly[d(G-C)] in 7.5 mM sodium cacodylate and 25% ethylene glycol can be readily converted to the left-handed (Z) conformation by the addition of 250 microM MnCl2 and this transition can be reversed by chelation of the Mn ions with EDTA or by addition of NaCl. This ability to obtain such reversible transitions in solvent and solute conditions which allow DNA-protein interactions and their assessment by c.d. permitted an analysis of the effect of purified histones, polyamino acids, protamine and polyamines on these transitions. Individual core histones H3, H4, H2a and H2b or protamine stabilised the Mn-induced Z form and prevented the transition to B DNA normally observed after chelation with EDTA or on dialysis to physiological salt concentrations. A similar suppression of Z leads to B transition was also achieved with poly-L-arginine (but not with poly-L-lysine). In contrast, histones H1 and H5 promoted the Z leads to B transition. Polyamines (spermine and spermidine) converted the B form to another right-handed (A) form which transformed to the Z form after the addition of EDTA and this Z form was restored to the B conformation on the addition of NaCl. These results suggest that sequence-dependent variations in the conformation of natural DNA may be modulated by interaction with histones and other basic cellular components and may provide a conformational basis for nucleosome formation and possibly for the control of gene expression.

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Year:  1983        PMID: 6641700      PMCID: PMC555340          DOI: 10.1002/j.1460-2075.1983.tb01639.x

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  36 in total

1.  Sequence-specific recognition of double helical nucleic acids by proteins.

Authors:  N C Seeman; J M Rosenberg; A Rich
Journal:  Proc Natl Acad Sci U S A       Date:  1976-03       Impact factor: 11.205

2.  The isolation and purification of the high mobility group (HMG) nonhistone chromosomal proteins.

Authors:  G H Goodwin; E W Johns
Journal:  Methods Cell Biol       Date:  1977       Impact factor: 1.441

3.  Fractionation of histones on molecular sieve matrices.

Authors:  C von Holt; W F Brandt
Journal:  Methods Cell Biol       Date:  1977       Impact factor: 1.441

4.  Spermine and spermidine-induced B to A transition of DNA in solution.

Authors:  E E Minyat; V I Ivanov; A M Kritzyn; L E Minchenkova; A K Schyolkina
Journal:  J Mol Biol       Date:  1979-03-05       Impact factor: 5.469

5.  Salt-induced co-operative conformational change of a synthetic DNA: equilibrium and kinetic studies with poly (dG-dC).

Authors:  F M Pohl; T M Jovin
Journal:  J Mol Biol       Date:  1972-06-28       Impact factor: 5.469

6.  The isolation and purification of histones.

Authors:  E W Johns
Journal:  Methods Cell Biol       Date:  1977       Impact factor: 1.441

7.  Interaction of metal ions with polynucleotides and related compounds. XV. Nuclear magnetic resonance studies of the binding of copper(II) to nucleotides and polynucleotides.

Authors:  N A Berger; G L Eichhorn
Journal:  Biochemistry       Date:  1971-05-11       Impact factor: 3.162

8.  A salt-induced conformational change in crystals of the synthetic DNA tetramer d(CpGpCpG).

Authors:  H R Drew; R E Dickerson; K Itakura
Journal:  J Mol Biol       Date:  1978-11-15       Impact factor: 5.469

9.  Cromatin and core particles formed from the inner histones and synthetic polydeoxyribonucleotides of defined sequence.

Authors:  R T Simpson; P Künzler
Journal:  Nucleic Acids Res       Date:  1979-04       Impact factor: 16.971

10.  Polypeptide phosphorylation in adenovirus-infected cells.

Authors:  W C Russell; G E Blair
Journal:  J Gen Virol       Date:  1977-01       Impact factor: 3.891

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  7 in total

1.  Concordance of experimentally mapped or predicted Z-DNA sites with positions of selected alternating purine-pyrimidine tracts.

Authors:  A K Konopka; J Reiter; M Jung; D A Zarling; T M Jovin
Journal:  Nucleic Acids Res       Date:  1985-03-11       Impact factor: 16.971

2.  Polyamine effects on purine-purine-pyrimidine triple helix formation by phosphodiester and phosphorothioate oligodeoxyribonucleotides.

Authors:  M Musso; M W Van Dyke
Journal:  Nucleic Acids Res       Date:  1995-06-25       Impact factor: 16.971

3.  Zinc Z-DNA.

Authors:  G V Fazakerley
Journal:  Nucleic Acids Res       Date:  1984-04-25       Impact factor: 16.971

4.  Detection of Z DNA binding proteins in tissue culture cells.

Authors:  I R Leith; R T Hay; W C Russell
Journal:  Nucleic Acids Res       Date:  1988-09-12       Impact factor: 16.971

5.  Immunological detection of left-handed Z DNA in isolated polytene chromosomes. Effects of ionic strength, pH, temperature and topological stress.

Authors:  M Robert-Nicoud; D J Arndt-Jovin; D A Zarling; T M Jovin
Journal:  EMBO J       Date:  1984-04       Impact factor: 11.598

6.  Zuotin, a putative Z-DNA binding protein in Saccharomyces cerevisiae.

Authors:  S Zhang; C Lockshin; A Herbert; E Winter; A Rich
Journal:  EMBO J       Date:  1992-10       Impact factor: 11.598

7.  Immunofluorescence localization of Z-DNA in chromosomes: quantitation by scanning microphotometry and computer-assisted image analysis.

Authors:  D J Arndt-Jovin; M Robert-Nicoud; P Baurschmidt; T M Jovin
Journal:  J Cell Biol       Date:  1985-10       Impact factor: 10.539

  7 in total

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