Literature DB >> 3477454

A two-dimensional 1H-NMR study of the dam methylase site: comparison between the hemimethylated GATC sequence, its unmethylated analogue and a hemimethylated CATG sequence. The sequence dependence of methylation upon base-pair lifetimes.

G V Fazakerley1, E Quignard, R Teoule, A Guy, W Guschlbauer.   

Abstract

We report two-dimensional NOE (NOESY) spectra on the sequence d(GCGATCATGG).d(CCATGATCGC) which contains the unmethylated dam site. As expected the DNA adopts a B-form conformation but appears to be distorted at the TG step of the second strand. This distorsion, probably bending, is not seen on the opposite strand. When the first strand is methylated on adenine in the GATC or CATG sequence the NOESY spectra indicate little or no change in the conformation. However the single strand-duplex exchange is slowed down to the slow-exchange region on a proton NMR time scale. We have assigned the exchangeable imino and cytidine amino resonances of the three duplexes. From the imino linewidths as a function of temperature, we observe that the unmethylated and the hemimethylated Gm6ATC duplexes melt normally from the ends. However, this is not so for the hemimethylated Cm6ATG duplex which, apart from the terminal base pairs, melts cooperatively and at higher temperature. In spectra recorded in H2O a second duplex is observed, for the Gm6ATC sequence, which we have not been able to identify. It is however unlikely to be a hairpin structure. Ultraviolet-melting curves also indicate the presence of two transitions for this duplex. The effect of methylation upon base-pair lifetimes has been studied by comparing the above three duplexes. Little effect is observed upon methylation in the GATC sequence but a drastic increase in the lifetimes of all base pairs is observed upon methylation in the CATG sequence.

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Year:  1987        PMID: 3477454     DOI: 10.1111/j.1432-1033.1987.tb13351.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  10 in total

1.  NMR studies for identification of dI:dG mismatch base-pairing structure in DNA.

Authors:  Y Oda; S Uesugi; M Ikehara; Y Kawase; E Ohtsuka
Journal:  Nucleic Acids Res       Date:  1991-10-11       Impact factor: 16.971

2.  The solution structure of a DNA hairpin containing a loop of three thymidines determined by nuclear magnetic resonance and molecular mechanics.

Authors:  Y Boulard; J Gabarro-Arpa; J A Cognet; M Le Bret; A Guy; R Téoule; W Guschlbauer; G V Fazakerley
Journal:  Nucleic Acids Res       Date:  1991-10-11       Impact factor: 16.971

3.  Allosteric and catalytic binding of S-adenosylmethionine to Escherichia coli DNA adenine methyltransferase monitored by 3H NMR.

Authors:  A Bergerat; W Guschlbauer; G V Fazakerley
Journal:  Proc Natl Acad Sci U S A       Date:  1991-08-01       Impact factor: 11.205

4.  Study of structure, base-pair opening kinetics and proton exchange mechanism of the d-(AATTGCAATT) self-complementary oligodeoxynucleotide in solution.

Authors:  M Kochoyan; G Lancelot; J L Leroy
Journal:  Nucleic Acids Res       Date:  1988-08-11       Impact factor: 16.971

5.  Theoretical study on the binding mechanism between N6-methyladenine and natural DNA bases.

Authors:  Qi-Xia Song; Zhen-Dong Ding; Jian-Hua Liu; Yan Li; Hai-Jun Wang
Journal:  J Mol Model       Date:  2012-11-09       Impact factor: 1.810

6.  The GTm6AC sequence is overwound and bent.

Authors:  G V Fazakerley; J Gabarro-Arpa; M Lebret; A Guy; W Guschlbauer
Journal:  Nucleic Acids Res       Date:  1989-04-11       Impact factor: 16.971

Review 7.  N6-Methyladenine: A Conserved and Dynamic DNA Mark.

Authors:  Zach Klapholz O'Brown; Eric Lieberman Greer
Journal:  Adv Exp Med Biol       Date:  2016       Impact factor: 2.622

8.  Specificity of DNA recognition in the nucleoprotein complex for site-specific recombination by Tn21 resolvase.

Authors:  S C Hall; S E Halford
Journal:  Nucleic Acids Res       Date:  1993-12-11       Impact factor: 16.971

9.  Dam methylase from Escherichia coli: kinetic studies using modified DNA oligomers: hemimethylated substrates.

Authors:  S Marzabal; S DuBois; V Thielking; A Cano; R Eritja; W Guschlbauer
Journal:  Nucleic Acids Res       Date:  1995-09-25       Impact factor: 16.971

10.  On the role of steric clashes in methylation control of restriction endonuclease activity.

Authors:  Karolina Mierzejewska; Matthias Bochtler; Honorata Czapinska
Journal:  Nucleic Acids Res       Date:  2015-12-03       Impact factor: 16.971

  10 in total

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