Literature DB >> 3011781

The effects of base analogue substitutions on the methylation by the EcoRI modification methylase of octadeoxyribonucleotides containing modified EcoRI recognition sequences.

C A Brennan, M D Van Cleve, R I Gumport.   

Abstract

We have examined the DNA-protein interactions involved in the recognition of a specific hexameric sequence, GAATTC, by the EcoRI modification methylase by using derivatives of an oligodeoxyribonucleotide that contain a variety of base analogues. The base analogues 2-aminopurine, 5-bromocytosine, 5-bromouracil, 2,6-diaminopurine, hypoxanthine, 5-methylcytosine, N6-methyladenine, and uracil were incorporated as single substitutions into the octadeoxyribonucleotide d(pG-G-A-A-T-T-C-C). The effects of the substitutions on the ability of the enzyme to methylate the modified substrates were monitored by determining the steady state kinetic values of the reaction in the presence of the cosubstrate, S-adenosylmethionine. The substitutions resulted in effects ranging from complete inactivity to enhanced reactivity. The enzyme exhibited Michaelis-Menten kinetics with those analogues that were active, whereas the octanucleotides containing hypoxanthine at the guanine site, N6-methyladenine at the first or 2-aminopurine at the second adenine site, or uracil at the second thymine site were completely inactive. The results are discussed in terms of the possible interactions between the methylase and its recognition sequence. In addition, the interactions are compared to those of the EcoRI restriction endonuclease, which has been similarly tested with the same analogue oligonucleotides. The results of that study are reported in an accompanying paper. Although both enzymes recognize the same sequence, they do so in different ways.

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Year:  1986        PMID: 3011781

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  28 in total

1.  Role of DNA minor groove interactions in substrate recognition by the M.SinI and M.EcoRII DNA (cytosine-5) methyltransferases.

Authors:  A Kiss; G Pósfai; G Zsurka; T Raskó; P Venetianer
Journal:  Nucleic Acids Res       Date:  2001-08-01       Impact factor: 16.971

2.  Substrate binding in vitro and kinetics of RsrI [N6-adenine] DNA methyltransferase.

Authors:  S S Szegedi; N O Reich; R I Gumport
Journal:  Nucleic Acids Res       Date:  2000-10-15       Impact factor: 16.971

3.  Effect of site-specific methylation on DNA modification methyltransferases and restriction endonucleases.

Authors:  M McClelland; M Nelson
Journal:  Nucleic Acids Res       Date:  1992-05-11       Impact factor: 16.971

4.  Dnmt3a-CD is less susceptible to bulky benzo[a]pyrene diol epoxide-derived DNA lesions than prokaryotic DNA methyltransferases.

Authors:  Olga V Lukashevich; Vladimir B Baskunov; Maria V Darii; Alexander Kolbanovskiy; Alexander A Baykov; Elizaveta S Gromova
Journal:  Biochemistry       Date:  2011-01-13       Impact factor: 3.162

5.  DNA containing the base analogue 2-aminoadenine: preparation, use as hybridization probes and cleavage by restriction endonucleases.

Authors:  A Chollet; E Kawashima
Journal:  Nucleic Acids Res       Date:  1988-01-11       Impact factor: 16.971

6.  Site-specific methylation: effect on DNA modification methyltransferases and restriction endonucleases.

Authors:  M Nelson; M McClelland
Journal:  Nucleic Acids Res       Date:  1991-04-25       Impact factor: 16.971

7.  Electrospray ionization mass spectrometric characterization of photocrosslinked DNA-EcoRI DNA methyltransferase complexes.

Authors:  D L Wong; J G Pavlovich; N O Reich
Journal:  Nucleic Acids Res       Date:  1998-01-15       Impact factor: 16.971

8.  Effect of site-specific methylation on DNA modification methyltransferases and restriction endonucleases.

Authors:  M Nelson; M McClelland
Journal:  Nucleic Acids Res       Date:  1989       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.  Synthesis of oligodeoxynucleotides containing 2-thiopyrimidine residues--a new protection scheme.

Authors:  R G Kuimelis; K P Nambiar
Journal:  Nucleic Acids Res       Date:  1994-04-25       Impact factor: 16.971

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