Literature DB >> 6299667

Eco RI* specificity and hydrogen bonding.

J M Rosenberg, P Greene.   

Abstract

Under standard conditions, Eco RI endonuclease uniquely recognizes the inverted repeat GAATTC. However, this specificity breaks down under non-standard conditions into what has been termed Eco RI* specificity, wherein many other sequences are recognized. We show here that the hydrolysis rates at all known Eco RI* sites can be summarized by the hierarchies: G much greater than A greater than T much greater than C at the first position, A much greater than [G,C] much greater than T at the second and third position, and the corresponding complements at the last three positions. This is consistent with a recognition model which assumes that there are two specific hydrogen bonds per base pair under standard conditions. One or more of these are randomly replaced by water under Eco RI* conditions and the position of a sequence within the appropriate hierarchy is primarily determined by the number of retained hydrogen bonds. These retained hydrogen bonds are common recognition features that can be identified by examining the DNA. The recognition points thereby identified for Eco RI all fall within the major groove of the DNA.

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Year:  1982        PMID: 6299667     DOI: 10.1089/dna.1.1982.1.117

Source DB:  PubMed          Journal:  DNA        ISSN: 0198-0238


  12 in total

1.  In vivo specificity of EcoRI DNA methyltransferase.

Authors:  D W Smith; S W Crowder; N O Reich
Journal:  Nucleic Acids Res       Date:  1992-11-25       Impact factor: 16.971

2.  Differences between EcoRI nonspecific and "star" sequence complexes revealed by osmotic stress.

Authors:  Nina Y Sidorova; Donald C Rau
Journal:  Biophys J       Date:  2004-10       Impact factor: 4.033

3.  Genetic analysis of the interaction of the insertion sequence IS903 transposase with its terminal inverted repeats.

Authors:  K M Derbyshire; L Hwang; N D Grindley
Journal:  Proc Natl Acad Sci U S A       Date:  1987-11       Impact factor: 11.205

4.  Site directed mutagenesis experiments suggest that Glu 111, Glu 144 and Arg 145 are essential for endonucleolytic activity of EcoRI.

Authors:  H Wolfes; J Alves; A Fliess; R Geiger; A Pingoud
Journal:  Nucleic Acids Res       Date:  1986-11-25       Impact factor: 16.971

Review 5.  Type II restriction endonucleases--a historical perspective and more.

Authors:  Alfred Pingoud; Geoffrey G Wilson; Wolfgang Wende
Journal:  Nucleic Acids Res       Date:  2014-05-30       Impact factor: 16.971

6.  Changes in solvation during DNA binding and cleavage are critical to altered specificity of the EcoRI endonuclease.

Authors:  C R Robinson; S G Sligar
Journal:  Proc Natl Acad Sci U S A       Date:  1998-03-03       Impact factor: 11.205

7.  A mammalian high mobility group protein recognizes any stretch of six A.T base pairs in duplex DNA.

Authors:  M J Solomon; F Strauss; A Varshavsky
Journal:  Proc Natl Acad Sci U S A       Date:  1986-03       Impact factor: 11.205

8.  Construction of bacteriophage T7 late promoters with point mutations and characterization by in vitro transcription properties.

Authors:  K A Chapman; R R Burgess
Journal:  Nucleic Acids Res       Date:  1987-07-10       Impact factor: 16.971

9.  Proton exchange and base-pair opening kinetics in 5'-d(CGCGAATTCGCG)-3' and related dodecamers.

Authors:  J G Moe; I M Russu
Journal:  Nucleic Acids Res       Date:  1990-02-25       Impact factor: 16.971

10.  Mutants of the EcoRI endonuclease with promiscuous substrate specificity implicate residues involved in substrate recognition.

Authors:  J Heitman; P Model
Journal:  EMBO J       Date:  1990-10       Impact factor: 11.598

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