Nucleotide sequence of the recognition site for the restriction-modification enzyme of Escherichia coli B.

Abstract:

:The nucleotide sequence of the recognition site for the restriction-modification enzyme of Escherichia coli B (SB site) has been determined. The recognition site is a 15-nucleotide sequence consisting of the trimer 5'TGA3', followed by an 8-nucleotide domain of variable sequence, which in turn is followed by tetramer 5'TGCT3'. The sequence has no 2-fold rotational symmetry. Single base changes in the constant nucleotide domains result in the loss of sensitivity to both restriction and modification. Our data are also consistent with modification occurring by methylation of two adenine residues per SB site: one on the adenine of the trimer 5'TGA3' and the other on the complementary strand on the adenine complementary to the first thymine of the tetramer 5'TGCT3'. All nine independently isolated spontaneous mutants at the SB1 site of bacteriophage f1 are caused by a G-to-T transversion. Mutations at the SB2 site are caused by various single base changes.

authors

Ravetch JV,Horiuchi K,Zinder ND

doi

10.1073/pnas.75.5.2266

subject

Has Abstract

pub_date

1978-05-01 00:00:00

pages

2266-70

issue

5

eissn

0027-8424

issn

1091-6490

journal_volume

75

pub_type

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