Studies on gene control regions XII. The functional significance of a lac operator constitutive mutation - PubMed (original) (raw)

Studies on gene control regions XII. The functional significance of a lac operator constitutive mutation

E F Fisher et al. Nucleic Acids Res. 1979.

Free PMC article

Abstract

The functional significance of a lac operator constitutive mutation has been determined. The transition adenine-thymine to guanine-cytosine was shown to be a constitutive mutation simply because thymine contains the functionally important 5-methyl group whereas cytosine does not. The remainder of the base pair is of no consequence. The experimental approach was to synthesize various modified operators containing cytosine, 5-methyl-cytosine, and 5-bromocytosine. The synthetic operator containing a guanine-cytosine base pair displays an eightfold reduction in stability with lac repressor whereas the operator containing 5-methylcytosine binds repressor at least as tightly as does the wild type sequence. Results published previously have shown that a similar decrease in stability of the repressor-operator complex can be obtained simply by substituting uracil for thymine or by inverting the base pair to thymine-adenine. All these results taken together implicate the thymine 5-methyl as the only important functional group recognized by the lac repressor at this base pair. Further confirmation of this conclusion was obtained by substitution of 5-bromocytosine and 5-bromouracil at this base pair. Both altered the stability of the repressor-operator complex by about the same percent suggesting that the bromine atom was the important determinant of complex stability for 5-bromopyrimidine analogs.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Biochemistry. 1976 May 4;15(9):1858-65 - PubMed
    1. Biochemistry. 1977 May 3;16(9):1765-72 - PubMed
    1. Nucleic Acids Res. 1977 Sep;4(9):3039-54 - PubMed
    1. Proc Natl Acad Sci U S A. 1977 Aug;74(8):3292-6 - PubMed
    1. Nucleic Acids Res. 1979 Jun 11;6(7):2583-99 - PubMed

Publication types

MeSH terms

Substances

LinkOut - more resources