TY - JOUR
T1 - Specificity of the Mnt protein
T2 - Independent effects of mutations at different positions in the operator
AU - Stormo, Gary D.
AU - Strobl, Stefan
AU - Yoshioka, Makoto
AU - Lee, John S.
PY - 1993/2/20
Y1 - 1993/2/20
N2 - The relative binding affinities of Mnt protein are determined for each possible base-pair at position 15 of the operator sequence, and for all combinations of G - C base-pairs at positions 15 and 17. The partitioning of each operator sequence is determined quantitatively with restriction enzymes. At position 15, the wild-type G - C base-pair provides the highest binding affinity but, unlike position 17, the primary distinction is between purine and pyrimidine bases on the top strand. The information content at position 15 is only about 0.16 bit. In comparison with previous measurements at position 17, it is determined that the interactions of the Mnt protein with positions 15 and 17 are independent, i.e. the specific binding energies for the two positions are additive. The relative binding affinities at position 17 are also determined in the background of a G to T mutation at position 5, the position equivalent to 17 on the other half of the symmetric operator. The relative affinities at position 17 are independent of whether position 5 is wild-type or mutant.
AB - The relative binding affinities of Mnt protein are determined for each possible base-pair at position 15 of the operator sequence, and for all combinations of G - C base-pairs at positions 15 and 17. The partitioning of each operator sequence is determined quantitatively with restriction enzymes. At position 15, the wild-type G - C base-pair provides the highest binding affinity but, unlike position 17, the primary distinction is between purine and pyrimidine bases on the top strand. The information content at position 15 is only about 0.16 bit. In comparison with previous measurements at position 17, it is determined that the interactions of the Mnt protein with positions 15 and 17 are independent, i.e. the specific binding energies for the two positions are additive. The relative binding affinities at position 17 are also determined in the background of a G to T mutation at position 5, the position equivalent to 17 on the other half of the symmetric operator. The relative affinities at position 17 are independent of whether position 5 is wild-type or mutant.
KW - DNA-protein interactions
KW - Mnt protein
KW - Protein-DNA recognition
KW - Specificity
UR - http://www.scopus.com/inward/record.url?scp=0027538479&partnerID=8YFLogxK
U2 - 10.1006/jmbi.1993.1088
DO - 10.1006/jmbi.1993.1088
M3 - Editorial
C2 - 8445649
AN - SCOPUS:0027538479
SN - 0022-2836
VL - 229
SP - 821
EP - 826
JO - Journal of Molecular Biology
JF - Journal of Molecular Biology
IS - 4
ER -