TY - JOUR
T1 - Sequence-specific high mobility group box factors recognize 10-12-base pair minor groove motifs
AU - Van Beest, Moniek
AU - Dooijes, Dennis
AU - Van De Wetering, Marc
AU - Kjaerulff, Søren
AU - Bonvin, Alexandre
AU - Nielsen, Olaf
AU - Clevers, Hans
PY - 2000
Y1 - 2000
N2 - Sequence-specific high mobility group (HMG) box factors bind and bend DNA via interactions in the minor groove. Three-dimensional NMR analyses have provided the structural basis for this interaction. The cognate HMG domain DNA motif is generally believed to span 6-8 bases. However, alignment of promoter elements controlled by the yeast genes ste11 and Rox1 has indicated strict conservation of a larger DNA motif. By site selection, we identify a highly specific 12-base pair motif for Ste11, AGAACAAAGAAA. Similarly, we show that Tcf1, MatMc, and Sox4 bind unique, highly specific DNA motifs of 12, 12, and 10 base pairs, respectively. Footprinting with a deletion mutant of Ste11 reveals a novel interaction between the 3' base pairs of the extended DNA motif and amino acids C-terminal to the HMG domain. The sequence-specific interaction of Ste11 with these 3' base pairs contributes significantly to binding and bending of the DNA motif.
AB - Sequence-specific high mobility group (HMG) box factors bind and bend DNA via interactions in the minor groove. Three-dimensional NMR analyses have provided the structural basis for this interaction. The cognate HMG domain DNA motif is generally believed to span 6-8 bases. However, alignment of promoter elements controlled by the yeast genes ste11 and Rox1 has indicated strict conservation of a larger DNA motif. By site selection, we identify a highly specific 12-base pair motif for Ste11, AGAACAAAGAAA. Similarly, we show that Tcf1, MatMc, and Sox4 bind unique, highly specific DNA motifs of 12, 12, and 10 base pairs, respectively. Footprinting with a deletion mutant of Ste11 reveals a novel interaction between the 3' base pairs of the extended DNA motif and amino acids C-terminal to the HMG domain. The sequence-specific interaction of Ste11 with these 3' base pairs contributes significantly to binding and bending of the DNA motif.
UR - http://www.scopus.com/inward/record.url?scp=0034282678&partnerID=8YFLogxK
U2 - 10.1074/jbc.M004102200
DO - 10.1074/jbc.M004102200
M3 - Article
C2 - 10867006
SN - 0021-9258
VL - 275
SP - 27266
EP - 27273
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 35
ER -