Site Name | Sequence | % Bound by FAX-1 | S.D. |
---|
DR1A |
AAGTCAaAAGTCA
| 53.3 | 13.6 |
DR1G |
AGGTCAaAGGTCA
| 42.1 | 11.8 |
DR1C |
ACGTCAaACGTCA
| 26.1 | 17.2 |
DR1T |
ATGTCAaATGTCA
| 29.8 | 1.9 |
DRNC |
AATTCAaAATTCA
| 0.4 | 0.2 |
MON1 |
AAGTCAaAATTTA
| 2.8 | 0.6 |
MON2 |
AATTTAaAAGTCA
| 4.5 | 1.0 |
HRSW |
AAGTCAaAATTCA
| 11.7 | 1.0 |
HRWS |
AATTCAaAAGTCA
| 10.5 | 0.9 |
DR2A |
AAGTCAaaAAGTCA
| 20.7 | 6.8 |
DR3A |
AAGTCAaaaAAGTCA
| 2.3 | 0.4 |
- The first column indicates the name used to refer to each sequence in the text. The second column shows the actual sequence tested. The third column indicates the percentage of the labeled DNA that was shifted to high mobility in EMSA experiments using FAX-1 protein. The fourth column indicates standard deviation for each set of EMSA experiments summarized. We evaluated the significance of the data using One-Way ANOVA and Fisher 95% Confidence Intervals for all pairwise comparisons. DR1A and DR1G were not significantly different from each other. DR1A was significantly different from all other sequences tested (p < 0.05). The difference between DR1G and DR1C or DR1T fell just outside the range of statistical significance. Binding data for MON1, MON2, DR3A, and DRNC sites were not significantly different from each. Pairwise differences between HRWS or HRSW and MON1 or MON2 were significant (p < 0.05).