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. 2007 Jul 25;8(7):R147. doi: 10.1186/gb-2007-8-7-r147

Table 1.

Systematic variation from consensus DR1-type PPRE

Percent binding strength PPRE position

1 2 3 4 5 6 7 8 9 10 11 12 13
PPARα
 Consensus (90-100) A/G G G T A/C A A A G G T C A
 Class I (60-90) T C G T G T C/G A/G G
 Class II (30-60) C T A/T A/C/G T T C/G C A/C/T T C/T
 Class III (0-30) A/C C/G T A/C A
PPARγ
 Consensus (90-100) A/G G G T C/G A A A G G T C A
 Class I (60-90) C/G A/T T G T C/G A/G/T G
 Class II (30-60) C/T A/T T A C C A/C/T C/T
 Class III (0-30) C A/C C/G/T G T A/C A
PPARβ/δ
 Consensus (90-100) A/G G G T C A A A G G T C A
 Class I (60-90) C/G G/T T G T G/T
 Class II (30-60) C A/T T A A A/T C/G A G/C/T
 Class III (0-30) T C A/C C/G/T C/G C/T C A/C A

The binding strengths of in vitro translated PPAR-RXR heterodimers to 39 systematic variations of the DR1-type consensus PPRE AGGTCAAAGGTCA were determined by gelshift assays in reference to this consensus PPRE. Based on their average binding strength, all variations are sorted into three classes.