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. 2003 Nov;133(3):1240–1250. doi: 10.1104/pp.103.023796

Table I.

Relative position of the analyzed restriction sites and methylation sensitivities of the enzymes (Nelson et al., 1993)

Enzyme Position Relative to TSSa Distance from IR Center Site Cutting Methylation Sensitivity Sequence Context
kb
Promoter region approximately 300/+1b
    TaiI-site a -79 ∼1.5 ACGT AmCGT CG
    TaiI-siteb -119 ∼1.6 ACGT AmCGT CG
    TaiI-sitec -130 ∼1.6 ACGT AmCGT CG
    Sau96-site a -163 ∼1.6 gGGTCCad GGWmCC, GGWCmC Nonsymmetrical
    Sau96I-siteb -175 ∼1.6 gGGACCa GGWmCC, GGWCmC Nonsymmetrical
    AluI -286 ∼1.7 tAGCTg AGmCT CWG
    NcoI -522 ∼2.0 CCATGG CmCATGG Nonsymmetrical
    HpaII -923 ∼2.4 CCGG CmCGG, mCCGG CG, CCG
    MspI -923 ∼2.4 CCGG mCCGG CCG
    CfoI -1146 ∼2.6 GCGC GmCGC CG
    SmaI -1636 ∼3.1 CCCGGG CCmCGGG CG
Transcribed region +1/+1,035c
    ClaI +37 ∼1.4 ATCGAT ATmCGAT CG
    BamI-II +881 ∼0.6 gGGATCCt GGATmCC Nonsymmetrical
    SmaI +884 ∼0.6 CCCGGG CCmCGGG CG
    Eco47III +1,211 ∼ 0.2 AGCGCT AGmCGCT CG

a TSS is at nucleotide +1, corresponding to 1,447 bp from the right border.

b The 35S cauliflower promoter securing efficient transcription is approximately 300 bp (Meyer et al., 1994).

c The polyadenylation site from the chalcon synthase gene (accession no. X03710) is at + 1,041, 408 bp from the right border.

d The small letters indicate nucleotides flanking the recognition site that are relevant to the methylation context.