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. 1999 Jan;19(1):296–306. doi: 10.1128/mcb.19.1.296

TABLE 1.

Ability of MCAT1 mutant oligonucleotides to compete for binding of LMC1Ba

Name Sequence LMC1B binding
MCAT1 tgCAAGTGTTGCATTCCTCTCTG +++
MCAT/SV40 tgCCTGACACACATTCCTCAGCT +
MCAT1-Emt tgCGACCCTTGCATTCCTCTCTG ++
MCAT1mt tgCAAGTGTTGCCCCACTCTCTG ++
mt1 tgGGAGTGTTGCATTCCTCTCTG ++
mt2 tgCAGTTGTTGCATTCCTCTCTG ++
mt3 tgCAAGGTTTGCATTCCTCTCTG +
mt4 tgCAAGTGGGGCATTCCTCTCTG +/−
mt5 tgCAAGTGTTTGATTCCTCTCTG
mt6 tgCAAGTGTTGCGGTCCTCTCTG +
mt7 tgCAAGTGTTGCATGGCTCTCTG ++
mt8 tgCAAGTGTTGCATTCGGCTCTG ++
mt9 tgCAAGTGTTGCATTCCTGGCTG ++
mt10 tgCAAGTGTTGCATTCCTCTGGG ++
MCAT2 tgCGCCGGGCACATTCCTGCTGC
a

Summary of results of competition analysis performed as shown in Fig. 1. +++, oligonucleotide competition as efficient as that of MCAT1 element; ++, efficient competition; +, weak competition; +/−, very weak competition; −, no competition. Cohesive termini are denoted by lowercase type (33). Mutated bases are underlined, and the core MCAT motifs are indicated by boldface type.