Table 1.

DNA oligomers used to create the β-globin gene variants by overlap-extension PCR

Oligomer*OrientationSequence (5′ → 3′)Position1-153
β5(ATC)b − TCTCCTCCTAAGTCAGGTG  
β5(TAG)c CACCTGACTTAGGAGGAGA 56 
β15(ATC)b − CCTTGCCCTACAGGGCAG  
β15(TAG)c CTGCCCTGTAGGGCAAGG 86 
β15(ATT)b − CCTTGCCTTACAGGGCAG  
β15(TAA)c CTGCCCTGTAAGGCAAGG 86 
β17(ATC)b − CGTTCACCTAGCCCCAC  
β17(TAG)c GTGGGGCTAGGTGAACG 94 
β26(ATC)b − CCAGGGCCTAACCACCAA  
β26(TAG)c TTGGTGGTTAGGCCCTGG 120 
Oligomer*OrientationSequence (5′ → 3′)Position1-153
β5(ATC)b − TCTCCTCCTAAGTCAGGTG  
β5(TAG)c CACCTGACTTAGGAGGAGA 56 
β15(ATC)b − CCTTGCCCTACAGGGCAG  
β15(TAG)c CTGCCCTGTAGGGCAAGG 86 
β15(ATT)b − CCTTGCCTTACAGGGCAG  
β15(TAA)c CTGCCCTGTAAGGCAAGG 86 
β17(ATC)b − CGTTCACCTAGCCCCAC  
β17(TAG)c GTGGGGCTAGGTGAACG 94 
β26(ATC)b − CCAGGGCCTAACCACCAA  
β26(TAG)c TTGGTGGTTAGGCCCTGG 120 
*

The number in the oligomer designations indicates the codon in which the nonsense mutation was introduced.

Minus signs indicate antisense; plus signs indicate sense.

Underlined sequences indicate the nonsense codons created by overlap-extension PCR.

F1-153

Distance (in nucleotides) between the oligomer sequence and the transcriptional initiation site of the human β-globin gene.

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