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. 2019 Aug 19;9:11960. doi: 10.1038/s41598-019-48130-3

Table 1.

Engineered sequences on donor DNA.

CpG position −58 −43 • −24 −19 *
Wild type DNA sequence ACCGTCCCTAGGTGAGCCGTCTTTCCACCAGGCCCCCGGCTCGGG--------AGGGCTGGAGCCGGG

Donor

DNA

AA ACAATCCCTAGGTGAGCAATCTTTCCACCAGCCCCCAAGCTAAGG--------AGGGCTCGAGCCGGG
AG ACAGTCCCTAGGTGAGCAGTCTTTCCACCAGCCCCCAGGCTAGGG--------AGGGCTCGAGCCGGG
CA ACCATCCCTAGGTGAGCCATCTTTCCACCAGCCCCCCAGCTCAGG--------AGGGCTCGAGCCGGG
CT ACCTTCCCTAGGTGAGCCTTCTTTCCACCAGCCCCCCTGCTCTGG--------AGGGCTCGAGCCGGG
TA ACTA TCCCTAGGTGAGCTATCTTTCCACCAGCCCCCTAGCTTAGG--------AGGGCTCGAGCCGGG
CpG position −470     *      −359   −326  −314  −290  −228   −203  −190
Wild type DNA sequence ACGG----- TCAATGGA------CCGA---GCGA--CCGA--CCGG---CCGT----ACGT---CCGT

Donor

DNA

CC ACCG----- TCCATGGA------CCCA---GCCA--CCCA--CCCG---CCCT----ACCT---CCCT
GG AGGG----- TCCATGGA------CGGA---GGGA--CGGA--CGGG---CGGT----AGGT---CGGT
CC/GG AGGG----- TCCATGGA------CCCA---GGGA--CCCA--CCCG---CCGT----AGGT---CCCT

The site is the PAM sequence for the sgRNA2/Cas9. *The sites are modified for the introduction of the restriction enzyme site as a reporter.