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. 1998 Feb 17;95(4):1398–1403. doi: 10.1073/pnas.95.4.1398

Table 2.

PNA-targeted mutagenesis of a chromosomal gene in mouse cells

Treatment supFG1 gene, mutants/total Frequency, ×10−5 cII gene, mutants/total Frequency, ×10−5
No oligo 7/74,093 9 2/51,868 4
PN-8 52/62,359 83 ND ND
PN-10 62/71,437 86 4/45,288 9
CP-10 10/73,185 14 4/49,846 8
RP-10 14/67,551 21 ND ND

The PNAs were introduced into mouse 3340 cells via SLO-mediated permeabilization. After 3–4 days, the cells were harvested for DNA preparation and rescue of the chromosomal shuttle vector. In each case, the frequency of mutant phage carrying mutations in the supFG1 and cII reporter genes was calculated. ND, not determined.