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. 2020 Feb 18;9(2):261. doi: 10.3390/plants9020261

Figure 1.

Figure 1

Quantitative RT-PCR assays of enzymes involved in double-strand break repair (DSBR) in UNG lines relative to wild-type: Fold change in transcript level is shown on the Y-axis. Error bars are standard deviation of three biological replicates. MSH1 and RECA2 are significantly transcriptionally upregulated in UNG lines relative to wild-type (5.60-fold increase and 3.19-fold increase, respectively. Unpaired, 2-tailed student’s t-test, * indicates p < 0.05). OSB1 is nearly significantly upregulated in UNG lines relative to wild-type (3.07-fold increase. Unpaired t-test p = 0.053).