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[Preprint]. 2024 Aug 6:2024.08.05.606388. [Version 1] doi: 10.1101/2024.08.05.606388

Fig 4. MLH1-KQQ fails to promote polar resolution of sequence divergence at bases 1 and 2, but not 7 and 8, whereas MLH1-566-3A shows a defect at each base.

Fig 4.

(A) Shown is the frequency of top strand base retention for WT, Mlh1−/−, Mlh1−/− + MLH1 (WT), Mlh1−/− + KQQ mESCs. WT samples as in Fig 2B. n=3. *p ≤ 0.05, **p ≤ 0.005, *** ≤ 0.001. WT vs. Mlh1−/−, unpaired t-test, Mlh1−/− vs. Mlh1−/− + MLH1 (WT) and Mlh1−/− + KQQ, unpaired t-tests with Holm-Sidak correction. (B) Frequency of top strand base retention for WT, Mlh1−/−, Mlh1−/− + MLH1 (WT), Mlh1−/− + 566–3A mESCs. WT samples as in Fig 2B. n=3. *p ≤ 0.05, **p ≤ 0.005, *** ≤ 0.001. WT vs. Mlh1−/−, unpaired t-test, Mlh1−/− vs. Mlh1−/− + MLH1 (WT) and Mlh1−/− + 566–3A, unpaired t-tests with Holm-Sidak correction. Data are represented as mean values ± SD.