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Table 1 KI efficiency in pig parthenogenetic embryos treated with small molecules

From: Modulation of cell cycle increases CRISPR-mediated homology-directed DNA repair

Treatment

Injected embryos

2-cell (%)

Blastocysts (%)

KI rate (%)

Control

466

77.52 ± 3.06ab

48.87 ± 4.84c

11.81 ± 1.84a

Irinotecan

(5 µM)

460

81.12 ± 2.46b

46.97 ± 4.62c

23.61 ± 2.50b

Docetaxel

(0.5 µM)

460

62.97 ± 3.36ab

19.14 ± 3.46b

23.61 ± 3.67b

Mitomycin C

(0.5 µM)

447

70.81 ± 4.98ab

18.31 ± 4.66b

22.22 ± 2.78b

Nocodazole

(0.1 µM)

302

75.53 ± 3.48ab

42.00 ± 4.59c

30.56 ± 1.39C

Irinotecan + Mitomycin C

120

70.83 ± 5.83ab

5.00 ± 1.67a

25.00 ± 25.00abc

Docetaxel + Nocodazole

184

56.14 ± 8.07a

16.14 ± 2.66b

30.56 ± 2.78C

  1. KI rates are ratios of blastocysts with HindIII-cut alleles to all blastocysts
  2. a,b,cDifferent letters indicate statistically significant differences between groups (mean ± SEM, P < 0.05)