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. 2019 Feb 21;12(3):545–556. doi: 10.1016/j.stemcr.2019.01.019

Table 2.

Effect of Kdm4a mRNA Injection and Melatonin Supplement on the Developmental Potential in Cloned Embryos of Cryopreserved Mouse Oocytes

Group Melatonin (μM) No. of NT Oocytes No. of 2-Cell Embryos (%)a No. of 4-Cell Embryos (%)b No. of 2-Cell Block Embryos (% ± SEM)b No. of Blastocysts (% ± SEM)b
SCNT-CROC 125 112 (90) 66 (59) 46 (42 ± 3.7)a 23 (20 ± 1.5)a
SCNT-CROC + M 10 125 114 (91) 81 (71) 33 (31 ± 3.7)a 44 (39 ± 1.2)b
SCNT-CROC + K 138 128 (98) 124 (94) 4 (3 ± 1.5)a 76 (59 ± 3.3)a
SCNT-CROC + K + M 10 138 123 (96) 119 (96) 4 (4 ± 1.8)a 91 (75 ± 3.3)b

SCNT-CROC, cloned embryos from somatic cell nuclear transfer using cryopreserved (vitrified/warmed) oocyte cytoplasm; M, treatment of melatonin; K, injection of lysine (K)-specific demethylase 4A (Kdm4a) mRNA (2 μg/μL). Within the same column, values with different superscript letters (a, b) are significantly different (p < 0.05; n = 5).

a

Based on the number of SCNT oocytes.

b

Based on the number of 2-cell embryos.