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A
Immunofluorescence of FLAG (red) and F‐actin (gray) in oocytes after microinjection of negative control or mouse Mos siRNAs combined with or without wild‐type human MOS or MOS variants mRNAs and culture in medium with 2.5 µM milrinone for 24 h, followed by release to maturation (n = 15–20 oocytes each group). Scale bar = 10 µm.
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B
The relative intensities of F‐actin were measured and compared among the indicated groups. The oocyte numbers for analyzed were labeled in each group. The box plot showing the F‐actin intensities distribution in each group quantified using Image J (n = 10–19/group).
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C
The immunofluorescence of F‐actin (red) and TPX2 (green) in WT and Erk1/2oo
−/− oocytes, using DAPI (blue) co‐staining (n = 15–20 oocytes for each group). The zoomed images of F‐actin are displayed in gray. Scale bar = 10 µm.
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D
The box plot summarizing the relative intensities of F‐actin between control and ERK1/2oo
−/− oocytes (n = 7–10 oocytes for each group).
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E
Representative bright‐field images showing the morphology of oocytes and embryos from wild‐type and ERK1/2oo
−/− mice. The MII oocyte, zygote, two‐cell, and blastocyst embryos were harvested in vivo at 14, 24, 48, and 96 h post‐hCG, respectively (n = 3 mice for each time points in two groups). Scale bar = 100 µm.
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F, G
Bar graphs shows the blastocyst percentage (F) and fragment percentage (G) in wild‐type (n = 51) and maternal ERK1/2 deletion embryos (n = 63).