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. 2022 Nov 28;24(2):e55778. doi: 10.15252/embr.202255778

Figure EV4. The phenotype of M1ap −/− mice.

Figure EV4

  • A–C
    Representative images of testes (A), the ratio of testis/body weight (B), and the sperm count per epididymis (C) from 8‐week‐old control and M1ap −/− mice. Each grid represents 1 mm in (A).
  • D
    Representative images of hematoxylin and eosin‐stained sections of testes and cauda epididymides from 8‐week‐old control and M1ap −/− mice. A magnified view of the boxed representative metaphase cell is shown in the lower left corner of the image of M1ap −/− mice. The blue arrow indicates unaligned chromosomes. Scale bars, 50 μm.
  • E
    Immunofluorescence staining of SYCP3 (red) and γH2AX (green) on spermatocyte spreads from 8‐week‐old control and M1ap −/− mice. Scale bars, 10 μm.
  • F
    The percentages of spermatocytes at each stage of meiotic prophase I in 8‐week‐old control and M1ap −/− mice.
  • G
    Quantification of nuclei with untouching XY chromosomes at pachytene.
  • H
    Immunofluorescence staining of SYCP3 (red) and MLH3 (green) in spermatocyte spreads from 8‐week‐old control and M1ap −/− mice. Scale bars, 10 μm.
  • I
    Number of MLH3 foci per cell.
  • J
    Meiotic metaphase I (MMI) spermatocytes stained with Giemsa. Scale bars, 10 μm.
  • K
    Number of bivalents per nucleus.
  • L
    Frequencies of nuclei with univalents.
  • M
    Frequencies of nuclei with only XY univalents, only autosome univalents, or both XY and autosome univalents.

Data information: (B and C), Data are presented as the mean ± SEM of three biological replicates. (F, G, I, and K–M) Data are presented as mean ± SEM. n shows the number of cells scored from at least three biological replicates. **P < 0.01; ***P < 0.001; ****P < 0.0001; NS, not significant; two‐tailed Student's t‐test.