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. 2020 Apr 8;15(4):e0230930. doi: 10.1371/journal.pone.0230930

Table 2. The cells and stages indicated by each number and their abbreviations.

Number Cell and stage Abbreviation (Stage)
1 preleptotene spermatocyte at stage VIII pL (VIII)
2 leptotene spermatocyte at stage X L (X)
3 zygotene spermatocyte at stage XII Z (XII)
4 pachytene spermatocyte at stage I P (I)
5 pachytene spermatocyte at stage V P (V)
6 pachytene spermatocyte at stage VIII P (VIII)
7 pachytene spermatocyte at stage X P (X)
8 M phase spermatocytes at stage XII M (XII)
9 round spermatid at stage I R (I)
10 round spermatid at stage V R (V)
11 round spermatid at stage VIII R (VIII)
12 elongated spermatid at stage X E (X)

While H3K4me2 was observed beginning in preleptotene cells (Fig 1-1B), the H3K4me3 signal was not detected between preleptotene cells to pachytene cells (Fig 1-2A, arrowheads 1–7). H3K4me3 was first detected in M-phase spermatocytes in stage XII seminiferous tubules (Fig 1-2A, arrowhead 8). The signal was broadly distributed on condensed chromosomes (Fig 1-2B, arrowhead 8). After meiosis II, the signal was detected in round spermatids at stages I to VIII, though there was no signal in the chromocenter (Fig 1-2A, arrowheads 9–11). In elongated spermatids, the signal was weak and widely detected in the whole nucleus (Fig 1-2A, arrowhead 12). Thus, localization of the H3K4me3 modification appeared later in meiosis, and the signal was weak compared to the H3K4me2 modification (Fig 1-2B).