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).