Cell cycle-driven epigenetic resetting maintains meristematic cell fate for shoot

演題

Cell cycle-driven epigenetic resetting maintains meristematic cell fate for shoot

講演者

Dr. Yuling Jiao (Peking University, China)

使用言語

English

日時

2026年9月8日(火曜日) 10：30～11：15

場所

L11

内容

Cell proliferation generally promotes differentiation, whereas proliferative quiescence maintains stem cell identity—a paradigm well-established in adult mammalian stem cells. Here, we report that in Arabidopsis bud precursor cells, meristematic cell fate maintenance depends on active cell- cycle progression. We identify two opposing mechanisms that balance H3K27me3 levels to regulate transcription of the shoot meristem marker gene SHOOT MERISTEMLESS (STM). On one hand, two classes of transcription factors recruit polycomb repressive complex 2 (PRC2) to epigenetically silence STM. Conversely, cell proliferation reduces H3K27me3 levels to counteract this silencing. We demonstrate that inhibiting cell division suppresses STM expression and promotes differentiation. The interplay between these forces establishes a cell cycle- coupled epigenetic resetting mechanism that sustains pluripotency. This cell fate switch is bistable; both modeling and experimental data confirm that prolonged quiescence triggers irreversible differentiation. We propose that in plants, sequence-dependent PRC2 recruitment enables precise silencing of fate-determining genes, while cell proliferation maintains pluripotency through periodic resetting of epigenetic marks.

問合せ先

Plant Growth Regulation
Umeda Masaaki (mumeda@bs.naist.jp)