Department of Plant Systems Biology, VIB, B-9052 Gent, Belgium.
Science. 2013 Nov 15;342(6160):860-3. doi: 10.1126/science.1240667. Epub 2013 Oct 24.
The quiescent center (QC) plays an essential role during root development by creating a microenvironment that preserves the stem cell fate of its surrounding cells. Despite being surrounded by highly mitotic active cells, QC cells self-renew at a low proliferation rate. Here, we identified the ERF115 transcription factor as a rate-limiting factor of QC cell division, acting as a transcriptional activator of the phytosulfokine PSK5 peptide hormone. ERF115 marks QC cell division but is restrained through proteolysis by the APC/C(CCS52A2) ubiquitin ligase, whereas QC proliferation is driven by brassinosteroid-dependent ERF115 expression. Together, these two antagonistic mechanisms delimit ERF115 activity, which is called upon when surrounding stem cells are damaged, revealing a cell cycle regulatory mechanism accounting for stem cell niche longevity.
静止中心 (QC) 通过创造一个微环境来维持其周围细胞的干细胞命运,在根发育中起着至关重要的作用。尽管被高度有丝分裂的活跃细胞包围,QC 细胞仍以低增殖率自我更新。在这里,我们确定 ERF115 转录因子是 QC 细胞分裂的限速因子,作为植物磺基肽 PSK5 激素的转录激活剂。ERF115 标记 QC 细胞分裂,但被 APC/C(CCS52A2)泛素连接酶的蛋白水解所抑制,而 QC 增殖则由油菜素内酯依赖性 ERF115 表达驱动。这两种拮抗机制共同限制了 ERF115 的活性,当周围的干细胞受到损伤时,就会调用这种活性,揭示了一个细胞周期调节机制,解释了干细胞生态位的长寿。