Jefri Heyman,Toon Cools,Filip Vandenbussche,Ken S. Heyndrickx,Jelle Van Leene,Ilse Vercauteren,Sandy Vanderauwera,Klaas Vandepoele,Geert De Jaeger,Dominique Van Der Straeten,Lieven De Veylder
出处
期刊:Science [American Association for the Advancement of Science] 日期:2013-10-25卷期号:342 (6160): 860-863被引量:318
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.