Arabidopsis RETINOBLASTOMA-RELATED Is Required for Stem Cell Maintenance, Cell Differentiation, and Lateral Organ Production

被引:136
作者
Borghi, Lorenzo [1 ]
Gutzat, Ruben [1 ]
Fuetterer, Johannes [1 ]
Laizet, Yec'han [1 ]
Hennig, Lars [1 ]
Gruissem, Wilhelm [1 ]
机构
[1] ETH, Dept Biol, CH-8092 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
GEMINIVIRUS REPLICATION PROTEIN; GENOME-WIDE IDENTIFICATION; INDUCIBLE GENE-EXPRESSION; SHOOT APICAL MERISTEM; SEVERE GROWTH DEFECTS; RB TUMOR-SUPPRESSOR; D-TYPE CYCLIN; DNA-REPLICATION; WUSCHEL EXPRESSION; OXIDATIVE STRESS;
D O I
10.1105/tpc.110.074591
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Several genes involved in the regulation of postembryonic organ initiation and growth have been identified. However, it remains largely unclear how developmental cues connect to the cell cycle. RETINOBLASTOMA RELATED (RBR) is a plant homolog of the tumor suppressor Retinoblastoma (pRb), which is a key regulator of the cell cycle. Using inducible RNA interference (RNAi) against Arabidopsis thaliana RBR (RBRi), we reduced RBR expression levels at different stages of plant development. Conditional reduction or loss of RBR function disrupted cell division patterns, promoted context-dependent cell proliferation, and negatively influenced establishment of cell differentiation. Several lineages of toti- and pluripotent cells, including shoot apical meristem stem cells, meristemoid mother cells, and procambial cells, failed to produce appropriately differentiated cells. Meristem activity was altered, leading to a disruption of the CLAVATA-WUSCHEL feedback loop and inhibition of lateral organ formation. Release of RBR from RNAi downregulation restored meristem activity. Gene profiling analyses soon after RBRi induction revealed that a change in RBR homeostasis is perceived as a stress, even before genes regulated by RBR-E2F become deregulated. The results establish RBR as a key cell cycle regulator required for coordination of cell division, differentiation, and cell homeostasis.
引用
收藏
页码:1792 / 1811
页数:20
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