State Key Laboratory of Plant Cell and Chromosome Engineering, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
Plant Signal Behav. 2012 Feb;7(2):182-3. doi: 10.4161/psb.18803. Epub 2012 Feb 1.
Control of final organ size is a fundamental and core process of development of all multicellular organisms, but the mechanisms that set the final size of determinate organs are largely unknown. In a recent study, we demonstrated that the Mediator complex subunit 25 (MED25/PFT1), which is involved in the transcriptional regulation of gene expression, controls the final size of determinate organs by restricting both cell proliferation and cell expansion. med25 mutants formed large organs with larger and slightly more cells, whereas plants overexpressing MED25 produced small organs due to a reduction in both cell number and cell size. Here, we show that a loss-of-function mutation in the Mediator complex subunit 8 (MED8) causes small flowers as a result of reduced cell expansion. Analysis of the med8 med25-2 double mutant reveals that MED8 acts independently of MED25 to regulate cell expansion and organ growth. Taken together, our findings show that MED8 and MED25 play an important role in regulating organ size. Further identification of upstream and downstream components of MED8 and MED25 will help understand how the Mediator complex is involved in organ size control in plants.
控制最终器官大小是所有多细胞生物发育的基本和核心过程,但决定器官最终大小的机制在很大程度上尚不清楚。在最近的一项研究中,我们证明了参与基因表达转录调控的中介复合物亚基 25(MED25/PFT1)通过限制细胞增殖和细胞扩张来控制确定性器官的最终大小。med25 突变体形成的大型器官具有更大且略微更多的细胞,而过量表达 MED25 的植物由于细胞数量和细胞大小减少而产生小器官。在这里,我们表明中介复合物亚基 8(MED8)的功能丧失突变导致花变小,这是由于细胞扩张减少所致。对 med8 med25-2 双突变体的分析表明,MED8 独立于 MED25 发挥作用以调节细胞扩张和器官生长。总之,我们的发现表明 MED8 和 MED25 在调节器官大小方面发挥着重要作用。进一步鉴定 MED8 和 MED25 的上游和下游成分将有助于了解中介复合物如何参与植物器官大小的控制。