Sridhar Vaniyambadi V, Surendrarao Anandkumar, Liu Zhongchi
Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, MD 20742, USA.
Development. 2006 Aug;133(16):3159-66. doi: 10.1242/dev.02498. Epub 2006 Jul 19.
The transcriptional repression of key regulatory genes is crucial for plant and animal development. Previously, we identified and isolated two Arabidopsis transcription co-repressors LEUNIG (LUG) and SEUSS (SEU) that function together in a putative co-repressor complex to prevent ectopic AGAMOUS (AG) transcription in flowers. Because neither LUG nor SEU possesses a recognizable DNA-binding motif, how they are tethered to specific target promoters remains unknown. Using the yeast two-hybrid assay and a co-immunoprecipitation assay, we showed that APETALA1 (AP1) and SEPALLATA3 (SEP3), both MADS box DNA-binding proteins, interacted with SEU. The AP1-SEU protein-protein interaction was supported by synergistic genetic interactions between ap1 and seu mutations. The role of SEU proteins in bridging the interaction between AP1/SEP3 and LUG to repress target gene transcription was further demonstrated in yeast and plant cells, providing important mechanistic insights into co-repressor function in plants. Furthermore, a direct in vivo association of SEU proteins with the AG cis-regulatory element was shown by chromatin immunoprecipitation. Accordingly, a reporter gene driven by the AG cis-element was able to respond to AP1- and SEP3-mediated transcriptional repression in a transient plant cell system when supplied with SEU and LUG. These results suggest that AP1 and SEP3 may serve as the DNA-binding partners of SEU/LUG. Our demonstration of the direct physical interaction between SEU and the C-terminal domain of SEP3 and AP1 suggests that AP1 and SEP3 MADS box proteins may interact with positive, as well as negative, regulatory proteins via their C-terminal domains, to either stimulate or repress their regulatory targets.
关键调控基因的转录抑制对动植物发育至关重要。此前,我们鉴定并分离出拟南芥中的两个转录共抑制因子LEUNIG(LUG)和SEUSS(SEU),它们在一个假定的共抑制复合物中共同发挥作用,以防止花中异位AGAMOUS(AG)转录。由于LUG和SEU均不具有可识别的DNA结合基序,它们如何与特定靶启动子相连仍不清楚。通过酵母双杂交试验和免疫共沉淀试验,我们发现MADS盒DNA结合蛋白APETALA1(AP1)和SEPALLATA3(SEP3)与SEU相互作用。ap1和seu突变之间的协同遗传相互作用支持了AP1-SEU蛋白-蛋白相互作用。SEU蛋白在桥接AP1/SEP3与LUG之间的相互作用以抑制靶基因转录中的作用在酵母和植物细胞中得到进一步证实,这为植物中共抑制因子的功能提供了重要的机制见解。此外,染色质免疫沉淀显示SEU蛋白与AG顺式调控元件在体内存在直接关联。因此,当提供SEU和LUG时,由AG顺式元件驱动的报告基因能够在瞬时植物细胞系统中对AP1和SEP3介导的转录抑制作出反应。这些结果表明,AP1和SEP3可能作为SEU/LUG的DNA结合伙伴。我们对SEU与SEP3和AP1的C末端结构域之间直接物理相互作用的证明表明,AP1和SEP3 MADS盒蛋白可能通过其C末端结构域与正调控蛋白以及负调控蛋白相互作用,以刺激或抑制其调控靶标。