In Arabidopsis, the feedback regulatory loop between CLAVATA3 (CLV3) signaling pathway and transcription factor, WUSCHEL (WUS) plays a significant role in shoot apical meristems (SAM) maintenance. Previously, CLV1/CLV2 heterodimers were supposed to perceive and transmit CLV3 signaling. Recent genetic analysis isolated a novel receptor kinase, CORYNE (CRN), which was found to be involved in the CLV3 pathway. Therefore, new hypothesis was put forward that CRN probably acts with CLV2 to transmit CLV3 in parallel with CLV1 based on genetic analysis. In our recent work, we took advantage of firefly luciferase complementation imaging (LCI) assay to analyze the interactions among CLV1, CLV2 and CRN in both Arabidopsis thaliana protoplasts and Nicotiana benthamiana leaves. We identified the physical interaction between CLV2 and CRN in the absence of CLV3 and found some interesting phenomenon such as CLV1, CLV2 and CRN may form a complex, and that CRN was able to form homodimers. These new observations make the relationships among these three proteins more complex than that indicated in two-parallel pathway model. Combining current genetic and our new biochemical evidence, a more possible and detailed model for CLV3 pathway was developed.The stem cells located in SAM constantly progress cell division and cell differentiation to generate all of the aboveground organs in plants. CLV3 signaling pathway negatively regulates the fate of stem cells and maintains the SAM size through repressing the homeodomain transcription factor, WUS, which promotes the stem cell differentiation.1-3 Current knowledge believes that CLV3 encodes a secreted extracellular peptide, 4 and CLV1 encodes a leucine-rich-repeat receptor-like kinase (LRR-RLK); CLV2 encodes a receptor-like protein (RLP) lacking a kinase domain. 5,6 Previous studies hypothesized that CLV1/ CLV2 heterodimers function as receptors to transmit CLV3 ligand signaling. 4,7 Recently, a new gene, CRN/SOL2, was isolated and predicted to encode membrane-associated kinase with a very short extracellular domain. Genetic evidences predicted that SOL2/CRN functions together with CLV2 in parallel with CLV1 in CLV3 signaling. 8,9 Accordingly new two-parallel pathway model was raised that: one uses CLV1 homodimers and the other uses CRN-CLV2 heterodimers. 8 In our recent work, we seek to analyze the interactions among these receptor proteins at biochemical level.Owing to the specific and limited expression patterns of these receptor proteins, it would be difficult to conduct biochemical analysis only using SAM due to its slight amount. Therefore, we took advantage of transient expression systems including Arabidopsis protoplasts and N. benthamiana leaves to analyze the interactions among CLV1, CLV2 and CRN using the newly developed LCI method, which is believed to have high signal-tonoise ratio and be able to detect dynamic interactions including membrane protein interactions.