Dissecting JACKDAW transcriptional regulatory module and protein– protein interaction domains
Embargo End Date2020-11-28
Permanent link to this recordhttp://hdl.handle.net/10754/660334
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AbstractMany biological processes are regulated via the action of interacting transcription factors. Together, these proteins form a complex regulatory network that will lead to different outcomes according to the DNA context of their target. The transcriptional regulator JACKDAW (JKD) together with the transcription factors SHR (SHORT-ROOT) and (SCARECROW) form a regulatory module that control a variety cell type specific targets to maintain the stem cell niche and regulate asymmetric cell division in the Arabidopsis root meristem. JKD functions is required to restrict the mobile transcription factor SHR to a single layer the endodermis by nuclear retention through association with SCR forming a ternary complex. Unpublished data from a yeast 2 hybrid screen indicated that JKD forms complexes with other transcriptional regulators involved either in growth or defense pathways, but the nature and the function of these interactions are yet to be elucidated. Here we validated these interactions using Yeast 2-Hybrid and Bimolecular fluorescence complementation (BiFC), which are widely used methods to study protein-protein interaction and can potentially provide valuable information in protein-complex composition. We also exploited these two approaches to determine interaction domains of JKD’s. However, the results from the Y2-H and BiFC assays showed inconsistent data. This hindered our ability to conclusively define the interacting JKD variants with various plant-specific transcriptional regulators. As JKD acts as a transcriptional regulator we tested JKD truncated variants on its target promoter pMYC2 using Dual-luciferase reporter assay in a plant-based expression. Our data indicated the significance of its ZF1 motif in mediating DNA binding. To assess whether JKD regulates its targets or in association with SCR and SHR we performed the same assay in a mammalian-based system to avoid plant transcriptional regulation. Our data indicate that based on the target DNA sequence, each of these TFs can either act either as an activator or repressor.