AUTHOR=Sun Yueming K. , Flematti Gavin R. , Smith Steven M. , Waters Mark T. 

TITLE=Reporter Gene-Facilitated Detection of Compounds in Arabidopsis Leaf Extracts that Activate the Karrikin Signaling Pathway

JOURNAL=Frontiers in Plant Science

VOLUME=7

YEAR=2016

URL=https://www.frontiersin.org/journals/plant-science/articles/10.3389/fpls.2016.01799

DOI=10.3389/fpls.2016.01799

ISSN=1664-462X

ABSTRACT=<p>Karrikins are potent germination stimulants generated by the combustion of plant matter. Treatment of <italic>Arabidopsis</italic> with karrikins triggers a signaling process that is dependent upon a putative receptor protein KARRIKIN INSENSITIVE 2 (KAI2). KAI2 is a homolog of DWARF 14 (D14), the receptor for endogenous strigolactone hormones. Genetic analyses suggest that KAI2 also perceives endogenous signal(s) that are not strigolactones. Activation of KAI2 by addition of karrikins to <italic>Arabidopsis</italic> plants induces expression of transcripts including <italic>D14-LIKE 2</italic> (<italic>DLK2</italic>). We constructed the synthetic reporter gene <italic>DLK2</italic>:<italic>LUC</italic> in <italic>Arabidopsis</italic>, which comprises the firefly luciferase gene (<italic>LUC</italic>) driven by the <italic>DLK2</italic> promoter. Here we describe a luminescence-based reporter assay with <italic>Arabidopsis</italic> seeds to detect chemical signals that can activate the KAI2 signaling pathway. We demonstrate that the <italic>DLK2</italic>:<italic>LUC</italic> assay can selectively and sensitively detect karrikins and a functionally similar synthetic strigolactone analog. Crucially we show that crude extracts from <italic>Arabidopsis</italic> leaves can also activate <italic>DLK2</italic>:<italic>LUC</italic> in a KAI2-dependent manner. Our work provides the first direct evidence for the existence of endogenous chemical signals that can activate the KAI2-mediated signaling pathway in <italic>Arabidopsis</italic>. This sensitive reporter system can now be used for the bioassay-guided purification and identification of putative endogenous KAI2 ligands or their precursors, and endogenous compounds that might modulate the KAI2 signaling pathway.</p>