Grant: Discovery Grants Program - Individual

MicroRNA156 (miR156) regulates numerous plant traits by silencing SQUAMOSA PROMOTER BINDING PROTEIN LIKE (SPL) transcription factors family. SPLs in turn regulate other downstream genes (target genes) that contain a SPL binding cis acting element. Thus, the propensity of miR156 to affect multiple plant traits is due to its ability to regulate a large network of downstream genes. So far, we have analyzed miR156 function in plants ranging from model plants to major crops, including Medicago sativa (alfalfa), where we found that miR156 affects forage yield and quality, plant architecture, flowering time, root development, nodulation, and abiotic stress tolerance by downregulating at least seven SPL genes. *We propose to expand this research by investigating the molecular basis for the multitude of roles that miR156 plays in alfalfa. We aim to associate each of miR156-silenced SPL genes and target genes to specific traits normally affected by miR156 in alfalfa. Analysis will involve molecular, genetic, phenotypic and physiological characterization of miR156 and SPL mis-expression alfalfa genotypes. We will identify SPL-regulated downstream genes through Next Generation RNA Sequencing (NGS), promoter analysis, and chromatin immunoprecipitation-qPCR (ChIP-qPCR), combined with phenotypic and physiological analyses of alfalfa plants with altered gene expression. The goal is to generate knowledge about the components of the miR156-SPL genetic network, ascribe functions to at least some of the SPL genes and target genes in alfalfa. Our objectives are:*1. To characterize role of miR156 and target SPL in abiotic stress, specifically drought, aluminum and salinity. The proposed research will use existing SPL silencing and overexpression alfalfa genotypes to test for abiotic stress tolerance, and determine which SPL (SPLs) is involved. We will conduct a range of physiological, phenotypic and molecular analyses to evaluate stress tolerance and characterize genes. *2. To assess the role of miR156/SPL module in determining root architecture, nodulation and nitrogen fixation in alfalfa. By characterizing plants with silenced or overexpressed miR156-targeted SPL genes, the proposed research will identify SPL genes responsible for above traits. *3. To identify SPL-regulated target genes involved in above traits. SPL RNAi plants showing the most visible morphological or physiological changes will be analysed by NGS to identify differentially expressed genes, which will be further assessed for SPL binding by ChIP-qPCR, and used for further molecular and phenotypic characterization using silencing and overexpression plants.*This research will deepen our understanding of the miR156-SPL gene regulatory network in alfalfa, and potentially other plants. The findings could be exploited to improve various alfalfa traits by gene editing or marker-assisted breeding.