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ARS Home » Plains Area » Fargo, North Dakota » Edward T. Schafer Agricultural Research Center » Cereal Crops Research » Research » Publications at this Location » Publication #389597

Research Project: Improvement of Biotic Stress Resistance in Durum and Hard Red Spring Wheat Using Genetics and Genomics

Location: Cereal Crops Research

Title: Map-based cloning of the Liguleless 1 gene regulating architecture in barley

Author
item Yang, Shengming
item Overlander-Chen, Megan
item Fiedler, Jason

Submitted to: Meeting Abstract
Publication Type: Abstract Only
Publication Acceptance Date: 12/13/2021
Publication Date: 1/10/2022
Citation: Yang, S., Overlander, M., Fiedler, J.D. 2022. Map-based cloning of the Liguleless 1 gene regulating architecture in barley [abstract]. Plant and Animal Genome Conference. Poster No.0315.

Interpretive Summary:

Technical Abstract: Crop architecture is important for light capture and tightly affects economic yield under field condition. In this study, we conducted map-based cloning of the Liguleless 1 (Lig 1) regulating leaf angle in barley. Loss-of-function mutant of Lig 1 obtained by fast neutron-mutagenesis is deficient in the formation of the ligule and auricle, resulting in smaller leaf angles. The compact architecture caused by erect leaves is desirable to increase yield with high planting density. Genetic mapping anchored the Lig 1 gene onto 2H within an '300-kb region. DNA sequencing indicated that a genomic deletion of 20-kb in the mutant occurred to the gene model HORVU.MOREX.r3.2HG0202650, which encodes a putative SQUAMOSA promoter-binding protein-like (SPL) transcription factor. Phylogenetic analysis suggested the SPL in barley might be a homolog of Zmlg1 and TaSPL8 regulating leaf angle in maize and wheat, respectively. Using CRISPR technology, we knocked out the SPL-encoding gene and phenocopied the Lig 1 mutant. Therefore, HORVU.MOREX.r3.2HG0202650 is indeed the Lig 1 gene. Cloning of Lig 1 demonstrated that the SPL transcription factor is conserved in monocots, providing a target for gene manipulation to maximize light interception capacity in high planting density.