Virus‐induced gene editing of stomatal regulators in Nicotiana benthamiana enables rapid functional genomics
Redeat Tibebu, Maria Elena Gamo, Evan E. Ellison, Erik A. Myers, Rishika Sahoo, Sydney R. Winecke, Grace D. Tan, James M. Fischer, Andrew D.B. Leakey, Daniel F. Voytas

TL;DR
A virus-based gene editing method in plants allows rapid study of genes controlling stomata, linking genetic changes to plant water use and resilience.
Contribution
A TRV-based gene editing platform enables rapid, heritable, and somatic genome editing of stomatal regulators in Nicotiana benthamiana.
Findings
Somatic and heritable genome editing was achieved in multiple stomatal regulator genes with up to 95% editing efficiency.
Mutations in stomatal genes caused gene-specific changes in stomatal density and leaf temperature.
A reporter system allowed visualization of virus-infected tissues for phenotyping edited plant sectors.
Abstract
Virus‐induced gene editing (VIGE) holds promise as a rapid and scalable approach for functional genomics in plants. Here, we apply a tobacco rattle virus (TRV)‐based single‐guide RNA (sgRNA) delivery system to target key regulators of stomatal development in Nicotiana benthamiana using transgenic Cas9‐expressing lines. sgRNAs fused to a mobile RNA element and co‐delivered with TRV enabled both somatic and heritable genome editing across orthologs of STOMAGEN, EPF2, YODA, and SPEECHLESS. Somatic editing frequencies reached up to 95%, and heritable tetra‐allelic mutations were recovered in multiple target genes. Mutants exhibited significant, gene‐specific changes in stomatal density, with corresponding effects on leaf temperature indicative of altered evaporative cooling. Additionally, sgRNAs fused to an AmCyan reporter enabled visualization of virus‐infected tissues, allowing stomatal…
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Taxonomy
TopicsPlant Virus Research Studies · CRISPR and Genetic Engineering · RNA regulation and disease
