Description:
We generated a 21-bp deletion in the miR156 target site of SPL-A13 using CRISPR. We crossed the resulting miR156-resistant allele (rSPL-A13) to Kronos and, in the segregating progeny, we selected plants homozygous for the 21-bp deletion without the CAS-9 transgene. The progeny of these plants are deposited here.