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. 2022 May 7;20:219. doi: 10.1186/s12951-022-01443-4

Fig. 6.

Fig. 6

Ds-MIRNA/SPc complex-mediated gene silencing in maize. a QRT-PCR assay for MIR164b and miR164b. The ds-MIR164b/SPc complex was applied to the root surface of maize every 24 h, and the samples were collected on 4 days after the treatment. Triplicate biological replicates were used for each treatment. The housekeeping gene ZmUBC was used as the reference gene. Different letters on columns indicate significant differences (Duncan’s multiple range test, P < 0.05). b QRT-PCR assay for target gene NAC1. c Photos of maize among various treatments. Scale bar: 1 cm. d Growth evaluation of roots by measuring lateral root number and density. Fifteen seedlings were used to collect the data. e Photos of maize ND101 (widely type) and transgenic maize overexpressing miR164e. Scale bar: 1 cm. f Growth evaluation of roots by measuring lateral root number and density. Thirteen seedlings were used to collect the data. The “n.s.” means no significance, and the “***” indicates significant differences according to the independent t test (P < 0.001)