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. 2020 May 25;71(18):5348–5364. doi: 10.1093/jxb/eraa209

Fig. 1.

Fig. 1.

Characterization of OsZHD2-D. (A) Root phenotypes at 8 DAG. Scale bar=1 cm. (B) Seminal root lengths of seedlings at 8 DAG that were grown under hydroponic culture conditions. n=13. (C) Lateral root lengths at the top 1 cm regions of seminal roots at 8 DAG. n>40. (D) Number of lateral roots at 8 DAG. n=7. (E) Density of lateral roots at the top 1 cm regions of seminal roots. n=7. Error bars show the SD. Statistical significance is indicated by *** (P<0.001). (F) Schematic diagram of the OsZHD2 genome and T-DNA insertion position in Line 3A-13017. T-DNA was inserted 5 kb downstream from the stop codon. (G) Transcript levels of OsZHD2 in the WT and the OsZHD2-D activation line. RNA samples were collected from leaf blades at the seedling stage. qRT-PCR was performed to measure the transcript levels using the gene-specific primers indicated by arrows in (F). n=4. Error bars show the SD. Statistical significance is indicated by *** (P<0.001).