Correction to: BMC Plant Biol 22, 102 (2022)

https://doi.org/10.1186/s12870-022-03487-y

Following publication of the original article [1], it was noted that due to a typesetting error Fig. 3 and Fig. 6 were captured incorrectly.

The correct figures and captions have been included in this correction, and the original article has been corrected.

Fig. 3
figure 1

Expression pattern and subcellular localization of SmAP2-17 protein. a Expression patterns of SmAP2-17 in the roots, stems, leaves, anthers, and shoots of S. matsudana and under salt stress were measured using qRT-PCR. b Subcellular localization of the SmAP2-17 protein. The 35S:EGFP-SmAP2-17 fusion construct and the nucleus localization marker 35S:H2B-RFP construct were co-transformed into tobacco epidermal leaves. The arrowhead indicates the merged signal (yellow) with EGFP (green) and RFP (red) co-located in the nucleus. Scale bar, 10 μm

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Fig. 6
figure 2

Relative expression levels of stress responsive marker genes and salinity responsive genes in WT and transgenic lines under normal conditions and after treatment with NaCl. a Relative expression levels of 15 genes in the WT and transgenic lines T-1 and T-15 under normal conditions. b Relative expression levels of 15 genes in the WT and transgenic lines T-1 and T-15 treated with 200 mM NaCl for 24 h. c Relative expression levels of 12 genes in the WT and transgenic lines Op T-3 and Op T-6 treated with 200 mM NaCl for 24 h. Data represent the mean ± SD of three biological replicates. *P < 0.05 and **P < 0.01 by Student’s t-test

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