Literature DB >> 35410127

Correction to: Overexpression of the Salix matsudana SmAP2-17 gene improves Arabidopsis salinity tolerance by enhancing the expression of SOS3 and ABI5.

Yanhong Chen1, Yuanhao Dai1, Yixin Li1, Jie Yang1, Yuna Jiang1, Guoyuan Liu1, Chunmei Yu1, Fei Zhong1, Bolin Lian1, Jian Zhang2.   

Abstract

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Year:  2022        PMID: 35410127      PMCID: PMC8996660          DOI: 10.1186/s12870-022-03552-6

Source DB:  PubMed          Journal:  BMC Plant Biol        ISSN: 1471-2229            Impact factor:   4.215


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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.
Fig. 3

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

Fig. 6

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

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

1.  Overexpression of the Salix matsudana SmAP2-17 gene improves Arabidopsis salinity tolerance by enhancing the expression of SOS3 and ABI5.

Authors:  Yanhong Chen; Yuanhao Dai; Yixin Li; Jie Yang; Yuna Jiang; Guoyuan Liu; Chunmei Yu; Fei Zhong; Bolin Lian; Jian Zhang
Journal:  BMC Plant Biol       Date:  2022-03-07       Impact factor: 5.260

  1 in total

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