Correction: The ILR3-NRTs/NIA1/SWEET12 module regulates nitrogen uptake and utilization in apple
Hong‑Liang Li, Ran‑Xin Liu, Xiang Wu, Xin‑Long Guo, Shan‑Shan Li, Tian‑Tian Wang, Yan‑Yan Guo, Xiao‑Fei Wang, Chun‑Xiang You
Abstract
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
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Taxonomy
TopicsPlant Physiology and Cultivation Studies
Correction **: ** Mol Horticulture 5, 57 (2025)
https://doi.org/10.1186/s43897-025-00172-0
Following the publication of the original article (Li et al. 2025), it is reported that the left and right panels of Fig. 7B were mistakenly duplicated due to a figure preparation error.
Incorrect Fig. 7 is:
Fig. 7. MdILR3 interacts with the promoter of MdSWEET12 to stimulate its transcription. A The EMSA assay was used to assess the interaction between MdILR3 and the MdSWEET12 promoter. The mutated probe of pMdSWEET12 contains a mutated G-box, where the sequence CACGTG is replaced by AAAAAA. B Y1H assays were used to determine the binding of MdILR3 to the promoter of MdSWEET12. C MdILR3-62SK and MdSWEET12-LUC were co-transformed into tobacco leaves, with varying colors indicating the intensity of the LUC signal. The image was obtained using a live imaging system (Xenogen, Alameda, CA, USA). D Relative expression level of GUS was determined. The 35S::MdILR3 construct was transiently introduced into transgenic calli containing the pMdSWEET12::GUS reporter. The mean ± SD of three independent replicates is represented by error bars, with significant differences marked by an asterisk (P < 0.05)
Correct Fig. 7 is:
Fig. 7. MdILR3 interacts with the promoter of MdSWEET12 to stimulate its transcription. A The EMSA assay was used to assess the interaction between MdILR3 and the MdSWEET12 promoter. The mutated probe of pMdSWEET12 contains a mutated G-box, where the sequence CACGTG is replaced by AAAAAA. B Y1H assays were used to determine the binding of MdILR3 to the promoter of MdSWEET12. C MdILR3-62SK and MdSWEET12-LUC were co-transformed into tobacco leaves, with varying colors indicating the intensity of the LUC signal. The image was obtained using a live imaging system (Xenogen, Alameda, CA, USA). D Relative expression level of GUS was determined. The 35S::MdILR3 construct was transiently introduced into transgenic calli containing the pMdSWEET12::GUS reporter. The mean ± SD of three independent replicates is represented by error bars, with significant differences marked by an asterisk (P < 0.05)
The original article (Li et al. 2025) has been updated.