| Literature DB >> 35410127 |
Yanhong Chen1, Yuanhao Dai1, Yixin Li1, Jie Yang1, Yuna Jiang1, Guoyuan Liu1, Chunmei Yu1, Fei Zhong1, Bolin Lian1, Jian Zhang2.
Abstract
Entities:
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
Fig. 3Expression 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. 6Relative 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