OsBBX11 on qSTS4 links to salt tolerance at the seeding stage in Oryza sativa L. ssp. Japonica
文献类型: 外文期刊
第一作者: Lei, Lei
作者: Lei, Lei;Lei, Lei;Cao, Liangzi;Ding, Guohua;Zhou, Jinsong;Luo, Yu;Bai, Liangming;Xia, Tianshu;Xie, Tingting;Yang, Guang;Sun, Shichen;Lai, Yongcai;Lei, Lei;Cao, Liangzi;Ding, Guohua;Zhou, Jinsong;Bai, Liangming;Sun, Shichen;Lei, Lei;Cao, Liangzi;Ding, Guohua;Zhou, Jinsong;Sun, Shichen;Lai, Yongcai;Chen, Lei;Wang, Jiangxu;Liu, Kai;Wang, Xueyang;Lei, Qingjun
作者机构:
关键词: japonica rice; seedling stage; salt tolerance; b-box zinc finger family protein; function characterization
期刊名称:FRONTIERS IN PLANT SCIENCE ( 影响因子:5.6; 五年影响因子:6.8 )
ISSN: 1664-462X
年卷期: 2023 年 14 卷
页码:
收录情况: SCI
摘要: Rice has been reported to be highly sensitive to salt stress at the seedling stage. However, the lack of target genes that can be used for improving salt tolerance has resulted in several saline soils unsuitable for cultivation and planting. To characterize new salt-tolerant genes, we used 1,002 F-2:3 populations derived from Teng-Xi144 and Long-Dao19 crosses as the phenotypic source to systematically characterize seedlings' survival days and ion concentration under salt stress. Utilizing QTL-seq resequencing technology and a high-density linkage map based on 4,326 SNP markers, we identified qSTS4 as a major QTL influencing seedling salt tolerance, which accounted for 33.14% of the phenotypic variation. Through functional annotation, variation detection and qRT-PCR analysis of genes within 46.9 Kb of qSTS4, it was revealed that there was one SNP in the promoter region of OsBBX11, which resulted in a significant response difference between the two parents to salt stress. Transgenic plants using knockout-based technology and demonstrated that Na+ and K+ in the roots of the functional-loss-type OsBBX11 were translocated largely to the leaves under 120 mmol/L NaCl compared with the wild-type, causing osbbx11 leaves to die after 12 days of salt stress due to an imbalance in osmotic pressure. In conclusion, this study identified OsBBX11 as a salt-tolerance gene, and one SNPs in the OsBBX11 promoter region can be used to identify its interacting transcription factors. This provides a theoretical basis for finding the molecular mechanism of OsBBX11 upstream and downstream regulation of salt tolerance and molecular design breeding in the future.
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