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PbGBF3 通过上调 PbAPL2 和 PbSDH1 以及降低 ABA 介导的盐敏感性增强梨的耐盐性。

PbGBF3 enhances salt response in pear by upregulating PbAPL2 and PbSDH1 and reducing ABA-mediated salt sensitivity.

机构信息

State Key Laboratory of Crop Genetics and Germplasm Enhancement, Centre of Pear Engineering Technology Research, Nanjing Agricultural University, Nanjing, China.

Centre of Pear Engineering Technology Research, Qingdao Agricultural University, Qingdao, China.

出版信息

Plant J. 2024 Sep;119(6):2837-2853. doi: 10.1111/tpj.16953. Epub 2024 Jul 29.

DOI:10.1111/tpj.16953
PMID:39073914
Abstract

Pear is a widely cultivated fruit crop, but its distribution and sustainable production are significantly limited by salt stress. This study used RNA-Seq time-course analysis, WGCNA, and functional enrichment analysis to uncover the molecular mechanisms underlying salt stress tolerance in Pyrus ussuriensis. We identified an ABA-related regulatory module, PbGBF3-PbAPL2-PbSDH1, as crucial in this response. PbGBF3, a bZIP transcription factor, enhances salt tolerance by upregulating PbAPL2 and PbSDH1. Overexpression of PbGBF3 improved salt tolerance in Pyrus communis calli and Arabidopsis, while silencing it reduced tolerance in Pyrus betulifolia. Functional assays showed that PbGBF3 binds to the promoters of PbAPL2 and PbSDH1, increasing their expression. PbAPL2 and PbSDH1, key enzymes in starch synthesis and the sorbitol pathway, respectively, enhance salt tolerance by increasing AGPase activity, soluble sugar content, and SDH activity, improving ROS scavenging and ion balance. Our findings suggest that the PbGBF3-PbAPL2 and PbGBF3-PbSDH1 modules positively regulate salt tolerance by enhancing ABA signaling and reducing ABA-mediated growth inhibition. These insights provide a foundation for developing salt-tolerant pear cultivars.

摘要

梨是一种广泛种植的水果作物,但它的分布和可持续生产受到盐胁迫的显著限制。本研究采用 RNA-Seq 时间序列分析、WGCNA 和功能富集分析,揭示了砂梨耐盐的分子机制。我们鉴定出一个与 ABA 相关的调控模块 PbGBF3-PbAPL2-PbSDH1,在该响应中起着关键作用。PbGBF3 是一个 bZIP 转录因子,通过上调 PbAPL2 和 PbSDH1 来增强耐盐性。PbGBF3 的过表达提高了西洋梨愈伤组织和拟南芥的耐盐性,而沉默则降低了山梨的耐盐性。功能分析表明,PbGBF3 结合到 PbAPL2 和 PbSDH1 的启动子上,增加它们的表达。PbAPL2 和 PbSDH1 分别是淀粉合成和山梨醇途径中的关键酶,通过增加 AGPase 活性、可溶性糖含量和 SDH 活性、改善 ROS 清除和离子平衡来增强耐盐性。我们的研究结果表明,PbGBF3-PbAPL2 和 PbGBF3-PbSDH1 模块通过增强 ABA 信号和减少 ABA 介导的生长抑制来正向调节耐盐性。这些发现为培育耐盐性梨品种提供了基础。

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