Institute of Nanfan & Seed Industry, Guangdong Academy of Science, Guangzhou, 510316, China.
Division of Plant Science and Technology, University of Missouri, Columbia, MO 65211, USA.
J Exp Bot. 2024 Feb 2;75(3):1051-1062. doi: 10.1093/jxb/erad404.
Identification and characterization of soybean germplasm and gene(s)/allele(s) for salt tolerance is an effective way to develop improved varieties for saline soils. Previous studies identified GmCHX1 (Glyma03g32900) as a major salt tolerance gene in soybean, and two main functional variations were found in the promoter region (148/150 bp insertion) and the third exon with a retrotransposon insertion (3.78 kb). In the current study, we identified four salt-tolerant soybean lines, including PI 483460B (Glycine soja), carrying the previously identified salt-sensitive variations at GmCHX1, suggesting new gene(s) or new functional allele(s) of GmCHX1 in these soybean lines. Subsequently, we conducted quantitative trait locus (QTL) mapping in a recombinant-inbred line population (Williams 82 (salt-sensitive) × PI 483460B) to identify the new salt tolerance loci/alleles. A new locus, qSalt_Gm18, was mapped on chromosome 18 associated with leaf scorch score. Another major QTL, qSalt_Gm03, was identified to be associated with chlorophyll content ratio and leaf scorch score in the same chromosomal region of GmCHX1 on chromosome 3. Novel variations in a STRE (stress response element) cis-element in the promoter region of GmCHX1 were found to regulate the salt-inducible expression of the gene in these four newly identified salt-tolerant lines including PI 483460B. This new allele of GmCHX1 with salt-inducible expression pattern provides an energy cost efficient (conditional gene expression) strategy to protect soybean yield in saline soils without yield penalty under non-stress conditions. Our results suggest that there might be no other major salt tolerance locus similar to GmCHX1 in soybean germplasm, and further improvement of salt tolerance in soybean may rely on gene-editing techniques instead of looking for natural variations.
鉴定和表征大豆种质资源和耐盐基因/等位基因是开发耐盐性土壤改良品种的有效方法。先前的研究鉴定出 GmCHX1(Glyma03g32900)是大豆中的一个主要耐盐基因,在启动子区域(148/150bp 插入)和第三外显子中有两个主要的功能变异,存在反转录转座子插入(3.78kb)。在本研究中,我们鉴定了四个耐盐性大豆品系,包括 PI 483460B(野生大豆),它们携带先前鉴定的 GmCHX1 中的盐敏感变异,表明这些大豆品系中存在新的基因或 GmCHX1 的新功能等位基因。随后,我们在重组自交系群体(Williams 82(盐敏感)×PI 483460B)中进行了数量性状位点(QTL)作图,以鉴定新的耐盐性基因座/等位基因。在与叶片灼伤评分相关的第 18 号染色体上,鉴定到一个新的基因座 qSalt_Gm18。另一个主要的 QTL,qSalt_Gm03,与第 3 号染色体上 GmCHX1 相同染色体区域的叶绿素含量比和叶片灼伤评分相关。在 GmCHX1 启动子区域的一个 STRE(应激反应元件)顺式元件中发现了新的变异,这些变异调节了包括 PI 483460B 在内的这四个新鉴定的耐盐性品系中基因的盐诱导表达。该 GmCHX1 的新等位基因具有盐诱导表达模式,为保护在盐渍土壤中的大豆产量提供了一种节能(条件性基因表达)策略,而在非胁迫条件下不会产生产量损失。我们的研究结果表明,大豆种质资源中可能没有其他与 GmCHX1 相似的主要耐盐性基因座,进一步提高大豆的耐盐性可能依赖于基因编辑技术,而不是寻找自然变异。