Table_5_Genome-wide identification and expression analysis of the U-box E3 ubiquitin ligase gene family related to salt tolerance in sorghum (Sorghum bicolor L.).xlsx

Plant U-box (PUB) E3 ubiquitin ligases play essential roles in many biological processes and stress responses, but little is known about their functions in sorghum (Sorghum bicolor L.). In the present study, 59 SbPUB genes were identified in the sorghum genome. Based on the phylogenetic analysis, the 59 SbPUB genes were clustered into five groups, which were also supported by the conserved motifs and structures of these genes. SbPUB genes were found to be unevenly distributed on the 10 chromosomes of sorghum. Most PUB genes (16) were found on chromosome 4, but there were no PUB genes on chromosome 5. Analysis of cis-acting elements showed that SbPUB genes were involved in many important biological processes, particularly in response to salt stress. From proteomic and transcriptomic data, we found that several SbPUB genes had diverse expressions under different salt treatments. To verify the expression of SbPUBs, qRT-PCR analyses also were conducted under salt stress, and the result was consistent with the expression analysis. Furthermore, 12 SbPUB genes were found to contain MYB-related elements, which are important regulators of flavonoid biosynthesis. These results, which were consistent with our previous multi-omics analysis of sorghum salt stress, laid a solid foundation for further mechanistic study of salt tolerance in sorghum. Our study showed that PUB genes play a crucial role in regulating salt stress, and might serve as promising targets for the breeding of salt-tolerant sorghum in the future.

植物U-box（PUB）E3泛素连接酶在众多生物学过程及胁迫反应中发挥着至关重要的作用，然而关于其在高粱（Sorghum bicolor L.）中的功能却鲜有研究。在本研究中，我们从高粱基因组中鉴定出59个SbPUB基因。基于系统发育分析，这59个SbPUB基因被划分为五个组，这一结论也得到了这些基因保守基序和结构的支持。研究发现，SbPUB基因在高粱的10条染色体上的分布并不均匀。大多数PUB基因（16个）位于第4染色体上，而第5染色体上则没有发现PUB基因。对顺式作用元件的分析表明，SbPUB基因参与了许多重要的生物学过程，特别是在盐胁迫响应中。通过蛋白质组学和转录组学数据，我们发现多个SbPUB基因在不同的盐处理条件下表现出多样化的表达模式。为验证SbPUBs的表达，我们在盐胁迫条件下进行了qRT-PCR分析，其结果与表达分析一致。此外，还发现12个SbPUB基因含有与MYB相关的元件，这些元件是类黄酮生物合成的重要调节因子。这些结果与我们对高粱盐胁迫的多组学分析一致，为深入探究高粱耐盐机制奠定了坚实基础。本研究揭示了PUB基因在调节盐胁迫中的关键作用，未来有望成为培育耐盐高粱的潜在靶标。