College of Biological and Agricultural Engineering, Jilin University, Changchun, China.
College of Plant Science, Jilin University, Changchun, China.
Plant Genome. 2024 Sep;17(3):e20504. doi: 10.1002/tpg2.20504. Epub 2024 Aug 28.
We aimed to identify HD-Zip (homologous domain leucine zipper) family genes based on the complete Sophora alopecuroides genome sequence. Eighty-six Sophora alopecuroides HD-Zip family (SaHDZ) genes were identified and categorized into four subclasses using phylogenetic analysis. Chromosome localization analysis revealed that these genes were distributed across 18 chromosomes. Gene structure and conserved motif analysis showed high similarity among members of the SaHDZ genes. Prediction analysis revealed 71 cis-acting elements in SaHDZ genes. Transcriptome and quantitative real-time polymerase chain reaction analyses showed that under salt stress, SaHDZ responded positively in S. alopecuroides, and that SaHDZ22 was significantly upregulated afterward. Functional verification experiments revealed that SaHDZ22 overexpression increased the tolerance of Arabidopsis to salt and osmotic stress. Combined with cis-acting element prediction and expression level analysis, HD-Zip family transcription factors may be involved in regulating the balance between plant growth and stress resistance under salt stress by modulating the expression of auxin and abscisic acid signaling pathway genes. The Sophora alopecuroides adenylate kinase protein (SaAKI) and S. alopecuroides tetrapeptide-like repeat protein (SaTPR; pCAMBIA1300-SaTPR-cLUC) expression levels were consistent with those of SaHDZ22, indicating that SaHDZ22 may coordinate with SaAKI and SaTPR to regulate plant salt tolerance. These results lay a foundation in understanding the salt stress response mechanisms of S. alopecuroides and provide a reference for future studies oriented toward exploring plant stress resistance.
我们旨在基于苦参完整基因组序列鉴定 HD-Zip(同源域亮氨酸拉链)家族基因。通过系统发育分析,鉴定了 86 个苦参 HD-Zip 家族(SaHDZ)基因,并分为四个亚类。染色体定位分析表明,这些基因分布在 18 条染色体上。基因结构和保守基序分析表明,SaHDZ 基因成员之间具有高度相似性。预测分析表明,SaHDZ 基因中存在 71 个顺式作用元件。转录组和定量实时聚合酶链反应分析表明,在盐胁迫下,苦参中的 SaHDZ 呈正响应,随后 SaHDZ22 显著上调。功能验证实验表明,SaHDZ22 的过表达提高了拟南芥对盐和渗透胁迫的耐受性。结合顺式作用元件预测和表达水平分析,HD-Zip 家族转录因子可能通过调节生长素和脱落酸信号通路基因的表达,参与调节植物在盐胁迫下生长和抗逆性之间的平衡。苦参腺苷酸激酶蛋白(SaAKI)和苦参四肽重复蛋白(SaTPR;pCAMBIA1300-SaTPR-cLUC)的表达水平与 SaHDZ22 一致,表明 SaHDZ22 可能与 SaAKI 和 SaTPR 协同调节植物的耐盐性。这些结果为理解苦参的盐胁迫响应机制奠定了基础,并为未来探索植物抗逆性的研究提供了参考。