Ming Meiling, Yi Mulin, Qin Chunyue, Yan Luyao, Sun Yuhan, Zhang Juan, Cao Fuliang, Fu Fangfang
State Key Laboratory of Tree Genetics and Breeding, Co-Innovation Center for Sustainable Forestry in Southern China, Nanjing Forestry University, Nanjing 210037, China.
Int J Mol Sci. 2025 May 21;26(10):4932. doi: 10.3390/ijms26104932.
SQUAMOSA promoter-binding protein-like (SPL) transcription factors specific to plants are vital for regulating growth, development, secondary metabolite biosynthesis, and responses to both biotic and abiotic stresses. Despite their importance, no systematic investigations or identifications of the SPL gene family in have been conducted. In this study, we identified 13 SPL genes within the reference genome, spanning seven chromosomes, and categorized these genes into six groups based on their phylogenetic relationships with SPL gene families. Our analysis of gene structure, conserved domains, motifs, and miR156 target predictions indicates that GbSPLs are highly conserved across evolutionary timelines. Furthermore, synteny analysis highlighted that dispersed duplication events have expanded the SPL gene family in . Examination of the cis-regulatory elements revealed that many genes possess motifs associated with light, hormones, and stress, implying their involvement in flavonoid biosynthesis and adaptation to environmental conditions. RNA-Seq and qRT-PCR expression profiles of genes across various tissues and low- and high-flavonoid leaves and during both short-term and long-term water stress illustrated their roles in flavonoid biosynthesis and responses to water stress. Subcellular localization experiments showed that GbSPL2 and GbSPL11 proteins are situated within the nucleus. Our research offers the first systematic characterization of the SPL gene family in , establishing a valuable foundation for understanding their evolutionary background and functional roles in flavonoid biosynthesis and water stress response.
植物特有的SQUAMOSA启动子结合蛋白样(SPL)转录因子对于调节生长、发育、次生代谢物生物合成以及对生物和非生物胁迫的响应至关重要。尽管它们很重要,但尚未对[具体物种名称未给出]中的SPL基因家族进行系统的研究或鉴定。在本研究中,我们在[具体物种名称未给出]参考基因组中鉴定出13个SPL基因,分布在七条染色体上,并根据它们与[具体物种名称未给出]SPL基因家族的系统发育关系将这些基因分为六组。我们对基因结构、保守结构域、基序和miR156靶标预测的分析表明,GbSPLs在进化时间线上高度保守。此外,共线性分析突出显示,分散重复事件使[具体物种名称未给出]中的SPL基因家族得以扩展。对顺式调控元件的研究表明,许多[具体物种名称未给出]基因具有与光、激素和胁迫相关的基序,这意味着它们参与类黄酮生物合成并适应环境条件。[具体物种名称未给出]基因在各种组织以及低黄酮和高黄酮叶片中以及短期和长期水分胁迫期间的RNA-Seq和qRT-PCR表达谱说明了它们在类黄酮生物合成和对水分胁迫响应中的作用。亚细胞定位实验表明,GbSPL2和GbSPL11蛋白位于细胞核内。我们的研究首次对[具体物种名称未给出]中的SPL基因家族进行了系统表征,为了解它们在类黄酮生物合成和水分胁迫响应中的进化背景和功能作用奠定了宝贵的基础。