Zhang Xiaohong, Dou Lingling, Pang Chaoyou, Song Meizhen, Wei Hengling, Fan Shuli, Wang Chengshe, Yu Shuxun
College of Agronomy, Northwest A&F University, Yangling, 712100, Shaanxi, People's Republic of China,
Mol Genet Genomics. 2015 Feb;290(1):115-26. doi: 10.1007/s00438-014-0901-x. Epub 2014 Aug 27.
SQUAMOSA promoter binding protein-like (SPL) genes encode plant-specific transcription factors that are involved in many fundamental developmental processes. Certain SPL genes contain sequences complementary to miR156, a microRNA (miRNA) that plays a role in modulating plant gene expression. In this study, 30 SPL genes were identified in the reference genome of Gossypium raimondii and 24 GhSPLs were cloned from Gossypium hirsutum. G. raimondii is regarded as the putative contributor of the D-subgenome of G. hirsutum. Comparative analysis demonstrated sequence conservation between GhSPLs and other plant species. GhSPL genes could be classified into seven subclades based on phylogenetic analysis, diverse intron-exon structure, and motif prediction. Within each subclade, genes shared a similar structure. Sequence and experimental analysis predicted that 18 GhSPL genes are putative targets of GhmiR156. Additionally, tissue-specific expression analysis of GhSPL genes showed that their spatiotemporal expression patterns during development progressed differently, with most genes having high transcript levels in leaves, stems, and flowers. Finally, overexpression of GhSPL3 and GhSPL18 in Arabidopsis plants demonstrated that these two genes are involved in the development of leaves and second shoots and play an integral role in promoting flowering. The flowering integrator GhSOC1 may bind to the promoter of GhSPL3 but not GhSPL18 to regulate flowering. In conclusion, our analysis of GhSPL genes will provide some gene resources and a further understanding of GhSPL3 and GhSPL18 function in flowering promotion. Furthermore, the comparative genomics and functional analysis deepened our understanding of GhSPL genes during upland cotton vegetative and reproductive growth.
类SQUAMOSA启动子结合蛋白(SPL)基因编码参与许多基本发育过程的植物特异性转录因子。某些SPL基因包含与miR156互补的序列,miR156是一种在调节植物基因表达中起作用的微小RNA(miRNA)。在本研究中,在雷蒙德氏棉的参考基因组中鉴定出30个SPL基因,并从陆地棉中克隆出24个GhSPL基因。雷蒙德氏棉被认为是陆地棉D亚基因组的假定贡献者。比较分析表明GhSPL与其他植物物种之间存在序列保守性。基于系统发育分析、不同的内含子-外显子结构和基序预测,GhSPL基因可分为七个亚分支。在每个亚分支内,基因具有相似的结构。序列和实验分析预测18个GhSPL基因是GhmiR156的假定靶标。此外,GhSPL基因的组织特异性表达分析表明,它们在发育过程中的时空表达模式不同,大多数基因在叶、茎和花中具有较高的转录水平。最后,在拟南芥植物中过表达GhSPL3和GhSPL18表明这两个基因参与叶和二级枝条的发育,并在促进开花中起重要作用。开花整合因子GhSOC1可能与GhSPL3的启动子结合,但不与GhSPL18的启动子结合以调节开花。总之,我们对GhSPL基因的分析将提供一些基因资源,并进一步了解GhSPL3和GhSPL18在促进开花中的功能。此外,比较基因组学和功能分析加深了我们对陆地棉营养生长和生殖生长过程中GhSPL基因的理解。