Tripathi Rajiv K, Goel Ridhi, Kumari Sweta, Dahuja Anil
Division of Biochemistry, Indian Agricultural Research Institute, New Delhi, India.
Department of Plant Science, McGill University, 21111 Rue Lakeshore, Sainte-Anne-de-Bellevue, QC, H9X 3V9, Canada.
Dev Genes Evol. 2017 Mar;227(2):101-119. doi: 10.1007/s00427-017-0574-7. Epub 2017 Jan 29.
SQUAMOSA Promoter-Binding Protein-Like (SPL) genes form a major family of plant-specific transcription factors and play an important role in plant growth and development. In this study, we report the identification of 41 SPL genes (GmSPLs) in the soybean genome. Phylogenetic analysis revealed that these genes were divided into five groups (groups 1-5). Further, exon/intron structure and motif composition revealed that the GmSPL genes are conserved within their same group. The N-terminal zinc finger 1 (Zn1) of the SBP domain was a CCCH (Cys3His1) and the C terminus zinc finger 2 (Zn2) was a CCHC (Cys2HisCys) type. The 41 GmSPL genes were distributed unevenly on 17 of the 20 chromosomes, with tandem and segmental duplication events. We found that segmental duplication has made an important contribution to soybean SPL gene family expansion. The Ka/Ks ratios revealed that the duplicated GmSPL genes evolved under the effect of purifying selection. In addition, 17 of the 41 GmSPLs were found as targets of miR156; these might be involved in their posttranscriptional regulation through miR156. Importantly, RLM-RACE analysis confirmed the GmmiR156-mediated cleavage of GmSPL2a transcript in 2-4 mm stage of soybean seed. Alternative splicing events in 9 GmSPLs were detected which produces transcripts and proteins of different lengths that may modulate protein signaling, binding, localization, stability, and other properties. Expression analysis of the soybean SPL genes in various tissues and different developmental stages of seed suggested distinct spatiotemporal patterns. Differences in the expression patterns of miR156-targeted and miR156-non-targeted soybean SPL genes suggest that miR156 plays key functions in soybean development. Our results provide an important foundation for further uncovering the crucial roles of GmSPLs in the development of soybean and other biological processes.
SQUAMOSA启动子结合蛋白样(SPL)基因构成了植物特有的转录因子的一个主要家族,并在植物生长发育中发挥重要作用。在本研究中,我们报告了在大豆基因组中鉴定出41个SPL基因(GmSPLs)。系统发育分析表明,这些基因被分为五组(第1 - 5组)。此外,外显子/内含子结构和基序组成表明,GmSPL基因在同一组内是保守的。SBP结构域的N端锌指1(Zn1)是CCCH(Cys3His1)型,C端锌指2(Zn2)是CCHC(Cys2HisCys)型。41个GmSPL基因不均匀地分布在20条染色体中的17条上,存在串联和片段重复事件。我们发现片段重复对大豆SPL基因家族的扩展做出了重要贡献。Ka/Ks比值表明,重复的GmSPL基因在纯化选择的作用下进化。此外,在41个GmSPLs中发现有17个是miR156的靶标;它们可能通过miR156参与其转录后调控。重要的是,RLM - RACE分析证实了GmmiR156在大豆种子2 - 4毫米阶段对GmSPL2a转录本的切割。检测到9个GmSPLs中的可变剪接事件,这些事件产生不同长度的转录本和蛋白质,可能调节蛋白质的信号传导、结合、定位、稳定性及其他特性。对大豆SPL基因在种子不同组织和不同发育阶段的表达分析表明其具有明显的时空模式。miR156靶向和非靶向的大豆SPL基因表达模式的差异表明,miR156在大豆发育中发挥关键作用。我们的结果为进一步揭示GmSPLs在大豆发育及其他生物学过程中的关键作用提供了重要基础。