Zhang Yu, Hu Qinghua, Zhai Xinyu, Tu Zhonghua, Wang Jing, Wang Minxin, Li Huogen
State Key Laboratory of Tree Genetics and Breeding, Co-Innovation Center for Sustainable Forestry in Southern China, Nanjing Forestry University, Nanjing 210037, China.
AoB Plants. 2024 Feb 20;16(2):plae008. doi: 10.1093/aobpla/plae008. eCollection 2024 Feb.
The plant-specific SQUAMOSA promoter-binding protein-like (SPL) transcription factors play a pivotal role in various developmental processes, including leaf morphogenesis and vegetative to reproductive phase transition. and are widely used in landscaping due to their tulip-like flowers and peculiar leaves. However, the gene family in has not been identified and systematically characterized. We systematically identified and characterized the family members in , including phylogeny, gene structure and syntenic analyses. Subsequently, we quantified the expression patterns of across various tissue sites through transcription-quantitative polymerase chain reaction (RT-qPCR) assays and identified the target gene, . Finally, we characterized the functions of via ectopic transformation. Altogether, 17 and 18 genes were genome-widely identified in and , respectively. All the 35 were grouped into 9 clades. Both species had three gene pairs arising from segmental duplication events, and the displayed high collinearity with the genome. RT-qPCR assays showed that genes were differentially expressed in different tissues, especially. Because is highly expressed in pistils and leaves, it was selected to describe the gene family of by ectopic expression. We showed that overexpression of in resulted in earlier flowering and fewer rosette leaves. Moreover, we observed that overexpression of in up-regulated the expression levels of four genes related to flower development. This study identified genes in and characterized the function of in advancing flower development.
植物特有的SQUAMOSA启动子结合蛋白样(SPL)转录因子在包括叶片形态发生和营养生长向生殖生长阶段转变在内的各种发育过程中起关键作用。[植物名称]因其郁金香状花朵和奇特的叶子而被广泛用于园林绿化。然而,[植物名称]中的[基因名称]基因家族尚未被鉴定和系统地表征。我们系统地鉴定并表征了[植物名称]中的[基因名称]家族成员,包括系统发育、基因结构和共线性分析。随后,我们通过转录定量聚合酶链反应(RT-qPCR)测定法量化了[基因名称]在各个组织部位的表达模式,并鉴定了靶基因[具体基因名称]。最后,我们通过异位转化表征了[具体基因名称]的功能。总共在[植物名称1]和[植物名称2]中分别全基因组鉴定出17个和18个[基因名称]基因。所有35个[基因名称]基因被分为9个进化枝。两个物种都有三个由片段重复事件产生的[基因名称]基因对,并且[植物名称1]的[基因名称]与[植物名称2]的基因组显示出高度共线性。RT-qPCR分析表明,[基因名称]基因在不同组织中差异表达,尤其是[具体组织]。由于[具体基因名称]在雌蕊和叶片中高度表达,因此选择它通过异位表达来描述[植物名称]的[基因名称]基因家族。我们表明,[具体基因名称]在[植物名称]中的过表达导致开花提前和莲座叶减少。此外,我们观察到[具体基因名称]在[植物名称]中的过表达上调了四个与花发育相关基因的表达水平。本研究鉴定了[植物名称]中的[基因名称]基因,并表征了[具体基因名称]在促进花发育中的功能。