Instituto de Biología Molecular y Celular de Plantas (CSIC-UPV), Valencia, Spain.
PMI R&D, Philip Morris Products S.A, Neuchâtel, Switzerland.
Plant Sci. 2023 Oct;335:111797. doi: 10.1016/j.plantsci.2023.111797. Epub 2023 Jul 17.
SQUAMOSA PROMOTER BINDING-LIKE (SPL) proteins constitute a large family of transcription factors known to play key roles in growth and developmental processes, including juvenile-to-adult and vegetative-to-reproductive phase transitions. This makes SPLs interesting targets for precision breeding in plants of the Nicotiana genus used as e.g. recombinant biofactories. We report the identification of 49 SPL genes in Nicotiana tabacum cv. K326 and 43 SPL genes in Nicotiana benthamiana LAB strain, which were classified into eight phylogenetic groups according to the SPL classification in Arabidopsis. Exon-intron gene structure and DNA-binding domains were highly conserved between homeologues and orthologues. Thirty of the NbSPL genes and 33 of the NtSPL genes were found to be possible targets of microRNA 156. The expression of SPL genes in leaves was analysed by RNA-seq at three different stages, revealing that genes not under miR156 control were in general constitutively expressed at high levels, whereas miR156-regulated genes showed lower expression, often developmentally regulated. We selected the N. benthamiana SPL13_1a gene as target for a CRISPR/Cas9 knock-out experiment. We show here that a full knock-out in this single gene leads to a significant delay in flowering time, a trait that could be exploited to increase biomass for recombinant protein production.
SQUAMOSA PROMOTER BINDING-LIKE (SPL) 蛋白构成了一个庞大的转录因子家族,已知它们在生长和发育过程中发挥着关键作用,包括从幼年到成年和营养生长到生殖生长的转变。这使得 SPL 成为用于重组生物工厂等的烟属植物精准育种的有趣目标。我们在烟草 cv. K326 中鉴定了 49 个 SPL 基因,在 Nicotiana benthamiana LAB 菌株中鉴定了 43 个 SPL 基因,根据拟南芥的 SPL 分类,这些基因被分为 8 个系统发育组。直系同源物和同源物之间的外显子-内含子基因结构和 DNA 结合域高度保守。发现 30 个 NbSPL 基因和 33 个 NtSPL 基因可能是 microRNA 156 的靶基因。通过 RNA-seq 在三个不同阶段分析叶片中的 SPL 基因表达,结果表明不受 miR156 调控的基因通常以高水平组成型表达,而受 miR156 调控的基因表达水平较低,通常受发育调控。我们选择了 N. benthamiana SPL13_1a 基因作为 CRISPR/Cas9 敲除实验的靶基因。我们在这里表明,该单个基因的完全敲除会导致开花时间显著延迟,这一特性可用于增加用于重组蛋白生产的生物量。