National Research Council of Italy, Institute of Biosciences and Bioresources, 80055 Portici, Naples, Italy.
Council for Agricultural Research and Economics, Research Centre for Genomics and Bioinformatics, 00178 Rome, Italy.
Plant Physiol. 2020 Jun;183(2):793-807. doi: 10.1104/pp.20.00037. Epub 2020 Mar 2.
RNA splicing is a fundamental mechanism contributing to the definition of the cellular protein population in any given environmental condition. DNA-DAMAGE REPAIR/TOLERATION PROTEIN111 (DRT111)/SPLICING FACTOR FOR PHYTOCHROME SIGNALING is a splicing factor previously shown to interact with phytochrome B and characterized for its role in splicing of pre-mRNAs involved in photomorphogenesis. Here, we show that DRT111 interacts with Arabidopsis () Splicing Factor1, involved in 3' splicing site recognition. Double- and triple-mutant analysis shows that DRT111 controls splicing of and acts upstream of the splicing factor SUPPRESSOR OF ABI3-ABI5. is highly expressed in seeds and stomata of Arabidopsis and is induced by long-term treatments of polyethylene glycol and abscisic acid (ABA). knock-out mutants are defective in ABA-induced stomatal closure and are hypersensitive to ABA during seed germination. Conversely, overexpressing plants show ABA-hyposensitive seed germination. RNA-sequencing experiments show that in dry seeds, DRT111 controls expression and splicing of genes involved in osmotic-stress and ABA responses, light signaling, and mRNA splicing, including targets of ABSCISIC ACID INSENSITIVE3 (ABI3) and PHYTOCHROME INTERACTING FACTORs (PIFs). Consistently, expression of the germination inhibitor , induced by ABI3 and PIF1, is upregulated in imbibed seeds of - mutants. Together, these results indicate that DRT111 controls sensitivity to ABA during seed development, germination, and stomatal movements, and integrates ABA- and light-regulated pathways to control seed germination.
RNA 剪接是一种基本机制,有助于在任何给定的环境条件下定义细胞的蛋白质群体。DNA 损伤修复/耐受蛋白 111(DRT111)/光敏色素信号转导剪接因子是一种剪接因子,先前已被证明与光敏色素 B 相互作用,并因其在涉及光形态发生的前体 mRNA 剪接中的作用而得到表征。在这里,我们表明 DRT111 与拟南芥()剪接因子 1 相互作用,该因子参与 3'剪接位点识别。双突变和三突变分析表明,DRT111 控制和的剪接,并作用于剪接因子 SUPPRESSOR OF ABI3-ABI5 的上游。在拟南芥的种子和气孔中高度表达,并受聚乙二醇和脱落酸(ABA)的长期处理诱导。的敲除突变体在 ABA 诱导的气孔关闭中存在缺陷,并且在种子萌发期间对 ABA 敏感。相反,过表达植物表现出 ABA 敏感的种子萌发。RNA-seq 实验表明,在干燥的种子中,DRT111 控制参与渗透胁迫和 ABA 反应、光信号以及 mRNA 剪接的基因的表达和剪接,包括 ABA 不敏感 3(ABI3)和光敏色素相互作用因子(PIFs)的靶标。一致地,由 ABI3 和 PIF1 诱导的萌发抑制剂的表达在突变体的吸胀种子中上调。总之,这些结果表明 DRT111 控制种子发育、萌发和气孔运动期间对 ABA 的敏感性,并整合 ABA 和光调节途径来控制种子萌发。