Hernando Carlos E, Sanchez Sabrina E, Mancini Estefanía, Yanovsky Marcelo J
Fundación Instituto Leloir, Instituto de Investigaciones Bioquímicas de Buenos Aires-Consejo Nacional de Investigaciones Científicas y Técnicas de Argentina, Buenos Aires, Argentina.
Molecular and Computational Biology Section, University of Southern California, Los Angeles, CA, 90089, USA.
BMC Genomics. 2015 Mar 17;16(1):192. doi: 10.1186/s12864-015-1399-2.
Methylation at arginine residues (R) is an important post-translational modification that regulates a myriad of essential cellular processes in eukaryotes, such as transcriptional regulation, RNA processing, signal transduction and DNA repair. Arginine methylation is catalyzed by a family of enzymes known as protein arginine methyltransferases (PRMTs). PRMTs are classified as Type I or Type II, depending on the position of the methyl group on the guanidine of the methylated arginine. Previous reports have linked symmetric R methylation to transcriptional repression, while asymmetric R methylation is generally associated with transcriptional activation. However, global studies supporting this conclusion are not available.
Here we compared side by side the physiological and molecular roles of the best characterized plant PRMTs, the Type II PRMT5 and the Type I PRMT4, also known as CARM1 in mammals. We found that prmt5 and prmt4a;4b mutants showed similar alterations in flowering time, photomorphogenic responses and salt stress tolerance, while only prmt5 mutants exhibited alterations in circadian rhythms. An RNA-seq analysis revealed that expression and splicing of many differentially regulated genes was similarly enhanced or repressed by PRMT5 and PRMT4s. Furthermore, PRMT5 and PRMT4s co-regulated the expression and splicing of key regulatory genes associated with transcription, RNA processing, responses to light, flowering, and abiotic stress tolerance, being candidates to mediate the physiological alterations observed in the mutants.
Our global analysis indicates that two of the most important Type I and Type II arginine methyltransferases, PRTM4 and PRMT5, have mostly overlapping as well as specific, but not opposite, roles in the global regulation of gene expression in plants.
精氨酸残基(R)甲基化是一种重要的翻译后修饰,可调节真核生物中众多基本的细胞过程,如转录调控、RNA加工、信号转导和DNA修复。精氨酸甲基化由一类称为蛋白质精氨酸甲基转移酶(PRMT)的酶催化。根据甲基化精氨酸胍基上甲基的位置,PRMT可分为I型或II型。先前的报道将对称R甲基化与转录抑制联系起来,而非对称R甲基化通常与转录激活相关。然而,尚无支持这一结论的全局性研究。
在这里,我们并排比较了植物中特征最明确的PRMT,即II型PRMT5和I型PRMT4(在哺乳动物中也称为CARM1)的生理和分子作用。我们发现,prmt5和prmt4a;4b突变体在开花时间、光形态建成反应和盐胁迫耐受性方面表现出相似的变化,而只有prmt5突变体在昼夜节律方面表现出变化。RNA测序分析表明,许多差异调节基因的表达和剪接受到PRMT5和PRMT4s的类似增强或抑制。此外,PRMT5和PRMT4s共同调节与转录、RNA加工、光反应、开花和非生物胁迫耐受性相关的关键调控基因的表达和剪接,它们是介导突变体中观察到的生理变化的候选者。
我们的全局性分析表明,两种最重要的I型和II型精氨酸甲基转移酶PRTM4和PRMT5在植物基因表达的全局调控中大多具有重叠以及特定但非相反的作用。