Sasaki Taku, Kanno Tatsuo, Liang Shih-Chieh, Chen Pao-Yang, Liao Wen-Wei, Lin Wen-Dar, Matzke Antonius J M, Matzke Marjori
Institute of Plant and Microbial Biology, Nangang District, Taipei 115, Taiwan.
Institute of Plant and Microbial Biology, Nangang District, Taipei 115, Taiwan
Genetics. 2015 Jun;200(2):523-35. doi: 10.1534/genetics.115.176438. Epub 2015 Mar 27.
Alternative splicing is prevalent in plants, but little is known about its regulation in the context of developmental and signaling pathways. We describe here a new factor that influences pre-messengerRNA (mRNA) splicing and is essential for embryonic development in Arabidopsis thaliana. This factor was retrieved in a genetic screen that identified mutants impaired in expression of an alternatively spliced GFP reporter gene. In addition to the known spliceosomal component PRP8, the screen recovered Arabidopsis RTF2 (AtRTF2), a previously uncharacterized, evolutionarily conserved protein containing a replication termination factor 2 (Rtf2) domain. A homozygous null mutation in AtRTF2 is embryo lethal, indicating that AtRTF2 is an essential protein. Quantitative RT-PCR demonstrated that impaired expression of GFP in atrtf2 and prp8 mutants is due to inefficient splicing of the GFP pre-mRNA. A genome-wide analysis using RNA sequencing indicated that 13-16% of total introns are retained to a significant degree in atrtf2 mutants. Considering these results and previous suggestions that Rtf2 represents an ubiquitin-related domain, we discuss the possible role of AtRTF2 in ubiquitin-based regulation of pre-mRNA splicing.
可变剪接在植物中普遍存在,但在发育和信号通路背景下其调控机制却鲜为人知。我们在此描述了一种影响前体信使核糖核酸(mRNA)剪接且对拟南芥胚胎发育至关重要的新因子。该因子是在一项遗传筛选中获得的,该筛选鉴定出在可变剪接的绿色荧光蛋白(GFP)报告基因表达中受损的突变体。除了已知的剪接体成分PRP8外,该筛选还获得了拟南芥RTF2(AtRTF2),这是一种以前未被表征的、进化上保守的蛋白质,含有复制终止因子2(Rtf2)结构域。AtRTF2中的纯合无效突变是胚胎致死的,这表明AtRTF2是一种必需蛋白。定量逆转录聚合酶链反应(RT-PCR)表明,atrtf2和prp8突变体中GFP表达受损是由于GFP前体mRNA剪接效率低下所致。使用RNA测序进行的全基因组分析表明,在atrtf2突变体中,13 - 16%的总内含子在很大程度上被保留。考虑到这些结果以及之前关于Rtf2代表泛素相关结构域的观点,我们讨论了AtRTF2在基于泛素的前体mRNA剪接调控中的可能作用。