Johnson Kaeli C M, Yu Yu, Gao Lei, Eng Ryan C, Wasteneys Geoffrey O, Chen Xuemei, Li Xin
Department of Botany, University of British Columbia, Vancouver, V6T 1Z4, Canada Michael Smith Laboratories, University of British Columbia, Vancouver, V6T 1Z4, Canada.
Institute for Integrative Genome Biology, Department of Botany and Plant Sciences, University of California Riverside, Riverside, CA 92521, USA.
J Exp Bot. 2016 Apr;67(8):2219-30. doi: 10.1093/jxb/erw020. Epub 2016 Feb 10.
Plants employ five DNA-dependent RNA polymerases (Pols) in transcription. One of these polymerases, Pol III, has previously been reported to transcribe 5S rRNA, tRNAs, and a number of small RNAs. However, in-depth functional analysis is complicated by the fact that knockout mutations in Pol subunits are typically lethal. Here, we report the characterization of the first known viable Pol III subunit mutant,nrpc7-1 This mutant was originally isolated from a forward genetic screen designed to identify enhancers of the autoimmune mutantsnc1, which contains a gain-of-function mutation in a nucleotide-binding leucine-rich repeat (NLR) immune receptor-encoding gene. Thenrpc7-1mutation occurs in an intron-exon splice site and results in intron retention in someNRPC7transcripts. There is a global disruption in RNA equilibrium innrpc7-1, exemplified by the altered expression of a number of RNA molecules, some of which are not reported to be transcribed by Pol III. There are developmental defects associated with the mutation, as homozygous mutant plants are dwarf, have stunted roots and siliques, and possess serrated leaves. These defects are possibly due to altered small RNA stability or activity. Additionally, thenrpc7-1mutation confers anNLR-specific alternative splicing defect that correlates with enhanced disease resistance, highlighting the importance of alternative splicing in regulating NLR activity. Altogether, these results reveal novel roles for Pol III in maintaining RNA homeostasis, adjusting the expression of a diverse suite of genes, and indirectly modulating gene splicing. Future analyses using thenrpc7-1mutant will be instrumental in examining other unknown Pol III functions.
植物在转录过程中使用五种依赖DNA的RNA聚合酶(Pol)。其中一种聚合酶Pol III,此前已有报道称其转录5S rRNA、tRNA和一些小RNA。然而,由于Pol亚基的敲除突变通常是致死性的,深入的功能分析变得复杂。在这里,我们报道了首个已知的存活的Pol III亚基突变体nrpc7-1的特征。该突变体最初是从一个正向遗传筛选中分离出来的,该筛选旨在鉴定自身免疫突变体nc1的增强子,nc1在一个编码核苷酸结合富含亮氨酸重复序列(NLR)免疫受体的基因中存在功能获得性突变。nrpc7-1突变发生在内含子-外显子剪接位点,导致一些NRPC7转录本中内含子保留。nrpc7-1中RNA平衡出现全局性破坏,表现为许多RNA分子的表达改变,其中一些并未报道由Pol III转录。该突变与发育缺陷相关,因为纯合突变体植株矮小,根和角果发育不良,叶片有锯齿。这些缺陷可能是由于小RNA稳定性或活性改变所致。此外,nrpc7-1突变赋予了一种NLR特异性的可变剪接缺陷,这与增强的抗病性相关,突出了可变剪接在调节NLR活性中的重要性。总之,这些结果揭示了Pol III在维持RNA稳态、调节多种基因表达以及间接调节基因剪接方面的新作用。使用nrpc7-1突变体进行的未来分析将有助于研究其他未知的Pol III功能。