Molecular and Environmental Plant Sciences, Texas A&M University, College Station, Texas 77843.
Department of Biochemistry and Biophysics, Texas A&M University, College Station, Texas 77843.
Plant Cell. 2017 Dec;29(12):3214-3233. doi: 10.1105/tpc.17.00331. Epub 2017 Nov 1.
Phosphorylation of the RNA polymerase II (Pol II) C-terminal domain (CTD) regulates transcription of protein-coding mRNAs and noncoding RNAs. CTD function in transcription of protein-coding RNAs has been studied extensively, but its role in plant noncoding RNA transcription remains obscure. Here, using knockdown lines ( ), we showed that CPL4 functions in genome-wide, conditional production of 3'-extensions of small nuclear RNAs (snRNAs) and biogenesis of novel transcripts from protein-coding genes downstream of the snRNAs (snRNA-downstream protein-coding genes [snR-DPGs]). Production of snR-DPGs required the Pol II snRNA promoter (PIIsnR), and plants showed increased read-through of the snRNA 3'-end processing signal, leading to continuation of transcription downstream of the snRNA gene. We also discovered an unstable, intermediate-length RNA from the locus ( ), whose expression originated from the 5' region of a protein-coding gene. Expression of the was driven by a PIIsnR and was conditionally 3'-extended to produce an mRNA. In the wild type, salt stress induced the snRNA-to-snR-DPG switch, which was associated with alterations of Pol II-CTD phosphorylation at the target loci. The snR-DPG transcripts occur widely in plants, suggesting that the transcriptional snRNA-to-snR-DPG switch may be a ubiquitous mechanism to regulate plant gene expression in response to environmental stresses.
RNA 聚合酶 II(Pol II)C 末端结构域(CTD)的磷酸化调节蛋白质编码 mRNA 和非编码 RNA 的转录。CTD 在蛋白质编码 RNA 转录中的功能已得到广泛研究,但在植物非编码 RNA 转录中的作用仍不清楚。在这里,我们使用 敲低系(),表明 CPL4 参与小核 RNA(snRNA)的全基因组条件性 3'-延伸和 snRNA 下游蛋白质编码基因(snRNA-downstream protein-coding genes [snR-DPGs])的新型转录本的生物发生。snR-DPG 的产生需要 Pol II snRNA 启动子(PIIsnR),而 植物表现出 snRNA 3'-末端加工信号的通读增加,导致 snRNA 基因下游的转录继续进行。我们还从 基因座发现了一种不稳定的、中等长度的 RNA(),其表达起源于一个蛋白质编码基因的 5'区域。的表达受 PIIsnR 驱动,并在条件下 3'-延伸以产生 mRNA。在野生型中,盐胁迫诱导了 snRNA 到 snR-DPG 的转换,这与靶基因座 Pol II-CTD 磷酸化的改变有关。snR-DPG 转录物在植物中广泛存在,这表明转录 snRNA-to-snR-DPG 转换可能是一种普遍的机制,可调节植物基因表达以响应环境胁迫。