a Department of Biology , Indiana University , Bloomington , Indiana , USA.
b Center for Genomics and Bioinformatics, Indiana University , Bloomington , Indiana , USA.
RNA Biol. 2018 Feb 1;15(2):269-279. doi: 10.1080/15476286.2017.1409930. Epub 2017 Dec 21.
Nuclear multisubunit RNA polymerases IV and V (Pol IV and Pol V) evolved in plants as specialized forms of Pol II. Their functions are best understood in the context of RNA-directed DNA methylation (RdDM), a process in which Pol IV-dependent 24 nt siRNAs direct the de novo cytosine methylation of regions transcribed by Pol V. Pol V has additional functions, independent of Pol IV and 24 nt siRNA biogenesis, in maintaining the repression of transposons and genomic repeats whose silencing depends on maintenance cytosine methylation. Here we report that Pol IV and Pol V play unexpected roles in defining the 3' boundaries of Pol II transcription units. Nuclear run-on assays reveal that in the absence of Pol IV or Pol V, Pol II occupancy downstream of poly A sites increases for approximately 12% of protein-coding genes. This effect is most pronounced for convergently transcribed gene pairs. Although Pols IV and V are detected near transcript ends of the affected Pol II - transcribed genes, their role in limiting Pol II read-through is independent of siRNA biogenesis or cytosine methylation for the majority of these genes. Interestingly, we observed that splicing was less efficient in pol IV or pol V mutant plants, compared to wild-type plants, suggesting that Pol IV or Pol V might affect pre-mRNA processing. We speculate that Pols IV and V (and/or their associated factors) play roles in Pol II transcription termination and pre-mRNA splicing by influencing polymerase elongation rates and/or release at collision sites for convergent genes.
核多亚基 RNA 聚合酶 IV 和 V(Pol IV 和 Pol V)是植物中作为 Pol II 的特化形式进化而来的。在 RNA 指导的 DNA 甲基化(RdDM)的背景下,它们的功能最容易理解,这是一个过程,其中 Pol IV 依赖性的 24nt siRNA 指导 Pol V 转录的区域的从头胞嘧啶甲基化。Pol V 具有与 Pol IV 和 24nt siRNA 生物发生无关的额外功能,在维持转座子和基因组重复的抑制中发挥作用,这些转座子和基因组重复的沉默依赖于维持胞嘧啶甲基化。在这里,我们报告 Pol IV 和 Pol V 在确定 Pol II 转录单位的 3'边界方面发挥了意想不到的作用。核运行试验表明,在缺乏 Pol IV 或 Pol V 的情况下,Pol II 在多聚 A 位点下游的占有率增加了大约 12%的编码蛋白基因。这种效应在转录方向相反的基因对中最为明显。尽管 Pols IV 和 V 被检测到受影响的 Pol II 转录基因的转录末端附近,但它们在限制 Pol II 通读中的作用独立于 siRNA 生物发生或大多数这些基因的胞嘧啶甲基化。有趣的是,与野生型植物相比,我们观察到在 pol IV 或 pol V 突变体植物中,剪接效率较低,这表明 Pol IV 或 Pol V 可能影响前体 mRNA 加工。我们推测 Pols IV 和 V(和/或它们的相关因子)通过影响聚合酶延伸率和/或在收敛基因的碰撞位点释放,在 Pol II 转录终止和前体 mRNA 剪接中发挥作用。