Non-coding RNA polymerases that silence transposable elements and reprogram gene expression in plants.

IF 3.6 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Transcription-Austin Pub Date : 2020-06-01 Epub Date: 2020-11-12 DOI:10.1080/21541264.2020.1825906
Bart Rymen, Laura Ferrafiat, Todd Blevins
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引用次数: 10

Abstract

Multisubunit RNA polymerase (Pol) complexes are the core machinery for gene expression in eukaryotes. The enzymes Pol I, Pol II and Pol III transcribe distinct subsets of nuclear genes. This family of nuclear RNA polymerases expanded in terrestrial plants by the duplication of Pol II subunit genes. Two Pol II-related enzymes, Pol IV and Pol V, are highly specialized in the production of regulatory, non-coding RNAs. Pol IV and Pol V are the central players of RNA-directed DNA methylation (RdDM), an RNA interference pathway that represses transposable elements (TEs) and selected genes. Genetic and biochemical analyses of Pol IV/V subunits are now revealing how these enzymes evolved from ancestral Pol II to sustain non-coding RNA biogenesis in silent chromatin. Intriguingly, Pol IV-RdDM regulates genes that influence flowering time, reproductive development, stress responses and plant-pathogen interactions. Pol IV target genes vary among closely related taxa, indicating that these regulatory circuits are often species-specific. Data from crops like maize, rice, tomato and Brassicarapa suggest that dynamic repositioning of TEs, accompanied by Pol IV targeting to TE-proximal genes, leads to the reprogramming of plant gene expression over short evolutionary timescales.

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植物中沉默转座因子和重编程基因表达的非编码RNA聚合酶。
多亚基RNA聚合酶(Pol)复合物是真核生物基因表达的核心机制。酶Pol I, Pol II和Pol III转录不同的核基因亚群。这个核RNA聚合酶家族通过Pol II亚基基因的复制在陆生植物中扩展。两种与Pol ii相关的酶,Pol IV和Pol V,是高度专门化的调节非编码rna的产生。Pol IV和Pol V是RNA定向DNA甲基化(RdDM)的核心参与者,RdDM是一种RNA干扰途径,可抑制转座因子(te)和选定基因。Pol IV/V亚基的遗传和生化分析现在揭示了这些酶如何从祖先Pol II进化到维持沉默染色质中的非编码RNA生物发生。有趣的是,Pol IV-RdDM调节影响开花时间、生殖发育、胁迫反应和植物与病原体相互作用的基因。Pol IV靶基因在密切相关的分类群中存在差异,表明这些调控回路通常具有物种特异性。来自玉米、水稻、番茄和芸苔等作物的数据表明,te的动态重新定位,伴随着Pol IV靶向te近端基因,导致植物基因表达在短进化时间尺度上的重编程。
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来源期刊
Transcription-Austin
Transcription-Austin BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
6.50
自引率
5.60%
发文量
9
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