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Unexpected Diversity of Chloroplast Noncoding RNAs as Revealed by Deep Sequencing of the Arabidopsis Transcriptome

机译:拟南芥转录组的深度测序揭示了叶绿体非编码RNA的意外多样性

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摘要

Noncoding RNAs (ncRNA) are widely expressed in both prokaryotes and eukaryotes. Eukaryotic ncRNAs are commonly micro- and small-interfering RNAs (18–25 nt) involved in posttranscriptional gene silencing, whereas prokaryotic ncRNAs vary in size and are involved in various aspects of gene regulation. Given the prokaryotic origin of organelles, the presence of ncRNAs might be expected; however, the full spectrum of organellar ncRNAs has not been determined systematically. Here, strand-specific RNA-Seq analysis was used to identify 107 candidate ncRNAs from Arabidopsis thaliana chloroplasts, primarily encoded opposite protein-coding and tRNA genes. Forty-eight ncRNAs were shown to accumulate by RNA gel blot as discrete transcripts in wild-type (WT) plants and/or the pnp1-1 mutant, which lacks the chloroplast ribonuclease polynucleotide phosphorylase (cpPNPase). Ninety-eight percent of the ncRNAs detected by RNA gel blot had different transcript patterns between WT and pnp1-1, suggesting cpPNPase has a significant role in chloroplast ncRNA biogenesis and accumulation. Analysis of materials deficient for other major chloroplast ribonucleases, RNase R, RNase E, and RNase J, showed differential effects on ncRNA accumulation and/or form, suggesting specificity in RNase-ncRNA interactions. 5′ end mapping demonstrates that some ncRNAs are transcribed from dedicated promoters, whereas others result from transcriptional read-through. Finally, correlations between accumulation of some ncRNAs and the symmetrically transcribed sense RNA are consistent with a role in RNA stability. Overall, our data suggest that this extensive population of ncRNAs has the potential to underpin a previously underappreciated regulatory mode in the chloroplast.
机译:非编码RNA(ncRNA)在原核生物和真核生物中广泛表达。真核ncRNA通常是微干扰和小干扰RNA(18-25 nt),参与转录后基因沉默,而原核ncRNA大小不一,涉及基因调控的各个方面。考虑到细胞器的原核起源,可能会出现ncRNA。然而,尚未系统地确定细胞器ncRNA的全谱。在这里,使用链特异性RNA-Seq分析来鉴定拟南芥叶绿体中的107个候选ncRNA,它们主要编码相反的蛋白质编码和tRNA基因。 RNA印迹显示,有48个ncRNA在野生型(WT)植物和/或缺少叶绿体核糖核酸酶多核苷酸磷酸化酶(cpPNPase)的pnp1-1突变体中作为离散转录本积累。 RNA凝胶印迹检测到的ncRNA中有98%在WT和pnp1-1之间具有不同的转录方式,表明cpPNPase在叶绿体ncRNA的生物发生和积累中具有重要作用。对其他主要叶绿体核糖核酸,RNase R,RNase E和RNase J缺乏材料的分析显示,它们对ncRNA积累和/或形式的影响不同,表明RNase-ncRNA相互作用具有特异性。 5'末端作图表明,某些ncRNA是从专用启动子转录的,而其他则是转录的通读。最后,某些ncRNA的积累与对称转录的有义RNA之间的相关性与RNA稳定性中的作用是一致的。总体而言,我们的数据表明,大量的ncRNA具有潜在的作用,可支持以前未充分认识的叶绿体调节模式。

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