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植物短沉默 RNA 的大型复杂网络证据。

Evidence for large complex networks of plant short silencing RNAs.

机构信息

The Sainsbury Laboratory, John Innes Centre, Norwich, United Kingdom.

出版信息

PLoS One. 2010 Mar 26;5(3):e9901. doi: 10.1371/journal.pone.0009901.

Abstract

BACKGROUND

In plants and animals there are many classes of short RNAs that carry out a wide range of functions within the cell; short silencing RNAs (ssRNAs) of 21-25 nucleotides in length are produced from double-stranded RNA precursors by the protein Dicer and guide nucleases and other proteins to their RNA targets through base pairing interactions. The consequence of this process is degradation of the targeted RNA, suppression of its translation or initiation of secondary ssRNA production. The secondary ssRNAs in turn could then initiate further layers of ssRNA production to form extensive cascades and networks of interacting RNA [1]. Previous empirical analysis in plants established the existence of small secondary ssRNA cascade [2], in which a single instance of this event occurred but it was not known whether there are other more extensive networks of secondary sRNA production.

METHODOLOGY/PRINCIPAL FINDINGS: We generated a network by predicting targets of ssRNA populations obtained from high-throughput sequencing experiments. The topology of the network shows it to have power law connectivity distribution, to be dissortative, highly clustered and composed of multiple components. We also identify protein families, PPR and ULP1, that act as hubs within the network. Comparison of the repetition of genomic sub-sequences of ssRNA length between Arabidopsis and E.coli suggest that the network structure is made possible by the underlying repetitiveness in the genome sequence.

CONCLUSIONS/SIGNIFICANCE: Together our results provide good evidence for the existence of a large, robust ssRNA interaction network with distinct regulatory function. Such a network could have a massive effect on the regulation of gene expression via mediation of transcript levels.

摘要

背景

在动植物中,有许多种类的短 RNA 分子在细胞内发挥着广泛的功能;长 21-25 个核苷酸的短沉默 RNA(ssRNA)是由双链 RNA 前体通过蛋白 Dicer 产生的,并通过碱基配对相互作用将核酶和其他蛋白引导到其 RNA 靶标上。这一过程的结果是靶向 RNA 的降解、其翻译的抑制或二级 ssRNA 产生的起始。二级 ssRNA 反过来又可以启动进一步的 ssRNA 产生层,形成广泛的级联和相互作用的 RNA 网络[1]。先前在植物中的经验分析确立了小的二级 ssRNA 级联的存在[2],其中单个事件发生,但尚不清楚是否存在其他更广泛的二级 sRNA 产生网络。

方法/主要发现:我们通过预测从高通量测序实验中获得的 ssRNA 群体的靶标来生成网络。网络的拓扑结构显示它具有幂律连接分布,是反关联的、高度聚类的,由多个组件组成。我们还鉴定了作为网络内枢纽的蛋白家族 PPR 和 ULP1。将 ssRNA 长度的基因组亚序列在拟南芥和大肠杆菌之间的重复进行比较,表明网络结构是由基因组序列的潜在重复性所决定的。

结论/意义:我们的研究结果共同为存在一个具有独特调节功能的大型稳健 ssRNA 相互作用网络提供了充分的证据。这样的网络可以通过调节转录本水平对基因表达的调控产生巨大的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2485/2845630/8eeee85f214a/pone.0009901.g001.jpg

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