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体内核 RNA 结构组学揭示了植物中转录后 mRNA 加工的 RNA 结构调控。

In vivo nuclear RNA structurome reveals RNA-structure regulation of mRNA processing in plants.

机构信息

Department of Cell and Developmental Biology, John Innes Centre, Norwich Research Park, Norwich, NR4 7UH, UK.

Key Laboratory of Molecular Epigenetics of the Ministry of Education, Northeast Normal University, Changchun, 130024, China.

出版信息

Genome Biol. 2021 Jan 4;22(1):11. doi: 10.1186/s13059-020-02236-4.

Abstract

BACKGROUND

mRNA processing is critical for gene expression. A challenge in regulating mRNA processing is how to recognize the actual mRNA processing sites, such as splice and polyadenylation sites, when the sequence content is insufficient for this purpose. Previous studies suggested that RNA structure affects mRNA processing. However, the regulatory role of RNA structure in mRNA processing remains unclear.

RESULTS

Here, we perform in vivo selective 2'-hydroxyl acylation analyzed by primer extension (SHAPE) chemical profiling on Arabidopsis and generate the in vivo nuclear RNA structure landscape. We find that nuclear mRNAs fold differently from cytosolic mRNAs across translation start and stop sites. Notably, we discover a two-nucleotide single-stranded RNA structure feature upstream of 5' splice sites that is strongly associated with splicing and the selection of alternative 5' splice sites. The regulatory role of this RNA structure feature is further confirmed by experimental validation. Moreover, we find the single-strandedness of branch sites is also associated with 3' splice site recognition. We also identify an RNA structure feature comprising two close-by single-stranded regions that is specifically associated with both polyadenylation and alternative polyadenylation events.

CONCLUSIONS

We successfully identify pre-mRNA structure features associated with splicing and polyadenylation at whole-genome scale and validate an RNA structure feature which can regulate splicing. Our study unveils a new RNA structure regulatory mechanism for mRNA processing.

摘要

背景

mRNA 加工对于基因表达至关重要。在调节 mRNA 加工时,面临的一个挑战是,当序列内容不足以实现此目的时,如何识别实际的 mRNA 加工位点,如剪接和多聚腺苷酸化位点。先前的研究表明,RNA 结构会影响 mRNA 加工。然而,RNA 结构在 mRNA 加工中的调节作用仍不清楚。

结果

在这里,我们对拟南芥进行了体内选择性 2'-羟基酰化分析引物延伸 (SHAPE) 化学分析,并生成了体内核 RNA 结构图谱。我们发现,跨翻译起始和终止位点,核 mRNA 的折叠方式与细胞质 mRNA 不同。值得注意的是,我们发现了 5'剪接位点上游的一个具有两个核苷酸的单链 RNA 结构特征,该特征与剪接和选择性 5'剪接位点的选择强烈相关。通过实验验证进一步证实了该 RNA 结构特征的调节作用。此外,我们发现分支位点的单链状态也与 3'剪接位点识别相关。我们还鉴定了一个包含两个附近单链区域的 RNA 结构特征,该特征与聚腺苷酸化和选择性聚腺苷酸化事件都相关。

结论

我们成功地在全基因组范围内识别出与剪接和多聚腺苷酸化相关的 pre-mRNA 结构特征,并验证了一个可以调节剪接的 RNA 结构特征。我们的研究揭示了一种新的 RNA 结构调节机制,用于 mRNA 加工。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6cc/7784297/90d0b3a3b7c1/13059_2020_2236_Fig1_HTML.jpg

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