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真核生物 TPP 核糖开关对涉及长距离碱基配对的可变剪接的调控。

Eukaryotic TPP riboswitch regulation of alternative splicing involving long-distance base pairing.

机构信息

Howard Hughes Medical Institute, Yale University, New Haven, CT 06520, USA.

出版信息

Nucleic Acids Res. 2013 Mar 1;41(5):3022-31. doi: 10.1093/nar/gkt057. Epub 2013 Feb 1.

DOI:10.1093/nar/gkt057
PMID:23376932
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3597705/
Abstract

Thiamin pyrophosphate (TPP) riboswitches are found in organisms from all three domains of life. Examples in bacteria commonly repress gene expression by terminating transcription or by blocking ribosome binding, whereas most eukaryotic TPP riboswitches are predicted to regulate gene expression by modulating RNA splicing. Given the widespread distribution of eukaryotic TPP riboswitches and the diversity of their locations in precursor messenger RNAs (pre-mRNAs), we sought to examine the mechanism of alternative splicing regulation by a fungal TPP riboswitch from Neurospora crassa, which is mostly located in a large intron separating protein-coding exons. Our data reveal that this riboswitch uses a long-distance (∼530-nt separation) base-pairing interaction to regulate alternative splicing. Specifically, a portion of the TPP-binding aptamer can form a base-paired structure with a conserved sequence element (α) located near a 5' splice site, which greatly increases use of this 5' splice site and promotes gene expression. Comparative sequence analyses indicate that many fungal species carry a TPP riboswitch with similar intron architecture, and therefore the homologous genes in these fungi are likely to use the same mechanism. Our findings expand the scope of genetic control mechanisms relying on long-range RNA interactions to include riboswitches.

摘要

硫胺素焦磷酸(TPP)核糖开关存在于所有三个生命领域的生物中。细菌中的例子通常通过终止转录或阻止核糖体结合来抑制基因表达,而大多数真核 TPP 核糖开关据预测通过调节 RNA 剪接来调节基因表达。鉴于真核 TPP 核糖开关的广泛分布及其在前体信使 RNA(pre-mRNA)中的位置的多样性,我们试图研究来自粗糙脉孢菌的真菌 TPP 核糖开关对可变剪接的调节机制,该核糖开关主要位于分离蛋白编码外显子的大内含子中。我们的数据表明,该核糖开关使用远距离(约 530-nt 分离)碱基配对相互作用来调节可变剪接。具体来说,TPP 结合适体的一部分可以与位于 5'剪接位点附近的保守序列元件 (α) 形成碱基配对结构,这大大增加了该 5'剪接位点的使用,并促进了基因表达。比较序列分析表明,许多真菌物种携带具有类似内含子结构的 TPP 核糖开关,因此这些真菌中的同源基因可能使用相同的机制。我们的发现扩展了依赖远距离 RNA 相互作用的遗传控制机制的范围,包括核糖开关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f80/3597705/c7b4daaa9637/gkt057f6p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f80/3597705/3b3b61484b44/gkt057f1p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f80/3597705/f3d4f3efefed/gkt057f2p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f80/3597705/6e1f4d205f9c/gkt057f3p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f80/3597705/16455dc67270/gkt057f4p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f80/3597705/303030a99ebb/gkt057f5p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f80/3597705/c7b4daaa9637/gkt057f6p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f80/3597705/3b3b61484b44/gkt057f1p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f80/3597705/f3d4f3efefed/gkt057f2p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f80/3597705/6e1f4d205f9c/gkt057f3p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f80/3597705/16455dc67270/gkt057f4p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f80/3597705/303030a99ebb/gkt057f5p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f80/3597705/c7b4daaa9637/gkt057f6p.jpg

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