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参与 3'剪接接头摆动机制的序列特征。

Sequence features involved in the mechanism of 3' splice junction wobbling.

机构信息

Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.

出版信息

BMC Mol Biol. 2010 May 7;11:34. doi: 10.1186/1471-2199-11-34.

DOI:10.1186/1471-2199-11-34
PMID:20459675
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2875228/
Abstract

BACKGROUND

Alternative splicing is an important mechanism mediating the diversified functions of genes in multicellular organisms, and such event occurs in around 40-60% of human genes. Recently, a new splice-junction wobbling mechanism was proposed that subtle modifications exist in mRNA maturation by alternatively choosing at 5'- GTNGT and 3'- NAGNAG, which created single amino acid insertion and deletion isoforms.

RESULTS

By browsing the Alternative Splicing Database information, we observed that most 3' alternative splice site choices occur within six nucleotides of the dominant splice site and the incidence significantly decreases further away from the dominant acceptor site. Although a lower frequency of alternative splicing occurs within the intronic region (alternative splicing at the proximal AG) than in the exonic region (alternative splicing at the distal AG), alternative AG sites located within the intronic region show stronger potential as the acceptor. These observations revealed that the choice of 3' splice sites during 3' splicing junction wobbling could depend on the distance between the duplicated AG and the branch point site (BPS). Further mutagenesis experiments demonstrated that the distance of AG-to-AG and BPS-to-AG can greatly influence 3' splice site selection. Knocking down a known alternative splicing regulator, hSlu7, failed to affect wobble splicing choices.

CONCLUSION

Our results implied that nucleotide distance between proximal and distal AG sites has an important regulatory function. In this study, we showed that occurrence of 3' wobble splicing occurs in a distance-dependent manner and that most of this wobble splicing is probably caused by steric hindrance from a factor bound at the neighboring tandem motif sequence.

摘要

背景

可变剪接是一种重要的机制,介导多细胞生物中基因的多样化功能,这种事件发生在大约 40-60%的人类基因中。最近,提出了一种新的剪接连接摆动机制,通过在 5'-GTNGT 和 3'-NAGNAG 处交替选择,存在 mRNA 成熟的细微修饰,从而产生单个氨基酸插入和缺失的同工型。

结果

通过浏览可变剪接数据库信息,我们观察到大多数 3' 可变剪接位点选择发生在主导剪接位点的六个核苷酸内,并且离主导受体位点越远,发生率显著降低。虽然内含子区域内的可变剪接(近端 AG 处的可变剪接)频率低于外显子区域(远端 AG 处的可变剪接),但位于内含子区域内的替代 AG 位点作为受体具有更强的潜力。这些观察结果表明,在 3' 剪接连接摆动过程中 3' 剪接位点的选择可能取决于重复的 AG 与分支点之间的距离(BPS)。进一步的突变实验表明,AG-AG 之间的距离和 BPS-AG 之间的距离可以极大地影响 3' 剪接位点的选择。敲低已知的可变剪接调节剂 hSlu7 未能影响摆动剪接的选择。

结论

我们的结果表明,近端和远端 AG 位点之间的核苷酸距离具有重要的调节功能。在这项研究中,我们表明,3' 摆动剪接的发生是一种距离依赖的方式,而且大多数这种摆动剪接可能是由结合在相邻串联基序序列上的因子引起的空间位阻造成的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19e0/2875228/a075ea6e2445/1471-2199-11-34-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19e0/2875228/15cfe4066639/1471-2199-11-34-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19e0/2875228/d863ad98c2e8/1471-2199-11-34-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19e0/2875228/2e6e6b7e1e24/1471-2199-11-34-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19e0/2875228/8dd83d165ba0/1471-2199-11-34-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19e0/2875228/a075ea6e2445/1471-2199-11-34-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19e0/2875228/15cfe4066639/1471-2199-11-34-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19e0/2875228/d863ad98c2e8/1471-2199-11-34-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19e0/2875228/2e6e6b7e1e24/1471-2199-11-34-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19e0/2875228/8dd83d165ba0/1471-2199-11-34-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19e0/2875228/a075ea6e2445/1471-2199-11-34-5.jpg

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