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一个外围元件组装了I组内含子自我剪接所必需的紧密核心结构。

A peripheral element assembles the compact core structure essential for group I intron self-splicing.

作者信息

Xiao Mu, Li Tingting, Yuan Xiaoyan, Shang Yuan, Wang Fu, Chen Shoudeng, Zhang Yi

机构信息

Department of Biotechnology, State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan, Hubei 430072, China.

出版信息

Nucleic Acids Res. 2005 Aug 12;33(14):4602-11. doi: 10.1093/nar/gki770. Print 2005.

DOI:10.1093/nar/gki770
PMID:16100381
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1185575/
Abstract

The presence of non-conserved peripheral elements in all naturally occurring group I introns underline their importance in ensuring the natural intron function. Recently, we reported that some peripheral elements are conserved in group I introns of IE subgroup. Using self-splicing activity as a readout, our initial screening revealed that one such conserved peripheral elements, P2.1, is mainly required to fold the catalytically active structure of the Candida ribozyme, an IE intron. Unexpectedly, the essential function of P2.1 resides in a sequence-conserved short stem of P2.1 but not in a long-range interaction associated with the loop of P2.1 that stabilizes the ribozyme structure. The P2.1 stem is indispensable in folding the compact ribozyme core, most probably by forming a triple helical interaction with two core helices, P3 and P6. Surprisingly, although the ribozyme lacking the P2.1 stem renders a loosely folded core and the loss of self-splicing activity requires two consecutive transesterifications, the mutant ribozyme efficiently catalyzes the first transesterification reaction. These results suggest that the intron self-splicing demands much more ordered structure than does one independent transesterification, highlighting that the universally present peripheral elements achieve their functional importance by enabling the highly ordered structure through diverse tertiary interactions.

摘要

所有天然存在的I组内含子中都存在非保守的外围元件,这突出了它们在确保天然内含子功能方面的重要性。最近,我们报道了一些外围元件在IE亚组的I组内含子中是保守的。以自我剪接活性作为读出指标,我们最初的筛选显示,其中一个这样的保守外围元件P2.1,主要是折叠念珠菌核酶(一种IE内含子)的催化活性结构所必需的。出乎意料的是,P2.1的基本功能存在于P2.1的一个序列保守的短茎中,而不是存在于与稳定核酶结构的P2.1环相关的长程相互作用中。P2.1茎在折叠紧密的核酶核心中是不可或缺的,很可能是通过与两个核心螺旋P3和P6形成三螺旋相互作用来实现的。令人惊讶的是,尽管缺少P2.1茎的核酶呈现出松散折叠的核心,并且自我剪接活性的丧失需要连续两次转酯反应,但突变核酶能有效地催化第一次转酯反应。这些结果表明,内含子自我剪接比一次独立的转酯反应需要更有序的结构,这突出了普遍存在的外围元件通过多样的三级相互作用实现高度有序的结构来发挥其功能重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0693/1185575/c6c10ba22e65/gki770f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0693/1185575/87700a18cf3d/gki770f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0693/1185575/bbfc406d7ff1/gki770f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0693/1185575/070316a71e43/gki770f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0693/1185575/47802aa1b87c/gki770f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0693/1185575/c6c10ba22e65/gki770f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0693/1185575/87700a18cf3d/gki770f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0693/1185575/bbfc406d7ff1/gki770f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0693/1185575/070316a71e43/gki770f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0693/1185575/47802aa1b87c/gki770f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0693/1185575/c6c10ba22e65/gki770f5.jpg

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本文引用的文献

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Nucleic Acids Res. 2005 Apr 20;33(7):2118-28. doi: 10.1093/nar/gki517. Print 2005.
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两个连续酯转移反应的协同作用:外源性鸟苷结合促进随后的ωG与I类内含子结合。
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