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互斥外显子转换的生物学影响。

Biological impact of mutually exclusive exon switching.

机构信息

Institute of Structural and Molecular Biology, University College London, Darwin Building, Gower Street, London, United Kingdom.

Department of Applied Physics, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, Bangi, Malaysia.

出版信息

PLoS Comput Biol. 2021 Mar 2;17(3):e1008708. doi: 10.1371/journal.pcbi.1008708. eCollection 2021 Mar.

Abstract

Alternative splicing can expand the diversity of proteomes. Homologous mutually exclusive exons (MXEs) originate from the same ancestral exon and result in polypeptides with similar structural properties but altered sequence. Why would some genes switch homologous exons and what are their biological impact? Here, we analyse the extent of sequence, structural and functional variability in MXEs and report the first large scale, structure-based analysis of the biological impact of MXE events from different genomes. MXE-specific residues tend to map to single domains, are highly enriched in surface exposed residues and cluster at or near protein functional sites. Thus, MXE events are likely to maintain the protein fold, but alter specificity and selectivity of protein function. This comprehensive resource of MXE events and their annotations is available at: http://gene3d.biochem.ucl.ac.uk/mxemod/. These findings highlight how small, but significant changes at critical positions on a protein surface are exploited in evolution to alter function.

摘要

可变剪接可以扩大蛋白质组的多样性。同源互斥外显子 (MXE) 起源于同一个祖先外显子,导致具有相似结构特性但序列改变的多肽。为什么有些基因会切换同源外显子,它们的生物学影响是什么?在这里,我们分析了 MXE 中序列、结构和功能变异性的程度,并报告了首次基于结构的来自不同基因组的 MXE 事件的生物学影响的大规模分析。MXE 特异性残基倾向于映射到单个结构域,高度富集在表面暴露的残基中,并聚集在或接近蛋白质功能位点。因此,MXE 事件可能保持蛋白质折叠,但改变蛋白质功能的特异性和选择性。该 MXE 事件及其注释的综合资源可在:http://gene3d.biochem.ucl.ac.uk/mxemod/ 获取。这些发现强调了在进化过程中,如何利用蛋白质表面关键位置的微小但显著的变化来改变功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95d6/7954323/8866ce4e6a04/pcbi.1008708.g001.jpg

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