Single-molecule fluorescence-based studies on the dynamics, assembly and catalytic mechanism of the spliceosome

被引:8
作者
Warnasooriya, Chandani
Rueda, David [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Ctr Clin, MRC, Dept Med,Sect Virol, London W12 0NN, England
基金
美国国家科学基金会; 英国医学研究理事会; 美国国家卫生研究院;
关键词
co-localization single-molecule spectroscopy (CoSMoS); dynamics; fluorescence resonance energy transfer (FRET); pre-mRNA splicing; single-molecule; fluorescence; splicessomal RNA; MESSENGER-RNA MOLECULES; SMALL NUCLEAR-RNA; GROUP-II INTRONS; CONFORMATIONAL DYNAMICS; U6; ACTIVATION; SNRNAS; STEPS; REVEALS; YEAST;
D O I
10.1042/BST20140105
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pre-mRNA (precursor mRNA) splicing is a key step in cellular gene expression where introns are excised and exons are ligated together to produce mature mRNA. This process is catalysed by the spliceosome, which consists of five snRNPs (small nuclear ribonucleoprotein particles) and numerous protein factors. Assembly of these snRNPs and associated proteins is a highly dynamic process, making it challenging to study the conformational rearrangements and spliceosome assembly kinetics in bulk studies. In the present review, we discuss recent studies utilizing techniques based on single-molecule detection that have helped overcome this challenge. These studies focus on the assembly dynamics and splicing kinetics in real-time, which help understanding of spliceosomal assembly and catalysis.
引用
收藏
页码:1211 / 1218
页数:8
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