School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney NSW 2052, Australia.
J Genet Genomics. 2012 Oct 20;39(10):535-43. doi: 10.1016/j.jgg.2012.08.002. Epub 2012 Sep 5.
As more information is gathered on the mechanisms of transcription and translation, it is becoming apparent that these processes are highly regulated. The formation of mRNA secondary and tertiary structures is one such regulatory process that until recently it has not been analysed in depth. Formation of these mRNA structures has the potential to enhance and inhibit alternative splicing of transcripts, and regulate rates and amount of translation. As this regulatory mechanism potentially impacts at both the transcriptional and translational level, while also potentially utilising the vast array of non-coding RNAs, it warrants further investigation. Currently, a variety of high-throughput sequencing techniques including parallel analysis of RNA structure (PARS), fragmentation sequencing (FragSeq) and selective 2-hydroxyl acylation analysed by primer extension (SHAPE) lead the way in the genome-wide identification and analysis of mRNA structure formation. These new sequencing techniques highlight the diversity and complexity of the transcriptome, and demonstrate another regulatory mechanism that could become a target for new therapeutic approaches.
随着越来越多的信息被收集到转录和翻译的机制中,人们越来越清楚地认识到这些过程是高度调控的。mRNA 二级和三级结构的形成就是这样一个调节过程,直到最近才对其进行了深入分析。这些 mRNA 结构的形成有可能增强和抑制转录本的选择性剪接,并调节翻译的速度和数量。由于这种调节机制可能同时在转录和翻译水平上产生影响,同时也可能利用大量的非编码 RNA,因此值得进一步研究。目前,包括 RNA 结构平行分析(PARS)、片段测序(FragSeq)和选择性 2-羟基酰化分析引物延伸(SHAPE)在内的各种高通量测序技术在鉴定和分析 mRNA 结构形成方面处于领先地位。这些新的测序技术突出了转录组的多样性和复杂性,并展示了另一种可能成为新治疗方法靶点的调节机制。