Inserm U1212, CNRS UMR5320, ARNA Laboratory, University of Bordeaux, Bordeaux Cedex, France.
RNA Biol. 2022 Jan;19(1):943-960. doi: 10.1080/15476286.2022.2100971.
In Eukarya, immature mRNA transcripts (pre-mRNA) often contain coding sequences, or exons, interleaved by non-coding sequences, or introns. Introns are removed upon , and further regulation of the retained exons leads to alternatively spliced mRNA. The reaction requires the stepwise assembly of the spliceosome, a macromolecular machine composed of small nuclear ribonucleoproteins (snRNPs). This review focuses on the early stage of spliceosome assembly, when U1 snRNP defines each intron 5'-splice site (5'ss) in the pre-mRNA. We first introduce the splicing reaction and the impact of alternative splicing on gene expression regulation. Thereafter, we extensively discuss splicing descriptors that influence the 5'ss selection by U1 snRNP, such as sequence determinants, and interactions mediated by U1-specific proteins or U1 small nuclear RNA (U1 snRNA). We also include examples of diseases that affect the 5'ss selection by U1 snRNP, and discuss recent therapeutic advances that manipulate U1 snRNP 5'ss selectivity with antisense oligonucleotides and small-molecule splicing switches.
在真核生物中,不成熟的 mRNA 转录本(pre-mRNA)通常包含编码序列,即外显子,被非编码序列,即内含子分隔开。内含子在被移除后,对保留的外显子的进一步调控会导致 mRNA 的可变剪接。这一反应需要剪接体的逐步组装,剪接体是由小核核糖核蛋白(snRNP)组成的大分子机器。这篇综述重点介绍了剪接体组装的早期阶段,此时 U1 snRNP 确定了 pre-mRNA 中每个内含子 5'剪接位点(5'ss)。我们首先介绍了剪接反应以及可变剪接对基因表达调控的影响。然后,我们广泛讨论了影响 U1 snRNP 对 5'ss 选择的剪接描述符,如序列决定因素,以及由 U1 特异性蛋白或 U1 小核 RNA(U1 snRNA)介导的相互作用。我们还包括了一些影响 U1 snRNP 对 5'ss 选择的疾病的例子,并讨论了最近利用反义寡核苷酸和小分子剪接开关来操纵 U1 snRNP 5'ss 选择性的治疗进展。