Department of Microbiology & Molecular Genetics, University of California, Irvine, CA, USA.
RNA Biol. 2009 Nov-Dec;6(5):526-30. doi: 10.4161/rna.6.5.9860. Epub 2009 Nov 18.
The splicing of nuclear pre-mRNAs is a fundamental process required for the expression of most metazoan genes. The majority of the approximately 25,000 genes encoded by the human genome has been shown to produce more than one kind of transcripts through alternative splicing. Alternative splicing of pre-mRNAs can lead to the production of multiple protein isoforms from a single gene, significantly enriching the proteomic diversity of higher eukaryotic organisms. Because regulation of this process determines the timing and location that a particular protein isoform is produced, changes of alternative splicing patterns have the potential to modulate many cellular activities. Consequently, pre-mRNA splicing must occur with a high degree of specificity and fidelity to ensure the appropriate expression of functional mRNAs. Here we review recent progress made in understanding the extent of alternative splicing within the human genome with particular emphasis on splicing fidelity.
核前体 mRNA 的剪接是大多数后生动物基因表达所必需的基本过程。已经表明,人类基因组中大约 25000 个编码基因中的大多数通过选择性剪接产生不止一种转录本。前体 mRNA 的选择性剪接可以从单个基因产生多种蛋白质同工型,从而显著丰富了高等真核生物的蛋白质组多样性。因为该过程的调节决定了特定蛋白质同工型产生的时间和位置,所以选择性剪接模式的变化有可能调节许多细胞活动。因此,前体 mRNA 的剪接必须具有高度的特异性和保真度,以确保功能性 mRNA 的适当表达。在这里,我们回顾了在理解人类基因组中选择性剪接的程度方面取得的最新进展,特别强调了剪接保真度。