Department of Molecular Biology, Cellular Biology and Biochemistry, Brown University, Providence, RI 02912, USA.
Semin Cell Dev Biol. 2012 May;23(3):281-8. doi: 10.1016/j.semcdb.2011.11.004. Epub 2011 Dec 8.
Post-transcriptional modifications such as RNA editing and splicing diversify the proteome while limiting the necessary size of the genome. Although splicing globally rearranges existing information within the transcript, the conserved process of adenosine-to-inosine RNA editing recodes the message through single nucleotide changes, often at very specific locations. Because inosine is interpreted as guanosine by the cellular machineries, editing effectively results in the substitution of a guanosine for an adenosine in the primary RNA sequence. Precise control of editing is dictated by duplex structures in the transcript, formed between the exonic region surrounding the editing site and cis regulatory elements often localized in a nearby intron, suggesting that editing must precede splicing. However, the precise relationship between these post-transcriptional processes remains unclear. Here we present general commonalities of RNA editing substrates and consequential predictions regarding the interaction between editing and splicing. We also discuss anomalies and interesting cases of RNA editing that confound our understanding of the relationship between these post-transcriptional processes.
转录后修饰,如 RNA 编辑和剪接,在使蛋白质组多样化的同时,限制了基因组的必要大小。虽然剪接全局地重新排列转录本内现有的信息,但保守的腺苷到肌苷 RNA 编辑过程通过单核苷酸变化对信息进行重新编码,通常在非常特定的位置。由于肌苷被细胞机制解释为鸟苷,因此编辑实际上导致在初级 RNA 序列中用鸟苷替换腺苷。编辑的精确控制由转录本中形成的双链结构决定,该结构位于编辑位点周围的外显子区域和通常位于附近内含子中的顺式调节元件之间,这表明编辑必须先于剪接。然而,这些转录后过程之间的确切关系仍不清楚。在这里,我们介绍了 RNA 编辑底物的一般共性,并对编辑和剪接之间的相互作用做出了相应的预测。我们还讨论了 RNA 编辑的异常和有趣案例,这些案例使我们对这些转录后过程之间的关系的理解变得复杂。