生物
聚腺苷酸
核糖核酸
计算生物学
转录后修饰
RNA编辑
RNA剪接
选择性拼接
遗传学
RNA结合蛋白
转录组
非编码RNA
基因表达
基因
信使核糖核酸
作者
Donny D. Licatalosi,Robert B. Darnell
摘要
mRNA repertoires can be diversified by many mechanisms, including alternative splicing and alternative polyadenylation. Technological advances are now allowing genome–wide insights into the extent of RNA processing, the actions of RNA–binding proteins and how regulation at the RNA level helps to control biological systems. In recent years views of eukaryotic gene expression have been transformed by the finding that enormous diversity can be generated at the RNA level. Advances in technologies for characterizing RNA populations are revealing increasingly complete descriptions of RNA regulation and complexity; for example, through alternative splicing, alternative polyadenylation and RNA editing. New biochemical strategies to map protein–RNA interactions in vivo are yielding transcriptome-wide insights into mechanisms of RNA processing. These advances, combined with bioinformatics and genetic validation, are leading to the generation of functional RNA maps that reveal the rules underlying RNA regulation and networks of biologically coherent transcripts. Together these are providing new insights into molecular cell biology and disease.
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