MRC Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, UK.
Mol Cell. 2012 Feb 24;45(4):447-58. doi: 10.1016/j.molcel.2011.12.021. Epub 2012 Jan 19.
A substantial amount of organismal complexity is thought to be encoded by enhancers which specify the location, timing, and levels of gene expression. In mammals there are more enhancers than promoters which are distributed both between and within genes. Here we show that activated, intragenic enhancers frequently act as alternative tissue-specific promoters producing a class of abundant, spliced, multiexonic poly(A)(+) RNAs (meRNAs) which reflect the host gene's structure. meRNAs make a substantial and unanticipated contribution to the complexity of the transcriptome, appearing as alternative isoforms of the host gene. The low protein-coding potential of meRNAs suggests that many meRNAs may be byproducts of enhancer activation or underlie as-yet-unidentified RNA-encoded functions. Distinguishing between meRNAs and mRNAs will transform our interpretation of dynamic changes in transcription both at the level of individual genes and of the genome as a whole.
大量的生物复杂性被认为是由增强子编码的,增强子决定了基因表达的位置、时间和水平。在哺乳动物中,增强子的数量多于启动子,它们分布在基因之间和内部。在这里,我们表明,激活的、基因内的增强子经常作为替代的组织特异性启动子发挥作用,产生一类丰富的、剪接的、多外显子的 poly(A)(+) RNA(meRNA),反映了宿主基因的结构。meRNA 为转录组的复杂性做出了重大而意外的贡献,作为宿主基因的替代异构体出现。meRNA 的低蛋白编码潜力表明,许多 meRNA 可能是增强子激活的副产物,或者是潜在的 RNA 编码功能。区分 meRNA 和 mRNA 将改变我们对单个基因和整个基因组转录动态变化的解释。