Institute of Genetic Medicine, Newcastle University, Newcastle, NE1 3BZ, UK.
Genes (Basel). 2014 Mar 14;5(1):235-53. doi: 10.3390/genes5010235.
Sequencing the human genome was a huge milestone in genetic research that revealed almost the total DNA sequence required to create a human being. However, in order to function, the DNA genome needs to be expressed as an RNA transcriptome. This article reviews how knowledge of genome sequence information has led to fundamental discoveries in how the transcriptome is processed, with a focus on new system-wide insights into how pre-mRNAs that are encoded by split genes in the genome are rearranged by splicing into functional mRNAs. These advances have been made possible by the development of new post-genome technologies to probe splicing patterns. Transcriptome-wide approaches have characterised a "splicing code" that is embedded within and has a significant role in deciphering the genome, and is deciphered by RNA binding proteins. These analyses have also found that most human genes encode multiple mRNA isoforms, and in some cases proteins, leading in turn to a re-assessment of what exactly a gene is. Analysis of the transcriptome has given insights into how the genome is packaged and transcribed, and is helping to explain important aspects of genome evolution.
人类基因组测序是遗传研究中的一个巨大里程碑,揭示了几乎所有创造人类所需的 DNA 序列。然而,为了发挥作用,DNA 基因组需要被表达为 RNA 转录组。本文综述了基因组序列信息的知识如何导致转录组处理方面的基本发现,重点是关于基因组中分裂基因编码的前体 mRNA 如何通过剪接重新排列成功能性 mRNA 的新的系统范围的见解。这些进展得益于开发新的后基因组技术来探测剪接模式。全转录组方法已经描述了一个“剪接代码”,它嵌入在基因组中,并在破译基因组方面具有重要作用,由 RNA 结合蛋白进行破译。这些分析还发现,大多数人类基因编码多个 mRNA 异构体,在某些情况下还编码蛋白质,这反过来又重新评估了基因的确切含义。对转录组的分析深入了解了基因组的包装和转录方式,并有助于解释基因组进化的重要方面。