Magnuson Brian, Bedi Karan, Ljungman Mats
Department of Radiation Oncology, University of Michigan Comprehensive Cancer Center, and Translational Oncology Program, University of Michigan, Ann Arbor, USA; Department of Environmental Health Sciences, School of Public Health, University of Michigan, Ann Arbor, USA.
Department of Radiation Oncology, University of Michigan Comprehensive Cancer Center, and Translational Oncology Program, University of Michigan, Ann Arbor, USA.
DNA Repair (Amst). 2016 Aug;44:81-86. doi: 10.1016/j.dnarep.2016.05.010. Epub 2016 May 16.
Our genome is protected from the introduction of mutations by high fidelity replication and an extensive network of DNA damage response and repair mechanisms. However, the expression of our genome, via RNA and protein synthesis, allows for more diversity in translating genetic information. In addition, the splicing process has become less stringent over evolutionary time allowing for a substantial increase in the diversity of transcripts generated. The result is a diverse transcriptome and proteome that harbor selective advantages over a more tightly regulated system. Here, we describe mechanisms in place that both safeguard the genome and promote translational diversity, with emphasis on post-transcriptional RNA processing.
我们的基因组通过高保真复制以及广泛的DNA损伤应答和修复机制网络来防止突变的引入。然而,通过RNA和蛋白质合成对基因组进行表达,使得在翻译遗传信息方面具有更多样性。此外,随着进化时间的推移,剪接过程变得不那么严格,从而使产生的转录本多样性大幅增加。其结果是形成了一个多样化的转录组和蛋白质组,与调控更为严格的系统相比具有选择优势。在这里,我们描述了既保护基因组又促进翻译多样性的机制,重点是转录后RNA加工。