Rehwinkel Jan, Raes Jeroen, Izaurralde Elisa
EMBL, Meyerhofstrasse 1, D-69117 Heidelberg, Germany.
Trends Biochem Sci. 2006 Nov;31(11):639-46. doi: 10.1016/j.tibs.2006.09.005. Epub 2006 Sep 28.
Recent genome-wide identification of nonsense-mediated mRNA decay (NMD) targets in yeast, fruitfly and human cells has provided insight into the biological functions and evolution of this mRNA quality control mechanism, revealing that NMD post-transcriptionally regulates an important fraction of the transcriptome. NMD targets are associated with a broad range of biological processes, but most of these targets are not encoded by orthologous genes across different species. Yeast and fruitfly NMD effectors regulate common targets in concert, but parallel pathways have evolved in humans, whereby NMD effectors have acquired additional functions. Thus, the phenotypic differences observed across species after inhibition of NMD are driven not only by the functional diversification of NMD effectors but also by changes in the repertoire of regulated genes.
最近在酵母、果蝇和人类细胞中对无义介导的mRNA衰变(NMD)靶点进行的全基因组鉴定,为深入了解这种mRNA质量控制机制的生物学功能和进化提供了线索,揭示了NMD在转录后对转录组的重要部分进行调控。NMD靶点与广泛的生物学过程相关,但这些靶点中的大多数并非由不同物种的直系同源基因编码。酵母和果蝇的NMD效应器协同调节共同的靶点,但在人类中已经进化出了平行途径,由此NMD效应器获得了额外的功能。因此,抑制NMD后在不同物种间观察到的表型差异不仅是由NMD效应器的功能多样化驱动的,也是由受调控基因库的变化驱动的。