Stegemann Sandra, Bock Ralph
Max-Planck-Institut für Molekulare Pflanzenphysiologie, D-14476 Potsdam-Golm, Germany.
Plant Cell. 2006 Nov;18(11):2869-78. doi: 10.1105/tpc.106.046466. Epub 2006 Nov 3.
Eukaryotic cells arose through the uptake of free-living bacteria by endosymbiosis and their gradual conversion into organelles (plastids and mitochondria). Capture of the endosymbionts was followed by massive translocation of their genes to the genome of the host cell. How genes were transferred from the (prokaryotic) organellar genome to the (eukaryotic) nuclear genome and how the genes became functional in their new eukaryotic genetic environment is largely unknown. Here, we report the successful experimental reconstruction of functional gene transfer between an organelle and the nucleus, a process that normally occurs only on large evolutionary timescales. In consecutive genetic screens, we first transferred a chloroplast genome segment to the nucleus and then selected for gene activation in the nuclear genome. We show that DNA-mediated gene transfer can give rise to functional nuclear genes if followed by suitable rearrangements in the nuclear genome. Acquisition of gene function involves (1) transcriptional activation by capture of the promoter of an upstream nuclear gene and (2) utilization of AT-rich noncoding sequences downstream of the plastid gene as RNA cleavage and polyadenylation sites. Our results reveal the molecular mechanisms of how organellar DNA transferred to the nucleus gives rise to functional genes and reproduce in the laboratory a key process in the evolution of eukaryotic cells.
真核细胞起源于通过内共生摄取自由生活的细菌,并逐渐将它们转化为细胞器(质体和线粒体)。捕获内共生体之后,其基因大量转移到宿主细胞的基因组中。基因是如何从(原核)细胞器基因组转移到(真核)核基因组的,以及这些基因如何在新的真核遗传环境中发挥功能,在很大程度上尚不清楚。在此,我们报告了细胞器与细胞核之间功能性基因转移的成功实验重建,这一过程通常仅在漫长的进化时间尺度上发生。在连续的遗传筛选中,我们首先将叶绿体基因组片段转移到细胞核,然后选择在核基因组中激活基因。我们表明,如果随后在核基因组中进行适当的重排,DNA介导的基因转移可以产生功能性核基因。基因功能的获得涉及(1)通过捕获上游核基因的启动子进行转录激活,以及(2)利用质体基因下游富含AT的非编码序列作为RNA切割和聚腺苷酸化位点。我们的结果揭示了细胞器DNA转移到细胞核后如何产生功能性基因的分子机制,并在实验室中重现了真核细胞进化中的一个关键过程。