Hein Anke, Polsakiewicz Monika, Knoop Volker
IZMB - Institut für Zelluläre und Molekulare Botanik, Abteilung Molekulare Evolution, Universität Bonn, Kirschallee 1, D-53115, Bonn, Germany.
BMC Evol Biol. 2016 Jan 25;16:23. doi: 10.1186/s12862-016-0589-0.
RNA editing by cytidine-to-uridine conversions is an essential step of RNA maturation in plant organelles. Some 30-50 sites of C-to-U RNA editing exist in chloroplasts of flowering plant models like Arabidopsis, rice or tobacco. We now predicted significantly more RNA editing in chloroplasts of early-branching angiosperm genera like Amborella, Calycanthus, Ceratophyllum, Chloranthus, Illicium, Liriodendron, Magnolia, Nuphar and Zingiber. Nuclear-encoded RNA-binding pentatricopeptide repeat (PPR) proteins are key editing factors expected to coevolve with their cognate RNA editing sites in the organelles.
With an extensive chloroplast transcriptome study we identified 138 sites of RNA editing in Amborella trichopoda, approximately the 3- to 4-fold of cp editing in Arabidopsis thaliana or Oryza sativa. Selected cDNA studies in the other early-branching flowering plant taxa furthermore reveal a high diversity of early angiosperm RNA editomes. Many of the now identified editing sites in Amborella have orthologues in ferns, lycophytes or hornworts. We investigated the evolution of CRR28 and RARE1, two known Arabidopsis RNA editing factors responsible for cp editing events ndhBeU467PL, ndhDeU878SL and accDeU794SL, respectively, all of which we now found conserved in Amborella. In a phylogenetically wide sampling of 65 angiosperm genomes we find evidence for only one single loss of CRR28 in chickpea but several independent losses of RARE1, perfectly congruent with the presence of their cognate editing sites in the respective cpDNAs.
Chloroplast RNA editing is much more abundant in early-branching than in widely investigated model flowering plants. RNA editing specificity factors can be traced back for more than 120 million years of angiosperm evolution and show highly divergent patterns of evolutionary losses, matching the presence of their target editing events.
胞苷到尿苷的转换介导的RNA编辑是植物细胞器中RNA成熟的关键步骤。在拟南芥、水稻或烟草等开花植物模式物种的叶绿体中,大约存在30 - 50个C到U的RNA编辑位点。我们现在预测,在无油樟、夏蜡梅、金鱼藻、金粟兰、八角、鹅掌楸、木兰、萍蓬草和姜等早期分支被子植物属的叶绿体中,RNA编辑位点要多得多。核编码的RNA结合五肽重复序列(PPR)蛋白是关键的编辑因子,预计会与其在细胞器中的同源RNA编辑位点共同进化。
通过广泛的叶绿体转录组研究,我们在无油樟中鉴定出138个RNA编辑位点,大约是拟南芥或水稻叶绿体编辑位点数量的3至4倍。对其他早期分支开花植物类群的cDNA研究进一步揭示了早期被子植物RNA编辑组的高度多样性。无油樟中现在鉴定出的许多编辑位点在蕨类植物、石松类植物或角苔类植物中有直系同源物。我们研究了CRR28和RARE1的进化,这两个已知的拟南芥RNA编辑因子分别负责叶绿体编辑事件ndhBeU467PL、ndhDeU878SL和accDeU794SL,我们现在发现它们在无油樟中都保守存在。在对65个被子植物基因组进行的系统发育广泛采样中,我们发现只有鹰嘴豆中CRR28发生了一次单一丢失的证据,但RARE1发生了几次独立丢失,这与它们各自叶绿体DNA中同源编辑位点的存在完全一致。
早期分支被子植物的叶绿体RNA编辑比广泛研究的模式开花植物丰富得多。RNA编辑特异性因子可以追溯到超过1.2亿年的被子植物进化历程,并且显示出高度不同的进化丢失模式,与它们靶标编辑事件的存在情况相匹配。