Institut de biologie moléculaire des plantes-CNRS, Université de Strasbourg, Strasbourg F-67084, France.
Proc Natl Acad Sci U S A. 2024 Nov 12;121(46):e2412221121. doi: 10.1073/pnas.2412221121. Epub 2024 Nov 6.
Over the course of evolution, land plant mitochondrial genomes have lost many transfer RNA (tRNA) genes and the import of nucleus-encoded tRNAs is essential for mitochondrial protein synthesis. By contrast, plastidial genomes of photosynthetic land plants generally possess a complete set of tRNA genes and the existence of plastidial tRNA import remains a long-standing question. The early vascular plants of the Selaginella genus show an extensive loss of plastidial tRNA genes while retaining photosynthetic capacity, and represent an ideal model for answering this question. Using purification, northern blot hybridization, and high-throughput tRNA sequencing, a global analysis of total and plastidial tRNA populations was undertaken in We confirmed the expression of all plastidial tRNA genes and, conversely, observed that nucleus-encoded tRNAs corresponding to these plastidial tRNAs were generally excluded from the chloroplasts. We then demonstrated a selective and differential plastidial import of around forty nucleus-encoded tRNA species, likely compensating for the insufficient coding capacity of plastidial-encoded tRNAs. In-depth analysis revealed differential import of tRNA isodecoders, leading to the identification of specific situations. This includes the expression and import of nucleus-encoded tRNAs expressed from plastidial or bacterial-like genes inserted into the nuclear genome. Overall, our results confirm the existence of molecular processes that enable tRNAs to be selectively imported not only into mitochondria, as previously described, but also into chloroplasts, when necessary.
在进化过程中,陆地植物的线粒体基因组丢失了许多转移 RNA(tRNA)基因,而细胞核编码的 tRNA 的输入对于线粒体蛋白质合成至关重要。相比之下,光合陆地植物的质体基因组通常拥有一套完整的 tRNA 基因,而质体 tRNA 输入的存在仍然是一个悬而未决的问题。卷柏属的早期维管植物表现出广泛的质体 tRNA 基因丢失,同时保留了光合作用能力,是回答这个问题的理想模型。通过纯化、 northern blot 杂交和高通量 tRNA 测序,对总 tRNA 和质体 tRNA 群体进行了全面分析,我们证实了所有质体 tRNA 基因的表达,相反,观察到与这些质体 tRNA 对应的细胞核编码的 tRNA 通常被排除在叶绿体之外。然后,我们证明了大约四十种细胞核编码的 tRNA 物种的选择性和差异质体输入,可能补偿了质体编码 tRNA 的不足编码能力。深入分析显示 tRNA 同功受体的差异输入,导致了特定情况的识别。这包括从插入核基因组的质体或细菌样基因表达的质体或细菌样基因表达和导入的细胞核编码的 tRNA。总的来说,我们的研究结果证实了存在分子过程,不仅可以选择性地将 tRNA 导入线粒体,如先前所述,而且在必要时还可以导入叶绿体。