Institute of Plant Molecular Biology (IBMP), CNRS and University of Strasbourg, 12 rue du Général Zimmer, 67084 Strasbourg, France.
Centre of Agricultural Biochemistry and Biotechnology (CABB), University of Agriculture, Faisalabad 38000, Pakistan.
Cells. 2019 Jun 13;8(6):583. doi: 10.3390/cells8060583.
We address here organellar genetic regulation and intercompartment genome coordination. We developed earlier a strategy relying on a tRNA-like shuttle to mediate import of nuclear transgene-encoded custom RNAs into mitochondria in plants. In the present work, we used this strategy to drive -cleaving hammerhead ribozymes into the organelles, to knock down specific mitochondrial RNAs and analyze the regulatory impact. In a similar approach, the tRNA mimic was used to import into mitochondria in the , an RNA associated with cytoplasmic male sterility in maize and possessing sequence identities with the mitochondrial RNA. In both cases, inducible expression of the transgenes allowed to characterise early regulation and signaling responses triggered by these respective manipulations of the organellar transcriptome. The results imply that the mitochondrial transcriptome is tightly controlled by a "buffering" mechanism at the early and intermediate stages of plant development, a control that is released at later stages. On the other hand, high throughput analyses showed that knocking down a specific mitochondrial mRNA triggered a retrograde signaling and an anterograde nuclear transcriptome response involving a series of transcription factor genes and small RNAs. Our results strongly support transcriptome coordination mechanisms within the organelles and between the organelles and the nucleus.
我们在这里探讨细胞器的遗传调控和隔室间基因组协调。我们之前开发了一种策略,依赖于 tRNA 样穿梭来介导核转基因编码的定制 RNA 进入植物线粒体。在本工作中,我们使用该策略将切割锤头核酶导入细胞器,敲低特定的线粒体 RNA,并分析调控影响。采用类似的方法,tRNA 模拟物被用于导入玉米细胞质雄性不育相关的 和 ,与线粒体 RNA 具有序列同一性。在这两种情况下,诱导转基因的表达允许对这些细胞器转录组各自操作所触发的早期调控和信号响应进行特征描述。结果表明,线粒体转录组在植物发育的早期和中期受到“缓冲”机制的严格控制,这种控制在后期被释放。另一方面,高通量分析表明,敲低特定的线粒体 mRNA 触发了逆行信号和前向核转录组反应,涉及一系列转录因子基因和小 RNA。我们的结果强烈支持细胞器内部以及细胞器和细胞核之间的转录组协调机制。