Plant Molecular Biology, Faculty of Biology, Ludwig-Maximilians-Universität München, D-82152 Planegg-Martinsried, Germany.
Centro Ricerca e Innovazione, Fondazione Edmund Mach, I-38010, San Michele all'Adige, Italy.
Plant Physiol. 2018 Jan;176(1):634-648. doi: 10.1104/pp.17.01545. Epub 2017 Nov 14.
DEAD-box RNA helicases (DBRHs) modulate RNA secondary structure, allowing RNA molecules to adopt the conformations required for interaction with their target proteins. RH50 is a chloroplast-located DBRH that colocalizes and is coexpressed with GUN1, a central factor in chloroplast-to-nucleus signaling. When combined with mutations that impair plastid gene expression (-, -, -, -, -, and -), and mutations evoke similar patterns of epistatic effects. These observations, together with the synergistic growth phenotype of the double mutant --, suggest that RH50 and GUN1 are functionally related and that this function is associated with plastid gene expression, in particular ribosome functioning. However, - itself is not a gun mutant, although-like -the - mutation suppresses the down-regulation of nuclear genes for photosynthesis induced by the - mutation. The RH50 protein comigrates with ribosomal particles, and is required for efficient translation of plastid proteins. RH50 binds to transcripts of the 23S-4.5S intergenic region and, in its absence, levels of the corresponding rRNA processing intermediate are strongly increased, implying that RH50 is required for the maturation of the 23S and 4.5S rRNAs. This inference is supported by the finding that loss of RH50 renders chloroplast protein synthesis sensitive to erythromycin and exposure to cold. Based on these results, we conclude that RH50 is a plastid rRNA maturation factor.
DEAD-box RNA 解旋酶(DBRHs)调节 RNA 二级结构,使 RNA 分子能够采用与其靶蛋白相互作用所需的构象。RH50 是一种位于叶绿体的 DBRH,与 GUN1 共定位并共表达,GUN1 是叶绿体到细胞核信号转导的核心因子。当与损害质体基因表达的突变(-、-、-、-、-和-)结合时,和 突变引起类似的上位性效应模式。这些观察结果,加上双突变体 -- 的协同生长表型,表明 RH50 和 GUN1 具有功能相关性,并且这种功能与质体基因表达相关,特别是核糖体功能相关。然而,-本身不是 gun 突变体,尽管像 - 一样,-突变抑制了由 - 突变诱导的光合作用核基因的下调。RH50 蛋白与核糖体颗粒共迁移,并且是质体蛋白有效翻译所必需的。RH50 结合到 23S-4.5S 基因间隔区的转录本上,并且在其不存在的情况下,相应的 rRNA 加工中间产物的水平强烈增加,这意味着 RH50 是 23S 和 4.5S rRNAs 成熟所必需的。这一推断得到了以下发现的支持:失去 RH50 使叶绿体蛋白合成对红霉素敏感,并使叶绿体蛋白合成对冷敏感。基于这些结果,我们得出结论,RH50 是一种质体 rRNA 成熟因子。