Molecular Biology of Plant Organelles, Ruhr University Bochum, Bochum, Germany.
Center for Synthetic Microbiology (SYNMIKRO) and Department of Chemistry, University of Marburg, Marburg, Germany.
J Exp Bot. 2024 Sep 27;75(18):5734-5749. doi: 10.1093/jxb/erae293.
In the chloroplast, the 54 kDa subunit of the signal recognition particle (cpSRP54) is involved in the post-translational transport of the light-harvesting chlorophyll a/b-binding proteins (LHCPs) and the co-translational transport of plastid-encoded subunits of the photosynthetic complexes to the thylakoid membrane. It forms a high-affinity complex with plastid-specific cpSRP43 for post-translational transport, while a ribosome-associated pool coordinates its co-translational function. CpSRP54 constitutes a conserved multidomain protein, comprising a GTPase (NG) and a methionine-rich (M) domain linked by a flexible region. It is further characterized by a plastid-specific C-terminal tail region containing the cpSRP43-binding motif. To characterize the physiological role of the various regions of cpSRP54 in thylakoid membrane protein transport, we generated Arabidopsis cpSRP54 knockout (ffc1-2) lines producing truncated cpSRP54 variants or a GTPase point mutation variant. Phenotypic characterization of the complementation lines demonstrated that the C-terminal tail region of cpSRP54 plays an important role exclusively in post-translational LHCP transport. Furthermore, we show that the GTPase activity of cpSRP54 plays an essential role in the transport pathways for both nuclear as well as plastid-encoded proteins. In addition, our data revealed that plants expressing cpSRP54 without the C-terminal region exhibit a strongly increased accumulation of a photosystem I assembly intermediate.
在叶绿体中,信号识别颗粒(cpSRP)的 54 kDa 亚基参与了光捕获叶绿素 a/b 结合蛋白(LHCP)的翻译后运输,以及质体编码的光合复合物亚基的共翻译运输到类囊体膜。它与质体特异性的 cpSRP43 形成高亲和力复合物,用于翻译后运输,而核糖体相关池协调其共翻译功能。CpSRP54 构成了一种保守的多结构域蛋白,包含一个 GTPase(NG)和一个富含甲硫氨酸的(M)结构域,通过一个柔性区域连接。它进一步的特点是质体特异性的 C 端尾部区域,包含 cpSRP43 结合基序。为了表征 cpSRP54 在类囊体膜蛋白运输中的各个区域的生理作用,我们生成了拟南芥 cpSRP54 敲除(ffc1-2)系,产生截短的 cpSRP54 变体或 GTPase 点突变变体。互补系的表型特征表明,cpSRP54 的 C 端尾部区域仅在翻译后 LHCP 运输中发挥重要作用。此外,我们表明,cpSRP54 的 GTPase 活性在核编码和质体编码蛋白的运输途径中都起着至关重要的作用。此外,我们的数据表明,表达没有 C 端区域的 cpSRP54 的植物表现出强烈增加的光系统 I 组装中间产物的积累。