Miranda-Laferte Erick, Barkovits Katalin, Rozanova Svitlana, Jordan Nadine, Marcus Katrin, Hidalgo Patricia
Institute of Biological Information Processing (IBI-1)- Molecular and Cellular Physiology, Forschungszentrum Jülich, Jülich, Germany.
Medizinisches Proteom-Center, Medical Faculty, Ruhr-University Bochum, Bochum, Germany.
Front Physiol. 2025 Apr 14;16:1555934. doi: 10.3389/fphys.2025.1555934. eCollection 2025.
The β-subunit (Cavβ) is a central component of the voltage-gated calcium channel complex. It lacks transmembrane domains and exhibits both channel-related and non-related functions. Previous studies have shown that, in the absence of the Cavα1 pore-forming subunit, electrostatic interactions between the N-terminus of Cavβ2e and the plasma membrane mediate its anchoring to the cell surface. Here, we demonstrate that, upon phospholipase C activation, Cavβ2e dissociates from the plasma membrane and homogeneously distributes between the cytosol and the nucleus. Mutagenesis analysis identified critical residues in the N-terminus of the protein, including a stretch of positively charged amino acids and a dileucine motif, which serve as nuclear import and export signals, respectively. Fusion of the Cavβ2e N-terminus to a trimeric YFP chimeric construct shows that this segment suffices for nuclear shuttling. Thus, the N-terminus of Cavβ2e emerges as a regulatory hotspot region controlling the subcellular localization of the protein. Quantitative mass spectrometry analysis revealed that the heterologous expression of a nuclear-enriched Cavβ2e mutant regulates gene expression. Our findings demonstrate the presence of active nuclear localization signals in Cavβ2e that enables its nuclear targeting and regulation of protein expression. Furthermore, they establish the membrane-associated Cavβ2e as a novel signaling mediator within the phospholipase C cascade.
β亚基(Cavβ)是电压门控钙通道复合物的核心组成部分。它缺乏跨膜结构域,具有与通道相关和不相关的功能。先前的研究表明,在没有形成孔道的Cavα1亚基的情况下,Cavβ2e的N端与质膜之间的静电相互作用介导了其在细胞表面的锚定。在此,我们证明,在磷脂酶C激活后,Cavβ2e从质膜解离,并均匀分布于细胞质和细胞核之间。诱变分析确定了该蛋白N端的关键残基,包括一段带正电荷的氨基酸序列和一个双亮氨酸基序,它们分别作为核输入和输出信号。将Cavβ2e的N端与三聚体黄色荧光蛋白(YFP)嵌合构建体融合表明,该片段足以进行核穿梭。因此,Cavβ2e的N端成为控制该蛋白亚细胞定位的调控热点区域。定量质谱分析表明,富含核的Cavβ2e突变体的异源表达可调节基因表达。我们的研究结果表明,Cavβ2e中存在活性核定位信号,使其能够进行核靶向并调节蛋白表达。此外,这些结果确立了膜相关的Cavβ2e作为磷脂酶C级联反应中的一种新型信号介质。