Institute of Botany, Heinrich Heine University, Düsseldorf 40225, Germany.
Institute of Botany, Heinrich Heine University, Düsseldorf 40225, Germany; Cluster of Excellence on Plant Science (CEPLAS), Heinrich Heine University, Düsseldorf 40225, Germany.
Eur J Cell Biol. 2023 Jun;102(2):151322. doi: 10.1016/j.ejcb.2023.151322. Epub 2023 May 18.
Many signaling processes rely on information decoding at the plasma membrane, and membrane-associated proteins and their complexes are fundamental for regulating this process. Still many questions exist as to how protein complexes are assembled and function at membrane sites to change identity and dynamics of membrane systems. Peripheral membrane proteins containing a calcium and phospholipid-binding C2-domain can act in membrane-related signaling by providing a tethering function so that protein complexes form. C2 domain proteins termed C2-DOMAIN ABSCISIC ACID-RELATED (CAR) proteins are plant-specific, and the functional relevance of this C2 domain protein subgroup is just emerging. The ten Arabidopsis CAR proteins CAR1 to CAR10 have a single C2 domain with a plant-specific insertion, the so-called "CAR-extra-signature" or also termed "sig domain". Via this "sig domain" CAR proteins can bind signaling protein complexes of different kinds and act in biotic and abiotic stress, blue light and iron nutrition. Interestingly, CAR proteins can oligomerize in membrane microdomains, and their presence in the nucleus can be linked with nuclear protein regulation. This shows that CAR proteins may play unprecedented roles in coordinating environmental responses and assembling required protein complexes to transmit information cues between plasma membrane and nucleus. The aim of this review is to summarize structure-function characteristics of the CAR protein family and assemble findings from CAR protein interactions and physiological functions. From this comparative investigation we extract common principles about the molecular operations that CAR proteins may fulfill in the cell. We also deduce functional properties of the CAR protein family based on its evolution and gene expression profiles. We highlight open questions and suggest novel avenues to prove and understand the functional networks and roles played by this protein family in plants.
许多信号转导过程依赖于质膜上的信息解码,而膜相关蛋白及其复合物是调节这一过程的基础。然而,关于蛋白复合物如何在膜位点组装和发挥功能,以改变膜系统的身份和动态,仍存在许多问题。含有钙和磷脂结合 C2 结构域的膜周蛋白可以通过提供连接功能来发挥膜相关信号转导作用,从而形成蛋白复合物。C2 结构域蛋白称为 C2-DOMAIN ABSCISIC ACID-RELATED (CAR) 蛋白,是植物特有的,这个 C2 结构域蛋白亚群的功能相关性才刚刚显现出来。拟南芥的 10 个 CAR 蛋白 CAR1 到 CAR10 都有一个单一的 C2 结构域,其中包含一个植物特异性的插入序列,即所谓的“CAR-extra-signature”或“sig 结构域”。通过这个“sig 结构域”,CAR 蛋白可以结合不同种类的信号蛋白复合物,并在生物和非生物胁迫、蓝光和铁营养中发挥作用。有趣的是,CAR 蛋白可以在膜微区寡聚化,它们在核内的存在可以与核蛋白调节相关联。这表明 CAR 蛋白可能在协调环境反应和组装所需的蛋白复合物以在质膜和核之间传递信息线索方面发挥前所未有的作用。本文综述了 CAR 蛋白家族的结构-功能特征,并总结了 CAR 蛋白相互作用和生理功能的研究结果。通过比较研究,我们提取了 CAR 蛋白可能在细胞中完成的分子操作的共同原则。我们还根据 CAR 蛋白的进化和基因表达谱推导出了 CAR 蛋白家族的功能特性。我们强调了一些悬而未决的问题,并提出了新的途径来证明和理解这个蛋白家族在植物中的功能网络和作用。