Ceder Mikaela M, Aggarwal Tanya, Hosseini Kimia, Maturi Varun, Patil Sourabh, Perland Emelie, Williams Michael J, Fredriksson Robert
Department of Pharmaceutical Biosciences, Molecular Neuropharmacology, Uppsala University, Uppsala, Sweden.
Department of Pharmacy, Drug Delivery, Uppsala University, Uppsala, Sweden.
Front Cell Dev Biol. 2020 Oct 14;8:580291. doi: 10.3389/fcell.2020.580291. eCollection 2020.
The number of transporter proteins that are not fully characterized is immense. Here, we used and human cell lines to perform a first in-depth characterization of CG4928, an ortholog to the human UNC93A, of which little is known. Solute carriers regulate and maintain biochemical pathways important for the body, and malfunctioning transport is associated with multiple diseases. Based on phylogenetic analysis, CG4928 is closely related to human UNC93A and has a secondary and a tertiary protein structure and folding similar to major facilitator superfamily transporters. Ubiquitous knockdown of causes flies to have a reduced secretion rate from the Malpighian tubules; altering potassium content in the body and in the Malpighian tubules, homologous to the renal system; and results in the development of edema. The edema could be rescued by using amiloride, a common diuretic, and by maintaining the flies on ion-free diets. CG4928-overexpressing cells did not facilitate the transport of sugars and amino acids; however, proximity ligation assay revealed that CG4928 co-localized with TASK channels. Overexpression of CG4928 resulted in induced apoptosis and cytotoxicity, which could be restored when cells were kept in high-sodium media. Furthermore, the basal membrane potential was observed to be disrupted. Taken together, the results indicate that CG4928 is of importance for generating the cellular membrane potential by an unknown manner. However, we speculate that it most likely acts as a regulator or transporter of potassium flows over the membrane.
尚未得到充分表征的转运蛋白数量极为庞大。在此,我们使用果蝇和人类细胞系,对CG4928进行了首次深入表征,它是人类UNC93A的直系同源物,目前人们对其了解甚少。溶质载体调节并维持对身体至关重要的生化途径,而转运功能失常与多种疾病相关。基于系统发育分析,CG4928与人类UNC93A密切相关,具有与主要易化子超家族转运蛋白相似的二级和三级蛋白质结构及折叠方式。对果蝇进行普遍的基因敲除会导致其马氏管的分泌率降低;改变身体和马氏管中的钾含量,马氏管与肾脏系统同源;并导致水肿的发生。使用常见利尿剂氨氯吡咪,以及让果蝇食用无离子饮食,可以缓解水肿。过表达CG4928的细胞并未促进糖类和氨基酸的转运;然而,邻近连接分析显示CG4928与TASK通道共定位。CG4928的过表达导致细胞凋亡和细胞毒性增加,当细胞置于高钠培养基中时,这种情况可以恢复。此外,还观察到基底膜电位受到破坏。综上所述,结果表明CG4928以未知方式对产生细胞膜电位具有重要作用。然而,我们推测它很可能作为膜上钾流的调节因子或转运体发挥作用。