Wiedmer Tabea, Teoh Shao Thing, Christodoulaki Eirini, Wolf Gernot, Tian Chengzhe, Sedlyarov Vitaly, Jarret Abigail, Leippe Philipp, Frommelt Fabian, Ingles-Prieto Alvaro, Lindinger Sabrina, Barbosa Barbara M G, Onstein Svenja, Klimek Christoph, Garcia Julio, Serrano Iciar, Reil Daniela, Santacruz Diana, Piotrowski Mary, Noell Stephen, Bueschl Christoph, Li Huanyu, Chi Gamma, Mereiter Stefan, Oliveira Tiago, Penninger Josef M, Sauer David B, Steppan Claire M, Viollet Coralie, Klavins Kristaps, Hannich J Thomas, Goldmann Ulrich, Superti-Furga Giulio
CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090, Vienna, Austria.
Boehringer Ingelheim Pharma GmbH & Co. KG, 88400, Biberach, Germany.
Mol Syst Biol. 2025 May 12. doi: 10.1038/s44320-025-00106-4.
Solute carrier (SLC) transporters govern most of the chemical exchange across cellular membranes and are integral to metabolic regulation, which in turn is linked to cellular function and identity. Despite their key role, individual functions of the SLC superfamily members were not evaluated systematically. We determined the metabolic and transcriptional profiles upon SLC overexpression in knock-out or wild-type isogenic cell backgrounds for 378 SLCs and 441 SLCs, respectively. Targeted metabolomics provided a fingerprint of 189 intracellular metabolites, while transcriptomics offered insights into cellular programs modulated by SLC expression. Beyond the metabolic profiles of 102 SLCs directly related to their known substrates, we identified putative substrates or metabolic pathway connections for 71 SLCs without previously annotated bona fide substrates, including SLC45A4 as a new polyamine transporter. By comparing the molecular profiles, we identified functionally related SLC groups, including some with distinct impacts on osmolyte balancing and glycosylation. The assessment of functionally related human genes presented here may serve as a blueprint for other systematic studies and supports future investigations into the functional roles of SLCs.
溶质载体(SLC)转运蛋白控制着细胞膜上的大部分化学物质交换,是代谢调节所不可或缺的,而代谢调节又与细胞功能和特性相关。尽管它们起着关键作用,但SLC超家族成员的个体功能尚未得到系统评估。我们分别在敲除或野生型同基因细胞背景下过表达378个和441个SLC后,测定了其代谢和转录谱。靶向代谢组学提供了189种细胞内代谢物的指纹图谱,而转录组学则深入了解了由SLC表达调节的细胞程序。除了102个与其已知底物直接相关的SLC的代谢谱外,我们还为71个此前未注释到真正底物的SLC确定了推定底物或代谢途径联系,包括将SLC45A4鉴定为一种新的多胺转运蛋白。通过比较分子谱,我们确定了功能相关的SLC组,包括一些对渗透剂平衡和糖基化有不同影响的组。本文对功能相关人类基因的评估可为其他系统研究提供蓝图,并支持未来对SLC功能作用的研究。