Metabolic mapping of the human solute carrier superfamily.

人类溶质载体超家族的代谢图谱

阅读:15
作者: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
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.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。