A substrate-based ontology for human solute carriers

被引:33
|
作者
Meixner, Eva [1 ]
Goldmann, Ulrich [1 ]
Sedlyarov, Vitaly [1 ]
Scorzoni, Stefania [1 ]
Rebsamen, Manuele [1 ]
Girardi, Enrico [1 ]
Superti-Furga, Giulio [1 ,2 ]
机构
[1] Austrian Acad Sci, CeMM Res Ctr Mol Med, Vienna, Austria
[2] Med Univ Vienna, Ctr Physiol & Pharmacol, Vienna, Austria
基金
欧洲研究理事会;
关键词
annotation; de-orphanization; ontology; SLCs; solute carriers; TRANSPORTERS; GROWTH; GENES;
D O I
10.15252/msb.20209652
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Solute carriers (SLCs) are the largest family of transmembrane transporters in the human genome with more than 400 members. Despite the fact that SLCs mediate critical biological functions and several are important pharmacological targets, a large proportion of them is poorly characterized and present no assigned substrate. A major limitation to systems-level de-orphanization campaigns is the absence of a structured, language-controlled chemical annotation. Here we describe a thorough manual annotation of SLCs based on literature. The annotation of substrates, transport mechanism, coupled ions, and subcellular localization for 446 human SLCs confirmed that similar to 30% of these were still functionally orphan and lacked known substrates. Application of a substrate-based ontology to transcriptomic datasets identified SLC-specific responses to external perturbations, while a machine-learning approach based on the annotation allowed us to identify potential substrates for several orphan SLCs. The annotation is available at . Given the increasing availability of large biological datasets and the growing interest in transporters, we expect that the effort presented here will be critical to provide novel insights into the functions of SLCs.
引用
收藏
页数:9
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