Systems Biology Analysis Reveals Eight SLC22 Transporter Subgroups, Including OATs, OCTs, and OCTNs
The SLC22 family of OATs, OCTs, and OCTNs is emerging as a central hub of endogenous physiology. Despite often being referred to as “drug” transporters, they facilitate the movement of metabolites and key signaling molecules. An in-depth reanalysis supports a reassignment of thes...
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doaj-a122de3f4c4e4ed38ebd80f6dfa82bd32020-11-25T02:57:38ZengMDPI AGInternational Journal of Molecular Sciences1422-00672020-03-01215179110.3390/ijms21051791ijms21051791Systems Biology Analysis Reveals Eight SLC22 Transporter Subgroups, Including OATs, OCTs, and OCTNsDarcy C. Engelhart0Jeffry C. Granados1Da Shi2Milton H. Saier Jr.3Michael E. Baker4Ruben Abagyan5Sanjay K. Nigam6Department of Biology, University of California San Diego, San Diego, CA 92093, USADepartment of Bioengineering, University of California San Diego, San Diego, CA 92093, USASchool of Pharmacy and Pharmaceutical Sciences, University of California San Diego, San Diego, CA 92093, USADepartment of Molecular Biology, Division of Biological Sciences, University of California San Diego, San Diego, CA 92093, USADepartment of Medicine, University of California San Diego, San Diego, CA 92093, USASchool of Pharmacy and Pharmaceutical Sciences, University of California San Diego, San Diego, CA 92093, USADepartment of Medicine, University of California San Diego, San Diego, CA 92093, USAThe SLC22 family of OATs, OCTs, and OCTNs is emerging as a central hub of endogenous physiology. Despite often being referred to as “drug” transporters, they facilitate the movement of metabolites and key signaling molecules. An in-depth reanalysis supports a reassignment of these proteins into eight functional subgroups, with four new subgroups arising from the previously defined OAT subclade: OATS1 (SLC22A6, SLC22A8, and SLC22A20), OATS2 (SLC22A7), OATS3 (SLC22A11, SLC22A12, and Slc22a22), and OATS4 (SLC22A9, SLC22A10, SLC22A24, and SLC22A25). We propose merging the OCTN (SLC22A4, SLC22A5, and Slc22a21) and OCT-related (SLC22A15 and SLC22A16) subclades into the OCTN/OCTN-related subgroup. Using data from GWAS, in vivo models, and in vitro assays, we developed an SLC22 transporter-metabolite network and similar subgroup networks, which suggest how multiple SLC22 transporters with mono-, oligo-, and multi-specific substrate specificity interact to regulate metabolites. Subgroup associations include: OATS1 with signaling molecules, uremic toxins, and odorants, OATS2 with cyclic nucleotides, OATS3 with uric acid, OATS4 with conjugated sex hormones, particularly etiocholanolone glucuronide, OCT with neurotransmitters, and OCTN/OCTN-related with ergothioneine and carnitine derivatives. Our data suggest that the SLC22 family can work among itself, as well as with other ADME genes, to optimize levels of numerous metabolites and signaling molecules, involved in organ crosstalk and inter-organismal communication, as proposed by the remote sensing and signaling theory.https://www.mdpi.com/1422-0067/21/5/1791transportersendogenous metabolismfunctional subgroupsslc22remote sensing and signalingdrug transportersgut microbiomechronic kidney disease |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Darcy C. Engelhart Jeffry C. Granados Da Shi Milton H. Saier Jr. Michael E. Baker Ruben Abagyan Sanjay K. Nigam |
spellingShingle |
Darcy C. Engelhart Jeffry C. Granados Da Shi Milton H. Saier Jr. Michael E. Baker Ruben Abagyan Sanjay K. Nigam Systems Biology Analysis Reveals Eight SLC22 Transporter Subgroups, Including OATs, OCTs, and OCTNs International Journal of Molecular Sciences transporters endogenous metabolism functional subgroups slc22 remote sensing and signaling drug transporters gut microbiome chronic kidney disease |
author_facet |
Darcy C. Engelhart Jeffry C. Granados Da Shi Milton H. Saier Jr. Michael E. Baker Ruben Abagyan Sanjay K. Nigam |
author_sort |
Darcy C. Engelhart |
title |
Systems Biology Analysis Reveals Eight SLC22 Transporter Subgroups, Including OATs, OCTs, and OCTNs |
title_short |
Systems Biology Analysis Reveals Eight SLC22 Transporter Subgroups, Including OATs, OCTs, and OCTNs |
title_full |
Systems Biology Analysis Reveals Eight SLC22 Transporter Subgroups, Including OATs, OCTs, and OCTNs |
title_fullStr |
Systems Biology Analysis Reveals Eight SLC22 Transporter Subgroups, Including OATs, OCTs, and OCTNs |
title_full_unstemmed |
Systems Biology Analysis Reveals Eight SLC22 Transporter Subgroups, Including OATs, OCTs, and OCTNs |
title_sort |
systems biology analysis reveals eight slc22 transporter subgroups, including oats, octs, and octns |
publisher |
MDPI AG |
series |
International Journal of Molecular Sciences |
issn |
1422-0067 |
publishDate |
2020-03-01 |
description |
The SLC22 family of OATs, OCTs, and OCTNs is emerging as a central hub of endogenous physiology. Despite often being referred to as “drug” transporters, they facilitate the movement of metabolites and key signaling molecules. An in-depth reanalysis supports a reassignment of these proteins into eight functional subgroups, with four new subgroups arising from the previously defined OAT subclade: OATS1 (SLC22A6, SLC22A8, and SLC22A20), OATS2 (SLC22A7), OATS3 (SLC22A11, SLC22A12, and Slc22a22), and OATS4 (SLC22A9, SLC22A10, SLC22A24, and SLC22A25). We propose merging the OCTN (SLC22A4, SLC22A5, and Slc22a21) and OCT-related (SLC22A15 and SLC22A16) subclades into the OCTN/OCTN-related subgroup. Using data from GWAS, in vivo models, and in vitro assays, we developed an SLC22 transporter-metabolite network and similar subgroup networks, which suggest how multiple SLC22 transporters with mono-, oligo-, and multi-specific substrate specificity interact to regulate metabolites. Subgroup associations include: OATS1 with signaling molecules, uremic toxins, and odorants, OATS2 with cyclic nucleotides, OATS3 with uric acid, OATS4 with conjugated sex hormones, particularly etiocholanolone glucuronide, OCT with neurotransmitters, and OCTN/OCTN-related with ergothioneine and carnitine derivatives. Our data suggest that the SLC22 family can work among itself, as well as with other ADME genes, to optimize levels of numerous metabolites and signaling molecules, involved in organ crosstalk and inter-organismal communication, as proposed by the remote sensing and signaling theory. |
topic |
transporters endogenous metabolism functional subgroups slc22 remote sensing and signaling drug transporters gut microbiome chronic kidney disease |
url |
https://www.mdpi.com/1422-0067/21/5/1791 |
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