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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Main Authors: Darcy C. Engelhart, Jeffry C. Granados, Da Shi, Milton H. Saier Jr., Michael E. Baker, Ruben Abagyan, Sanjay K. Nigam
Format: Article
Language:English
Published: MDPI AG 2020-03-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/21/5/1791
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spelling 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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