Pregled bibliografske jedinice broj: 651794
Molecular characterization of zebrafish Oatp1d1 (Slco1d1), a novel Organic anion transporting polypeptide
Molecular characterization of zebrafish Oatp1d1 (Slco1d1), a novel Organic anion transporting polypeptide // The Journal of biological chemistry, 288 (2013), 47; 33894-33911 doi:10.1074/jbc.M113.518506 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 651794 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Molecular characterization of zebrafish Oatp1d1 (Slco1d1), a novel Organic anion transporting polypeptide
Autori
Popović, Marta ; Žaja, Roko ; Fent, Karl ; Smital, Tvrtko
Izvornik
The Journal of biological chemistry (0021-9258) 288
(2013), 47;
33894-33911
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
OATP/Oatp; zebrafish Oatp1d1; phylogeny; substrate specificity; physiological role
Sažetak
Organic anion transporting polypeptide (OATP/Oatp) superfamily includes group of polyspecific transporters that mediate transport of large amphipathic, mostly anionic molecules across cell membranes of eukaryotes. OATPs/Oatps are involved in disposition and elimination of numerous physiological and foreign compounds. However, in non-mammalian species functional properties of Oatps remain unknown. We aimed to elucidate the role of Oatp1d1 in zebrafish to gain insights into the functional and structural evolution of the OATP1/Oatp1 superfamily. We show that diversification of the OATP1/Oatp1 family occurs after the emergence of jawed fish and that OATP1A/Oatp1a and OATP1B/Oatp1b subfamilies appeared at the root of tetrapods. The Oatp1d subfamily emerged in teleosts and is absent in tetrapods. The zebrafish Oatp1d1 is similar to mammalian OATP1A/Oatp1a and OATP1B/Oatp1b members, with the main physiological role in transport and balance of steroid hormones. Oatp1d1 activity is dependent upon pH gradient which could indicate bicarbonate exchange as a mode of transport. Our analysis of evolutionary conservation and structural properties revealed that: (i) H79 in the intracellular loop 3 is conserved within OATP1/Oatp1 family and is crucial for the transport activity ; (ii) N-glycosylation impacts membrane targeting and is conserved within the OATP1/Oatp1 family with N122, N133, N499 and N512 residues involved ; (iii) evolutionary conserved CRAC motif is important for membrane localization ; and (iv) Oatp1d1 is present in dimeric and possibly oligomeric form in the cell membrane. In conclusion, we describe the first detailed characterization of a new Oatp transporter in zebrafish, offering important insights into the functional evolution of OATP1/Oatp1 family and the physiological role of Oatp1d1.
Izvorni jezik
Engleski
Znanstvena područja
Biologija
POVEZANOST RADA
Projekti:
098-0982934-2745 - Ekotoksikološko značenje ABC transportnih proteina u vodenih organizama (Smital, Tvrtko, MZOS ) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE