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Critical impact of different conserved endoplasmic retention mofits and dopamine receptor interacting proteins (DRIPs) on intracellular localization and trafficking of the D2 dopamine receptor (D2-R) isoforms
ID Blagotinšek Cokan, Kaja (Author), ID Mavri, Maša (Author), ID Rutland, Catrin (Author), ID Glisić, Sanja (Author), ID Sencanski, Milan (Author), ID Vrecl, Milka (Author), ID Kubale, Valentina (Author)

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Abstract
The type 2 dopamine receptor D2 (D2-R), member of the G protein-coupled receptor (GPCR) superfamily, exists in two isoforms, short (D2S-R) and long (D2L-R). They differ by an additional 29 amino acids (AA) in the third cytoplasmic loop (ICL3) of the D2L-R. These isoforms differ in their intracellular localization and trafficking functionality, as D2L-R possesses a larger intracellular pool, mostly in the endoplasmic reticulum (ER). This review focuses on the evolutionarily conserved motifs in the ICL3 of the D2-R and proteins interacting with the ICL3 of both isoforms, specifically with the 29 AA insert. These motifs might be involved in D2-R exit from the ER and have an impact on cell-surface and intracellular localization and, therefore, also play a role in the function of dopamine receptor signaling, ligand binding and possible homo/heterodimerization. Our recent bioinformatic data on potential new interaction partners for the ICL3 of D2-Rs are also presented. Both are highly relevant, and have clinical impacts on the pathophysiology of several diseases such as Parkinson’s disease, schizophrenia, Tourette’s syndrome, Huntington’s disease, manic depression, and others, as they are connected to a variety of essential motifs and differences in communication with interaction partners.

Language:English
Keywords:D2 dopamine receptor, intracellular trafficking, endoplasmic reticulum, retention motifs, ICL3, interacting partners
Work type:Article
Typology:1.02 - Review Article
Organization:VF - Veterinary Faculty
Publication status:Published
Publication version:Version of Record
Year:2020
Number of pages:18 str.
Numbering:Vol. 10, iss. 10, art. 1355
PID:20.500.12556/RUL-134373 This link opens in a new window
UDC:577
ISSN on article:2218-273X
DOI:10.3390/biom10101355 This link opens in a new window
COBISS.SI-ID:29478403 This link opens in a new window
Publication date in RUL:12.01.2022
Views:956
Downloads:189
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BLAGOTINŠEK COKAN, Kaja, MAVRI, Maša, RUTLAND, Catrin, GLISIĆ, Sanja, SENCANSKI, Milan, VRECL, Milka and KUBALE, Valentina, 2020, Critical impact of different conserved endoplasmic retention mofits and dopamine receptor interacting proteins (DRIPs) on intracellular localization and trafficking of the D$_2$ dopamine receptor (D$_2$-R) isoforms. Biomolecules [online]. 2020. Vol. 10, no. 10,  1355. [Accessed 5 April 2025]. DOI 10.3390/biom10101355. Retrieved from: https://repozitorij.uni-lj.si/IzpisGradiva.php?lang=eng&id=134373
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Record is a part of a journal

Title:Biomolecules
Shortened title:Biomolecules
Publisher:MDPI AG
ISSN:2218-273X
COBISS.SI-ID:519952921 This link opens in a new window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:01.10.2020

Projects

Funder:ARRS - Slovenian Research Agency
Project number:P4-0053
Name:Endokrini, imunski in encimski odzivi pri zdravih in bolnih živalih

Funder:ARRS - Slovenian Research Agency
Project number:BI-RS/20-21-045

Funder:ARRS - Slovenian Research Agency
Funding programme:Young researchers

Funder:MESTD - Ministry of Education, Science and Technological Development of Republic of Serbia
Funding programme:Basic Research (BR or ON)
Project number:173001
Name:Application of the EIIP/ISM bioinformatics platform in discovery of novel therapeutic targets and potential therapeutic molecules

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