dc.contributor.author
Gorinski, Nataliya
dc.contributor.author
Sigrist, Stephan
dc.contributor.author
Bijata, Monika
dc.contributor.author
Prasad, Sonal
dc.contributor.author
Wirth, Alexander
dc.contributor.author
Galil, Dalia Abdel
dc.contributor.author
Zeug, Andre
dc.contributor.author
Bazovkina, Daria
dc.contributor.author
Kondaurova, Elena
dc.contributor.author
Kulikova, Elizabeth
dc.date.accessioned
2019-09-12T09:52:38Z
dc.date.available
2019-09-12T09:52:38Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/25532
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-25302
dc.description.abstract
The serotonergic system and in particular serotonin 1A receptor (5-HT1AR) are implicated in major depressive disorder (MDD). Here we demonstrated that 5-HT1AR is palmitoylated in human and rodent brains, and identified ZDHHC21 as a major palmitoyl acyltransferase, whose depletion reduced palmitoylation and consequently signaling functions of 5-HT1AR. Two rodent models for depression-like behavior show reduced brain ZDHHC21 expression and attenuated 5-HT1AR palmitoylation. Moreover, selective knock-down of ZDHHC21 in the murine forebrain induced depression-like behavior. We also identified the microRNA miR-30e as a negative regulator of Zdhhc21 expression. Through analysis of the post-mortem brain samples in individuals with MDD that died by suicide we find that miR-30e expression is increased, while ZDHHC21 expression, as well as palmitoylation of 5-HT1AR, are reduced within the prefrontal cortex. Our study suggests that downregulation of 5-HT1AR palmitoylation is a mechanism involved in depression, making the restoration of 5-HT1AR palmitoylation a promising clinical strategy for the treatment of MDD.
en
dc.format.extent
14 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
G protein-coupled receptors
en
dc.subject.ddc
500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie::576 Genetik und Evolution
dc.title
Attenuated palmitoylation of serotonin receptor 5-HT1A affects receptor function and contributes to depression-like behaviors
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
3924
dcterms.bibliographicCitation.doi
10.1038/s41467-019-11876-5
dcterms.bibliographicCitation.journaltitle
Nature Communications
dcterms.bibliographicCitation.originalpublishername
Nature Publishing Group UK
dcterms.bibliographicCitation.originalpublisherplace
London
dcterms.bibliographicCitation.volume
10
dcterms.bibliographicCitation.url
https://doi.org/10.1038/s41467-019-11876-5
refubium.affiliation
Biologie, Chemie, Pharmazie
refubium.affiliation.other
Institut für Biologie / Arbeitsbereich Genetik

refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
2041-1723
refubium.resourceType.provider
WoS-Alert