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NTR: beta-arrestin-dependent dopamine receptor signaling pathway #28005
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@pgaudet For annotation review, is the proposal to make dopamine receptor signaling pathway do_not_annotate or obsolete or something else? Thanks. |
The PMID:25671228 figure above is about D2R whereas PMID:35688404 D1R. As indicated in PMID:28328745, G-protein independent arrestin signaling is quite varied regarding both upstream (many different 7TM receptors) and downstream (kinase and non-kinase). Perhaps we could do: |
This looks good to me. @hattrill ? |
Hi https://pubmed.ncbi.nlm.nih.gov/21711983/ - if so I will use it and maybe try to curate that experimental paper. Or is there a beta-arrestin/AKT/GSK signaling pathway that I have missed and therefore could state that the DRs pos reg the beta-arrestin/AKT/GSK signaling pathway Thanks |
@raymond91125 Can you please create that new term? |
+[Term] |
Following up on #26959
After discussion with @hattrill we agree that we should look into creating a new term under 'GO:0007166 cell surface signaling pathway', based on the paper @raymond91125 cited, PMID: 25671228, and also PMID:35688404.
One problem is that there are no general beta-arrestin or GSK3 signaling pathway terms in GO, so no 'module' we can reuse. Beta-arrestin a an adaptor that seem to activate may different proteins; can a a pathway in which the receptor binds beta-arrestin be defined unambiguously?
The mechanism of signaling is not clear: PMID: 25671228, mentions PP2, Akt and GSK3A, while
PMID:35688404 mentions Akt, PI3K, MAP kinases but not GSK3
Are these the same pathway?
The first step would be with it to review the direct annotations to GO:0007212 dopamine receptor signaling pathway (39 EXP) and see if they can be made more precise with existing terms, or if we already need a new term.
@raymond91105 can you please set up an annotation review?
Thanks, Pascale
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