MURAL - Maynooth University Research Archive Library

    Protein Kinase A-mediated Phosphorylation of serine 357 of the mouse Prostacyclin Receptor Regulates Its coupling to Gs-, to Gi- and to Gq-coupled Effector Signalling*

    Lawler, Orlaith A. and Miggin, Sinead and Kinsella, B. Therese (2001) Protein Kinase A-mediated Phosphorylation of serine 357 of the mouse Prostacyclin Receptor Regulates Its coupling to Gs-, to Gi- and to Gq-coupled Effector Signalling*. Journal of Biological Chemistry, 276 (36). pp. 33596-33607. ISSN 0021-9258

    Download (671kB) | Preview

    Share your research

    Twitter Facebook LinkedIn GooglePlus Email more...

    Add this article to your Mendeley library


    The prostacyclin receptor (IP) is primarily coupled to Gαs-dependent activation of adenylyl cyclase; however, a number of studies indicate that the IP may couple to other secondary effector systems perhaps in a species-specific manner. In the current study, we investigated the specificity of G protein:effector coupling by the mouse (m) IP overexpressed in human embryonic kidney 293 cells and endogenously expressed in murine erythroleukemia cells. The mIP exhibited efficient Gαs coupling and concentration-dependent increases in cAMP generation in response to the IP agonist cicaprost; however, mIP also coupled to G α (i) decreasing the levels of cAMP in forskolin-treated cells. mIP coupling to G α (i) was pertussis toxin-sensitive and was dependent on protein kinase (PK) A activation status. In addition, the mIP coupled to phospholipase C (PLC) activation in a pertussis toxin-insensitive, α (i)-, G β γ -, and PKC-independent but in a Gαq- and PKA-dependent manner. Whole cell phosphorylation assays demonstrated that the mIP undergoes cicaprost-induced PKA phosphorylation. mIP(S357A), a site-directed mutant of mIP, efficiently coupled to Gαs but failed to couple to Gα(i) or to efficiently couple to Gα(q):PLC. Moreover, mIP(S357A) did not undergo cicaprost-induced phosphorylation confirming that Ser(357) is the target residue for PKA-dependent phosphorylation. Finally, co-precipitation experiments permitted the detection of Gαs, Gα(i), and Gα(q) in the immunoprecipitates of mIP, whereas only Gαs was co-precipitated with mIP(S357A) indicating that Ser(357) of mIP is essential for Gα(i) and Gα(q) interaction. Moreover, inhibition of PKA blocked co-precipitation of mIP with Gα(i) or Gα(q). Taken together our data indicate that the mIP, in addition to coupling to Gαs, couples to Gα(i) and Gα(q); however, Gα(i) and Gα(q) coupling is dependent on initial cicaprost-induced mIP:Gαs coupling and phosphorylation of mIP by cAMP-dependent PKA where Ser(357) was identified as the target residue for PKA phosphorylation.

    Item Type: Article
    Keywords: Protein; Kinase; A-mediated Phosphorylation; serine 357; mouse; Prostacyclin Receptor; coupling; Gs-; Gi-; Gq-; Effector Signalling;
    Academic Unit: Faculty of Science and Engineering > Biology
    Item ID: 12645
    Identification Number:
    Depositing User: Sinead Miggin
    Date Deposited: 27 Mar 2020 11:43
    Journal or Publication Title: Journal of Biological Chemistry
    Publisher: American Society for Biochemistry and Molecular Biology
    Refereed: Yes
    Use Licence: This item is available under a Creative Commons Attribution Non Commercial Share Alike Licence (CC BY-NC-SA). Details of this licence are available here

    Repository Staff Only(login required)

    View Item Item control page


    Downloads per month over past year

    Origin of downloads