Differential Coupling of m2 and m4 Muscarinic Receptors to Inhibition of Adenylyl Cyclase by G and G Subunits
We compared the G-protein requirements for coupling of human and chicken m2 and m4 muscarinic acetylcholine receptors (mAChRs) to inhibition of adenylyl cyclase, using a luciferase reporter gene under the transcriptional control of a cAMP response element as a sensitive monitor of intracellular cAMP...
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Veröffentlicht in: | The Journal of biological chemistry 1995-07, Vol.270 (27), p.16070 |
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container_issue | 27 |
container_start_page | 16070 |
container_title | The Journal of biological chemistry |
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creator | Jacques C. Migeon Sarabeth L. Thomas Neil M. Nathanson |
description | We compared the G-protein requirements for coupling of human and chicken m2 and m4 muscarinic acetylcholine receptors (mAChRs)
to inhibition of adenylyl cyclase, using a luciferase reporter gene under the transcriptional control of a cAMP response element
as a sensitive monitor of intracellular cAMP levels. Previously, we used this system to demonstrate that the chick m4 receptor
preferentially coupled to G i α-2 and G o α over G i α-1 and G i α-3. We found that both the chick and human m2 mAChRs can couple to G i α-1, G i α-2, G i α-3, and G o α, while the human m4 mAChR preferentially couples to G i α-2 and G o α. Both the G and G forms of the G o α subunit were effective in reconstituting coupling of the m2 and m4 mAChRs to inhibit adenylyl cyclase activity. The m2 and
m4 mAChRs thus couple to inhibition of adenylyl cyclase by overlapping but different sets of G-protein α subunits. |
doi_str_mv | 10.1074/jbc.270.27.16070 |
format | Article |
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to inhibition of adenylyl cyclase, using a luciferase reporter gene under the transcriptional control of a cAMP response element
as a sensitive monitor of intracellular cAMP levels. Previously, we used this system to demonstrate that the chick m4 receptor
preferentially coupled to G i α-2 and G o α over G i α-1 and G i α-3. We found that both the chick and human m2 mAChRs can couple to G i α-1, G i α-2, G i α-3, and G o α, while the human m4 mAChR preferentially couples to G i α-2 and G o α. Both the G and G forms of the G o α subunit were effective in reconstituting coupling of the m2 and m4 mAChRs to inhibit adenylyl cyclase activity. The m2 and
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to inhibition of adenylyl cyclase, using a luciferase reporter gene under the transcriptional control of a cAMP response element
as a sensitive monitor of intracellular cAMP levels. Previously, we used this system to demonstrate that the chick m4 receptor
preferentially coupled to G i α-2 and G o α over G i α-1 and G i α-3. We found that both the chick and human m2 mAChRs can couple to G i α-1, G i α-2, G i α-3, and G o α, while the human m4 mAChR preferentially couples to G i α-2 and G o α. Both the G and G forms of the G o α subunit were effective in reconstituting coupling of the m2 and m4 mAChRs to inhibit adenylyl cyclase activity. The m2 and
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to inhibition of adenylyl cyclase, using a luciferase reporter gene under the transcriptional control of a cAMP response element
as a sensitive monitor of intracellular cAMP levels. Previously, we used this system to demonstrate that the chick m4 receptor
preferentially coupled to G i α-2 and G o α over G i α-1 and G i α-3. We found that both the chick and human m2 mAChRs can couple to G i α-1, G i α-2, G i α-3, and G o α, while the human m4 mAChR preferentially couples to G i α-2 and G o α. Both the G and G forms of the G o α subunit were effective in reconstituting coupling of the m2 and m4 mAChRs to inhibit adenylyl cyclase activity. The m2 and
m4 mAChRs thus couple to inhibition of adenylyl cyclase by overlapping but different sets of G-protein α subunits.</abstract><pub>American Society for Biochemistry and Molecular Biology</pub><pmid>7608168</pmid><doi>10.1074/jbc.270.27.16070</doi></addata></record> |
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title | Differential Coupling of m2 and m4 Muscarinic Receptors to Inhibition of Adenylyl Cyclase by G and G Subunits |
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