Molecular details of cAMP generation in mammalian cells: A tale of two systems

被引:259
作者
Kamenetsky, Margarita
Middelhaufe, Sabine
Bank, Erin M.
Levin, Lonny R. [1 ]
Buck, Jochen
Steegborn, Clemens
机构
[1] Cornell Univ, Joan & Sanford I Weill Med Coll, Dept Pharmacol, New York, NY 10021 USA
[2] Ruhr Univ Bochum, Dept Physiol Chem, D-44801 Bochum, Germany
关键词
cAMP signaling; class III nucleoticlyl cyclases; enzyme regulation; soluble adenylyl cyclases; transmembrane adenylyl cyclases;
D O I
10.1016/j.jmb.2006.07.045
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The second messenger cAMP has been extensively studied for half century but the plethora of regulatory mechanisms controlling cAMP synthesis in mammalian cells is just beginning to be revealed. mammalian cells, cAMP is produced by two evolutionary related families of adenylyl cyclases, soluble adenylyl cyclases (sAC) and transmembrane adenylyl cyclases (tmAC). These two enzyme families serve distinct physiological functions. They share a conserved overall architecture in their catalytic domains and a common catalytic mechanism, but they differ their sub-cellular localizations and responses to various regulators. The major regulators of tmACs are heterotrimeric G proteins, which transduce extracellular signals via G protein-coupled receptors. sAC enzymes, in contrast, are regulated by the intracellular signaling molecules bicarbonate and calcium. Here, we discuss and compare the biochemical, structural and regulatory characteristics of the two mammalian AC families. This comparison reveals the mechanisms underlying their different properties but also illustrates many unifying themes for these evolutionary related signaling enzymes. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:623 / 639
页数:17
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