Antithetical modes of and the Ca 2+ sensors targeting in ANF-RGC and ROS-GC1 membrane guanylate cyclases

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Abstract

The membrane guanylate cyclase family has been branched into three subfamilies: natriuretic peptide hormone surface receptors, Ca 2+-modulated neuronal ROS-GC, and Ca 2+-modulated odorant surface receptor ONE-GC. The first subfamily is solely modulated by the extracellularly-generated hormonal signals; the second, by the intracellularly-generated sensory and sensory-linked signals; and the third, by combination of these two. The present study defines a new paradigm and a new mechanism of Ca 2+ signaling. (1) It demonstrates for the first time that ANF-RGC, the prototype member of the surface receptor subfamily, is stimulated by free [Ca 2+] i. The stimulation occurs via myristoylated form of neurocalcin δ, and both the guanylate cyclase and the calcium sensor neurocalcin δ are present in the glomerulosa region of the adrenal gland. (2) The EF-2, EF-3 and EF-4 hands of GCAP1 sense the progressive increment of [Ca 2+] i and with a K 1/2 of 100 nM turn ROS-GC1 "OFF". In total reversal, the same EF hands upon sensing the progressive increment of [Ca 2+] i with K 1/2 turn ONE-GC "ON". The findings suggest a universal Ca 2+-modulated signal transduction theme of the membrane guanylate cyclase family; demonstrate that signaling of ANF-RGC occurs by the peptide hormones and also by [Ca 2+] i signals; that for the Ca 2+ signal transduction, ANF-RGC functions as a two-component transduction system consisting of the Ca 2+ sensor neurocalcin δ and the transducer ANF-RGC; and that the neurocalcin δ in this case expands beyond its NCS family. Furthermore, the study shows a novel mechanism of the [Ca 2+] i sensor GCAP1 where it acts as an antithetical NCS for the signaling mechanisms of ROS-GC1 and ONE-GC. © 2012 Duda, Peretzev, Koch and Sharma.

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Duda, T., Pertzev, A., Koch, K. W., & Sharma, R. K. (2012). Antithetical modes of and the Ca 2+ sensors targeting in ANF-RGC and ROS-GC1 membrane guanylate cyclases. Frontiers in Molecular Neuroscience, (MARCH), 1–16. https://doi.org/10.3389/fnmol.2012.00044

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