Abstract
A sequel to these authors' earlier comprehensive reviews which covered the field of mammalian membrane guanylate cyclase (MGC) from its origin to the year 2010, this article contains 13 sections. The first is historical and covers MGC from the year 1963–1987, summarizing its colorful developmental stages from its passionate pursuit to its consolidation. The second deals with the establishment of its biochemical identity. MGC becomes the transducer of a hormonal signal and founder of the peptide hormone receptor family, and creates the notion that hormone signal transduction is its sole physiological function. The third defines its expansion. The discovery of ROS-GC subfamily is made and it links ROS-GC with the physiology of phototransduction. Sections ROS-GC, a Ca2+-Modulated Two Component Transduction System to Migration Patterns and Translations of the GCAP Signals Into Production of Cyclic GMP are Different cover its biochemistry and physiology. The noteworthy events are that augmented by GCAPs, ROS-GC proves to be a transducer of the free Ca2+ signals generated within neurons; ROS-GC becomes a two-component transduction system and establishes itself as a source of cyclic GMP, the second messenger of phototransduction. Section ROS-GC1 Gene Linked Retinal Dystrophies demonstrates how this knowledge begins to be translated into the diagnosis and providing the molecular definition of retinal dystrophies. Section Controlled By Low and High Levels of [Ca2+]i, ROS-GC1 is a Bimodal Transduction Switch discusses a striking property of ROS-GC where it becomes a “[Ca2+]i bimodal switch” and transcends its signaling role in other neural processes. In this course, discovery of the first CD-GCAP (Ca2+-dependent guanylate cyclase activator), the S100B protein, is made. It extends the role of the ROS-GC transduction system beyond the phototransduction to the signaling processes in the synapse region between photoreceptor and cone ON-bipolar cells; in section Ca2+-Modulated Neurocalcin δ ROS-GC1 Transduction System Exists in the Inner Plexiform Layer (IPL) of the Retinal Neurons, discovery of another CD-GCAP, NCδ, is made and its linkage with signaling of the inner plexiform layer neurons is established. Section ROS-GC Linkage With Other Than Vision-Linked Neurons discusses linkage of the ROS-GC transduction system with other sensory transduction processes: Pineal gland, Olfaction and Gustation. In the next, section Evolution of a General Ca2+-Interlocked ROS-GC Signal Transduction Concept in Sensory and Sensory-Linked Neurons, a theoretical concept is proposed where “Ca2+-interlocked ROS-GC signal transduction” machinery becomes a common signaling component of the sensory and sensory-linked neurons. Closure to the review is brought by the conclusion and future directions.
Highlights
In addition to cyclic AMP and inositol triphosphate (IP3), cyclic GMP is an omnipresent intracellular second messenger of prokaryotes and eukaryotes
GCAP2 remains bound to this ROSGC1 as its activator. These results prove that the two guanylate cyclase activating proteins (GCAPs) signal rod outer segment (ROS)-GC1 activation through different modes and the differences reside in the spatial characteristics of ROS-GC1; and because orientations of the two domains of their signal origins are different, their migration pathways are different: GCAP1 downstream from M445-L456 and L503-I522 to the P808-K1054
An extraordinary characteristic about the neurocalcin δ (NCδ) binding domain in ROS-GC is that it resides directly within the catalytic domain (CCD) (Venkataraman et al, 2008). This finding demonstrated that NCδ-modulated Ca2+ signaling of ROS-GC1 occurs through a new model, its principles are (1) NCδ directly interacts with CCD; (2) it does not require the adjacent N-terminally located α-helical dimerization domain structural element for its interaction; (3) the CCD module, housing the site, is intrinsically active, i.e., it has basal guanylate cyclase activity
Summary
In addition to cyclic AMP and inositol triphosphate (IP3), cyclic GMP is an omnipresent intracellular second messenger of prokaryotes and eukaryotes. A hormonally-dependent membrane guanylate cyclase existed in the mammalian cells; it was a transducer of specific hormonal signals and cyclic GMP was their second messenger.
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