Neuronal calcium sensor-1
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Neuronal calcium sensor-1 (NCS-1) also known as frequenin homolog (Drosophila) (freq) is a protein that is encoded by the FREQ gene in humans.[1] NCS-1 is a member of the neuronal calcium sensor family,[2] a class of EF hand containing calcium-myristoyl-switch proteins.[3]
Contents
Function
NCS-1 regulates synaptic transmission,[4] helps control the dynamics of nerve terminal growth,[5][6][4] is critical for some forms of learning and memory in C. elegans[7] and mammals,[8] regulates corticohippocampal plasticity; and enhancing levels of NCS-1 in the mouse dentate gyrus increases spontaneous exploration of safe environments,[8]potentially linking NCS-1 to curiosity.[9]
NCS-1 is a calcium sensor, not a calcium buffer (chelator); thus it is a high-affinity, low-capacity, calcium-binding protein.
Frq can substitute for calmodulin in some situations. It is thought to be associated with neuronal secretory vesicles and regulate neurosecretion.
- It is the Ca2+-sensing subunit of the yeast phosphatidylinositol (PtdIns)-4-OH kinase, PIK1
- It binds to many proteins, some in calcium dependent and some in calcium independent ways, and switches many of the targets "on" (some off).
- Calcineurin (protein phosphatase 2B)
- GRK2 (G-protein-coupled receptor kinase 2)
- D2 dopamine receptor
- IL1RAPL1 (interleukin-1 receptor accessory protein-like 1 protein)
- PI4KIIIβ (type III phosphatidylinositol 4-kinase β)
- IP3 receptor (this activity is inhibited by lithium - a drug used for the treatment of bipolar disorder)[10]
- 3',5'-cyclic nucleotide phosphodiesterases
- ARF1 (ADP Ribosylation factor 1)
- A type (Kv4.3; Shal-related subfamily, member 3) voltage-gated potassium channels
- Nitric oxide synthase
- TRPC5 channel[11]
- Ric8a[12]
- Frq modulates Ca2+ entry through a functional interaction with the α1 voltage-gated Ca2+-channel subunit.[4]
Structure
NCS-1 is a globular protein consisting of ten alpha-helices. Four pairs of alpha-helices each form independent 12-amino-acid loops containing a negatively charged calcium binding domain known as an EF-hand. However, only three of these EF hands are functional in NCS-1 (the most N-terminal EF hand does not bind calcium). NCS-1 also contains at least two known protein binding domains, and a large surface exposed hydrophobic crevice containing EF-hands three and four. There is a myristoylation motif at the N-terminus that presumably allows NCS-1 to associate with lipid membranes.
Clinical significance
The expression of NCS-1 increases in bipolar disorder and some forms of schizophrenia[13] and decreases in inflammatory bowel disease.[14] NCS-1 has also been linked with Autism.[15] In addition NCS-1 is significant in intelligence in creating curiosity by its function on dopamine D2 receptors in the dentate gyrus, increasing memory for complex tasks. http://www.physorg.com/news172174436.html
History
NCS-1 was originally discovered in Drosophila as a gain-of-function mutation associated with frequency-dependent increases in neurotransmission.[16] A role in neurotransmission was later confirmed in Drosophila using frq null mutants.[4] Work in bovine chromaffin cells demonstrated that NCS-1 is also a modulator of neurotransmission in mammals.[17] The designation 'NCS-1' came from the assumption that the protein was expressed only in neuronal cell types, which is not the case.[18]
References
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Further reading
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