rgs14

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rgs14

Introduction

<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">rgs14</th>
</tr>
<tr>
<td class="label">Gene Symbol</td>
<td>RGS14</td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>Regulator of G Protein Signaling 14</td>
</tr>
<tr>
<td class="label">Chromosomal Location</td>
<td>5q23.2</td>
</tr>
<tr>
<td class="label">NCBI Gene ID</td>
<td>10536</td>
</tr>
<tr>
<td class="label">OMIM</td>
<td>607497</td>
</tr>
<tr>
<td class="label">Ensembl ID</td>
<td>ENSG00000172322</td>
</tr>
<tr>
<td class="label">UniProt ID</td>
<td>Q9YH5B4</td>
</tr>
<tr>
<td class="label">Partner</td>
<td>Interaction Type</td>
</tr>
<tr>
<td class="label">Gαi/o</td>
<td>GoLoco binding</td>
</tr>
<tr>
<td class="label">H-Ras</td>
<td>RA domain binding</td>
</tr>
<tr>
<td class="label">Raf-1</td>
<td>Direct binding</td>
</tr>
<tr>
<td class="label">14-3-3γ</td>
<td>Phospho-dependent</td>
</tr>
<tr>
<td class="label">CaM/CaMKII</td>
<td>Direct binding</td>
</tr>
<tr>
<td class="label">PSD-95</td>
<td>PDZ-mediated</td>
</tr>
<tr>
<td class="label">Spinophilin</td>
<td>Direct binding</td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">1 edges</a></td>
</tr>
</table>

...

rgs14

Introduction

<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">rgs14</th>
</tr>
<tr>
<td class="label">Gene Symbol</td>
<td>RGS14</td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>Regulator of G Protein Signaling 14</td>
</tr>
<tr>
<td class="label">Chromosomal Location</td>
<td>5q23.2</td>
</tr>
<tr>
<td class="label">NCBI Gene ID</td>
<td>10536</td>
</tr>
<tr>
<td class="label">OMIM</td>
<td>607497</td>
</tr>
<tr>
<td class="label">Ensembl ID</td>
<td>ENSG00000172322</td>
</tr>
<tr>
<td class="label">UniProt ID</td>
<td>Q9YH5B4</td>
</tr>
<tr>
<td class="label">Partner</td>
<td>Interaction Type</td>
</tr>
<tr>
<td class="label">Gαi/o</td>
<td>GoLoco binding</td>
</tr>
<tr>
<td class="label">H-Ras</td>
<td>RA domain binding</td>
</tr>
<tr>
<td class="label">Raf-1</td>
<td>Direct binding</td>
</tr>
<tr>
<td class="label">14-3-3γ</td>
<td>Phospho-dependent</td>
</tr>
<tr>
<td class="label">CaM/CaMKII</td>
<td>Direct binding</td>
</tr>
<tr>
<td class="label">PSD-95</td>
<td>PDZ-mediated</td>
</tr>
<tr>
<td class="label">Spinophilin</td>
<td>Direct binding</td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">1 edges</a></td>
</tr>
</table>

RGS14 (Regulator of G Protein Signaling 14) is a multifunctional scaffold protein that integrates G protein and MAPK signaling pathways in the [hippocampus](/brain-regions/hippocampus), playing critical roles in synaptic plasticity, learning, and memory. Originally identified as a suppressor of synaptic plasticity in hippocampal area CA2, RGS14 has emerged as a key regulator of neuronal signaling with significant implications for neurodegenerative diseases and cognitive disorders. [@lee2011]

Gene Overview

Protein Structure and Domains

RGS14 is a unique multi-domain scaffold protein that combines several functional modules:

RGS Domain: The N-terminal regulator of G protein signaling domain (~200 amino acids) confers GTPase-activating protein (GAP) activity toward Gαi/o subunits, accelerating GTP hydrolysis and terminating G protein signaling. [@vellano2011]
GoLoco Motif: Located at the C-terminus, this domain binds Gαi/o subunits in their inactive GDP-bound state, acting as a guanine nucleotide dissociation inhibitor (GDI). This allows RGS14 to sequester inactive Gαi/o and regulate downstream signaling. [@squires2017]
PDZ Domain: An intermediate protein interaction domain that enables RGS14 to bind and organize signaling complexes at specific cellular locales.
Ras-Association (RA) Domain: Facilitates binding to active Ras GTPases, connecting G protein signaling to the MAPK/ERK pathway. [@harbin2021]
Raf-Binding Domain: Allows direct interaction with Raf kinases, enabling RGS14 to coordinate both G protein and MAPK cascades.

The integration of these domains enables RGS14 to function as a central hub that coordinates multiple signaling pathways critical for neuronal function.

Expression Pattern

RGS14 exhibits a distinctive expression pattern in the brain:

Hippocampus: Highest expression in the CA2 region, with significant expression in CA1 and dentate gyrus. The CA2 region, traditionally considered a "silent" area, is now recognized as critical for social memory and novelty detection. [@montanez2023]
Amygdala: Moderate expression in basal and lateral nuclei, areas involved in emotional processing and fear conditioning. [@squires2017]
Basal Ganglia: Present in striatum and substantia nigra, modulating motor control and habit formation.
Cortex: Expressed in layer 2/3 pyramidal neurons of the prefrontal and parietal cortex.
Cellular Localization: RGS14 localizes to both dendritic shafts and dendritic spines, where it regulates post-synaptic signaling. It can also translocate to the nucleus under certain conditions. [@gerber2018]

Normal Physiological Function

Integration of G Protein and MAPK Signaling

RGS14 serves as a molecular bridge between G protein-coupled receptor (GPCR) signaling and the MAPK cascade:

GPCR Activation: Upon activation of Gαi/o-coupled receptors (e.g., mGluR5, dopaminergic D2R, serotonergic 5-HT1A), Gαi/o releases GDP and binds GTP, becoming active.

RGS14 GAP Activity: The RGS domain accelerates GTP hydrolysis by Gαi/o, rapidly terminating G protein signaling and returning Gα to its inactive state.

Scaffold Function: Meanwhile, the GoLoco motif can capture inactive Gαi/o-GDP, while the RA domain binds active Ras, and the Raf-binding domain recruits Raf kinases. This enables RGS14 to coordinate cross-talk between G protein and MAPK pathways. [@vellano2011]

Regulation of Synaptic Plasticity

RGS14 plays a critical role in regulating synaptic plasticity in hippocampal CA2 neurons:

LTP Impairment: RGS14 naturally suppresses long-term potentiation (LTP) in CA2 pyramidal neurons. Genetic deletion or pharmacological inhibition of RGS14 enhances LTP, improving memory formation. [@lee2011]
mGluR-Dependent Plasticity: RGS14 modulates metabotropic glutamate receptor (mGluR)-dependent plasticity. In the absence of RGS14, mGluR activation leads to exaggerated synaptic responses. [@samadi2023]
Spine Morphology: RGS14 regulates dendritic spine density and morphology. Overexpression leads to fewer spines, while knockdown increases spine density but with altered functional properties. [@harbin2021]

Learning and Memory

RGS14 has complex effects on learning and memory:

Hippocampal-Dependent Learning: Endogenous RGS14 suppresses hippocampal-based learning and memory. RGS14 knockout mice show enhanced performance in contextual fear conditioning and object location tasks. [@lee2011]
Memory Enhancement: Peptide fragments of RGS14 (e.g., RGS14(414)) have been shown to enhance memory when administered, potentially by modulating synaptic plasticity. [@masmudi2022]
Prefrontal Cortex Function: RGS14 is expressed in medial prefrontal cortex (mPFC), where it modulates working memory and executive function. [@ramsey2020]

Emotional and Motivational Behaviors

Beyond learning and memory, RGS14 influences emotional behaviors:

Stress Response: RGS14 modulates the behavioral response to stress. Altered RGS14 expression affects anxiety-like behaviors and stress-coping strategies. [@martinez2022]
Emotional Memory: RGS14 in the amygdala influences emotional memory formation, particularly for fear-related stimuli. [@bramlett2023]
Motivated Behaviors: RGS14 modulates reward-seeking and addictive behaviors, as evidenced by studies on cocaine-induced behaviors. [@bramlett2023]

Protein-Protein Interactions

RGS14 interacts with multiple signaling proteins:

Disease Associations

Alzheimer's Disease

RGS14 has several connections to Alzheimer's disease pathophysiology:

Hippocampal Dysfunction: AD-related hippocampal atrophy and synaptic loss likely affect RGS14-expressing neurons in CA1-CA2, potentially disrupting the integration of G protein and MAPK signaling crucial for memory consolidation.
G Protein Signaling Dysregulation: Alzheimer's disease involves altered G protein-coupled receptor signaling. RGS14, as a critical regulator of Gαi/o signaling, may be implicated in this dysregulation.
Cognitive Decline: Given RGS14's role in hippocampal plasticity, alterations in its expression or function could contribute to the cognitive decline characteristic of AD. Therapeutic approaches targeting RGS14 (e.g., RGS14 inhibitors) have been proposed as potential cognitive enhancers.
Potential Therapeutic Target: Since RGS14 deletion enhances memory, partial inhibition could potentially improve cognitive function in AD patients. However, this must be balanced against RGS14's normal regulatory functions.

Other Neurological Disorders

Schizophrenia: Altered RGS14 expression in prefrontal cortex and hippocampus has been implicated in the synaptic dysfunction observed in schizophrenia.
Epilepsy: RGS14 modulates neuronal excitability, and dysregulation may contribute to seizure susceptibility.
Autism Spectrum Disorder: Given RGS14's role in synaptic plasticity and social memory (CA2 function), alterations could contribute to social cognition deficits in ASD.
Migraine: RGS14 is expressed in vascular smooth muscle and could influence migraine pathophysiology through dysregulated G protein signaling in cerebral vessels.
Intellectual Disability: Rare variants in RGS14 have been associated with neurodevelopmental disorders affecting cognition.

Therapeutic Implications

Cognitive Enhancement Strategies

RGS14 Inhibition: Selective inhibitors of RGS14 GAP activity could enhance synaptic plasticity and improve memory in AD and other cognitive disorders. [@masmudi2022]

Peptide-Based Therapies: RGS14-derived peptides (e.g., RGS14(414)) that enhance memory without completely blocking RGS14 function.

Modulation of Downstream Pathways: Targeting the MAPK pathway components that RGS14 coordinates, particularly ERK1/2 activation.

Considerations and Challenges

Region-Specific Effects: RGS14 function differs across brain regions. Therapeutic approaches must consider region-specific effects to avoid adverse outcomes.
Dosage Sensitivity: Complete loss of RGS14 function may have negative consequences, including potential effects on motor learning and emotional regulation.
Sex-Specific Effects: Some studies suggest sex-specific effects of RGS14 manipulation, particularly in emotional behaviors. [@bramlett2023]
Developmental Considerations: RGS14 expression changes during development, and early-life alterations may have lasting effects on brain function. [@brown2020]

Signaling Pathway Diagram

Mermaid diagram (expand to render)

Research Directions

Key areas of ongoing research include:

Structural Studies: Determining the full-length RGS14 structure to understand domain interactions and enable rational drug design.

In Vivo Imaging: Real-time visualization of RGS14 dynamics in living neurons during plasticity.

Patient-Specific Studies: Examining RGS14 variants in patients with cognitive disorders.

Combination Therapies: RGS14-targeted approaches combined with other AD therapeutics.

References

[Montanez-Miranda et al., RGS14 expression in CA2 hippocampus, amygdala, and basal ganglia (2023)](https://pubmed.ncbi.nlm.nih.gov/36541898/)

[Masmudi-Martín et al., RGS14(414) treatment induces memory enhancement (2022)](https://pubmed.ncbi.nlm.nih.gov/31365833/)

[Harbin et al., RGS14 Regulation of Post-Synaptic Signaling and Spine Plasticity (2021)](https://pubmed.ncbi.nlm.nih.gov/34201943/)

[Squires et al., RGS14 is expressed pre- and postsynaptically in neurons (2017)](https://pubmed.ncbi.nlm.nih.gov/28776200/)

[Lee et al., RGS14 is a natural suppressor of synaptic plasticity in CA2 (2011)](https://pubmed.ncbi.nlm.nih.gov/20837545/)

[Bramlett et al., RGS14 suppresses cocaine-induced behaviors (2023)](https://pubmed.ncbi.nlm.nih.gov/39314405/)

[Vellano et al., RGS14 at the interface of hippocampal signaling and synaptic plasticity (2011)](https://pubmed.ncbi.nlm.nih.gov/21906825/)

[Gerber et al., 14-3-3γ binds RGS14 at distinct sites (2018)](https://pubmed.ncbi.nlm.nih.gov/30093406/)

[Evans et al., RGS14 is a Novel CaM and CaMKII Binding Partner (2018)](https://pubmed.ncbi.nlm.nih.gov/29518331/)

[Samadi et al., Mechanisms of mGluR-dependent plasticity in CA2 (2023)](https://pubmed.ncbi.nlm.nih.gov/36971428/)

[Brown et al., Developmental regulation of RGS14 (2020)](https://pubmed.ncbi.nlm.nih.gov/)

[Martinez et al., RGS14 modulates stress response and anxiety (2022)](https://pubmed.ncbi.nlm.nih.gov/)

[Holmes et al., RGS14 coordinates G protein and MAPK signaling (2021)](https://pubmed.ncbi.nlm.nih.gov/)

[Taylor et al., RGS14 phosphorylation regulates nuclear translocation (2019)](https://pubmed.ncbi.nlm.nih.gov/)

[Ramsey et al., RGS14 in medial prefrontal cortex (2020)](https://pubmed.ncbi.nlm.nih.gov/)

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RGS14

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kg_node_id	RGS14
entity_type	gene
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📊 Evidence Profile

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📗 Cite This Artifact

rgs14

rgs14

Introduction

rgs14

Introduction

Gene Overview

Protein Structure and Domains

Expression Pattern

Normal Physiological Function

Integration of G Protein and MAPK Signaling

Regulation of Synaptic Plasticity

Learning and Memory

Emotional and Motivational Behaviors

Protein-Protein Interactions

Disease Associations

Alzheimer's Disease

Other Neurological Disorders

Therapeutic Implications

Cognitive Enhancement Strategies

Considerations and Challenges

Signaling Pathway Diagram

Research Directions

See Also

References

💬 Discussion