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5-HT3B

Previous and Unofficial Names
5-HT3B
5-HT3B
Structural Information
Species TM AA Chromosomal Location Gene Name Reference
Human 4 441 11q23.1 HTR3B 22,32
Rat 4 437 8q23 Htr3b 89
Mouse 4 437 9 B Htr3b 89
Contents:
Previous and Unofficial Names
Structural Information
Database Links
Tissue Distribution
Physiological Consequences of Altering Gene Expression
Clinically-Relevant Mutations
Gene Expression and Pathophysiology
Biologically Significant Variants
Subunit Comments
Database Links
ChEMBL Target 11305 (Hs), 11765 (Mm), 11885 (Rn)
Ensembl ENSG00000149305 (Hs), ENSMUSG00000008590 (Mm), ENSRNOG00000006920 (Rn)
Entrez Gene 9177 (Hs), 57014 (Mm), 58963 (Rn)
GeneCards HTR3B (Hs)
HomoloGene 38131 (Hs)
OMIM 604654 (Hs)
PharmGKB Gene PA29556 (Hs)
RefSeq Nucleotide NM_006028 (Hs), NM_020274 (Mm), NM_022189 (Rn)
RefSeq Protein NP_006019 (Hs), NP_064670 (Mm), NP_071525 (Rn)
UniGene Hs. 241377 (Hs)
UniProt O95264 (Hs), Q9JHJ5 (Mm), Q9JJ16 (Rn)
Wikipedia 5-HT3B
Search for 3D structures on the PDB
Search using keywords: 5-HT3 receptors 5-HT3B Search using accession numbers: Q9JJ16 || Q9JHJ5 || O95264
Tissue Distribution
Amygdala, caudate nucleus, hippocampus, thalamus.
Species:  Human
Technique:  Northern Blot
References:  22
Cerebral cortex including occipital, frontal and temporal regions, amygdala, hippocampus and testis.
Species:  Human
Technique:  PCR-based detection
References:  32
Amygdala, hippocampus, caudate nucleus, small intestine, colon and kidney.
Species:  Human
Technique:  RT-PCR
References:  37
Submucous plexus neurones.
Species:  Human
Technique:  Immunohistochemistry
References:  81
Brain, small intestine, colon.
Species:  Mouse
Technique:  RT-PCR
References:  90
Neurones of the myenteric and submucous plexus, mucosal epithelial cells of the intestinal crypts.
Species:  Mouse
Technique:  In situ hybridisation
References:  81
The 5-HT3B subunit is co-expressed with the 5-HT3A subunit in a subpopulation of superior cervical, nodose and dorsal root ganglion neurones. Nodose and dorsal root ganglion neurones co-expressing the 5-HT3A and 5-HT3B subunits have been demonstrated to project centrally to the nucleus tractus solitarius and superficial layers of the spinal cord, respectively.
Species:  Rat
Technique:  In situ hybridisation
References:  96
Restricted subpopulation of neurones in the pyramidal and molecular layers of the hippocampus.
Species:  Rat
Technique:  Immunohistochemistry
References:  97
Hippocampal interneurones.
Species:  Rat
Technique:  Immunohistochemistry
References:  98
Pyramidal neurones in the CA2, CA3 and to a lesser extent CA1 fields of the hippocampus. Large neurones in the hilus (CA4) of the hippocampus.
Species:  Human
Technique:  Immunohistochemistry
References:  78
Hippocampus (CA1 and dentate gyrus) and cerebral cortex.
Species:  Rat
Technique:  Immunohistochemistry
References:  99
Nodose, trigeminal, superior cervical and dorsal root ganglia.
Species:  Rat
Technique:  Immunohistochemistry
References:  99
Nodose, trigeminal, superior cervical and dorsal root ganglia.
Species:  Mouse
Technique:  Immunohistochemistry
References:  99
Physiological Consequences of Altering Gene Expression
Despite the existence of 5-HT3B subunit mRNA in neuroblastoma cell lines, the introduction of the rat 5-HT3B subunit by transient transfection of mouse NB41A3 cells causes 5-HT to become less potent as an activator of 5-HT3 receptors native to the cell line and alters the kinetics of 5-HT activated currents. Introduction of the 5-HT3B subunit also abolishes the 5-HT induced increase in intracellular Ca2+ concentration seen in untransfected NB41A3 cells.
Species:  Mouse
Tissue:  NB41A3 cells
Technique:  Transient transfection of the rat 5-HT3B subunit
References:  60
Clinically-Relevant Mutations
Disease:  Bipolar affective disease
OMIM:  125480
Comments:  This deletion in the promotor region of the HTR3B gene is underrepresented in a sample of patients suffering from bipolar depression.
References:  91
Click column headers to sort
Type Species Molecular location Reference
Deletion Human -100 to -102AAG 91
Disease:  Major depression (female)
OMIM:  608516
Role:  5-HT3B has been associated with major female depression in genetic analyses.
Comments:  This polymorphism occurs at a significantly reduced frequency in female patients suffering from major depression and also patients with bipolar disorder, consistent with a protective influence of the variant allele.
References:  92
Click column headers to sort
Type Species Molecular location Reference
Missense Human Y129S 92
Disease:  Emesis.
Comments:  This deletion variant in the promotor region of the HTR3B gene increases promoter activity in vitro and has been associated with an increased incidence of paroxetine-induced nausea, and with an increased frequency of vomiting caused by chemotherapy in patients receiving 5-HT3 receptor antagonists as anti-emetic therapy.
References:  93-95
Click column headers to sort
Type Species Molecular location Reference
Deletion Human -100 to -102AAG 94-95
Gene Expression and Pathophysiology
Downregulation of mRNA encoding the 5-HT3B subunit as a consequence of the knockout of SERT.
Tissue or cell type:  Myenteric neurones
Pathophysiology:  Downregulation of mRNA encoding the 5-HT3B subunit as a consequence of the knockout of SERT is associated with an increase in the EC50 for 5-HT in myenteric neurones.
Species:  Mouse
Technique:  Whole cell patch clamp.
References:  90
Biologically Significant Variants
The human 5-HT3B(S156R) polymorphism causes enhanced functional responses to 5-HT mediated by heteromeric 5-HT3AB receptors.
Amino acids:  441
Type:  Single nucleotide polymorphism
Species:  Human
References:  100
The human 5-HT3B(Y129S) polymorphism causes decreased desensitisation, decreased inactivation rate, and a 7-fold increase in the mean channel open time of heteromeric 5-HT3AB receptors compared to receptors incorporating the Y129 variant.
Amino acids:  441
Type:  Single nucleotide polymorphism
Species:  Human
References:  39
The human 5-HT3B(I143T) polymorphism causes reduced functional responses to 5-HT mediated by heteromeric 5-HT3AB receptors and is associated with decreased cell surface expression.
Amino acids:  441
Type:  Single nucleotide polymorphism
Species:  Human
References:  101
Subunit Comments
The 5-HT3B subunit does not function as a homo-oligomer in recombinant expression systems and is retained in the endoplasmic reticulum [88]. Association with the 5-HT3A subunit facilitates trafficking of 5-HT3B to the plasma membrane as a heteromeric complex [88] with the suggested stoichiometry (5-HT3A)2(5-HT3B)3 [25]. Variants of the human 5-HT3B subunit canonical form have been postulated to exist in the intestine (the canonical form) and brain due to alternative promoters with the HTR3B gene that initiate transcription at different start sites [37]. One brain specific isoform (brain transcript 1) is predicted to differ from the canonical 5-HT3B subunit only within the signal peptide, whereas the second (brain transcript 2) is predicted to lack a large section of the extracellular N-terminal domain [37].

To cite this receptor data page, please use the following:

Sarah C. R. Lummis , Nicholas M. Barnes, Tim G. Hales, Beate Niesler, John A. Peters.
5-HT3 receptors: 5-HT3B. Last modified on 2010-07-01. Accessed on 2010-09-10. IUPHAR database (IUPHAR-DB), http://www.iuphar-db.org/DATABASE/ObjectDisplayForward?objectId=374.


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