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Relevance to Autism

Genetic association has been found between the PTGS2 gene and autism in a Korean population cohort (Yoo et al., 2008).

Molecular Function

The encoded protein is a key enzyme for prostaglandin synthesis. It has prostagl andin-endoperoxide synthase activity.

External Links

        

References

Type
Title
Type of Disorder
Associated Disorders
Author, Year
Primary
Association between PTGS2 polymorphism and autism spectrum disorders in Korean trios.
ASD
Support
Integrating de novo and inherited variants in 42
ASD
Support
Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes
ASD
Highly Cited
Suppression of intestinal polyposis in Apc delta716 knockout mice by inhibition of cyclooxygenase 2 (COX-2).
Highly Cited
COX-2, a synaptically induced enzyme, is expressed by excitatory neurons at postsynaptic sites in rat cerebral cortex.
Recent Recommendation
Autism-related behaviors in the cyclooxygenase-2-deficient mouse model.
Recent Recommendation
PGE2 glycerol ester, a COX-2 oxidative metabolite of 2-arachidonoyl glycerol, modulates inhibitory synaptic transmission in mouse hippocampal neurons.
Recent Recommendation
Contribution of inducible nitric oxide synthase and cyclooxygenase-2 to apoptosis induction in smooth chorion trophoblast cells of human fetal memb...

Rare

Variant ID
Variant Type
Allele Change
Residue Change
Inheritance Pattern
Inheritance Association
Family Type
Author, Year
 GEN205R001 
 synonymous_variant 
 c.1731C>T 
 p.Val577= 
 De novo 
  
  
 GEN205R002 
 inframe_deletion 
 c.1613_1615del 
 p.Gly538del 
 De novo 
  
 Simplex 

Common

Variant ID
Polymorphism
SNP ID
Allele Change
Residue Change
Population Origin
Population Stage
Author, Year
 GEN205C001 
 intron_variant 
 rs2745557 
 c.52+150T>C 
  
 Korean 
 Discovery 
Chromosome
CNV Locus
CNV Type
# of studies
Animal Model
1
Duplication
 44
 
1
Deletion
 2
 
1
Deletion
 2
 
1
Deletion
 1
 
1
Deletion
 3
 
1
Deletion-Duplication
 19
 

Model Summary

Mutants show increased ambulatory activity, increased repetitive digging, and increased anxiety. Changes in gene expression are also evident, especially in males.

References

Type
Title
Author, Year
Primary
Autism-related behaviors in the cyclooxygenase-2-deficient mouse model.

M_PTGS2_1_KI_HM

Model Type: Genetic
Model Genotype: Homozygous
Mutation: Ptgs2^Y385F (also known as Ptgs^2tm1.1Fun) mice are a genetic mouse model for selective COX2 (i.e., PTGS2) inactivation, which was created by a targeted point mutation of the Ptgs2 gene, resulting in a Y385F amino acid substitution, which results in the complete inhibition of COX2 activity (Yu et al., 2006).
Allele Type: LOF Knockin
Strain of Origin:
Genetic Background:
ES Cell Line:
Mutant ES Cell Line:
Model Source: Jackson Laboratory

M_PTGS2_1_KI_HM

Category
Entity
Quantity
Experimental Paradigm
Age at Testing
General locomotor activity: ambulatory activity1
Increased
Description: Mutants showed an increasein distance traveled compared to controls.
Exp Paradigm: NA
 Open field test
 4-6 weeks
Grip strength1
Decreased
Description: Mutants showed an increase in fall percentage compared to controls.
Exp Paradigm: NA
 Inverted grid test
 4-6 weeks
General locomotor activity: ambulatory activity1
Increased
Description: Mutants showed an increasein distance traveled compared to controls.
Exp Paradigm: NA
 Open field test
 8-11 weeks
Repetitive digging1
Increased
Description: Mutants showed an increase in the number of marbles buried compared to controls. moreover, male mutants showed a significant increase in the digging time and female mutants showed a trend towards an increase in the digging time (p=0.068) compared to controls.
Exp Paradigm: NA
 Marble-burying test
 8-11 weeks
Repetitive digging1
Increased
Description: Mutants showed an increase in the digging time and the number of marbles buried compared to controls.
Exp Paradigm: NA
 Marble-burying test
 4-6 weeks
Social approach1
Decreased
Description: Mutants showed a decrease in time spent in chamber containing a novel mouse compared to controls. however, mutants showed no change in time spent sniffing the novel mouse compared to controls.
Exp Paradigm: NA
 Three-chamber social approach test
 8-11 weeks
Anxiety1
Increased
Description: Mutants showed a decrease in time spent in the center of open field test compared to controls.
Exp Paradigm: NA
 Open field test
 8-11 weeks
Gene expression1
Decreased
Description: Mutants showed a decrease in expression of glo1, grm5, and mmp9 compared to controls.
Exp Paradigm: NA
 Quantitative pcr (qrt-pcr)
 P8
Gene expression1
Increased
Description: Mutants showed an increase in wnt2 expression compared to controls.
Exp Paradigm: NA
 Quantitative pcr (qrt-pcr)
 P8
Gene expression1
Decreased
Description: Mutants showed a decrease in glo1 expression compared to controls.
Exp Paradigm: NA
 Quantitative pcr (qrt-pcr)
 P8
Anxiety1
 No change
 Open field test
 4-6 weeks
Anxiety1
 No change
 Open field test
 8-11 weeks
Gene expression1
 No change
 Quantitative pcr (qrt-pcr)
 P8
Grip strength1
 No change
 Inverted grid test
 4-6 weeks
Grip strength1
 No change
 Inverted grid test
 8-11 weeks
Social approach1
 No change
 Three-chamber social approach test
 4-6 weeks
Social approach1
 No change
 Three-chamber social approach test
 8-11 weeks
 Not Reported: Circadian sleep/wake cycle, Communications, Developmental profile, Immune response, Learning & memory, Maternal behavior, Neuroanatomy / ultrastructure / cytoarchitecture, Neurophysiology, Physiological parameters, Seizure, Sensory


Interactor Symbol Interactor Name Interactor Organism Entrez ID Uniprot ID Interaction Type Evidence Reference
LMAN2L lectin, mannose-binding 2-like 81562 Q9H0V9 IP; LC-MS/MS
Huttlin EL , et al. 2015
MIR101-1 microRNA 101-1 406893 Luciferase reporter assay
Shao Y , et al. 2015

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