Pglyrp2-knockout mice were shown to exhibit altered expression of the autism risk gene c-Met, as well as sex-dependent changes in social behavior, similar to mice with manipulated microbiota (Arentsen et al., 2016).
Molecular Function
This gene encodes a peptidoglycan recognition protein, which belongs to the N-acetylmuramoyl-L-alanine amidase 2 family. This protein hydrolyzes the link between N-acetylmuramoyl residues and L-amino acid residues in bacterial cell wall glycopeptides, and thus may play a scavenger role by digesting biologically active peptidoglycan into biologically inactive fragments.
External Links
References
Type
Title
Type of Disorder
Associated Disorders
Author, Year
Primary
The bacterial peptidoglycan-sensing molecule Pglyrp2 modulates brain development and behavior.
Pglyrp2 knockout mice have abnormal expression of the brain circuit formation markers, Met and BDNF, and synaptogenesis marker, Syp. Pglyrp2 knockout mice exhibit increased social approach for male and female mice in three-chamber tests.
References
Type
Title
Author, Year
Primary
The bacterial peptidoglycan-sensing molecule Pglyrp2 modulates brain development and behavior.
Model Type:
Genetic
Model Genotype:
Homozygous
Mutation:
A construct containing EGFP-floxed Neo cassette is introduced inframe downstream to the start codon in exon 1, which results in a null allele after removing the Neo gene by Cre.
Allele Type: Targeted (Knock Out)
Strain of Origin: Not specified
Genetic Background: C57BL/6
ES Cell Line: 129S4/SvJae-Tg(Prm-cre)70Og
Mutant ES Cell Line: Model Source: Jax Lab
Description: Increased gene expression of met or syp in the prefrontal cortex of pglyrp2 nulls and in the amygdala of female nulls or in the prefrontal cortex and striatum of female nulls, respectively
Exp Paradigm: Rt-qpcr: met, bdnf, syp
Description: Decreased gene expression of met or bdnf in the striatum of pglyrp2 null female mice or male mice, respectively
Exp Paradigm: Rt-qpcr: met, bdnf, syp