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 Animal Model >> null >> M_MECP2_57_KI_HE_GABRB3-CRE Construct Details
 Model Details :M_MECP2_57_KI_HE_GABRB3-CRE
 
Model Type RESCUE-Genetic
Model Genotype Hemizygous
Mutation Male knockin mice harboring an arginine-to-cysteine missense R306 mutation in Mecp2 (Mecp2^R306C), a common allele in Rett syndrome patients together with Advillin-Cre (Advillin-Cre; Mecp2^C/y). Male Advillin-Cre; Mecp2^C/y mice were intraperitoneally injected at P5 with AAV.FLEx.GABRB3.mCHERRY to restore GABRB3 expression selectively in peripheral somatosensory neurons. Mecp2^R306C littermate mice lacking the Advillin-Cre allele and injected with AAV.FLEx.GABRB3.mCHERRY served as a control together with wild-type littermates with and without the Advillin-Cre allele. Intraperitoneal injection of Advillin-Cre; Mecp2^R306C mice, but not Mecp2^R306C mice lacking the Advillin-Cre allele, with AAV.FLEx.GABRB3.mCHERRY led to transduction of all types of DRG sensory neurons. Wildtype controls were Mecp2^R/y male littermates injected with AAV.FLEx.GABRB3.mCHERRY.
Allele Type ASD LOF knockin
Strain of Origin Not specified
Genetic Background C57BL/6J
ES Cell Line
Mutant ES Cell Line 129/Ola E14 TG2a mouse ES cells
Model Source Michael Greenberg; Lyst et al., 2013; PMID 23770565
Reference Orefice LL , et al. 2019
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