کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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6263956 | 1613943 | 2013 | 11 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Research ReportCorrecting deregulated Fxyd1 expression ameliorates a behavioral impairment in a mouse model of Rett syndrome Research ReportCorrecting deregulated Fxyd1 expression ameliorates a behavioral impairment in a mouse model of Rett syndrome](/preview/png/6263956.png)
Rett syndrome (RTT) is an X-linked neurodevelopmental disorder caused by mutations in the MECP2. Several genes have been shown to be MECP2 targets. We previously identified FXYD1 (encoding phospholemman; a protein containing the motif phenylalanine-X-tyrosine-aspartate), a gene encoding a transmembrane modulator of the Na, K-ATPase (NKA) enzyme, as one of them. In the absence of MECP2, FXYD1 expression is increased in the frontal cortex (FC) of both RTT patients and Mecp2Bird null mice. Here, we show that Fxyd1 mRNA levels are also increased in the FC and hippocampus (HC) of male mice carrying a truncating mutation of the Mecp2 gene (Mecp2308). To test the hypothesis that some of the behavioral phenotypes seen in these Mecp2 mutants could be ameliorated by genetically preventing the Fxyd1 response to MECP2 deficiency, we crossed Fxyd1 null male mice with Mecp2308 heterozygous females and behaviorally tested the adult male offspring. Mecp2308 mice had impaired HC-dependent novel location recognition, and this impairment was rescued by deletion of both Fxyd1 alleles. No other behavioral or sensorimotor impairments were rescued. These results indicate that reducing FXYD1 levels improves a specific cognitive impairment in MECP2-deficient mice.
⺠Fxyd1 expression increased in frontal cortex of Mecp2308 mutant male mice. ⺠Fxyd1 mRNA levels increased in hippocampus of Mecp2308 mutant male mice. ⺠Mecp2308 mutant mice have impaired hippocampus-dependent novel location recognition. ⺠This impairment is rescued by deletion of the Fxyd1 gene.
Journal: Brain Research - Volume 1496, 16 February 2013, Pages 104-114