کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
4312542 1612965 2014 4 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Impaired sensorimotor gating in Fmr1 knock out and Fragile X premutation model mice
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب رفتاری
پیش نمایش صفحه اول مقاله
Impaired sensorimotor gating in Fmr1 knock out and Fragile X premutation model mice
چکیده انگلیسی


• FMR1 KO Fragile X syndrome model mice show impaired prepulse inhibition (PPI).
• CGG repeat knockin FXTAS model mice show impaired prepulse inhibition.
• These prepulse inhibition abnormalities in CGG knockin mice are age-dependent.
• Fmr1 KO and CGG knockin animals share an impaired PPI phenotype.

Fragile X syndrome (FXS) is a common inherited cause of intellectual disability that results from a CGG repeat expansion in the FMR1 gene. Large repeat expansions trigger both transcriptional and translational suppression of Fragile X protein (FMRP) production. Fragile X-associated Tremor/Ataxia Syndrome (FXTAS) is an allelic neurodegenerative disease caused by smaller “pre-mutation” CGG repeat expansions that enhance FMR1 transcription but lead to translational inefficiency and reduced FMRP expression in animal models. Sensorimotor gating as measured by pre-pulse inhibition (PPI) is altered in both FXS patients and Fmr1 knock out (KO) mice. Similarly, FXTAS patients have demonstrated PPI deficits. Recent work suggests there may be overlapping synaptic defects between Fmr1 KO and CGG knock-in premutation mouse models (CGG KI). We therefore sought to interrogate PPI in CGG KI mice. Using a quiet PPI protocol more akin to human testing conditions, we find that Fmr1 KO animals have significantly impaired PPI. Using this same protocol, we find CGG KI mice demonstrate an age-dependent impairment in PPI compared to wild type (WT) controls. This study describes a novel phenotype in CGG KI mice that can be used in future therapeutic development targeting premutation associated symptoms.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Behavioural Brain Research - Volume 267, 1 July 2014, Pages 42–45
نویسندگان
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