Progranulin is an FMRP target that influences macroorchidism but not behaviour in a mouse model of Fragile X Syndrome

dc.contributor.authorLife, Benjamin
dc.contributor.authorBettio, Luis E. B.
dc.contributor.authorGantois, Ilse
dc.contributor.authorChristie, Brian R.
dc.contributor.authorLeavitt, Blair R.
dc.date.accessioned2024-01-04T19:31:46Z
dc.date.available2024-01-04T19:31:46Z
dc.date.copyright2023en_US
dc.date.issued2023
dc.descriptionThe authors would like to thank Ge Lu and Alissandra de Moura Gomes for their technical expertise in collecting tissue from Fmr1 KO and wild-type mice. We are also grateful to Dr. Terri Petkau for developing the Golgi-cox protocol used in this manuscript.en_US
dc.description.abstractA growing body of evidence has implicated progranulin in neurodevelopment and indicated that aberrant progranulin expression may be involved in neurodevelopmental disease. Specifically, increased progranulin expression in the prefrontal cortex has been suggested to be pathologically relevant in male Fmr1 knockout (Fmr1 KO) mice, a mouse model of Fragile X Syndrome (FXS). Further investigation into the role of progranulin in FXS is warranted to determine if therapies that reduce progranulin expression represent a viable strategy for treating patients with FXS. Several key knowledge gaps remain. The mechanism of increased progranulin expression in Fmr1 KO mice is poorly understood and the extent of progranulin's involvement in FXS-like phenotypes in Fmr1 KO mice has been incompletely explored. To this end, we have performed a thorough characterization of progranulin expression in Fmr1 KO mice. We find that the phenomenon of increased progranulin expression is post-translational and tissue-specific. We also demonstrate for the first time an association between progranulin mRNA and FMRP, suggesting that progranulin mRNA is an FMRP target. Subsequently, we show that progranulin over-expression in Fmr1 wild-type mice causes reduced repetitive behaviour engagement in females and mild hyperactivity in males but is largely insufficient to recapitulate FXS-associated behavioural, morphological, and electrophysiological abnormalities. Lastly, we determine that genetic reduction of progranulin expression on an Fmr1 KO background reduces macroorchidism but does not alter other FXS-associated behaviours or biochemical phenotypes.en_US
dc.description.reviewstatusRevieweden_US
dc.description.scholarlevelFacultyen_US
dc.description.sponsorshipThis work was partially supported by the British Columbia Children’s Hospital Research Institute’s Brain, Behaviour and Development research theme.en_US
dc.identifier.citationLife, B., Bettio, L. E. B., Gantois, I., Christie, B. R., & Leavitt, B. R. (2023). Progranulin is an FMRP target that influences macroorchidism but not behaviour in a mouse model of Fragile X Syndrome. Current Research in Neurobiology, 5, 100094. https://doi.org/10.1016/j.crneur.2023.100094en_US
dc.identifier.urihttps://doi.org/10.1016/j.crneur.2023.100094
dc.identifier.urihttp://hdl.handle.net/1828/15791
dc.language.isoenen_US
dc.publisherCurrent Research in Neurobiologyen_US
dc.subjectProgranulinen_US
dc.subjectFragile X Syndromeen_US
dc.subjectAutism spectrum disorderen_US
dc.subjectNeurodevelopmenten_US
dc.subjectMouse modelsen_US
dc.titleProgranulin is an FMRP target that influences macroorchidism but not behaviour in a mouse model of Fragile X Syndromeen_US
dc.typeArticleen_US

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