Abstract
In the Fmr1 knockout mice, a model for fragile X mental retardation syndrome, the levels of regulator of G-protein signaling (Rgs) 4 but not Rgs2 mRNA were considerably reduced (65% from control) in the cerebral cortex and hippocampal CA1 region. The expression of Rgs4 was normal in animals lacking a related protein, FXR2P, indicating that the decrease in Rgs4 expression was specific for the absence of FMRP, and suggests a role for FMRP in G-protein signaling.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Animals, Newborn
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Brain / growth & development
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Brain / metabolism*
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Fragile X Mental Retardation Protein
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Gene Expression / physiology*
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In Situ Hybridization / methods
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Mice
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Mice, Knockout
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Nerve Tissue Proteins / deficiency*
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Nerve Tissue Proteins / genetics
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RGS Proteins / genetics
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RGS Proteins / metabolism*
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RNA, Messenger / metabolism
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RNA-Binding Proteins / genetics
Substances
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Fmr1 protein, mouse
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Nerve Tissue Proteins
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RGS Proteins
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RNA, Messenger
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RNA-Binding Proteins
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Fragile X Mental Retardation Protein
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RGS4 protein