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- W2898814165 abstract "Fragile X syndrome (FXS) is caused by the loss of fragile X mental retardation protein (FMRP), an RNA binding protein whose deficiency impacts many brain functions, including differentiation of adult neural stem cells (aNSCs). However, the mechanism by which FMRP influences these processes remains unclear. Here, we performed ribosome profiling and transcriptomic analysis of aNSCs in parallel from wild-type and Fmr1 knockout mice. Our data revealed diverse gene expression changes at both mRNA and translation levels. Many mitosis and neurogenesis genes were dysregulated primarily at the mRNA level, while numerous synaptic genes were mostly dysregulated at the translation level. Translational buffering, whereby changes in ribosome association with mRNA are compensated by alterations in RNA abundance, was also evident. Knockdown of NECDIN, an FMRP-repressed transcriptional factor, rescued neuronal differentiation. In addition, we discovered that FMRP regulates mitochondrial mRNA expression and energy homeostasis. Thus, FMRP controls diverse transcriptional and posttranscriptional gene expression programs critical for neural differentiation." @default.
- W2898814165 created "2018-11-09" @default.
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- W2898814165 date "2018-10-29" @default.
- W2898814165 modified "2023-09-30" @default.
- W2898814165 title "Regulatory discrimination of mRNAs by FMRP controls mouse adult neural stem cell differentiation" @default.
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- W2898814165 doi "https://doi.org/10.1073/pnas.1809588115" @default.
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- W2898814165 hasPublicationYear "2018" @default.
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