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FMRP Control of Ribosome Translocation Promotes Chromatin Modifications and Alternative Splicing of Neuronal Genes Linked to Autism
Silencing of FMR1 and loss of its gene product, FMRP, results in fragile X syndrome (FXS). FMRP binds brain mRNAs and inhibits polypeptide elongation. Using ribosome profiling of the hippocampus, we find that ribosome footprint levels in Fmr1-deficient tissue mostly reflect changes in RNA abundance....
Autores principales: | Shah, Sneha, Molinaro, Gemma, Liu, Botao, Wang, Ruijia, Huber, Kimberly M., Richter, Joel D. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7179797/ https://www.ncbi.nlm.nih.gov/pubmed/32234480 http://dx.doi.org/10.1016/j.celrep.2020.02.076 |
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