Microarray Identification of FMRP-Associated Brain mRNAs and Altered mRNA Translational Profiles in Fragile X Syndrome

Fragile X syndrome results from the absence of the RNA binding FMR protein. Here, mRNA was coimmunoprecipitated with the FMRP ribonucleoprotein complex and used to interrogate microarrays. We identified 432 associated mRNAs from mouse brain. Quantitative RT-PCR confirmed some to be >60-fold enric...

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Veröffentlicht in:Cell 2001-11, Vol.107 (4), p.477-487
Hauptverfasser: Brown, Victoria, Jin, Peng, Ceman, Stephanie, Darnell, Jennifer C., O'Donnell, William T., Tenenbaum, Scott A., Jin, Xiaokui, Feng, Yue, Wilkinson, Keith D., Keene, Jack D., Darnell, Robert B., Warren, Stephen T.
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Sprache:eng
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Zusammenfassung:Fragile X syndrome results from the absence of the RNA binding FMR protein. Here, mRNA was coimmunoprecipitated with the FMRP ribonucleoprotein complex and used to interrogate microarrays. We identified 432 associated mRNAs from mouse brain. Quantitative RT-PCR confirmed some to be >60-fold enriched in the immunoprecipitant. In parallel studies, mRNAs from polyribosomes of fragile X cells were used to probe microarrays. Despite equivalent cytoplasmic abundance, 251 mRNAs had an abnormal polyribosome profile in the absence of FMRP. Although this represents
ISSN:0092-8674
1097-4172
DOI:10.1016/S0092-8674(01)00568-2