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The fragile X mental retardation protein is associated with ribosomes

Nature Genetics volume 12, pages 91–93 (1996)Cite this article

Abstract

Fragile X mental retardation syndrome is one of the most common human genetic diseases. Patients carry a methylated expansion of a CGG repeat resulting in the silencing of the FMR1 gene1–5 that codes for a heterogeneous set of proteins (FMRP)6–9. FMRP is abundant in neurons and is also widely expressed, albeit at different levels, in various human and mouse tissues. FMRP is cytoplasmic6,7 and contains two conserved RNA-binding domains, suggesting a possible involvement in RNA metabolism10–12. However, its function remains unknown. To understand the possible role(s) of FMRP in cellular processes, we investigated its association with cellular structures. We observed that FMRP cosediments with polyribosomes after ultracentrifugation in sucrose density gradients. Following the dissociation of ribosomes into their components, we found that FMRP is associated with the ribosomal 60S subunit and possesses the characteristics of a nonintegral ribosomal protein. Immunofluorescence studies reveal a tight colocalisation of FMRP with cytoplasmic ribosomes in NIH 3T3 and HeLa cells and in primary cultures of neurons, confirming our biochemical observations. We propose that fragile X mental retardation might result from defects in the translational machinery due to the absence of FMRP.

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Author notes

  1. Edouard W. Khandjian: Correspondence should be addressed to E.W.K.

Authors and Affiliations

  1. Unité de recherche en génétique humaine et moléculaire, Hôpital Saint-François d'Assise, Québec, G1L 315, Canada

    Edouard W. Khandjian, François Corbin & François Rousseau

  2. Département de biochimie, Faculté de médecine, Université Lavaly,

    Edouard W. Khandjian, François Corbin & François Rousseau

  3. Organogel Canada Ltée, Québec, Canada

    Stephane Woerly

Authors
  1. Edouard W. Khandjian
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  2. François Corbin
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  3. Stephane Woerly
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  4. François Rousseau
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Khandjian, E., Corbin, F., Woerly, S. et al. The fragile X mental retardation protein is associated with ribosomes. Nat Genet 12, 91–93 (1996). https://doi.org/10.1038/ng0196-91

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