Abstract
Fragile X mental retardation is caused by the absence of FMRP, an RNA-binding protein found in a large mRNP complex. Although there is evidence that FMRP exists as a homo-multimer, additional proteins have been identified that associate with FMRP in the mRNP. The autosomal paralogs of FMRP, FXR1P, and FXR2P, associate with FMRP, as do nucleolin and NUFIP1, all RNA binding proteins. Using cell lines that were stably transfected with Flag-Fmr1, we identiffed an additional protein that coimmunoprecipitares with FMRP. The approximately 50 kDa protein was identified by mass spectrometry as mouse Y box-binding protein 1 (YB1), which is 97% identical to the core mRNP protein p50, an RNA-binding protein. An anti-p50 antiserum recognized the 50 kDa protein, confirming the identification. The association of the FMRP-mRNP with a Y box protein, the latter commonly found in mRNPs, further suggests the involvement of FMRP in translation modulation.
Original language | English (US) |
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Pages (from-to) | 904-908 |
Number of pages | 5 |
Journal | Biochemical and Biophysical Research Communications |
Volume | 279 |
Issue number | 3 |
DOIs | |
State | Published - Dec 29 2000 |
Externally published | Yes |
Keywords
- FMR1
- FMRP
- Fragile X syndrome
- MRNP
- YB1
- p50
ASJC Scopus subject areas
- Biophysics
- Biochemistry
- Molecular Biology
- Cell Biology