Identification of mouse YB1/p50 as a component of the FMRP-associated mRNP particle

被引:70
作者
Ceman, S
Nelson, R
Warren, ST
机构
[1] Emory Univ, Sch Med, Howard Hughes Med Inst, Rollins Res Ctr, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Dept Biochem, Atlanta, GA 30322 USA
[3] Emory Univ, Sch Med, Dept Pediat, Atlanta, GA 30322 USA
[4] Emory Univ, Sch Med, Dept Genet, Atlanta, GA 30322 USA
关键词
fragile X syndrome; FMRP; FMR1; mRNP; p50; YB1;
D O I
10.1006/bbrc.2000.4035
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 identified an additional protein that coimmunoprecipitates 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 kTPa 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. (C) 2000 Academic Press.
引用
收藏
页码:904 / 908
页数:5
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