82-FIP, a novel FMRP (Fragile X Mental Retardation Protein) interacting protein, shows a cell cycle-dependent intracellular localization

被引:58
作者
Bardoni, B
Castets, M
Huot, ME
Schenck, A
Adinolfi, S
Corbin, F
Pastore, A
Khandjian, EW
Mandel, JL
机构
[1] ULP, INSERM, CNRS, Inst Genet & Biol Mol & Cellulaire, F-67404 Illkirch Graffenstaden, France
[2] CHUQ, Hop St Francois Assise, Ctr Rech, Unite Rech Genet Humaine & Mol, Quebec City, PQ G1L 3L5, Canada
[3] Natl Inst Med Res, London NW7 1AA, England
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
D O I
10.1093/hmg/ddg181
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
FMRP is an RNA binding protein whose absence produces pathological manifestations of the fragile-X syndrome. FMRP is a component of mRNP complexes found in association with actively translating polyribosomes, RNA complexes trafficking in neurites, RNA granules in cytoplasm and, in Drosophila, with the RNAi machinery. We report here the identification and characterization of a novel FMRP-interacting protein associated to polyribosomes as a component of mRNP complexes containing FMRP. We named this protein 82-FIP (82-kD FMRP Interacting Protein). FMRP interacts with 82-FIP through a novel interaction motif located in its N-terminal region. The distribution of 82-FIP in different areas of the brain is very similar to that of FMRP. However, unlike FMRP, 82-FIP is found in both nucleus and cytoplasm in some neurons, while it appears only cytoplasmic in others. Subcellular distribution of 82-FIP is cell cycle-dependent in cultured cells, suggesting that the composition of some FMRP-containing RNP complexes may be cell cycle-modulated.
引用
收藏
页码:1689 / 1698
页数:10
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