RNAs that interact with the Fragile X syndrome RNA binding protein FMRP

被引:71
|
作者
Sung, YJ
Conti, J
Currie, JR
Brown, WT
Denman, RB
机构
[1] New York State Inst Basic Res Dev Disabil, Dept Mol Biol, Staten Isl, NY 10314 USA
[2] New York State Inst Basic Res Dev Disabil, Dept Human Genet, Staten Isl, NY 10314 USA
关键词
D O I
10.1006/bbrc.2000.3405
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
The Fragile X protein FMRP is an RNA binding protein whose targets are not well known; yet, these RNAs may play an integral role in the disease's etiology, Using a biotinylated-FMRP affinity resin, we isolated RNAs from the parietal cortex of a normal adult that bound FMRP, These RNAs were amplified by differential display (DDRT-PCR) and cloned and their identities determined. Nine candidate RNAs were isolated; five RNAs, including FMR1 mRNA, encoded known proteins. Four others were novel. The specificity of binding was demonstrated for each candidate RNA. The domains required for binding a subset of the RNAs were delineated using FMRP truncation mutant proteins and it was shown that only the KH2 domain was required for binding. Binding occurred independently of homoribopolymer binding to the C-terminal arginine-glycine-rich region (RGG box), suggesting that FMRP may bind multiple RNAs simultaneously. (C) 2000 Academic Press.
引用
收藏
页码:973 / 980
页数:8
相关论文
共 50 条
  • [21] FMRP expression as a potential prognostic indicator in fragile X syndrome.
    Tassone, F
    Hagerman, RJ
    Ikle, D
    Dyer, PN
    Lampe, M
    Willemsen, R
    Oostra, BA
    Taylor, AK
    AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) : A321 - A321
  • [22] Biology of the fragile X mental retardation protein, an RNA-binding protein
    Khandjian, EW
    BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE, 1999, 77 (04): : 331 - 342
  • [23] The Fragile X Syndrome-Related Protein, FMRP, Modulates Innate Immune Gene Expression in Macrophages
    Vail, Krystal J.
    Patrick, Kristin L.
    Watson, Robert
    Fischer, Tracy
    FASEB JOURNAL, 2022, 36
  • [24] Co-regulation of mRNA translation by TDP-43 and Fragile X Syndrome protein FMRP
    Majumder, Pritha
    Chu, Jen-Fei
    Chatterjee, Biswanath
    Swamy, Krishna B. S.
    Shen, Che-Kun James
    ACTA NEUROPATHOLOGICA, 2016, 132 (05) : 721 - 738
  • [25] Loss of the fragile X syndrome protein FMRP results in misregulation of nonsense-mediated mRNA decay
    Tatsuaki Kurosaki
    Naoto Imamachi
    Christoph Pröschel
    Shuhei Mitsutomi
    Rina Nagao
    Nobuyoshi Akimitsu
    Lynne E. Maquat
    Nature Cell Biology, 2021, 23 : 40 - 48
  • [26] Co-regulation of mRNA translation by TDP-43 and Fragile X Syndrome protein FMRP
    Pritha Majumder
    Jen-Fei Chu
    Biswanath Chatterjee
    Krishna B. S. Swamy
    Che-Kun James Shen
    Acta Neuropathologica, 2016, 132 : 721 - 738
  • [27] Loss of the fragile X syndrome protein FMRP results in misregulation of nonsense-mediated mRNA decay
    Kurosaki, Tatsuaki
    Imamachi, Naoto
    Proschel, Christoph
    Mitsutomi, Shuhei
    Nagao, Rina
    Akimitsu, Nobuyoshi
    Maquat, Lynne E.
    NATURE CELL BIOLOGY, 2021, 23 (01) : 40 - 48
  • [28] Detection and Quantification of the Fragile X Mental Retardation Protein 1 (FMRP)
    LaFauci, Giuseppe
    Adayev, Tatyana
    Kascsak, Richard
    Brown, W. Ted
    GENES, 2016, 7 (12):
  • [29] Fragile X Mental Retardation Protein FMRP Binds mRNAs in the Nucleus
    Kim, Miri
    Bellini, Michel
    Ceman, Stephanie
    MOLECULAR AND CELLULAR BIOLOGY, 2009, 29 (01) : 214 - 228
  • [30] The RNA binding protein FMRP: new connections and missing links
    Schaeffer, C
    Beaulande, M
    Ehresmann, C
    Ehresmann, B
    Moine, H
    BIOLOGY OF THE CELL, 2003, 95 (3-4) : 221 - 228