Staufen- and FMRP-containing neuronal RNPs are structurally and functionally related to somatic P bodies

被引:286
作者
Barbee, Scott A.
Estes, Patricia S.
Cziko, Anne-Marie
Hillebrand, Jens
Luedeman, Rene A.
Coller, Jeff M.
Johnson, Nick
Howlett, Iris C.
Geng, Cuiyun
Ueda, Ryu
Brand, Andrea H.
Newbury, Sarah F.
Wilhelm, James E.
Levine, Richard B.
Nakamura, Akira
Parker, Roy [1 ]
Ramaswami, Mani
机构
[1] Univ Arizona, Dept Mol & Cellular Biol, Tucson, AZ 85721 USA
[2] Univ Arizona, ARL Div Neurobiol, Tucson, AZ 85721 USA
[3] Univ Arizona, Howard Hughes Med Inst, Tucson, AZ 85721 USA
[4] Univ Dublin Trinity Coll, Smurfit Inst Genet & TCIN, Dublin 2, Ireland
[5] Univ Texas, Inst Mol & Cellular Biol, Sect Mol Cell & Dev Biol, Austin, TX 78712 USA
[6] Univ Cambridge, Dept Genet, Cambridge CB2 1QR, England
[7] Univ Cambridge, Wellcome CRC Inst, Cambridge CB2 1QR, England
[8] Univ Newcastle, Sch Med, Inst Cell & Mol Biosci, Newcastle Upon Tyne, Tyne & Wear, England
[9] Univ Calif San Diego, Sect Cell & Dev Biol, Div Biol Sci, La Jolla, CA 92093 USA
[10] RIKEN, Ctr Dev Biol, Lab Germline Dev, Chuo Ku, Kobe, Hyogo 6500047, Japan
[11] Natl Inst Genet, Invertebrate Genet Lab, Genet Strains Res Ctr, Mishima, Shizuoka 4118540, Japan
基金
英国医学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
D O I
10.1016/j.neuron.2006.10.028
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Local control of mRNA translation modulates neuronal development, synaptic plasticity, and memory formation. A poorly understood aspect of this control is the role and composition of ribonucleoprotein (RNP) particles that mediate transport and translation of neuronal RNAs. Here, we show that staufen- and FMRP-containing RNPs in Drosophila neurons contain proteins also present in somatic "P bodies," including the RNA-degradative enzymes Dcp1p and Xrn1p/Pacman and crucial components of miRNA (argonaute), NMD (Upf1p), and general translational repression (Dhh1p/Me31B) pathways. Drosophila Me31B is shown to participate (1) with an FMRP-associated, P body protein (Scd6p/trailer hitch) in FMRP-driven, argonaute-dependent translational repression in developing eye imaginal discs; (2) in dendritic elaboration of larval sensory neurons; and (3) in bantam miRNA-mediated translational repression in wing imaginal discs. These results argue for a conserved mechanism of translational control critical to neuronal function and open up new experimental avenues for understanding the regulation of mRNA function within neurons.
引用
收藏
页码:997 / 1009
页数:13
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