Identification of Synaptic Targets of Drosophila Pumilio

被引:37
作者
Chen, Gengxin [1 ]
Li, Wanhe [1 ,2 ]
Zhang, Qing-Shuo [1 ]
Regulski, Michael [1 ]
Sinha, Nishi [1 ]
Barditch, Jody [1 ]
Tully, Tim [1 ]
Krainer, Adrian R. [1 ]
Zhang, Michael Q. [1 ]
Dubnau, Josh [1 ]
机构
[1] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
[2] SUNY Stony Brook, Grad Program Mol & Cellular Biol, Stony Brook, NY 11794 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1371/journal.pcbi.1000026
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Drosophila Pumilio (Pum) protein is a translational regulator involved in embryonic patterning and germline development. Recent findings demonstrate that Pum also plays an important role in the nervous system, both at the neuromuscular junction (NMJ) and in long-term memory formation. In neurons, Pum appears to play a role in homeostatic control of excitability via down regulation of para, a voltage gated sodium channel, and may more generally modulate local protein synthesis in neurons via translational repression of eIF-4E. Aside from these, the biologically relevant targets of Pum in the nervous system remain largely unknown. We hypothesized that Pum might play a role in regulating the local translation underlying synapse-specific modifications during memory formation. To identify relevant translational targets, we used an informatics approach to predict Pum targets among mRNAs whose products have synaptic localization. We then used both in vitro binding and two in vivo assays to functionally confirm the fidelity of this informatics screening method. We find that Pum strongly and specifically binds to RNA sequences in the 3'UTR of four of the predicted target genes, demonstrating the validity of our method. We then demonstrate that one of these predicted target sequences, in the 3'UTR of discs large (dlg1), the Drosophila PSD95 ortholog, can functionally substitute for a canonical NRE (Nanos response element) in vivo in a heterologous functional assay. Finally, we show that the endogenous dlg1 mRNA can be regulated by Pumilio in a neuronal context, the adult mushroom bodies (MB), which is an anatomical site of memory storage.
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页数:14
相关论文
共 41 条
[1]   Maternal Pumilio acts together with Nanos in germline development in Drosophila embryos [J].
Asaoka-Taguchi, M ;
Yamada, M ;
Nakamura, A ;
Hanyu, K ;
Kobayashi, S .
NATURE CELL BIOLOGY, 1999, 1 (07) :431-437
[2]   Neuronal homeostasis through translational control [J].
Baines, RA .
MOLECULAR NEUROBIOLOGY, 2005, 32 (02) :113-121
[3]   Binding specificity and mRNA targets of a C-elegans PUF protein, FBF-1 [J].
Bernstein, D ;
Hook, B ;
Hajarnavis, A ;
Opperman, L ;
Wickens, M .
RNA, 2005, 11 (04) :447-458
[4]   Regulation of synapse structure and function by the Drosophila tumor suppressor gene dlg [J].
Budnik, V ;
Koh, YH ;
Guan, B ;
Hartmann, B ;
Hough, C ;
Woods, D ;
Gorczyca, M .
NEURON, 1996, 17 (04) :627-640
[5]   Discs-large (DLG) is clustered by presynaptic innervation and regulates postsynaptic glutamate receptor subunit composition in Drosophila [J].
Chen, KY ;
Featherstone, DE .
BMC BIOLOGY, 2005, 3 (1)
[6]   Engineering RNA sequence specificity of Pumilio repeats [J].
Cheong, Cheorn-Gil ;
Hall, Traci M. Tanaka .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (37) :13635-13639
[7]  
Clarke PA, 1999, METH MOL B, V118, P1
[8]   Associative learning disrupted by impaired G(s) signaling in Drosophila mushroom bodies [J].
Connolly, JB ;
Roberts, IJH ;
Armstrong, JD ;
Kaiser, K ;
Forte, M ;
Tully, T ;
OKane, CJ .
SCIENCE, 1996, 274 (5295) :2104-2107
[9]   DISCRETE SEQUENCE ELEMENTS CONTROL POSTERIOR POLE ACCUMULATION AND TRANSLATIONAL REPRESSION OF MATERNAL CYCLIN-B RNA IN DROSOPHILA [J].
DALBY, B ;
GLOVER, DM .
EMBO JOURNAL, 1993, 12 (03) :1219-1227
[10]   The staufen/pumilio pathway is involved in Drosophila long-term memory [J].
Dubnau, J ;
Chiang, AS ;
Grady, L ;
Barditch, J ;
Gossweiler, S ;
McNeil, J ;
Smith, P ;
Buldoc, F ;
Scott, R ;
Certa, U ;
Broger, C ;
Tully, T .
CURRENT BIOLOGY, 2003, 13 (04) :286-296