An Unbiased Expression Screen for Synaptogenic Proteins Identifies the LRRTM Protein Family as Synaptic Organizers

被引:291
作者
Linhoff, Michael W. [1 ,2 ,3 ]
Lauren, Juha [4 ,5 ,6 ]
Cassidy, Robert M. [1 ,3 ]
Dobie, Frederick A. [1 ,3 ]
Takahashi, Hideto [1 ,3 ]
Nygaard, Haakon B. [4 ,5 ]
Airaksinen, Matti S. [6 ]
Strittmatter, Stephen M. [4 ,5 ]
Craig, Ann Marie [1 ,2 ,3 ]
机构
[1] Univ British Columbia, Brain Res Ctr, Vancouver, BC V6T 2B5, Canada
[2] Washington Univ, Sch Med, Dept Anat & Neurobiol, St Louis, MO 63110 USA
[3] Univ British Columbia, Dept Psychiat, Vancouver, BC V6T 2B5, Canada
[4] Yale Univ, Sch Med, Dept Neurol, New Haven, CT 06520 USA
[5] Yale Univ, Sch Med, Dept Neurobiol, New Haven, CT 06520 USA
[6] Univ Helsinki, Ctr Neurosci, FIN-00014 Helsinki, Finland
关键词
ADHESION-LIKE MOLECULES; RICH REPEAT PROTEINS; LENGTH CDNA CLONING; FULL-LENGTH; EXCITATORY SYNAPSES; INHIBITORY SYNAPSES; CAP-TRAPPER; NEUROLIGINS; RECEPTOR; PROMOTES;
D O I
10.1016/j.neuron.2009.01.017
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Delineating the molecular basis of synapse development is crucial for understanding brain function. Cocultures of neurons with transfected fibroblasts have demonstrated the synapse-promoting activity of candidate molecules. Here, we performed an unbiased expression screen for synaptogenic proteins in the coculture assay using custom-made cDNA libraries. Reisolation of NGL-3/LRRC4B and neuroligin-2 accounts for a minority of positive clones, indicating that current understanding of mammalian synaptogenic proteins is incomplete. We identify LRRTM1 as a transmembrane protein that induces presynaptic differentiation in contacting axons. All four LRRTM family members exhibit synaptogenic activity, LRRTMs localize to excitatory synapses, and artificially induced clustering of LRRTMs mediates postsynaptic differentiation. We generate LRRTM1(-/-) mice and reveal altered distribution of the vesicular glutamate transporter VGLUT1, confirming an in vivo synaptic function. These results suggest a prevalence of LRR domain proteins in trans-synaptic signaling and provide a cellular basis for the reported linkage of LRRTM1 to handedness and schizophrenia.
引用
收藏
页码:734 / 749
页数:16
相关论文
共 56 条
[1]   Sequence variants in SLITRK1 are associated with Tourette's syndrome [J].
Abelson, JF ;
Kwan, KY ;
O'Roak, BJ ;
Baek, DY ;
Stillman, AA ;
Morgan, TM ;
Mathews, CA ;
Pauls, DA ;
Rasin, MR ;
Gunel, M ;
Davis, NR ;
Ercan-Sencicek, AG ;
Guez, DH ;
Spertus, JA ;
Leckman, JF ;
Dure, LS ;
Kurlan, R ;
Singer, HS ;
Gilbert, DL ;
Farhi, A ;
Louvi, A ;
Lifton, RP ;
Sestan, N ;
State, MW .
SCIENCE, 2005, 310 (5746) :317-320
[2]   Genetic analysis of synaptic target recognition and assembly [J].
Ackley, BD ;
Jin, YS .
TRENDS IN NEUROSCIENCES, 2004, 27 (09) :540-547
[3]   Postsynaptic EphrinB3 promotes shaft glutamatergic synapse formation [J].
Aoto, Jason ;
Ting, Pamela ;
Maghsoodi, Bita ;
Xu, Nanjie ;
Henkemeyer, Mark ;
Chen, Lu .
JOURNAL OF NEUROSCIENCE, 2007, 27 (28) :7508-7519
[4]   Identification and characterization of Slitrk, a novel neuronal transmembrane protein family controlling neurite outgrowth [J].
Aruga, J ;
Mikoshiba, K .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2003, 24 (01) :117-129
[5]   Role of β-catenin in synaptic vesicle localization and presynaptic assembly [J].
Bamji, SX ;
Shimazu, K ;
Kimes, N ;
Huelsken, J ;
Birchmeier, W ;
Lu, B ;
Reichardt, LF .
NEURON, 2003, 40 (04) :719-731
[6]   SynCAM, a synaptic adhesion molecule that drives synapse assembly [J].
Biederer, T ;
Sara, Y ;
Mozhayeva, M ;
Atasoy, D ;
Liu, XR ;
Kavalali, ET ;
Südhof, TC .
SCIENCE, 2002, 297 (5586) :1525-1531
[7]   Mixed-culture assays for analyzing neuronal synapse formation [J].
Biederer, Thomas ;
Scheiffele, Peter .
NATURE PROTOCOLS, 2007, 2 (03) :670-676
[8]  
Carninci P, 1999, METHOD ENZYMOL, V303, P19
[9]   High-efficiency full-length cDNA cloning by biotinylated CAP trapper [J].
Carninci, P ;
Kvam, C ;
Kitamura, A ;
Ohsumi, T ;
Okazaki, Y ;
Itoh, M ;
Kamiya, M ;
Shibata, K ;
Sasaki, N ;
Izawa, M ;
Muramatsu, M ;
Hayashizaki, Y ;
Schneider, C .
GENOMICS, 1996, 37 (03) :327-336
[10]   Control of excitatory and inhibitory synapse formation by neuroligins [J].
Chih, B ;
Engelman, H ;
Scheiffele, P .
SCIENCE, 2005, 307 (5713) :1324-1328