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An unbiased expression screen for synaptogenic proteins identifies the LRRTM protein family as synaptic organizers.


ABSTRACT: 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.

SUBMITTER: Linhoff MW 

PROVIDER: S-EPMC2746109 | biostudies-literature | 2009 Mar

REPOSITORIES: biostudies-literature

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An unbiased expression screen for synaptogenic proteins identifies the LRRTM protein family as synaptic organizers.

Linhoff Michael W MW   Laurén Juha J   Cassidy Robert M RM   Dobie Frederick A FA   Takahashi Hideto H   Nygaard Haakon B HB   Airaksinen Matti S MS   Strittmatter Stephen M SM   Craig Ann Marie AM  

Neuron 20090301 5


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 syna  ...[more]

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