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The Journal of Neuroscience, 2001, 21:RC161:1-5
RAPID COMMUNICATION
Synapse Formation between Central Neurons Requires Postsynaptic
Expression of the MEN1 Tumor Suppressor Gene
Ronald E.
van Kesteren1,
Naweed I.
Syed2,
David W.
Munno2,
Jildau
Bouwman1,
Zhong-Ping
Feng2,
Wijnand P. M.
Geraerts1, and
August B.
Smit1
1 Department of Molecular and Cellular Neurobiology,
Research Institute Neurosciences, Vrije Universiteit, 1081HV
Amsterdam, The Netherlands, and 2 Respiratory and
Neuroscience Research Groups, Faculty of Medicine, University of
Calgary, Alberta, Canada T2N 4N1
Synapse formation is a crucial step in the development of neuronal
circuits and requires precise coordination of presynaptic and
postsynaptic activities. However, molecular mechanisms that control the
formation of functionally mature synaptic contacts, in particular
between central neurons, remain poorly understood. To identify genes
that are involved in the formation of central synapses, we made use of
molluscan neurons that in culture form synaptic contacts between their
somata (soma-soma synapses) in the absence of neurite outgrowth. Using
single-cell mRNA differential display, we have identified a molluscan
homolog of the multiple endocrine neoplasia type 1 (MEN1) tumor suppressor gene encoding the transcription
factor menin as a gene that is upregulated during synapse formation.
In vitro antisense knock-down of MEN1
mRNA blocks the formation of mature synapses between different types of
identified central neurons. Moreover, immunocytochemistry and cell-specific knock-down of MEN1 mRNA show that
postsynaptic but not presynaptic expression is required for synapses to
form. Together, our data demonstrate that menin is a synaptogenic
factor that is critically involved in a general postsynaptic mechanism
of synapse formation between central neurons.
Key words:
synaptogenesis; soma-soma synapse; gene expression; MEN1 tumor suppressor gene; menin; transcription factor; antisense knock-down
Copyright © Society for Neuroscience 0270-6474//$05.00/0
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