adhesion complexes at cns synapses
DESCRIPTION
Regulation of synaptic adhesion complexes by alternative splicing Peter Scheiffele, Columbia University, NY. Adhesion complexes at CNS synapses. adhesion molecules represent one of the most important morphogenic determinants in all tissues - PowerPoint PPT PresentationTRANSCRIPT
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Regulation of synaptic adhesion complexesby alternative splicing
Peter Scheiffele, Columbia University, NY
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Adhesion complexes at CNS synapses
- adhesion molecules represent one of the most important morphogenic determinants in all tissues
- central regulators for cell polarization, migration, and for three-dimensional organization
- cell adhesion complexes are dynamically regulated to alter cellular architecture and function
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Adhesion complexes mediate cell-cell interactions at multiple synaptic sub-domains
peri-active zones• synaptic growth• endocytic zone active zone /
postsynaptic density- synaptic transmission- alignment & recruitment
NectinsCadherinsFasII(Still life)
EphA4Glt-1
ProtocadherinsNeuroligins
presynaptic terminal
glia
postsynaptic terminal
neuron-glia junction• transmitter uptake• signaling• spine morphogenesis
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Branching, tiling(repulsive self-
recognition)
Laminarspecificity
Potential roles for adhesion molecules in local regulation of connectivity
Subcellularspecificity
Cell typespecificity
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promoter promoter
1 2 4 53 6 9 107b
7a
8 1112 13 1415 16 17 18 21201922b
22a
23
Neurexin-1 genomic locus
DSCAM genomic locus
Protocadherin genomic locus
Cadherin-related
Neuronal Receptor (CNR)
Variable (1) Constant (1) Constant (1)Variable (1)Single exon genes
1 2 3 5 7 8 10 12 1311 14 15 16 18 20 2119 22 23 24
exon4 exon6 exon9 exon17
TM
Alternative splicing is one of the key processes that increases the diversity of cell adhesion molecules
Families of surface molecules encoded by multiple genes:olfactory receptors, classical cadherins, immunoglobulin-domain proteins, leucine-rich repeat proteins
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-neurexin
-neurexin
• three neurexin genes in mice (NRX1,2,3)• alternative promoter choice generates 2 transcripts per gene ( and NRX)• alternative splicing at 5 sites generates more than 1,000 variants (Ushkaryov et al., 1992)
Neurexins
Neuroligins
• four genes in mouse, five in human• further isoforms are generated by alternative splicing at two sites in the extracellular
domain (Ichtchenko et al. 1995, 1996) • neuroligins are postsynaptic adhesion molecules, interact with postsynaptic scaffolding
molecules (Irie et al., 1997, Song et al 1999)• inactivating mutations in NL3 and NL4 are associated with autism-spectrum disorders
and mental retardation (Jaimain et al. 2003, Laumonnier et al 2004)
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Adhesion complexes mediate cell-cell interactions at multiple synaptic sub-domains
peri-active zones• synaptic growth• endocytic zone active zone /
postsynaptic density- synaptic transmission- alignment & recruitment
NectinsCadherinsFasII(Still life)
EphA4Glt-1
Neuroligins
presynaptic terminal
glia
postsynaptic terminal
neuron-glia junction• transmitter uptake• signaling• spine morphogenesis
Neurexins
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Outline
1. Subcellular localization of neuroligins and neurexins at hippocampal synapses
2. Analysis of splice isoforms-specific functions
3. Mechanisms that control alternative splicing
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Freeze-fracture replica immuno-EM
Quick-freezing in helium
Freeze-fracture and platinum/carbon shadowing
SDS digestion andimmuno-gold labeling
Kazushi Fujimoto, J. Cell Sci., 108:3443-3449, 1995Elaine BudreckRyuichi Shigemoto
5 nm gold: pan-neuroligin10 nm gold: PSD95
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10 nm gold: GABA-A R beta 2 subunit 5 nm gold: neuroligin-2
Neuroligins are closely associated with neurotransmitter receptors in the postsynaptic membrane
Elaine Budreck, Ryuichi Shigemoto
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GFP-beta-Neurexin-1 mice
pan-neurexinantibodies
Chiye AokiFrancisco G. Scholl
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Model of the synaptic Neuroligin-Neurexin adhesion complex
postsynaptic:Neuroligin
presynaptic:Neurexin
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Neurexin and neuroligin genes encode large numbers of splice variants
-NRX
-NRX
GPLTKKHTDDLGDNDGAEDE GNRWSNSTK
NL1
NL2
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Selectivity of neuroligins for glutamatergic and GABAergic synapses
1 2
GlutamatergicAxon
GABAergicAxon
Dendrite
1 2
PresynapticReceptors?
(Song et al. 1999; Prange et al, 2004; Varoqueaux et al., 2004, Graf et al. 2004)
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Neuroligin variants generated by alternative splicing
GPLTKKHTDDLGDNDGAEDE GNRWSNSTK
Leora Gollan
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Ben Chih
% o
verla
p
Pun
cta/
10µ
m
VG
AT
: VG
lut1
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Alternative splicing controls localization of neuroligin-2
VGAT : VGlut1
Ben Chih, Leora Gollan
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Ben Chih
NL1B
VGlut1 : VGAT
Presence of the B insertion is sufficient to preventactivity of neuroligin-2 towards GABAergic axons
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Synaptic selectivity of NL splice variants
GABAergicaxon
dendrite
Specific Neurexinisoforms?glutamatergic
axon
insertion A: localization and function at GABAergic contacts
insertion B: localization and function at glutamatergic contacts B insertion is dominant
NL1B NL1ANL2A
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NL1A
NL1B
NL2A
NRX4(-) NRX4(+)
NL NL NL
Fc-control
NX-Fc NX-FcFc
Neuroligin-1 splice variants differ in their interactions with neurexin-1 isoforms
Ben Chih similar findings: Boucard et al., 2005; Graf et al. 2006
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Candidate neurexins for interactions at GABAergic synapses
GABAergicaxon
dendrite
glutamatergicaxon
NRXNRX4(+)NRX4(-)
NL1B NL1ANL2A
+? ?
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Selective function for neurexin variants in GABAergic postsynaptic differentiation
PSD95
gephyrin
Ben Chih
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GABAergicaxon
dendrite
glutamatergicaxon
NRXNRX4(+)NRX4(-)
NL1B NL1ANL2A
+? ?
vGlut1 VGAT
Ben Chih
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postsynaptic:Neuroligin
presynaptic:Neurexin
• alternative splicing of neuroligin-1 and -2 regulates localization and function at GABAergic vs. glutamatergic contacts
• neurexin splice variants that interact selectively with the GABAergic neuroligin variants selectively induce GABAergic postsynaptic differentiation
• alternative splicing underlies selective trans-synaptic interactions of the neuroligin - neurexin complex
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What is the spatial and temporal regulation of Neurexin splicing?
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What is the spatial and temporal regulation of Neurexin splicing?
a) Cell-type specific expression of splicing factors
b) Dynamic regulation by post-translational modifications, e.g. phosphorylation
Dynamic alterations in neurexin splicing have been reported, e.g. in response to growth factor signaling, seizure or ischemia (Patzke and Ernsberger, 2000; Gorecki et al. 1999, Sun et al. 2000)
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Leora Gollan
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A quantitative assay for neurexin splicing
Leora Gollan
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Splice reporters with inactivated donor and acceptor sites
Leora Gollan
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Processing of splice reporter RNAs in hippocampal neurons
RF
PG
FP
mer
ge
DNA transfection
RNA delivery
Leora Gollan
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1. specific introns are retained in cytoplasmic neurexin-1 mRNA
2. unspliced RNA delivered into the cytoplasm of hippocampal neurons can be processed by the cellular machinery
is the neurexin-1 mRNA processed through a cytoplasmic splicing mechanism?
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RNA processing in mechanically isolated axons
Leora Gollan
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Cytoplasmic splicing of synaptic proteins would provide a novel mechanism for local modifications of cell function
In the neuroligin-neurexin complex alternative splicing regulates selective adhesive interactions
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Candidate mechanisms for cytoplasmic neurexin mRNA processing
Non-conventional cytoplasmic mechanism: Ire1p - cleavagetRNA ligase - exon joining
Sidrauski, Walter and colleagues
Cytoplasmic mechanism using conventional machinery: Glanzer et al. PNAS 102(46):16859-64 suggested splicing-like mRNA processing in dendrites
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AcknowledgementsBen Chih (Genentech)Leora GollanElaine BudreckFrancisco Gomez-Scholl (Univ. Seville)
Collaborators:Ryuichi Shigemoto (NIPS, Okazaki)Chiye Aoki (NYU)
Support: NIDANINDSIrma T. Hirschl FundThe John Merck FundThe Simons FoundationSearle Scholar ProgramAlfred P. Sloan FoundationJoseph and Esther Klingenstein FundNational Alliance for Autism Research
(POSTER: Wednesday 715.13/B25)