Cited by 6RNA regulation and diseaseCellular transport and secretionNeuroscience and Neuropharmacology Research

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Stochastic RNA editing of the Complexin C-terminus within single neurons regulates neurotransmitter release

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Abstract

Neurotransmitter release requires assembly of the SNARE complex fusion machinery, with multiple SNARE-binding proteins regulating when and where synaptic vesicle fusion occurs. The presynaptic protein Complexin (Cpx) controls spontaneous and evoked neurotransmitter release by modulating SNARE complex zippering. Although the central SNARE-binding helix is essential, post-translational modifications to Cpx's C-terminal membrane-binding amphipathic helix regulate its ability to control synaptic vesicle fusion. Here, we demonstrate that RNA editing of the Cpx C-terminus modifies its ability to clamp SNARE-mediated fusion and alters presynaptic output. RNA editing of Cpx across single neurons is stochastic, generating up to eight edit variants that fine tune neurotransmitter release by altering the subcellular localization and clamping properties of the protein. Similar stochastic editing rules for other synaptic genes were observed, indicating editing variability at single adenosines and across multiple mRNAs generates unique synaptic proteomes within the same population of neurons to fine tune presynaptic output.

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Research works printed but not linked: 60

  1. Sauvola, 2021, SNARE regulatory proteins in synaptic vesicle fusion and recycling, Front. Mol. Neurosci., 14, 10.3389/fnmol.2021.733138 · DOI
  2. Rizo, 2022, Molecular mechanisms underlying neurotransmitter release, Annu. Rev. Biophys., 51, 377, 10.1146/annurev-biophys-111821-104732 · DOI
  3. Quiñones-Frías, 2021, Function of Drosophila Synaptotagmins in membrane trafficking at synapses, Cell. Mol. Life Sci., 78, 4335, 10.1007/s00018-021-03788-9 · DOI
  4. Jorquera, 2012, Complexin controls spontaneous and evoked neurotransmitter release by regulating the timing and properties of synaptotagmin activity, J. Neurosci., 32, 18234, 10.1523/JNEUROSCI.3212-12.2012 · DOI
  5. Bera, 2022, Molecular determinants of complexin clamping and activation function, Elife, 11, 10.7554/eLife.71938 · DOI
  6. Malsam, 2020, Complexin Suppresses Spontaneous Exocytosis by Capturing the Membrane-Proximal Regions of VAMP2 and SNAP25, Cell Rep., 32, 10.1016/j.celrep.2020.107926 · DOI
  7. Huntwork, 2007, A complexin fusion clamp regulates spontaneous neurotransmitter release and synaptic growth, Nat. Neurosci., 10, 1235, 10.1038/nn1980 · DOI
  8. Hobson, 2011, Complexin maintains vesicles in the primed state in C. elegans, Curr. Biol., 21, 106, 10.1016/j.cub.2010.12.015 · DOI
  9. Martin, 2011, Complexin has opposite effects on two modes of synaptic vesicle fusion, Curr. Biol., 21, 97, 10.1016/j.cub.2010.12.014 · DOI
  10. Cho, 2015, Phosphorylation of Complexin by PKA Regulates Activity-Dependent Spontaneous Neurotransmitter Release and Structural Synaptic Plasticity, Neuron, 88, 749, 10.1016/j.neuron.2015.10.011 · DOI
  11. Robinson, 2018, Nitric oxide-mediated posttranslational modifications control neurotransmitter release by modulating complexin farnesylation and enhancing its clamping ability, PLoS Biol., 16, 10.1371/journal.pbio.2003611 · DOI
  12. Choi, 2014, Miniature neurotransmission regulates Drosophila synaptic structural maturation, Neuron, 82, 618, 10.1016/j.neuron.2014.03.012 · DOI
  13. Lottermoser, 2023, Complexin membrane interactions: implications for synapse evolution and function, J. Mol. Biol., 435, 10.1016/j.jmb.2022.167774 · DOI
  14. Buhl, 2013, Differential regulation of evoked and spontaneous neurotransmitter release by C-terminal modifications of complexin, Mol. Cell. Neurosci., 52, 161, 10.1016/j.mcn.2012.11.009 · DOI
  15. Cho, 2010, Comparative analysis of Drosophila and mammalian complexins as fusion clamps and facilitators of neurotransmitter release, Mol. Cell. Neurosci., 45, 389, 10.1016/j.mcn.2010.07.012 · DOI
  16. Nishikura, 2016, A-to-I editing of coding and non-coding RNAs by ADARs, Nat. Rev. Mol. Cell Biol., 17, 83, 10.1038/nrm.2015.4 · DOI · Paper page
  17. Hoopengardner, 2003, Nervous system targets of RNA editing identified by comparative genomics, Science, 301, 832, 10.1126/science.1086763 · DOI · Paper page
  18. Radhakrishnan, 2021, Symmetrical arrangement of proteins under release-ready vesicles in presynaptic terminals, Proc. Natl. Acad. Sci. USA, 118, 10.1073/pnas.2024029118 · DOI
  19. Reim, 2005, Structurally and functionally unique complexins at retinal ribbon synapses, J. Cell Biol., 169, 669, 10.1083/jcb.200502115 · DOI
  20. Varadi, 2022, AlphaFold Protein Structure Database: massively expanding the structural coverage of protein-sequence space with high-accuracy models, Nucleic Acids Res., 50, D439, 10.1093/nar/gkab1061 · DOI · Paper page
  21. Snead, 2014, Membrane curvature sensing by the C-terminal domain of complexin, Nat. Commun., 5, 4955, 10.1038/ncomms5955 · DOI
  22. Gong, 2016, C-terminal domain of mammalian complexin-1 localizes to highly curved membranes, Proc. Natl. Acad. Sci. USA, 113, E7590, 10.1073/pnas.1609917113 · DOI
  23. Gautier, 2008, HELIQUEST: a web server to screen sequences with specific alpha-helical properties, Bioinformatics, 24, 2101, 10.1093/bioinformatics/btn392 · DOI
  24. Aponte-Santiago, 2020, Synaptic properties and plasticity mechanisms of invertebrate tonic and phasic neurons, Front. Physiol., 11, 10.3389/fphys.2020.611982 · DOI
  25. Johansen, 1989, Stereotypic morphology of glutamatergic synapses on identified muscle cells of Drosophila larvae, J. Neurosci., 9, 710, 10.1523/JNEUROSCI.09-02-00710.1989 · DOI
  26. Jetti, 2023, Molecular logic of synaptic diversity between Drosophila tonic and phasic motoneurons, Neuron, 10.1016/j.neuron.2023.07.019 · DOI
  27. Bulat, 2014, Presynaptic CK2 promotes synapse organization and stability by targeting Ankyrin2, J. Cell Biol., 204, 77, 10.1083/jcb.201305134 · DOI
  28. Wragg, 2013, Synaptic vesicles position complexin to block spontaneous fusion, Neuron, 77, 323, 10.1016/j.neuron.2012.11.005 · DOI
  29. Makke, 2018, A mechanism for exocytotic arrest by the Complexin C-terminus, Elife, 7, 10.7554/eLife.38981 · DOI
  30. Courtney, 2022, The complexin C-terminal amphipathic helix stabilizes the fusion pore open state by sculpting membranes, Nat. Struct. Mol. Biol., 29, 97, 10.1038/s41594-021-00716-0 · DOI
  31. Malsam, 2009, The carboxy-terminal domain of complexin I stimulates liposome fusion, Proc. Natl. Acad. Sci. USA, 106, 2001, 10.1073/pnas.0812813106 · DOI
  32. Liang, 2022, Complexin-1 and synaptotagmin-1 compete for binding sites on membranes containing PtdInsP2, Biophys. J., 121, 3370, 10.1016/j.bpj.2022.08.023 · DOI
  33. Bulgari, 2023, Ca2+ and cAMP open differentially dilating synaptic fusion pores, J. Cell Sci., 136, jcs261026, 10.1242/jcs.261026 · DOI
  34. Yoshihara, 2005, Retrograde signaling by Syt 4 induces presynaptic release and synapse-specific growth, Science, 310, 858, 10.1126/science.1117541 · DOI
  35. Shi, 2021, Phosphorylation of Syntaxin-1a by casein kinase 2α regulates pre-synaptic vesicle exocytosis from the reserve pool, J. Neurochem., 156, 614, 10.1111/jnc.15161 · DOI
  36. Bao, 2018, Dynamics and number of trans-SNARE complexes determine nascent fusion pore properties, Nature, 554, 260, 10.1038/nature25481 · DOI
  37. Domanska, 2009, Single vesicle millisecond fusion kinetics reveals number of SNARE complexes optimal for fast SNARE-mediated membrane fusion, J. Biol. Chem., 284, 32158, 10.1074/jbc.M109.047381 · DOI
  38. Hua, 2001, Three SNARE complexes cooperate to mediate membrane fusion, Proc. Natl. Acad. Sci. USA, 98, 8065, 10.1073/pnas.131214798 · DOI
  39. Foletti, 2000, Phosphorylated syntaxin 1 is localized to discrete domains along a subset of axons, J. Neurosci., 20, 4535, 10.1523/JNEUROSCI.20-12-04535.2000 · DOI
  40. Shi, 2012, SNARE proteins: one to fuse and three to keep the nascent fusion pore open, Science, 335, 1355, 10.1126/science.1214984 · DOI
  41. Bennett, 1993, Casein kinase II phosphorylates the synaptic vesicle protein p65, J. Neurosci., 13, 1701, 10.1523/JNEUROSCI.13-04-01701.1993 · DOI
  42. Shata, 2007, Phosphorylated synaphin/complexin found in the brain exhibits enhanced SNARE complex binding, Biochem. Biophys. Res. Commun., 354, 808, 10.1016/j.bbrc.2007.01.064 · DOI
  43. Robinson, 2016, ADAR-mediated RNA editing suppresses sleep by acting as a brake on glutamatergic synaptic plasticity, Nat. Commun., 7, 10.1038/ncomms10512 · DOI
  44. Li, 2014, The ADAR RNA editing enzyme controls neuronal excitability in Drosophila melanogaster, Nucleic Acids Res., 42, 1139, 10.1093/nar/gkt909 · DOI
  45. Maldonado, 2013, Adar is essential for optimal presynaptic function, Mol. Cell. Neurosci., 52, 173, 10.1016/j.mcn.2012.10.009 · DOI
  46. Shumate, 2021, RNA editing-mediated regulation of calcium-dependent activator protein for secretion (CAPS1) localization and its impact on synaptic transmission, J. Neurochem., 158, 182, 10.1111/jnc.15372 · DOI
  47. Birk, 2023, Temperature-dependent RNA editing in octopus extensively recodes the neural proteome, Cell, 186, 2544, 10.1016/j.cell.2023.05.004 · DOI
  48. Sommer, 1991, RNA editing in brain controls a determinant of ion flow in glutamate-gated channels, Cell, 67, 11, 10.1016/0092-8674(91)90568-J · DOI · Paper page
  49. Graveley, 2011, The developmental transcriptome of Drosophila melanogaster, Nature, 471, 473, 10.1038/nature09715 · DOI
  50. Sapiro, 2019, Illuminating spatial A-to-I RNA editing signatures within the Drosophila brain, Proc. Natl. Acad. Sci. USA, 116, 2318, 10.1073/pnas.1811768116 · DOI
  51. Palladino, 2000, A-to-I pre-mRNA editing in Drosophila is primarily involved in adult nervous system function and integrity, Cell, 102, 437, 10.1016/S0092-8674(00)00049-0 · DOI
  52. Tran, 2019, Widespread RNA editing dysregulation in brains from autistic individuals, Nat. Neurosci., 22, 25, 10.1038/s41593-018-0287-x · DOI
  53. Schindelin, 2012, Fiji: an open-source platform for biological-image analysis, Nat. Methods, 9, 676, 10.1038/nmeth.2019 · DOI · Paper page
  54. Robinson, 2011, Integrative genomics viewer, Nat. Biotechnol., 29, 24, 10.1038/nbt.1754 · DOI · Paper page
  55. Wang, 2020, iCn3D, a web-based 3D viewer for sharing 1D/2D/3D representations of biomolecular structures, Bioinformatics, 36, 131, 10.1093/bioinformatics/btz502 · DOI
  56. Gratz, 2014, Highly specific and efficient CRISPR/Cas9-catalyzed homology-directed repair in Drosophila, Genetics, 196, 961, 10.1534/genetics.113.160713 · DOI
  57. Port, 2016, Augmenting CRISPR applications in Drosophila with tRNA-flanked sgRNAs, Nat. Methods, 13, 852, 10.1038/nmeth.3972 · DOI
  58. Ali, 2011, Assaying locomotor, learning, and memory deficits in Drosophila models of neurodegeneration, J. Vis. Exp., 10.3791/2504-v · DOI
  59. Kashima, 2017, Hyperactive locomotion in a Drosophila model is a functional readout for the synaptic abnormalities underlying fragile X syndrome, Sci. Signal., 10, 10.1126/scisignal.aai8133 · DOI
  60. Nichols, 2012, Methods to assay Drosophila behavior, J. Vis. Exp., 10.3791/3795-v · DOI

Metadata

Authors
Brija, E. A., Guan, Z., Jetti, S. K., & Littleton, J. T.
Affiliations
Massachusetts Institute of Technology (US)
Corresponding author
Littleton, J. Troy
Venue
Cell Reports
Publisher
Elsevier BV
Published
2023-09
Volume
42
Issue
9
Pages
113152
ISSN
2211-1247 (ISSN-L)
OpenAlex
W4386818208
Cited by
6
References
1
Citations by year
2026: 1 · 2025: 5
FWCI
0.53
Type
journal article
Language
en
Open access
Locations
  • Cell Reports (publishedVersion, cc-by-nc-nd)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion, cc-by-nc-nd)
  • PubMed Central (submittedVersion, cc-by)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • NINDS (NS40296)
  • Indiana University
  • National Science Foundation (1122374)
  • JPB Foundation
  • National Institutes of Health (P40OD018537)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA regulation and disease
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Keywords
RNA editing, complexin, SNARE complex, synaptic vesicle fusion, neurotransmitter release, presynaptic proteins, single neurons, synaptic proteome, subcellular localization

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