Your browser doesn't support javascript.
loading
Electrical synapse structure requires distinct isoforms of a postsynaptic scaffold.
Michel, Jennifer Carlisle; Grivette, Margaret M B; Harshfield, Amber T; Huynh, Lisa; Komons, Ava P; Loomis, Bradley; McKinnis, Kaitlan; Miller, Brennen T; Nguyen, Ethan Q; Huang, Tiffany W; Lauf, Sophia; Michel, Elias S; Michel, Mia E; Kissinger, Jane S; Marsh, Audrey J; Crow, William E; Kaye, Lila E; Lasseigne, Abagael M; Lukowicz-Bedford, Rachel M; Farnsworth, Dylan R; Martin, E Anne; Miller, Adam C.
Afiliación
  • Michel JC; Institute of Neuroscience, Department of Biology, University of Oregon, Eugene, Oregon, United States of America.
  • Grivette MMB; Institute of Neuroscience, Department of Biology, University of Oregon, Eugene, Oregon, United States of America.
  • Harshfield AT; Institute of Neuroscience, Department of Biology, University of Oregon, Eugene, Oregon, United States of America.
  • Huynh L; Institute of Neuroscience, Department of Biology, University of Oregon, Eugene, Oregon, United States of America.
  • Komons AP; Institute of Neuroscience, Department of Biology, University of Oregon, Eugene, Oregon, United States of America.
  • Loomis B; Institute of Neuroscience, Department of Biology, University of Oregon, Eugene, Oregon, United States of America.
  • McKinnis K; Institute of Neuroscience, Department of Biology, University of Oregon, Eugene, Oregon, United States of America.
  • Miller BT; Institute of Neuroscience, Department of Biology, University of Oregon, Eugene, Oregon, United States of America.
  • Nguyen EQ; Institute of Neuroscience, Department of Biology, University of Oregon, Eugene, Oregon, United States of America.
  • Huang TW; Institute of Neuroscience, Department of Biology, University of Oregon, Eugene, Oregon, United States of America.
  • Lauf S; Institute of Neuroscience, Department of Biology, University of Oregon, Eugene, Oregon, United States of America.
  • Michel ES; Institute of Neuroscience, Department of Biology, University of Oregon, Eugene, Oregon, United States of America.
  • Michel ME; Institute of Neuroscience, Department of Biology, University of Oregon, Eugene, Oregon, United States of America.
  • Kissinger JS; Institute of Neuroscience, Department of Biology, University of Oregon, Eugene, Oregon, United States of America.
  • Marsh AJ; Institute of Neuroscience, Department of Biology, University of Oregon, Eugene, Oregon, United States of America.
  • Crow WE; Institute of Neuroscience, Department of Biology, University of Oregon, Eugene, Oregon, United States of America.
  • Kaye LE; Institute of Neuroscience, Department of Biology, University of Oregon, Eugene, Oregon, United States of America.
  • Lasseigne AM; Institute of Neuroscience, Department of Biology, University of Oregon, Eugene, Oregon, United States of America.
  • Lukowicz-Bedford RM; Institute of Neuroscience, Department of Biology, University of Oregon, Eugene, Oregon, United States of America.
  • Farnsworth DR; Institute of Neuroscience, Department of Biology, University of Oregon, Eugene, Oregon, United States of America.
  • Martin EA; Institute of Neuroscience, Department of Biology, University of Oregon, Eugene, Oregon, United States of America.
  • Miller AC; Institute of Neuroscience, Department of Biology, University of Oregon, Eugene, Oregon, United States of America.
PLoS Genet ; 19(11): e1011045, 2023 Nov.
Article en En | MEDLINE | ID: mdl-38011265
Electrical synapses are neuronal gap junction (GJ) channels associated with a macromolecular complex called the electrical synapse density (ESD), which regulates development and dynamically modifies electrical transmission. However, the proteomic makeup and molecular mechanisms utilized by the ESD that direct electrical synapse formation are not well understood. Using the Mauthner cell of zebrafish as a model, we previously found that the intracellular scaffolding protein ZO1b is a member of the ESD, localizing postsynaptically, where it is required for GJ channel localization, electrical communication, neural network function, and behavior. Here, we show that the complexity of the ESD is further diversified by the genomic structure of the ZO1b gene locus. The ZO1b gene is alternatively initiated at three transcriptional start sites resulting in isoforms with unique N-termini that we call ZO1b-Alpha, -Beta, and -Gamma. We demonstrate that ZO1b-Beta and ZO1b-Gamma are broadly expressed throughout the nervous system and localize to electrical synapses. By contrast, ZO1b-Alpha is expressed mainly non-neuronally and is not found at synapses. We generate mutants in all individual isoforms, as well as double mutant combinations in cis on individual chromosomes, and find that ZO1b-Beta is necessary and sufficient for robust GJ channel localization. ZO1b-Gamma, despite its localization to the synapse, plays an auxiliary role in channel localization. This study expands the notion of molecular complexity at the ESD, revealing that an individual genomic locus can contribute distinct isoforms to the macromolecular complex at electrical synapses. Further, independent scaffold isoforms have differential contributions to developmental assembly of the interneuronal GJ channels. We propose that ESD molecular complexity arises both from the diversity of unique genes and from distinct isoforms encoded by single genes. Overall, ESD proteomic diversity is expected to have critical impacts on the development, structure, function, and plasticity of electrical transmission.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Pez Cebra / Sinapsis Eléctricas Límite: Animals Idioma: En Revista: PLoS Genet Asunto de la revista: GENETICA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Pez Cebra / Sinapsis Eléctricas Límite: Animals Idioma: En Revista: PLoS Genet Asunto de la revista: GENETICA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos