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Transcriptional control of visual neural circuit development by GS homeobox 1.
Schmidt, Alexandra R; Placer, Haiden J; Muhammad, Ishmael M; Shephard, Rebekah; Patrick, Regina L; Saurborn, Taylor; Horstick, Eric J; Bergeron, Sadie A.
  • Schmidt AR; Department of Biology, West Virginia University, Morgantown, West Virgina, United States of America.
  • Placer HJ; Department of Biology, West Virginia University, Morgantown, West Virgina, United States of America.
  • Muhammad IM; Department of Biology, West Virginia University, Morgantown, West Virgina, United States of America.
  • Shephard R; Department of Biology, West Virginia University, Morgantown, West Virgina, United States of America.
  • Patrick RL; Department of Biology, West Virginia University, Morgantown, West Virgina, United States of America.
  • Saurborn T; Department of Biology, West Virginia University, Morgantown, West Virgina, United States of America.
  • Horstick EJ; Department of Biology, West Virginia University, Morgantown, West Virgina, United States of America.
  • Bergeron SA; Department of Neuroscience, West Virginia University, Morgantown, West Virgina, United States of America.
PLoS Genet ; 20(4): e1011139, 2024 Apr.
Article en En | MEDLINE | ID: mdl-38669217
ABSTRACT
As essential components of gene expression networks, transcription factors regulate neural circuit assembly. The homeobox transcription factor encoding gene, gs homeobox 1 (gsx1), is expressed in the developing visual system; however, no studies have examined its role in visual system formation. In zebrafish, retinal ganglion cell (RGC) axons that transmit visual information to the brain terminate in ten arborization fields (AFs) in the optic tectum (TeO), pretectum (Pr), and thalamus. Pretectal AFs (AF1-AF9) mediate distinct visual behaviors, yet we understand less about their development compared to AF10 in the TeO. Using gsx1 zebrafish mutants, immunohistochemistry, and transgenic lines, we observed that gsx1 is required for vesicular glutamate transporter, Tg(slc17a6bDsRed), expression in the Pr, but not overall neuron number. gsx1 mutants have normal eye morphology, yet they exhibit impaired visual ability during prey capture. RGC axon volume in the gsx1 mutant Pr and TeO is reduced, and AF7 that is active during feeding is missing which is consistent with reduced hunting performance. Timed laser ablation of Tg(slc17a6bDsRed)-positive cells reveals that they are necessary for AF7 formation. This work is the first to implicate gsx1 in establishing cell identity and functional neural circuits in the visual system.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Células Ganglionares de la Retina / Pez Cebra / Animales Modificados Genéticamente / Proteínas de Homeodominio / Regulación del Desarrollo de la Expresión Génica / Proteínas de Pez Cebra Límite: Animals Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Células Ganglionares de la Retina / Pez Cebra / Animales Modificados Genéticamente / Proteínas de Homeodominio / Regulación del Desarrollo de la Expresión Génica / Proteínas de Pez Cebra Límite: Animals Idioma: En Año: 2024 Tipo del documento: Article