Cargando…
A common evolutionary origin for the ON- and OFF-edge motion detection pathways of the Drosophila visual system
Synaptic circuits for identified behaviors in the Drosophila brain have typically been considered from either a developmental or functional perspective without reference to how the circuits might have been inherited from ancestral forms. For example, two candidate pathways for ON- and OFF-edge motio...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4496578/ https://www.ncbi.nlm.nih.gov/pubmed/26217193 http://dx.doi.org/10.3389/fncir.2015.00033 |
_version_ | 1782380429495500800 |
---|---|
author | Shinomiya, Kazunori Takemura, Shin-ya Rivlin, Patricia K. Plaza, Stephen M. Scheffer, Louis K. Meinertzhagen, Ian A. |
author_facet | Shinomiya, Kazunori Takemura, Shin-ya Rivlin, Patricia K. Plaza, Stephen M. Scheffer, Louis K. Meinertzhagen, Ian A. |
author_sort | Shinomiya, Kazunori |
collection | PubMed |
description | Synaptic circuits for identified behaviors in the Drosophila brain have typically been considered from either a developmental or functional perspective without reference to how the circuits might have been inherited from ancestral forms. For example, two candidate pathways for ON- and OFF-edge motion detection in the visual system act via circuits that use respectively either T4 or T5, two cell types of the fourth neuropil, or lobula plate (LOP), that exhibit narrow-field direction-selective responses and provide input to wide-field tangential neurons. T4 or T5 both have four subtypes that terminate one each in the four strata of the LOP. Representatives are reported in a wide range of Diptera, and both cell types exhibit various similarities in: (1) the morphology of their dendritic arbors; (2) their four morphological and functional subtypes; (3) their cholinergic profile in Drosophila; (4) their input from the pathways of L3 cells in the first neuropil, or lamina (LA), and by one of a pair of LA cells, L1 (to the T4 pathway) and L2 (to the T5 pathway); and (5) their innervation by a single, wide-field contralateral tangential neuron from the central brain. Progenitors of both also express the gene atonal early in their proliferation from the inner anlage of the developing optic lobe, being alone among many other cell type progeny to do so. Yet T4 receives input in the second neuropil, or medulla (ME), and T5 in the third neuropil or lobula (LO). Here we suggest that these two cell types were originally one, that their ancestral cell population duplicated and split to innervate separate ME and LO neuropils, and that a fiber crossing—the internal chiasma—arose between the two neuropils. The split most plausibly occurred, we suggest, with the formation of the LO as a new neuropil that formed when it separated from its ancestral neuropil to leave the ME, suggesting additionally that ME input neurons to T4 and T5 may also have had a common origin. |
format | Online Article Text |
id | pubmed-4496578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-44965782015-07-27 A common evolutionary origin for the ON- and OFF-edge motion detection pathways of the Drosophila visual system Shinomiya, Kazunori Takemura, Shin-ya Rivlin, Patricia K. Plaza, Stephen M. Scheffer, Louis K. Meinertzhagen, Ian A. Front Neural Circuits Neuroscience Synaptic circuits for identified behaviors in the Drosophila brain have typically been considered from either a developmental or functional perspective without reference to how the circuits might have been inherited from ancestral forms. For example, two candidate pathways for ON- and OFF-edge motion detection in the visual system act via circuits that use respectively either T4 or T5, two cell types of the fourth neuropil, or lobula plate (LOP), that exhibit narrow-field direction-selective responses and provide input to wide-field tangential neurons. T4 or T5 both have four subtypes that terminate one each in the four strata of the LOP. Representatives are reported in a wide range of Diptera, and both cell types exhibit various similarities in: (1) the morphology of their dendritic arbors; (2) their four morphological and functional subtypes; (3) their cholinergic profile in Drosophila; (4) their input from the pathways of L3 cells in the first neuropil, or lamina (LA), and by one of a pair of LA cells, L1 (to the T4 pathway) and L2 (to the T5 pathway); and (5) their innervation by a single, wide-field contralateral tangential neuron from the central brain. Progenitors of both also express the gene atonal early in their proliferation from the inner anlage of the developing optic lobe, being alone among many other cell type progeny to do so. Yet T4 receives input in the second neuropil, or medulla (ME), and T5 in the third neuropil or lobula (LO). Here we suggest that these two cell types were originally one, that their ancestral cell population duplicated and split to innervate separate ME and LO neuropils, and that a fiber crossing—the internal chiasma—arose between the two neuropils. The split most plausibly occurred, we suggest, with the formation of the LO as a new neuropil that formed when it separated from its ancestral neuropil to leave the ME, suggesting additionally that ME input neurons to T4 and T5 may also have had a common origin. Frontiers Media S.A. 2015-07-09 /pmc/articles/PMC4496578/ /pubmed/26217193 http://dx.doi.org/10.3389/fncir.2015.00033 Text en Copyright © 2015 Shinomiya, Takemura, Rivlin, Plaza, Scheffer and Meinertzhagen. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Shinomiya, Kazunori Takemura, Shin-ya Rivlin, Patricia K. Plaza, Stephen M. Scheffer, Louis K. Meinertzhagen, Ian A. A common evolutionary origin for the ON- and OFF-edge motion detection pathways of the Drosophila visual system |
title | A common evolutionary origin for the ON- and OFF-edge motion detection pathways of the Drosophila visual system |
title_full | A common evolutionary origin for the ON- and OFF-edge motion detection pathways of the Drosophila visual system |
title_fullStr | A common evolutionary origin for the ON- and OFF-edge motion detection pathways of the Drosophila visual system |
title_full_unstemmed | A common evolutionary origin for the ON- and OFF-edge motion detection pathways of the Drosophila visual system |
title_short | A common evolutionary origin for the ON- and OFF-edge motion detection pathways of the Drosophila visual system |
title_sort | common evolutionary origin for the on- and off-edge motion detection pathways of the drosophila visual system |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4496578/ https://www.ncbi.nlm.nih.gov/pubmed/26217193 http://dx.doi.org/10.3389/fncir.2015.00033 |
work_keys_str_mv | AT shinomiyakazunori acommonevolutionaryoriginfortheonandoffedgemotiondetectionpathwaysofthedrosophilavisualsystem AT takemurashinya acommonevolutionaryoriginfortheonandoffedgemotiondetectionpathwaysofthedrosophilavisualsystem AT rivlinpatriciak acommonevolutionaryoriginfortheonandoffedgemotiondetectionpathwaysofthedrosophilavisualsystem AT plazastephenm acommonevolutionaryoriginfortheonandoffedgemotiondetectionpathwaysofthedrosophilavisualsystem AT schefferlouisk acommonevolutionaryoriginfortheonandoffedgemotiondetectionpathwaysofthedrosophilavisualsystem AT meinertzhageniana acommonevolutionaryoriginfortheonandoffedgemotiondetectionpathwaysofthedrosophilavisualsystem AT shinomiyakazunori commonevolutionaryoriginfortheonandoffedgemotiondetectionpathwaysofthedrosophilavisualsystem AT takemurashinya commonevolutionaryoriginfortheonandoffedgemotiondetectionpathwaysofthedrosophilavisualsystem AT rivlinpatriciak commonevolutionaryoriginfortheonandoffedgemotiondetectionpathwaysofthedrosophilavisualsystem AT plazastephenm commonevolutionaryoriginfortheonandoffedgemotiondetectionpathwaysofthedrosophilavisualsystem AT schefferlouisk commonevolutionaryoriginfortheonandoffedgemotiondetectionpathwaysofthedrosophilavisualsystem AT meinertzhageniana commonevolutionaryoriginfortheonandoffedgemotiondetectionpathwaysofthedrosophilavisualsystem |