Literature DB >> 19469853

Conservation of arthropod midline netrin accumulation revealed with a cross-reactive antibody provides evidence for midline cell homology.

Wendy Simanton1, Stephanie Clark, Anthony Clemons, Caitlin Jacowski, Adrienne Farrell-VanZomeren, Paul Beach, William E Browne, Molly Duman-Scheel.   

Abstract

Although many similarities in arthropod CNS development exist, differences in axonogenesis and the formation of midline cells, which regulate axon growth, have been observed. For example, axon growth patterns in the ventral nerve cord of Artemia franciscana differ from that of Drosophila melanogaster. Despite such differences, conserved molecular marker expression at the midline of several arthropod species indicates that midline cells may be homologous in distantly related arthropods. However, data from additional species are needed to test this hypothesis. In this investigation, nerve cord formation and the putative homology of midline cells were examined in distantly related arthropods, including: long- and short-germ insects (D. melanogaster, Aedes aeygypti, and Tribolium castaneum), branchiopod crustaceans (A. franciscana and Triops longicauditus), and malacostracan crustaceans (Porcellio laevis and Parhyale hawaiensis). These comparative analyses were aided by a cross-reactive antibody generated against the Netrin (Net) protein, a midline cell marker and regulator of axonogenesis. The mechanism of nerve cord formation observed in Artemia is found in Triops, another branchiopod, but is not found in the other arthropods examined. Despite divergent mechanisms of midline cell formation and nerve cord development, Net accumulation is detected in a well-conserved subset of midline cells in branchiopod crustaceans, malacostracan crustaceans, and insects. Notably, the Net accumulation pattern is also conserved at the midline of the amphipod P. hawaiensis, which undergoes split germ-band development. Conserved Net accumulation patterns indicate that arthropod midline cells are homologous, and that Nets function to regulate commissure formation during CNS development of Tetraconata.

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Year:  2009        PMID: 19469853      PMCID: PMC2749990          DOI: 10.1111/j.1525-142X.2009.00328.x

Source DB:  PubMed          Journal:  Evol Dev        ISSN: 1520-541X            Impact factor:   1.930


  29 in total

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Authors:  Scott R Wheeler; James B Skeath
Journal:  Gene Expr Patterns       Date:  2005-04-09       Impact factor: 1.224

3.  ROBO directs axon crossing of segmental boundaries by suppressing responsiveness to relocalized Netrin.

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4.  Crustacean appendage evolution associated with changes in Hox gene expression.

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Journal:  Nature       Date:  1997-08-14       Impact factor: 49.962

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Authors:  R Harris; L M Sabatelli; M A Seeger
Journal:  Neuron       Date:  1996-08       Impact factor: 17.173

6.  The Tribolium columnar genes reveal conservation and plasticity in neural precursor patterning along the embryonic dorsal-ventral axis.

Authors:  Scott R Wheeler; Michelle L Carrico; Beth A Wilson; James B Skeath
Journal:  Dev Biol       Date:  2005-03-15       Impact factor: 3.582

7.  frazzled encodes a Drosophila member of the DCC immunoglobulin subfamily and is required for CNS and motor axon guidance.

Authors:  P A Kolodziej; L C Timpe; K J Mitchell; S R Fried; C S Goodman; L Y Jan; Y N Jan
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8.  Stages of embryonic development in the amphipod crustacean, Parhyale hawaiensis.

Authors:  William E Browne; Alivia L Price; Matthias Gerberding; Nipam H Patel
Journal:  Genesis       Date:  2005-07       Impact factor: 2.487

9.  Cell lineage of the midline cells in the amphipod crustacean Orchestia cavimana (Crustacea, Malacostraca) during formation and separation of the germ band.

Authors:  M Gerberding; G Scholtz
Journal:  Dev Genes Evol       Date:  1999-02       Impact factor: 0.900

10.  Analysis of molecular marker expression reveals neuronal homology in distantly related arthropods.

Authors:  M Duman-Scheel; N H Patel
Journal:  Development       Date:  1999-06       Impact factor: 6.868

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  14 in total

1.  Ablation of a single cell from eight-cell embryos of the amphipod crustacean Parhyale hawaiensis.

Authors:  Anastasia R Nast; Cassandra G Extavour
Journal:  J Vis Exp       Date:  2014-03-16       Impact factor: 1.355

Review 2.  Midline axon guidance in the Drosophila embryonic central nervous system.

Authors:  LaFreda J Howard; Haley E Brown; Benjamin C Wadsworth; Timothy A Evans
Journal:  Semin Cell Dev Biol       Date:  2017-11-27       Impact factor: 7.727

3.  Slit/Robo-mediated axon guidance in Tribolium and Drosophila: divergent genetic programs build insect nervous systems.

Authors:  Timothy A Evans; Greg J Bashaw
Journal:  Dev Biol       Date:  2012-01-08       Impact factor: 3.582

4.  Aedes aegypti: an emerging model for vector mosquito development.

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Journal:  Cold Spring Harb Protoc       Date:  2010-10-01

5.  Fixation and preparation of developing tissues from Aedes aegypti.

Authors:  Anthony Clemons; Morgan Haugen; Ellen Flannery; Kristopher Kast; Caitlin Jacowski; David Severson; Molly Duman-Scheel
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6.  Culturing and egg collection of Aedes aegypti.

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7.  Immunohistochemical analysis of protein expression during Aedes aegypti development.

Authors:  Anthony Clemons; Ellen Flannery; Kristopher Kast; David Severson; Molly Duman-Scheel
Journal:  Cold Spring Harb Protoc       Date:  2010-10-01

8.  A prominent requirement for single-minded and the ventral midline in patterning the dorsoventral axis of the crustacean Parhyale hawaiensis.

Authors:  Mario A Vargas-Vila; Roberta L Hannibal; Ronald J Parchem; Paul Z Liu; Nipam H Patel
Journal:  Development       Date:  2010-09-15       Impact factor: 6.868

9.  Redeployment of a conserved gene regulatory network during Aedes aegypti development.

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Journal:  Dev Biol       Date:  2016-06-21       Impact factor: 3.582

10.  Functional genetic characterization of salivary gland development in Aedes aegypti.

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