Literature DB >> 16965768

A genomic view of the sea urchin nervous system.

R D Burke1, L M Angerer, M R Elphick, G W Humphrey, S Yaguchi, T Kiyama, S Liang, X Mu, C Agca, W H Klein, B P Brandhorst, M Rowe, K Wilson, A M Churcher, J S Taylor, N Chen, G Murray, D Wang, D Mellott, R Olinski, F Hallböök, M C Thorndyke.   

Abstract

The sequencing of the Strongylocentrotus purpuratus genome provides a unique opportunity to investigate the function and evolution of neural genes. The neurobiology of sea urchins is of particular interest because they have a close phylogenetic relationship with chordates, yet a distinctive pentaradiate body plan and unusual neural organization. Orthologues of transcription factors that regulate neurogenesis in other animals have been identified and several are expressed in neurogenic domains before gastrulation indicating that they may operate near the top of a conserved neural gene regulatory network. A family of genes encoding voltage-gated ion channels is present but, surprisingly, genes encoding gap junction proteins (connexins and pannexins) appear to be absent. Genes required for synapse formation and function have been identified and genes for synthesis and transport of neurotransmitters are present. There is a large family of G-protein-coupled receptors, including 874 rhodopsin-type receptors, 28 metabotropic glutamate-like receptors and a remarkably expanded group of 161 secretin receptor-like proteins. Absence of cannabinoid, lysophospholipid and melanocortin receptors indicates that this group may be unique to chordates. There are at least 37 putative G-protein-coupled peptide receptors and precursors for several neuropeptides and peptide hormones have been identified, including SALMFamides, NGFFFamide, a vasotocin-like peptide, glycoprotein hormones and insulin/insulin-like growth factors. Identification of a neurotrophin-like gene and Trk receptor in sea urchin indicates that this neural signaling system is not unique to chordates. Several hundred chemoreceptor genes have been predicted using several approaches, a number similar to that for other animals. Intriguingly, genes encoding homologues of rhodopsin, Pax6 and several other key mammalian retinal transcription factors are expressed in tube feet, suggesting tube feet function as photosensory organs. Analysis of the sea urchin genome presents a unique perspective on the evolutionary history of deuterostome nervous systems and reveals new approaches to investigate the development and neurobiology of sea urchins.

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Year:  2006        PMID: 16965768      PMCID: PMC1950334          DOI: 10.1016/j.ydbio.2006.08.007

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  153 in total

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Review 2.  Evolution of the vertebrate neurotrophin and Trk receptor gene families.

Authors:  F Hallböök
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3.  Gap junctional communication in the vibration-sensitive response of sea anemones.

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Journal:  Neuron       Date:  1999-02       Impact factor: 17.173

5.  Initial analysis of immunochemical cell surface properties, location and formation of the serotonergic apical ganglion in sea urchin embryos.

Authors:  S Yaguchi; K Kanoh; S Amemiya; H Katow
Journal:  Dev Growth Differ       Date:  2000-10       Impact factor: 2.053

Review 6.  Evolution of eyes.

Authors:  R D Fernald
Journal:  Curr Opin Neurobiol       Date:  2000-08       Impact factor: 6.627

7.  Distinct phenotypes of mutant mice lacking agrin, MuSK, or rapsyn.

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8.  Homeobrain, a novel paired-like homeobox gene is expressed in the Drosophila brain.

Authors:  U Walldorf; A Kiewe; M Wickert; M Ronshaugen; W McGinnis
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9.  Spatially restricted expression of PlOtp, a Paracentrotus lividus orthopedia-related homeobox gene, is correlated with oral ectodermal patterning and skeletal morphogenesis in late-cleavage sea urchin embryos.

Authors:  M Di Bernardo; S Castagnetti; D Bellomonte; P Oliveri; R Melfi; F Palla; G Spinelli
Journal:  Development       Date:  1999-05       Impact factor: 6.868

10.  SpSoxB1, a maternally encoded transcription factor asymmetrically distributed among early sea urchin blastomeres.

Authors:  A P Kenny; D Kozlowski; D W Oleksyn; L M Angerer; R C Angerer
Journal:  Development       Date:  1999-12       Impact factor: 6.868

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  96 in total

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Authors:  Sharleen Yuan; Brian D Burrell
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2.  A database of mRNA expression patterns for the sea urchin embryo.

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Journal:  Dev Biol       Date:  2006-08-22       Impact factor: 3.582

Review 3.  Molecular evolution of the vertebrate mechanosensory cell and ear.

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Journal:  Int J Dev Biol       Date:  2007       Impact factor: 2.203

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Authors:  Marsha L Pierce; Michael D Weston; Bernd Fritzsch; Harrison W Gabel; Gary Ruvkun; Garrett A Soukup
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Authors:  Sam Dupont; William Thorndyke; Michael C Thorndyke; Robert D Burke
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Journal:  Development       Date:  2009-04       Impact factor: 6.868

7.  Deep evolutionary origins of neurobiology: Turning the essence of 'neural' upside-down.

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Journal:  Commun Integr Biol       Date:  2009

8.  Sea urchin tube feet are photosensory organs that express a rhabdomeric-like opsin and PAX6.

Authors:  Michael P Lesser; Karen L Carleton; Stefanie A Böttger; Thomas M Barry; Charles W Walker
Journal:  Proc Biol Sci       Date:  2011-03-30       Impact factor: 5.349

Review 9.  Gene, cell, and organ multiplication drives inner ear evolution.

Authors:  Bernd Fritzsch; Karen L Elliott
Journal:  Dev Biol       Date:  2017-09-01       Impact factor: 3.582

10.  A putative 'pre-nervous' endocannabinoid system in early echinoderm development.

Authors:  G A Buznikov; L A Nikitina; V V Bezuglov; M E Y Francisco; G Boysen; I N Obispo-Peak; R E Peterson; E R Weiss; H Schuel; B R S Temple; A L Morrow; J M Lauder
Journal:  Dev Neurosci       Date:  2009-11-12       Impact factor: 2.984

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