Literature DB >> 21624360

Neurogenesis in the water flea Daphnia magna (Crustacea, Branchiopoda) suggests different mechanisms of neuroblast formation in insects and crustaceans.

Petra Ungerer1, Bo Joakim Eriksson, Angelika Stollewerk.   

Abstract

Within euarthropods, the morphological and molecular mechanisms of early nervous system development have been analysed in insects and several representatives of chelicerates and myriapods, while data on crustaceans are fragmentary. Neural stem cells (neuroblasts) generate the nervous system in insects and in higher crustaceans (malacostracans); in the remaining euarthropod groups, the chelicerates (e.g. spiders) and myriapods (e.g. millipedes), neuroblasts are missing. In the latter taxa, groups of neural precursors segregate from the neuroectoderm and directly differentiate into neurons and glial cells. In all euarthropod groups, achaete-scute homologues are required for neuroblast/neural precursor group formation. In the insects Drosophila melanogaster and Tribolium castaneum achaete-scute homologues are initially expressed in clusters of cells (proneural clusters) in the neuroepithelium but expression becomes restricted to the future neuroblast. Subsequently genes such as snail and prospero are expressed in the neuroblasts which are required for asymmetric division and differentiation. In contrast to insects, malacostracan neuroblasts do not segregate into the embryo but remain in the outer neuroepithelium, similar to vertebrate neural stem cells. It has been suggested that neuroblasts are present in another crustacean group, the branchiopods, and that they also remain in the neuroepithelium. This raises the questions how the molecular mechanisms of neuroblast selection have been modified during crustacean and insect evolution and if the segregation or the maintenance of neuroblasts in the neuroepithelium represents the ancestral state. Here we take advantage of the recently published Daphnia pulex (branchiopod) genome and identify genes in Daphnia magna that are known to be required for the selection and asymmetric division of neuroblasts in the fruit fly D. melanogaster. We unambiguously identify neuroblasts in D. magna by molecular marker gene expression and division pattern. We show for the first time that branchiopod neuroblasts divide in the same pattern as insect and malacostracan neuroblasts. Furthermore, in contrast to D. melanogaster, neuroblasts are not selected from proneural clusters in the branchiopod. Snail rather than ASH is the first gene to be expressed in the nascent neuroblasts suggesting that ASH is not required for the selection of neuroblasts as in D. melanogaster. The prolonged expression of ASH in D. magna furthermore suggests that it is involved in the maintenance of the neuroblasts in the neuroepithelium. Based on these and additional data from various representatives of arthropods we conclude that the selection of neural precursors from proneural clusters as well as the segregation of neural precursors represents the ancestral state of neurogenesis in arthropods. We discuss that the derived characters of malacostracans and branchiopods - the absence of neuroblast segregation and proneural clusters - might be used to support or reject the possible groupings of paraphyletic crustaceans.
Copyright © 2011 Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Year:  2011        PMID: 21624360     DOI: 10.1016/j.ydbio.2011.05.662

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


  11 in total

1.  Larval neurogenesis in the copepod Tigriopus californicus (Tetraconata, Multicrustacea).

Authors:  Hendrikje Hein; Gerhard Scholtz
Journal:  Dev Genes Evol       Date:  2018-04-12       Impact factor: 0.900

2.  Analysis of snail genes in the crustacean Parhyale hawaiensis: insight into snail gene family evolution.

Authors:  Roberta L Hannibal; Alivia L Price; Ronald J Parchem; Nipam H Patel
Journal:  Dev Genes Evol       Date:  2012-03-31       Impact factor: 0.900

Review 3.  A flexible genetic toolkit for arthropod neurogenesis.

Authors:  Angelika Stollewerk
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2016-01-05       Impact factor: 6.237

Review 4.  The evolution of early neurogenesis.

Authors:  Volker Hartenstein; Angelika Stollewerk
Journal:  Dev Cell       Date:  2015-02-23       Impact factor: 12.270

5.  Spatiotemporal regulation of nervous system development in the annelid Capitella teleta.

Authors:  Abhinav Sur; Craig R Magie; Elaine C Seaver; Néva P Meyer
Journal:  Evodevo       Date:  2017-08-01       Impact factor: 2.250

6.  Development of an efficient RNA interference method by feeding for the microcrustacean Daphnia.

Authors:  Charles A Schumpert; Jeffry L Dudycha; Rekha C Patel
Journal:  BMC Biotechnol       Date:  2015-10-07       Impact factor: 2.563

7.  Serotonin-immunoreactivity in the ventral nerve cord of Pycnogonida--support for individually identifiable neurons as ancestral feature of the arthropod nervous system.

Authors:  Georg Brenneis; Gerhard Scholtz
Journal:  BMC Evol Biol       Date:  2015-07-10       Impact factor: 3.260

8.  The 'ventral organs' of Pycnogonida (Arthropoda) are neurogenic niches of late embryonic and post-embryonic nervous system development.

Authors:  Georg Brenneis; Gerhard Scholtz
Journal:  PLoS One       Date:  2014-04-15       Impact factor: 3.240

9.  Embryonic neurogenesis in Pseudopallene sp. (Arthropoda, Pycnogonida) includes two subsequent phases with similarities to different arthropod groups.

Authors:  Georg Brenneis; Angelika Stollewerk; Gerhard Scholtz
Journal:  Evodevo       Date:  2013-11-29       Impact factor: 2.250

10.  Development and staging of the water flea Daphnia magna (Straus, 1820; Cladocera, Daphniidae) based on morphological landmarks.

Authors:  Beate Mittmann; Petra Ungerer; Marleen Klann; Angelika Stollewerk; Carsten Wolff
Journal:  Evodevo       Date:  2014-03-18       Impact factor: 2.250

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.