Literature DB >> 10402954

Segment polarity genes in neuroblast formation and identity specification during Drosophila neurogenesis.

K M Bhat1.   

Abstract

The relatively simple central nervous system (CNS) of the Drosophila embryo provides a useful model system for investigating the mechanisms that generate and pattern complex nervous systems. Central to the generation of different types of neurons by precursor neuroblasts is the initial specification of neuroblast identity and the Drosophila segment polarity genes, genes that specify regions within a segment or repeating unit of the Drosophila embryo, have emerged recently as significant players in this process. During neurogenesis the segment polarity genes are expressed in the neuroectodermal cells from which neuroblasts delaminate and they continue to be expressed in neuroblasts and their progeny. Loss-of-function mutations in these genes lead to a failure in the formation of neuroblasts and/or specification of neuroblast identity. Results from several recent studies suggest that regulatory interactions between segment polarity genes during neurogenesis lead to an increase in the number of neuroblasts and specification of different identities to neuroblasts within a population of cells.

Entities:  

Mesh:

Year:  1999        PMID: 10402954     DOI: 10.1002/(SICI)1521-1878(199906)21:6<472::AID-BIES4>3.0.CO;2-W

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  34 in total

1.  Single-cell mapping of neural and glial gene expression in the developing Drosophila CNS midline cells.

Authors:  Scott R Wheeler; Joseph B Kearney; Amaris R Guardiola; Stephen T Crews
Journal:  Dev Biol       Date:  2006-04-24       Impact factor: 3.582

2.  Wingless activity in the precursor cells specifies neuronal migratory behavior in the Drosophila nerve cord.

Authors:  Krishna Moorthi Bhat
Journal:  Dev Biol       Date:  2007-09-17       Impact factor: 3.582

3.  Ancestry-independent fate specification and plasticity in the developmental timing of a typical Drosophila neuronal lineage.

Authors:  Ivana Gaziova; Krishna Moorthi Bhat
Journal:  Development       Date:  2008-12-15       Impact factor: 6.868

4.  A neurodegenerative disease affecting synaptic connections in Drosophila mutant for the tumor suppressor morphogen Patched.

Authors:  Michal Gazi; Baragur V Shyamala; Krishna Moorthi Bhat
Journal:  Dev Biol       Date:  2009-07-25       Impact factor: 3.582

5.  Roles of Hox genes in the patterning of the central nervous system of Drosophila.

Authors:  Alicia Estacio-Gómez; Fernando J Díaz-Benjumea
Journal:  Fly (Austin)       Date:  2013-12-05       Impact factor: 2.160

Review 6.  Programmed cell death acts at different stages of Drosophila neurodevelopment to shape the central nervous system.

Authors:  Filipe Pinto-Teixeira; Nikolaos Konstantinides; Claude Desplan
Journal:  FEBS Lett       Date:  2016-07-28       Impact factor: 4.124

7.  Differential effects of Drosophila mastermind on asymmetric cell fate specification and neuroblast formation.

Authors:  Barry Yedvobnick; Anumeha Kumar; Padmashree Chaudhury; Jonathan Opraseuth; Nathan Mortimer; Krishna Moorthi Bhat
Journal:  Genetics       Date:  2004-03       Impact factor: 4.562

8.  Patched regulation of axon guidance is by specifying neural identity in the Drosophila nerve cord.

Authors:  Tanuja T Merianda; Vandana Botta; Krishna Moorthi Bhat
Journal:  Dev Genes Evol       Date:  2005-03-08       Impact factor: 0.900

9.  Segment-specific neuronal subtype specification by the integration of anteroposterior and temporal cues.

Authors:  Daniel Karlsson; Magnus Baumgardt; Stefan Thor
Journal:  PLoS Biol       Date:  2010-05-11       Impact factor: 8.029

10.  Single cell cultures of Drosophila neuroectodermal and mesectodermal central nervous system progenitors reveal different degrees of developmental autonomy.

Authors:  Karin Lüer; Gerhard M Technau
Journal:  Neural Dev       Date:  2009-08-03       Impact factor: 3.842

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.