Literature DB >> 1703680

Genes required for specifying cell fates in Drosophila embryonic sensory nervous system.

Y N Jan1, L Y Jan.   

Abstract

The nervous system contains a diverse group of cells. Specification of the correct cell fate is obviously important for the proper function of the nervous system, yet how are the fates of different neurons determined during development? Very little is known about the underlying molecular mechanisms used in the mammalian nervous system. How, for example, are certain cells directed to form pyramidal cells rather than local interneurons? In the fruit fly Drosophila melanogaster, and the nematode Caenorhabditis elegans, some progress has been made in studying neuronal fate determination. For instance, in Drosophila, a number of genes acting at different levels have been found to control this process. They function to (1) endow a subset of the ectodermal cells in the early embryo with the potential to become neuronal precursors, (2) commit some of these cells to the fate of neuronal precursors, (3) specify the identity of these neuronal precursors, and (4) specify the identity of the individual progeny cells of a neuronal precursor. In this review, we discuss first the rationale of the genetic approach, then outline the working hypothesis and, finally, briefly describe the genes known to be involved in the formation of the sensory nervous system in Drosophila. We also discuss the prospects for extrapolating these molecular mechanisms and principles to vertebrate and invertebrate neural development.

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Year:  1990        PMID: 1703680     DOI: 10.1016/0166-2236(90)90083-m

Source DB:  PubMed          Journal:  Trends Neurosci        ISSN: 0166-2236            Impact factor:   13.837


  27 in total

1.  The Enhancer of split [E(spl)] locus of Drosophila encodes seven independent helix-loop-helix proteins.

Authors:  C Delidakis; S Artavanis-Tsakonas
Journal:  Proc Natl Acad Sci U S A       Date:  1992-09-15       Impact factor: 11.205

2.  The Drosophila couch potato gene: an essential gene required for normal adult behavior.

Authors:  H J Bellen; H Vaessin; E Bier; A Kolodkin; D D'Evelyn; S Kooyer; Y N Jan
Journal:  Genetics       Date:  1992-06       Impact factor: 4.562

3.  Two closely linked Drosophila POU domain genes are expressed in neuroblasts and sensory elements.

Authors:  T Dick; X H Yang; S L Yeo; W Chia
Journal:  Proc Natl Acad Sci U S A       Date:  1991-09-01       Impact factor: 11.205

4.  Mediation of NGF signaling by post-translational inhibition of HES-1, a basic helix-loop-helix repressor of neuronal differentiation.

Authors:  A Ström; P Castella; J Rockwood; J Wagner; M Caudy
Journal:  Genes Dev       Date:  1997-12-01       Impact factor: 11.361

5.  Sequential emergence of the evenly spaced microchaetes on the notum of Drosophila.

Authors:  Kazuya Usui; Ken-Ichi Kimura
Journal:  Rouxs Arch Dev Biol       Date:  1993-12

6.  Regulatory signals and signal molecules in early neurogenesis of Drosophila melanogaster.

Authors:  José A Campos-Ortega; Marc Haenlin
Journal:  Rouxs Arch Dev Biol       Date:  1992-02

7.  Patterns of cell death in the embryonic antenna of the grasshopper Schistocerca gregaria.

Authors:  George Boyan; Philip Graf; Erica Ehrhardt
Journal:  Dev Genes Evol       Date:  2018-03-06       Impact factor: 0.900

Review 8.  The role of BETA2/NeuroD1 in the development of the nervous system.

Authors:  Jang-Hyeon Cho; Ming-Jer Tsai
Journal:  Mol Neurobiol       Date:  2004-08       Impact factor: 5.590

9.  The WRPW motif of the hairy-related basic helix-loop-helix repressor proteins acts as a 4-amino-acid transcription repression and protein-protein interaction domain.

Authors:  A L Fisher; S Ohsako; M Caudy
Journal:  Mol Cell Biol       Date:  1996-06       Impact factor: 4.272

10.  Csx: a murine homeobox-containing gene specifically expressed in the developing heart.

Authors:  I Komuro; S Izumo
Journal:  Proc Natl Acad Sci U S A       Date:  1993-09-01       Impact factor: 11.205

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