Document Detail


The CNS midline cells coordinate proper cell cycle progression and identity determination of the Drosophila ventral neuroectoderm.
MedLine Citation:
PMID:  11071757     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The CNS midline cells, specified by the single-minded (sim) gene, are required for the proper patterning of the ventral CNS and epidermis, which are derived from the Drosophila ventral neuroectoderm. Defects in the sim mutant are characterized by the loss of the gene expression, which is required for the proper formation of the ventral neurons and epidermis, and by a decrease in the spacing of longitudinal and commissural axon tracks. Molecular and cellular mechanisms for these defects were analyzed to elucidate the precise role of the CNS midline cells in proper patterning of the ventral neuroectoderm during embryonic neurogenesis. These analyses showed that the ventral neuroectoderm in the sim mutant fails to carry out its proper formation and characteristic cell division cycle. This resulted in the loss of the dividing neuroectodermal cells that are located ventral to the CNS midline. The CNS midline cells are also required for the cell cycle-independent expression of the neural and epidermal markers. This indicates that the CNS midline cells are essential for the establishment and maintenance of the ventral epidermal and neuronal cell lineage by cell-cell interaction. On the other hand, the CNS midline cells do not cause extensive cell death in the ventral neuroectoderm. This study indicates that the CNS midline cells play important roles in the coordination of the proper cell cycle progression and the correct identity determination of the adjacent ventral neuroectoderm along the dorsoventral axis.
Authors:
J Chang; I O Kim; J S Ahn; J S Kwon; S H Jeon; S H Kim
Related Documents :
20066107 - Shaping morphogen gradients by proteoglycans.
19906847 - Sanpodo: a context-dependent activator and inhibitor of notch signaling during asymmetr...
12100887 - Cell movements during gastrulation: snail dependent and independent pathways.
2387237 - Origin and organization of the zebrafish fate map.
19873357 - Pacemakers in nitella : iii. electrical alternans.
7640407 - Morphological and morphometrical features of the corpus albicans in the course of the p...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Developmental biology     Volume:  227     ISSN:  0012-1606     ISO Abbreviation:  Dev. Biol.     Publication Date:  2000 Nov 
Date Detail:
Created Date:  2000-12-08     Completed Date:  2001-01-04     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0372762     Medline TA:  Dev Biol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  307-23     Citation Subset:  IM    
Copyright Information:
Copyright 2000 Academic Press.
Affiliation:
Department of Chemistry, Konkuk University, Seoul, 143-701, Korea.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Animals
Apoptosis / genetics
Basic Helix-Loop-Helix Transcription Factors
Body Patterning / genetics
Cell Cycle
Cell Division
Central Nervous System / cytology,  embryology*
DNA-Binding Proteins / genetics*
Drosophila / embryology*,  genetics*
Drosophila Proteins
Ectoderm / cytology
Gene Expression Regulation, Developmental
Genes, Insect*
Genetic Markers
In Situ Hybridization
Models, Biological
Mutation
Nuclear Proteins / genetics*
Chemical
Reg. No./Substance:
0/Basic Helix-Loop-Helix Transcription Factors; 0/DNA-Binding Proteins; 0/Drosophila Proteins; 0/Genetic Markers; 0/Nuclear Proteins; 0/sim protein, Drosophila

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Mutational analysis of endothelin receptor b1 (rose) during neural crest and pigment pattern develop...
Next Document:  The murine gene, Traube, is essential for the growth of preimplantation embryos.