Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
21
pubmed:dateCreated
1999-11-24
pubmed:abstractText
The myogenic factor D-MEF2 is required for the proper differentiation of muscle cells during Drosophila embryogenesis and the correct patterning of indirect flight muscles assembled during later metamorphosis. In addition to these essential myogenic functions, mutant D-mef2 adult females are weakly fertile and produce defective eggs. D-MEF2 is expressed in nurse and follicle cells of the wild-type egg chamber. We have analyzed the D-mef2 oogenic phenotype and show that the gene is required for the normal patterning and differentiation of the centripetally migrating follicle cells that are crucial for development of the anterior chorionic structures. D-mef2 alleles exhibit a genetic interaction with a dominant-negative allele of thick veins (tkv), which encodes a type I receptor of the Decapentaplegic-signaling pathway. tkv RNA is overexpressed in D-mef2 mutant egg chambers, and, conversely, forced expression of D-mef2 represses tkv expression. These results indicate a role for D-MEF2 in the regulation of tkv gene expression and Decapentaplegic signal transduction that are essential for proper determination and/or differentiation of the anterior follicle cells. Additionally, they demonstrate a vital function for the D-MEF2 transcription factor in multiple genetic pathways during Drosophila development.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-2924351, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-3467201, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-3722280, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-7540118, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-7556894, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-7688122, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-7691414, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-7697719, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-7697720, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-7700357, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-7729689, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-7791898, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-7839146, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-7915669, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-8101173, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-8178370, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-8223268, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-8625842, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-8647437, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-8698232, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-8722779, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-9012496, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-9034334, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-9367443, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-9553046, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-9621427, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-9694800, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-9732552, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-9814706, http://linkedlifedata.com/resource/pubmed/commentcorrection/10518546-9882489
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0027-8424
pubmed:author
pubmed:issnType
Print
pubmed:day
12
pubmed:volume
96
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
11889-94
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:10518546-Animals, pubmed-meshheading:10518546-DNA-Binding Proteins, pubmed-meshheading:10518546-Drosophila, pubmed-meshheading:10518546-Drosophila Proteins, pubmed-meshheading:10518546-Endonucleases, pubmed-meshheading:10518546-Female, pubmed-meshheading:10518546-Gene Expression Regulation, Developmental, pubmed-meshheading:10518546-Genes, Insect, pubmed-meshheading:10518546-Genotype, pubmed-meshheading:10518546-Muscle Development, pubmed-meshheading:10518546-Muscles, pubmed-meshheading:10518546-Mutagenesis, pubmed-meshheading:10518546-Myogenic Regulatory Factors, pubmed-meshheading:10518546-Oogenesis, pubmed-meshheading:10518546-Ovum, pubmed-meshheading:10518546-Phenotype, pubmed-meshheading:10518546-Protein-Serine-Threonine Kinases, pubmed-meshheading:10518546-Receptors, Cell Surface, pubmed-meshheading:10518546-Signal Transduction, pubmed-meshheading:10518546-Transcription Factors
pubmed:year
1999
pubmed:articleTitle
Oogenic function of the myogenic factor D-MEF2: negative regulation of the decapentaplegic receptor gene thick veins.
pubmed:affiliation
Center for Molecular and Structural Biology, Department of Cell Biology and Anatomy, Medical University of South Carolina, 86 Jonathan Lucas Street, Charleston, SC 29425, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't