Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2001-2-22
pubmed:abstractText
The decapentaplegic (dpp) gene directs numerous developmental events in Drosophila melanogaster. dpp encodes a member of the Transforming Growth Factor-beta family of secreted signaling molecules. At this time, mechanisms of dpp signaling have not yet been fully described. Therefore we conducted a genetic screen for new dpp signaling pathway components. The screen exploited a transvection-dependent dpp phenotype: heldout wings. The screen generated 30 mutations that appear to disrupt transvection at dpp. One of the mutations is a translocation with a recessive lethal breakpoint in cytological region 23C1-2. Genetic analyses identified a number of mutations allelic to this breakpoint. The 23C1-2 complementation group includes several mutations in the newly discovered gene lilliputian (lilli). lilli mutations that disrupt the transvection-dependent dpp phenotype are also dominant maternal enhancers of recessive embryonic lethal alleles of dpp and screw. lilli zygotic mutant embryos exhibit a partially ventralized phenotype similar to dpp embryonic lethal mutations. Phylogenetic analyses revealed that lilli encodes the only Drosophila member of a family of transcription factors that includes the human genes causing Fragile-X mental retardation (FMR2) and Burkitt's Lymphoma (LAF4). Taken together, the genetic and phylogenetic data suggest that lilli may be an activator of dpp expression in embryonic dorsal-ventral patterning and wing development.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-10353905, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-10409512, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-10588740, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-10655223, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-10731132, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-10767313, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-1989880, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-2120113, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-2296575, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-3447015, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-3467201, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-6804094, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-6806814, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-7705627, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-7768443, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-8330541, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-8770593, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-8852848, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-9205057, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-9233580, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-9272957, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-9299237, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-9475739, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-9502724, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-9529255, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-9636086, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-9808577, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-9810230, http://linkedlifedata.com/resource/pubmed/commentcorrection/11156991-9827795
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0016-6731
pubmed:author
pubmed:issnType
Print
pubmed:volume
157
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
717-25
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:11156991-Alleles, pubmed-meshheading:11156991-Amino Acid Sequence, pubmed-meshheading:11156991-Animals, pubmed-meshheading:11156991-Burkitt Lymphoma, pubmed-meshheading:11156991-Chromosome Mapping, pubmed-meshheading:11156991-Crosses, Genetic, pubmed-meshheading:11156991-Drosophila Proteins, pubmed-meshheading:11156991-Drosophila melanogaster, pubmed-meshheading:11156991-Fragile X Mental Retardation Protein, pubmed-meshheading:11156991-Gene Expression Regulation, Developmental, pubmed-meshheading:11156991-Genes, Dominant, pubmed-meshheading:11156991-Genes, Recessive, pubmed-meshheading:11156991-Insect Proteins, pubmed-meshheading:11156991-Models, Genetic, pubmed-meshheading:11156991-Molecular Sequence Data, pubmed-meshheading:11156991-Mutation, pubmed-meshheading:11156991-Nerve Tissue Proteins, pubmed-meshheading:11156991-Nuclear Proteins, pubmed-meshheading:11156991-Phenotype, pubmed-meshheading:11156991-Phylogeny, pubmed-meshheading:11156991-RNA-Binding Proteins, pubmed-meshheading:11156991-Signal Transduction, pubmed-meshheading:11156991-Transcription Factors
pubmed:year
2001
pubmed:articleTitle
A screen for modifiers of decapentaplegic mutant phenotypes identifies lilliputian, the only member of the Fragile-X/Burkitt's Lymphoma family of transcription factors in Drosophila melanogaster.
pubmed:affiliation
Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't