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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
1992-10-7
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pubmed:databankReference |
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M79310,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M81118,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M95192,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S49473,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S49475,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X65112,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X65113,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X66097,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X66098,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X72830
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pubmed:abstractText |
The mechanosensory bristles of adult Drosophila are composed of four cells that, in most cases, are progeny of a single sensory organ precursor (SOP) cell. Two sister cells in this lineage, the trichogen and tormogen, produce the external shaft and socket of the bristle, respectively. Loss-of-function mutations of Hairless (H) confer two distinct mutant phenotypes on adult bristles. The bristle loss phenotype results from the failure to specify and/or execute the SOP cell fate; the double socket phenotype results from the transformation of the trichogen (shaft) cell into a second tormogen (socket) cell. We have found that the H gene encodes a novel basic protein with a predicted molecular mass of 109 kD. Basal levels of expression of a transgene (P[Hs-H]) in which the H protein-coding region is under the control of the Hsp70 promoter are sufficient to provide full rescue of H mutant phenotypes. Heat shock treatment of P[Hs-H] transgenic animals as late larvae and early pupae produces a tormogen-to-trichogen (double shaft) cell fate transformation, as well as bristle multiplication and loss phenotypes very similar to those caused by loss-of-function mutations in the neurogenic gene Notch. Our results indicate that the SOP cell fate requires H to antagonize the activity of the neurogenic group of genes and that the expression of distinct cell fates by the trichogen/tormogen sister cell pair depends on an asymmetry in their levels of H+ activity or in their thresholds for response to H.
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Sep
|
pubmed:issn |
0890-9369
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
6
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1752-69
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:1516831-Amino Acid Sequence,
pubmed-meshheading:1516831-Animals,
pubmed-meshheading:1516831-Base Sequence,
pubmed-meshheading:1516831-Cell Differentiation,
pubmed-meshheading:1516831-Cloning, Molecular,
pubmed-meshheading:1516831-Drosophila,
pubmed-meshheading:1516831-Drosophila Proteins,
pubmed-meshheading:1516831-Molecular Sequence Data,
pubmed-meshheading:1516831-Promoter Regions, Genetic,
pubmed-meshheading:1516831-Proteins,
pubmed-meshheading:1516831-Recombinant Fusion Proteins,
pubmed-meshheading:1516831-Restriction Mapping,
pubmed-meshheading:1516831-Sense Organs,
pubmed-meshheading:1516831-Transcription Factors
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pubmed:year |
1992
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pubmed:articleTitle |
The Drosophila gene Hairless encodes a novel basic protein that controls alternative cell fates in adult sensory organ development.
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pubmed:affiliation |
Department of Biology, University of California, San Diego, La Jolla 92093-0322.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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