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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
1994-12-23
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pubmed:abstractText |
Homeobox genes are expressed with a specific spatial and temporal order, which is essential for pattern formation during the early development of both invertebrates and vertebrates. Here we show that widespread ectopic expression of the Hoxa-1 (Hox 1.6) gene directed by a human beta-actin promoter in transgenic mice is embryolethal and produces abnormal phenotypes in a subset of domains primarily located in anterior regions. Interestingly, this abnormal development in the Hoxa-1 transgenic mice is associated with ectopic expression of the Hoxb-1 (Hox 2.9) gene in select hindbrain regions. At gestation day 9.5, two domains of strong Hoxb-1 expression are found in the anterior region of the hindbrains of Hoxa-1 transgenic embryos. One region represents the normal pattern of Hoxb-1 expression in rhombomere 4 and its associated migrating neural crest cells, while another major domain of Hoxb-1 expression consistently appears in rhombomere 2. Similar ectopic domains of beta-galactosidase activity are detected in dual transgenic embryos containing both beta-actin/Hoxa-1 transgene and a Hoxb-1/lacZ reporter construct. Expression of another lacZ reporter gene that directs beta-galactosidase activity predominantly in rhombomere 2 is suppressed in the Hoxa-1 transgenic embryos. We have also detected weaker and variable ectopic Hoxb-1 expression in rhombomeres 1, 3 and 6. No ectopic Hoxb-1 expression is detected in rhombomere 5 and the expression of Hoxa-3 and Krox-20 in this region is unchanged in the Hoxa-1 transgenic embryos. While no obvious change in the morphology of the trigeminal or facial-acoustic ganglia is evident, phenotypic changes do occur in neurons that emanate from rhombomeres 2 and 3 in the Hoxa-1 transgenic embryos. Additionally, alterations in the pattern of Hoxa-2 and Hoxb-1 expression in a subpopulation of neural crest cells migrating from the rhombomere 2 region are detected in these transgenics. Taken together, these data suggest that ectopic Hoxa-1 expression can reorganize select regions of the developing hindbrain by inducing partial transformations of several rhombomeres into a rhombomere-4-like identity.
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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
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pubmed:issn |
0950-1991
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
120
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pubmed:geneSymbol |
Hoxa-1,
Hoxa-2,
Hoxb-1
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2431-42
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:7956823-Actins,
pubmed-meshheading:7956823-Animals,
pubmed-meshheading:7956823-Base Sequence,
pubmed-meshheading:7956823-Gene Expression Regulation,
pubmed-meshheading:7956823-Genes, Homeobox,
pubmed-meshheading:7956823-Immunohistochemistry,
pubmed-meshheading:7956823-In Situ Hybridization,
pubmed-meshheading:7956823-Mice,
pubmed-meshheading:7956823-Mice, Transgenic,
pubmed-meshheading:7956823-Molecular Sequence Data,
pubmed-meshheading:7956823-Morphogenesis,
pubmed-meshheading:7956823-Nervous System,
pubmed-meshheading:7956823-Neural Crest,
pubmed-meshheading:7956823-Promoter Regions, Genetic,
pubmed-meshheading:7956823-Rhombencephalon,
pubmed-meshheading:7956823-Transformation, Genetic
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pubmed:year |
1994
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pubmed:articleTitle |
Ectopic Hoxa-1 induces rhombomere transformation in mouse hindbrain.
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pubmed:affiliation |
Department of Toxicology and Pathology, Roche Research Center, Hoffmann-La Roche, Nutley, New Jersey 07110.
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pubmed:publicationType |
Journal Article
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