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BMC Developmental Biology
Article . 2006 . Peer-reviewed
License: CC BY
Data sources: Crossref
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BMC Developmental Biology
Article
License: CC BY
Data sources: UnpayWall
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PubMed Central
Other literature type . 2006
License: CC BY
Data sources: PubMed Central
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The Hlx homeobox transcription factor is required early in enteric nervous system development

Authors: Bates, M; Dunagan, D; Welch, L; Kaul, A; Harvey, RP;

The Hlx homeobox transcription factor is required early in enteric nervous system development

Abstract

Abstract Background Development of the enteric nervous system (ENS) requires interactions between migrating neural crest cells and the nascent gastrointestinal tract that are dependent upon genes expressed by both cell compartments. Hlx, a homeobox transcription factor gene that is expressed in mouse intestinal and hepatic mesenchyme, is required for normal embryonic growth of intestine and liver, and the Hlx-/- genotype is embryonic lethal. We hypothesized that Hlx is required for ENS development. Results Enteric neurons were identified in Hlx+/+ and Hlx-/- mouse embryos by immunostaining of embryo sections for the neural markers PGP9.5 and Phox2b, or by staining for β-galactosidase in whole-mount embryos containing the dopamine β-hydroxylase-nLacZ transgene. In Hlx+/+ embryos, neural crest cells/enteric neurons have moved from the stomach into the intestine by E10.5. By contrast, neural crest cells/enteric neurons remain largely restricted to the lateral stomach mesenchyme of Hlx-/- embryos, with only a few scattered neural crest cells/enteric neurons in the intestine between E10.5–16.5. Conclusion The Hlx homeobox transcription factor is required for early aspects of ENS development.

Keywords

Male, 570, Time Factors, 1.1 Normal biological development and functioning, Knockout, 610, 32 Biomedical and Clinical Sciences, Mice, Transgenic, Dopamine beta-Hydroxylase, Inbred C57BL, 3105 Genetics, Transgenic, Enteric Nervous System, Mesoderm, Mice, anzsrc-for: 32 Biomedical and Clinical Sciences, Genetics, Animals, Developmental, anzsrc-for: 31 Biological Sciences, Pediatric, Homeodomain Proteins, Mice, Knockout, Neurons, anzsrc-for: 42 Health sciences, Liver Disease, Neurosciences, Gene Expression Regulation, Developmental, Stem Cell Research, beta-Galactosidase, Immunohistochemistry, Gastrointestinal Tract, Mice, Inbred C57BL, anzsrc-for: 3105 Genetics, Gene Expression Regulation, anzsrc-for: 11 Medical and Health Sciences, Lac Operon, Neurological, anzsrc-for: 06 Biological Sciences, Congenital Structural Anomalies, Female, Digestive Diseases, 31 Biological Sciences, Research Article, Transcription Factors

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
22
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