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PMID:17596284

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Citation

Ferri, AL, Lin, W, Mavromatakis, YE, Wang, JC, Sasaki, H, Whitsett, JA and Ang, SL (2007) Foxa1 and Foxa2 regulate multiple phases of midbrain dopaminergic neuron development in a dosage-dependent manner. Development 134:2761-9

Abstract

The role of transcription factors in regulating the development of midbrain dopaminergic (mDA) neurons is intensively studied owing to the involvement of these neurons in diverse neurological disorders. Here we demonstrate novel roles for the forkhead/winged helix transcription factors Foxa1 and Foxa2 in the specification and differentiation of mDA neurons by analysing the phenotype of Foxa1 and Foxa2 single- and double-mutant mouse embryos. During specification, Foxa1 and Foxa2 regulate the extent of neurogenesis in mDA progenitors by positively regulating Ngn2 (Neurog2) expression. Subsequently, Foxa1 and Foxa2 regulate the expression of Nurr1 (Nr4a2) and engrailed 1 in immature neurons and the expression of aromatic l-amino acid decarboxylase and tyrosine hydroxylase in mature neurons during early and late differentiation of midbrain dopaminergic neurons. Interestingly, genetic evidence indicates that these functions require different gene dosages of Foxa1 and Foxa2. Altogether, our results demonstrate that Foxa1 and Foxa2 regulate multiple phases of midbrain dopaminergic neuron development in a dosage-dependent manner.

Links

PubMed Online version:10.1242/dev.000141

Keywords

Animals; Basic Helix-Loop-Helix Transcription Factors/genetics; Cell Differentiation/genetics; Dopamine/metabolism; Female; Gene Dosage/physiology; Gene Expression Regulation, Developmental; Hepatocyte Nuclear Factor 3-alpha/genetics; Hepatocyte Nuclear Factor 3-alpha/metabolism; Hepatocyte Nuclear Factor 3-alpha/physiology; Hepatocyte Nuclear Factor 3-beta/genetics; Hepatocyte Nuclear Factor 3-beta/metabolism; Hepatocyte Nuclear Factor 3-beta/physiology; Homeodomain Proteins/genetics; Male; Mesencephalon/embryology; Mesencephalon/metabolism; Mice; Mice, Transgenic; Models, Biological; Nerve Tissue Proteins/genetics; Neurons/cytology; Neurons/metabolism; Pregnancy; Stem Cells/cytology; Stem Cells/metabolism; Transcription Factors/genetics

Significance

Annotations

Gene product Qualifier GO ID GO term name Evidence Code with/from Aspect Notes Status


See also

References

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