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FoxP1 promotes midbrain identity in embryonic stem cell‐derived dopamine neurons by regulating Pitx3
Author(s) -
Konstantoulas Constantine James,
Parmar Malin,
Li Meng
Publication year - 2010
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.2010.06650.x
Subject(s) - embryonic stem cell , stem cell , biology , induced pluripotent stem cell , cellular differentiation , microbiology and biotechnology , homeobox protein nanog , dopamine , neuroscience , genetics , gene
J. Neurochem. (2010) 113 , 836–847. Abstract The robust generation of midbrain dopamine neurons from embryonic stem cells and patient‐specific induced pluripotent stem cells is a prospective tool for the development of new drugs and cell based therapies, and investigations into the aetiology of Parkinson’s disease. To achieve this, it is crucial to identify the fate‐determining regulatory factors that influence dopamine cell fate decision and the underlying molecular machinery. We identified FoxP1 as a novel marker for midbrain dopamine neurons. Enforced expression of FoxP1 in embryonic stem cells actuates the expression of Pitx3, a homeobox protein that is exclusively expressed in midbrain dopaminergic neurons and is required for their differentiation and survival during development and from embryonic stem cells in vitro . We show that FoxP1 can be recruited to the Pitx3 locus in embryonic stem cells and regulate Pitx3 promoter activity in a dual‐luciferase assay. This transcriptional regulation of Pitx3 by FoxP1 depends on the presence of two high affinity binding sites in the distal Pitx3 promoter, through which FoxP1 directly binds as demonstrated by chromatin immunoprecipitation and electrophoretic mobility shift assay. Thus, this study demonstrates for the first time a transcription regulatory role for FoxP1 on the Pitx3 gene in mammalian stem cells.