4.7 Article

Neurogenin 2 is required for the development of ventral midbrain dopaminergic neurons

Journal

DEVELOPMENT
Volume 133, Issue 3, Pages 495-505

Publisher

COMPANY OF BIOLOGISTS LTD
DOI: 10.1242/dev.02223

Keywords

proneural genes; cell fate specification; differentiation; Sox2; Nurr1; stem cells; Parkinson's disease

Funding

  1. Medical Research Council [MC_U117570528, MC_U117570533] Funding Source: researchfish
  2. MRC [MC_U117570528, MC_U117570533] Funding Source: UKRI
  3. Medical Research Council [MC_U117570533, MC_U117570528] Funding Source: Medline
  4. Parkinson's UK [G-4068] Funding Source: Medline

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Proneural genes are crucial regulators of neurogenesis and subtype specification in many areas of the nervous system; however, their function in dopaminergic neuron development is unknown. We report that proneural genes have an intricate pattern of expression in the ventricular zone of the ventral midbrain, where mesencephalic dopaminergic neurons are generated. Neurogenin 2 (Ngn2) and Mash1 are expressed in the ventral midline, while Ngn1, Nyn2 and Mash1 are co-localized more laterally in the ventricular zone. Ngn2 is also expressed in an intermediate zone immediately adjacent to the ventricular zone at the ventral midline. To examine the function of these genes, we analyzed mutant mice in which one or two of these genes were deleted (Ngn1, Ngn2 and Mash1) or substituted (Mash1 in the Ngn2 locus). Our results demonstrate that Ngn2 is required for the differentiation of Sox2(+) ventricular zone progenitors into Nurr1(+) postmitotic dopaminergic neuron precursors in the intermediate zone, and that it is also likely to be required for their subsequent differentiation into tyrosine hydroxylase-positive dopaminergic neurons in the marginal zone. Although Mash1 normally has no detectable function in dopaminergic neuron development, it could partially rescue the generation of dopaminergic neuron precursors in the absence of Ngn2. These results demonstrate that Ngn2 is uniquely required for the development of midbrain dopaminergic neurons.

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