The transcription factor BCL11A defines distinct subsets of midbrain dopaminergic neurons

Midbrain dopaminergic (mDA) neurons are diverse in their projection targets, effect on behavior, and susceptibility to neurodegeneration. Little is known about the molecular mechanisms establishing this diversity during development. We show that the transcription factor BCL11A is expressed in a subset of mDA neurons in the developing and adult murine brain and in a subpopulation of pluripotent-stem-cell-derived human mDA neurons. By combining intersectional labeling and viral-mediated tracing, we demonstrate that Bcl11a-expressing mDA neurons form a highly specific subcircuit within the murine dopaminergic system. In the substantia nigra, the Bcl11a-expressing mDA subset is particularly vulnerable to neurodegeneration upon a-synuclein overexpression or oxidative stress. Inactivation of Bcl11a in murine mDA neurons increases this susceptibility further, alters the distribution of mDA neurons, and results in deficits in skilled motor behavior. In summary, BCL11A defines mDA subpopulations with highly distinctive characteristics and is required for establishing and maintaining their normal physiology.

Automated summary

The transcription factor BCL11A is expressed in subsets of murine and human dopamine neurons, forming specific subcircuits within the dopamine system. These Bcl11a-expressing neurons are vulnerable to neurodegeneration, as inactivation of Bcl11a increases susceptibility and results in motor behavior deficits. BCL11A is crucial for establishing and maintaining the physiological characteristics of dopamine neuron subpopulations.