An increasing number of diseases of the brain are being linked to deviations from the normally carefully calibrated balance between excitatory and inhibitory neuronal activities. A critical choice point for establishing this inhibitory/excitatory neuronal balance is governed by the transcription factor Ptf1a. Ptf1a is a bHLH transcription factor that is required for GABAergic inhibitory neurons in the dorsal spinal cord, cerebellum, and retina. In the absence of Ptf1a, neural progenitor cells fail to generate inhibitory neurons and aberrantly assume an excitatory neuronal phenotype. Uncovering the transcriptional control of Ptf1a expression and the function of its downstream targets will provide molecular insight into developmental processes regulating the neuronal circuitry in multiple regions of the central nervous system. Because of the timing and the mechanism of PTf1a function, it provides a unique opportunity to uncover the molecular mechanisms that couple neuronal differentiation and neuronal subtype specification. Identification of cis-regulatory sequences in the Ptf1a gene locus revealed separable elements controlling transcription initiation, autoregulation, restriction to dI4/dIL progenitors, and downregulation as the cells differentiate to inhibitory neurons. In addition, direct targets of Ptf1a have been identified that serve as candidates for mediating inhibitory neuronal identity while suppressing excitatory neuron identity. The goal of the current project is to build on these findings to 1) identify trans-acting upstream factors and signaling pathways that function through the cis-regulatory sequences to regulate Ptf1a, and 2) determine the function of a downstream target of Ptf1a in specification of interneurons in the dorsal horn, cerebellum, and retina. Success in this program will impact understanding of how stem/progenitor cells transition to mature cell types and generate the neuronal diversity required for circuit formation. Identifying the pathways that direct cells down a specific lineage may have therapeutic value in stem cell manipulation and treatment of neurological disorders.
Alterations in the balance of inhibitory and excitatory neurons are thought to underlie diverse neurological disorders from epilepsy to autism to hyperalgesia. Ptf1a is an essential regulator of this balance in multiple regions of the nervous system, and thus, factors and signaling pathways regulating Ptf1a and regulated by Ptf1a will control the formation of these balanced neuronal networks. Pathways identified here may serve as targets for manipulating the fate of stem cells for regenerative purposes, and are likely to provide fundamental principles of gene regulation common to developing systems.
|Goodson, Noah B; Nahreini, Jhenya; Randazzo, Grace et al. (2018) Prdm13 is required for Ebf3+ amacrine cell formation in the retina. Dev Biol 434:149-163|
|Mona, Bishakha; Uruena, Ana; Kollipara, Rahul K et al. (2017) Repression by PRDM13 is critical for generating precision in neuronal identity. Elife 6:|
|Mona, Bishakha; Avila, John M; Meredith, David M et al. (2016) Regulating the dorsal neural tube expression of Ptf1a through a distal 3' enhancer. Dev Biol 418:216-225|
|Lai, Helen C; Seal, Rebecca P; Johnson, Jane E (2016) Making sense out of spinal cord somatosensory development. Development 143:3434-3448|
|Russ, Jeffrey B; Borromeo, Mark D; Kollipara, Rahul K et al. (2015) Misexpression of ptf1a in cortical pyramidal cells in vivo promotes an inhibitory peptidergic identity. J Neurosci 35:6028-37|
|Borromeo, Mark D; Meredith, David M; Castro, Diogo S et al. (2014) A transcription factor network specifying inhibitory versus excitatory neurons in the dorsal spinal cord. Development 141:2803-12|
|Tran, Tracy S; Carlin, Edward; Lin, Ruihe et al. (2013) Neuropilin2 regulates the guidance of post-crossing spinal commissural axons in a subtype-specific manner. Neural Dev 8:15|
|Chang, Joshua C; Meredith, David M; Mayer, Paul R et al. (2013) Prdm13 mediates the balance of inhibitory and excitatory neurons in somatosensory circuits. Dev Cell 25:182-95|
|Meredith, David M; Borromeo, Mark D; Deering, Tye G et al. (2013) Program specificity for Ptf1a in pancreas versus neural tube development correlates with distinct collaborating cofactors and chromatin accessibility. Mol Cell Biol 33:3166-79|
|Johnson, Jane E; Macdonald, Raymond J (2011) Notch-independent functions of CSL. Curr Top Dev Biol 97:55-74|
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