We are investigating how the central nervous system (CNS) is assembled during embryonic development. This is has several potential human health benefits relevant to the NIH mission. First, the treatment of many neurological disorders would benefit from a method for generating specific types of neurons from the patient's own induced pluripotent stem (IPS) cells. Second, many psychiatric disorders arise in part from developmental defects. Generating therapeutic tools to treat these types of disorders will require a detailed understanding of how each neuronal subtype is normally formed. We have been investigating this question in the model organism Drosophila, which has been profoundly important for discovering mechanisms of neurogenesis relevant in mammals. Much is currently known about how neural progenitors acquire their spatial identity (e.g. forebrain vs. hindbrain) but we still know very little about how they sequentially produce different cell types. We previously identified a series of transcription factors that specify temporal identity within the Drosophila nervous system. Here we focus on three related questions in embryonic progenitors (Aims 1-3) and conclude with the first analysis of temporal identity in a newly discovered Drosophila post- embryonic neural progenitor that shares features with the primate outer ventricular zone progenitor (Aim 4).
In Aim 1, we will determine whether the Hunchback transcription factor acts transiently in progenitors or continuously in post-mitotic neurons to specify """"""""first-born"""""""" temporal identity. Because the mammalian Hunchback ortholog Ikaros has a similar role in specifying early-born retinal ganglion cell fates, this aim has the potential to hep design therapeutic treatments to replace a cell type essential for human vision.
In Aim 2, we follow up on results from the previous funding period showing that neural progenitors lose competence over time to form early-born neuron subtypes in response to a pulse of Hunchback expression. We will determine the mechanism of """"""""progressive loss of competence"""""""" in these progenitors, aided by the identification of a nuclear protein whose expression mimics the competence window, and whose prolonged expression can extend the competence window.
In Aim 3, we initiate work on a new """"""""Type II"""""""" neural stem cell that we and others recently discovered. Each brain lobe contains 8 type II neuroblasts that divide asymmetrically to produce a series of """"""""intermediate neural progenitors (INPs) that each also divide asymmetrically to make a sequence of 10-12 neurons. We will characterize the relationship between neuroblast or INP birthorder and the production of distinct neural subtypes. We have recently identified transcription factors expressed in sequentially in INPs, and we will determine if they specify temporal identity in these sublineages.

Public Health Relevance

The proposed project is relevant to public health because understanding how spatial and temporal cues are integrated by single progenitors to generate unique neuronal subtypes will help guide stem cell therapy for replacing neurons lost to traumatic brain injury (TBI), stroke, disease, or age-related degeneration. Thus, the proposed research is relevant to NIH's mission to reduce the burden to society arising from prevalent environmental and genetic brain disorders.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37HD027056-22
Application #
8646935
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Henken, Deborah B
Project Start
1989-09-01
Project End
2017-03-31
Budget Start
2014-04-01
Budget End
2015-03-31
Support Year
22
Fiscal Year
2014
Total Cost
Indirect Cost
Name
University of Oregon
Department
Neurosciences
Type
Graduate Schools
DUNS #
City
Eugene
State
OR
Country
United States
Zip Code
97403
Tomorsky, Johanna; DeBlander, Leah; Kentros, Clifford G et al. (2017) TU-Tagging: A Method for Identifying Layer-Enriched Neuronal Genes in Developing Mouse Visual Cortex. eNeuro 4:
Doe, Chris Q (2017) Temporal Patterning in the Drosophila CNS. Annu Rev Cell Dev Biol 33:219-240
Manning, Laurina; Doe, Chris Q (2017) Immunofluorescent antibody staining of intact Drosophila larvae. Nat Protoc 12:1-14
Hirono, Keiko; Kohwi, Minoree; Clark, Matt Q et al. (2017) The Hunchback temporal transcription factor establishes, but is not required to maintain, early-born neuronal identity. Neural Dev 12:1
Walsh, Kathleen T; Doe, Chris Q (2017) Drosophila embryonic type II neuroblasts: origin, temporal patterning, and contribution to the adult central complex. Development 144:4552-4562
Farnsworth, Dylan R; Doe, Chris Q (2017) Opportunities lost and gained: Changes in progenitor competence during nervous system development. Neurogenesis (Austin) 4:e1324260
Syed, Mubarak Hussain; Mark, Brandon; Doe, Chris Q (2017) Playing Well with Others: Extrinsic Cues Regulate Neural Progenitor Temporal Identity to Generate Neuronal Diversity. Trends Genet 33:933-942
Syed, Mubarak Hussain; Mark, Brandon; Doe, Chris Q (2017) Steroid hormone induction of temporal gene expression in Drosophila brain neuroblasts generates neuronal and glial diversity. Elife 6:
Joy, Tasha; Hirono, Keiko; Doe, Chris Q (2015) The RanGEF Bj1 promotes prospero nuclear export and neuroblast self-renewal. Dev Neurobiol 75:485-93
Farnsworth, Dylan R; Bayraktar, Omer Ali; Doe, Chris Q (2015) Aging Neural Progenitors Lose Competence to Respond to Mitogenic Notch Signaling. Curr Biol 25:3058-68

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