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In JoVE (1)
Other Publications (5)
Articles by Rajiv Dixit in JoVE
Efficient Gene Delivery into Multiple CNS Territories Using In Utero Electroporation
Rajiv Dixit1, Fuqu Lu2, Robert Cantrup1, Nicole Gruenig1,2, Lisa Marie Langevin1, Deborah M. Kurrasch2, Carol Schuurmans1
1Department of Biochemistry and Molecular Biology, Hotchkiss Brain Institute, Alberta Children’s Hospital Research Institute, University of Calgary, 2Department of Medical Genetics, Alberta Children’s Hospital Research Institute, Hotchkiss Brain Institute, University of Calgary
In utero electroporation allows for rapid gene delivery in a spatially- and temporally-controlled manner in the developing central nervous system (CNS). Here we describe a highly adaptable in utero electroporation protocol that can be used to deliver expression constructs into multiple embryonic CNS domains, including the telencephalon, diencephalon and retina.
Other articles by Rajiv Dixit on PubMed
Case 11-2004: a Boy with Rash, Edema, and Hypertension
The New England Journal of Medicine. Sep, 2004 | Pubmed ID: 15356317
Case 28-2005: a Case of Systemic Necrotizing Vasculitis
The New England Journal of Medicine. Dec, 2005 | Pubmed ID: 16339106
Ascl1 Participates in Cajal-Retzius Cell Development in the Neocortex
Cerebral Cortex (New York, N.Y. : 1991). Nov, 2011 | Pubmed ID: 21467208
Cajal-Retzius cells are essential pioneer neurons that guide neuronal migration in the developing neocortex. During development, Cajal-Retzius cells arise from distinct progenitor domains that line the margins of the dorsal telencephalon, or pallium. Here, we show that the proneural gene Ascl1 is expressed in Cajal-Retzius cell progenitors in the pallial septum, ventral pallium, and cortical hem. Using a short-term lineage trace, we demonstrate that it is primarily the Ascl1-expressing progenitors in the pallial septum and ventral pallium that differentiate into Cajal-Retzius cells. Accordingly, we found a small, albeit significant reduction in the number of Reelin(+) and Trp73(+) Cajal-Retzius cells in the Ascl1(-/-) neocortex. Conversely, using a gain-of-function approach, we found that Ascl1 induces the expression of both Reelin, a Cajal-Retzius marker, and Tbr1, a marker of pallial-derived neurons, in a subset of early-stage pallial progenitors, an activity that declines over developmental time. Taken together, our data indicate that the proneural gene Ascl1 is required and sufficient to promote the differentiation of a subset of Cajal-Retzius neurons during early neocortical development. Notably, this is the first study that reports a function for Ascl1 in the pallium, as this gene is best known for its role in specifying subpallial neuronal identities.
Zac1 Plays a Key Role in the Development of Specific Neuronal Subsets in the Mouse Cerebellum
Neural Development. 2011 | Pubmed ID: 21592321
The cerebellum is composed of a diverse array of neuronal subtypes. Here we have used a candidate approach to identify Zac1, a tumor suppressor gene encoding a zinc finger transcription factor, as a new player in the transcriptional network required for the development of a specific subset of cerebellar nuclei and a population of Golgi cells in the cerebellar cortex.
Hip Fracture: a Complex Illness Among Complex Patients
Annals of Internal Medicine. Jan, 2012 | Pubmed ID: 22213508
