Dissertation/Thesis Abstract

Tbr1 and Fezf2 regulate alternate corticofugal neuronal identities during neocortical development
by McKenna, William L., Ph.D., University of California, Santa Cruz, 2010, 81; 3442827
Abstract (Summary)

The molecular mechanisms regulating fate divergence of closely related, but distinct, layer 6 corticothalamic and layer 5 subcerebral projection neurons are largely unknown. We present evidence for central transcriptional mechanisms that regulate fate specification of corticothalamic (layer 6) and subcerebral (layer 5) projection neurons. We found that TBR1 promotes the identity of corticothalamic neurons and represses subcerebral fates through reducing expression of Fezf2 and CTIP2. These conclusions are based on: (1) In Tbr-/- mice, the number of cells expressing layer 6 markers was reduced, and the number of cells expressing layer 5 markers was increased. Early-born (birthdated on E11.5) neurons ectopically expressed subcerebral neuronal markers, and extended their axons into subcerebral targets; (2) Ectopic Tbr1 expression in layer 5 neurons prevented them from extending axons into brain stem and the spinal cord; (3) ChIP analysis using TBR1 antibodies showed that TBR1 bound to a conserved region in the Fezf2 gene; (4) Analysis of Fezf2 mutants and Tbr -/-; Fezf2-/- compound mutants provided evidence that Fezf2 blocks corticothalamic fate in layer 5 by reducing Tbr1 expression in subcerebral neurons. All neocortical regions appear to use this core transcriptional program to specify corticothalamic (layer 6) and subcerebral (layer 5) projection neurons.

Indexing (document details)
Advisor: Chen, Bin
Commitee:
School: University of California, Santa Cruz
School Location: United States -- California
Source: DAI-B 72/04, Dissertation Abstracts International
Source Type: DISSERTATION
Subjects: Molecular biology, Neurosciences, Cellular biology
Keywords: Cerebral cortex, Neocortical development
Publication Number: 3442827
ISBN: 978-1-124-47868-5
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