Interactions between Pax6, Barhl2 and Shh in the early patterning of the mammalian diencephalon
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Date
27/06/2016Author
Parish, Elisa Victoria
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Abstract
Diencephalic development requires the transcription factors Pax6 and Barhl2 in
order to proceed correctly. Both genes are necessary for the normal development of
the organizer region known as the zona limitans intrathalamica (ZLI). The ZLI goes
on to pattern the diencephalon via its secretion of the morphogen Shh, which inhibits
the expression of Pax6. These findings suggest that interactions between Pax6,
Barhl2 and Shh may be involved in the control of diencephalic development. This
project aims to characterise these interactions and investigate their roles.
The expression domains of Pax6 and Barhl2 were mapped during the early
development of the mouse diencephalon. Qualitative approaches were employed to
confirm the high complementarity of their expression domains and obtain evidence
of a mutually repressive relationship existing between the two genes. The findings
from a quantitative analysis suggested that this inhibition is incomplete within the
thalamus. Investigations using the Pax6-null mutant mouse confirmed that in the
absence of Pax6 the thalamic Barhl2 expression domain expands beyond the
ventricular zone, the site of thalamic neurogenesis.
The influence of Shh signalling on the expression of Pax6 and Barhl2 was
investigated via a gain-of-function approach utilising in utero electroporation to
activate the Shh pathway. This led to a downregulation of both Pax6 and Barhl2
within the thalamus.
In Shh loss-of-function experiments drug treatment with the Shh antagonist
vismodegib led to an upregulation of Barhl2 and the loss of the GABAergic pTh-R
in the Pax6-null mutant thalamus, but not in the wild type thalamus, suggesting that
Pax6 and Shh may be required to inhibit Barhl2 in order for GABAergic
neurogenesis to proceed. Barhl2 expression was detected in the Shh-null mutant
mouse confirming that, in contrast with their homologues in Drosophila, Shh may be
expressed downstream of Barhl2.
Together these findings have been used to develop a novel model of thalamic
development in which Barhl2 induces ZLI development, inhibition of Barhl2 by
Pax6 restricts its expansion, and secretion of Shh by the ZLI then goes on to inhibit
Pax6 and Barhl2 in the pTh-R while mutual repression between Pax6 and Barhl2
modulates neurogenesis in the more caudal regions of the thalamic neuroepithelium.