While there is much evidence to support this model, a number of recent studies have indicated that the specification of the forebrain (an anterior structure, presumed to be induced by the initial signal in the activation-transformation model) requires additional regulatory inputs as well. New work by scientists in the Laboratory for Organogenesis and Neurogenesis (Group Director, Yoshiki Sasai) at the RIKEN Center for Developmental Biology (CDB; Kobe, Japan) showing anterior neural specifying activity in the African clawed frog, Xenopus laevis, lends weight to the revisionist argument.
In an article published in the July 13 issue of Developmental Cell, Takayuki Onai et al. report that XsalF, the Xenopus homolog of spalt, a homeotic gene known to function in anterior-posterior segment identity in Drosophila, regulates the expression of forebrain and midbrain-specific genes. A series of experiments in which XsalF was misexpressed, deleted and its function blocked, showed direct linkage between XsalF expression and forebrain/midbrain identity.
XsalF was originally identified in a screen of the frog anterior neural plate, a structure that appears early in neural development. Sequencing of the gene, and analysis of the timing and spatial pattern of its expression showed that it codes a transcription factor related to Spalt and is expressed in the incipient forebrain and midbrain at precisely those developmental stages when brain regions are specified. When members of the Sasai lab overexpressed the gene by injecting its mRNA into early embryos, they found it caused the expanded expression of genes specific to anterior brain regions while suppressing the expression of more posterior markers.
Onai et al. next went on to test the effects of the loss of XsalF function. Disabling the gene by the deletion of functional domains resulted in embryos with significant reductions in anterior neural structures. Conditional loss-of-function experiments showed that the gene's expression was required in the early and mid neurula stages, when the developing brain undergoes regionalization. They then confirmed the specificity of this requirement for XsalF by injecting morpholinos (short nucleotide chains that block the function of a targeted gene), which gave similar results to the earlier loss-of-function studies.
These preliminary findings prompted the lab to look into the molecular mechanisms behind XsalF's anterior specifying activity, which they suspected was linked to the inhibition of the Wnt cascade (a signaling pathway that posteriorizes neural tissues). They focused on two factors, GSKβ and Tcf3, known to antagonize Wnt signaling in certain contexts, and found that the expression of both factors was dependent on XsalF. Gain- and loss-of-function studies reconfirmed the connection between XsalF and these Wnt antagonists, showing that XsalF alters the receptivity of anterior neural cells to Wnt signaling by regulating the expression of GSKβ and Tcf3, making these cells resistant to the posteriorizing effects of Wnt.
The signaling networks at work in this competitive regional determination appear to be intricate and involved in two linked, but distinct, aspects of regions-specific transcriptional regulation -- the switching on of fore- and midbrain-specific genes, and the suppression of posterior genes. The Sasai lab now plans to conduct further studies to develop a detailed model for understanding both the direct and mediated effects of XsalF in neural patterning.
Journal
Developmental Cell