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doi: 10.1242/10.1242/dev.00328
1 Division of Developmental Biology, Children's Hospital Research Foundation,
Cincinnati, OH 45229-3039, USA
2 Wallenberg Neuroscience Center, Division of Neurobiology, Lund University,
Solvegatan 17, BMC A11, S-221 84 Lund, Sweden
3 Howard Hughes Medical Institute, The Salk Institute, 10010 North Torrey Pines
Road, La Jolla, CA 92037, USA
* Author for correspondence (e-mail: kenneth.campbell{at}chmcc.org)
Accepted 12 December 2002
We have examined the role of Tlx, an orphan nuclear receptor, in dorsal-ventral patterning of the mouse telencephalon. Tlx is expressed broadly in the ventricular zone, with the exception of the dorsomedial and ventromedial regions. The expression spans the pallio-subpallial boundary, which separates the dorsal (i.e. pallium) and ventral (i.e. subpallium) telencephalon. Despite being expressed on both sides of the pallio-subpallial boundary, Tlx homozygous mutants display alterations in the development of this boundary. These alterations include a dorsal shift in the expression limits of certain genes that abut at the pallio-subpallial boundary as well as the abnormal formation of the radial glial palisade that normally marks this boundary. The Tlx mutant phenotype is similar to, but less severe than, that seen in Small eye (i.e. Pax6) mutants. Interestingly, removal of one allele of Pax6 on the homozygous Tlx mutant background significantly worsens the phenotype. Thus Tlx and Pax6 cooperate genetically to regulate the establishment of the pallio-subpallial boundary. The patterning defects in the Tlx mutant telencephalon result in a loss of region-specific gene expression in the ventral-most pallial region. This correlates well with the malformation of the lateral and basolateral amygdala in Tlx mutants, both of which have been suggested to derive from ventral portions of the pallium.
Key words: Acetylcholine esterase, Amygdala, DLX, GSH2, MASH1, Neurogenin 2, NR2E1, Pallium, Pallio-subpallial boundary, Subpallium, Tailless, Ventral pallium, Mouse
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