Removal of Pax6 partially rescues the loss of ventral structures in Shh null mice

被引:18
作者
Fuccillo, Marc
Rutlin, Michael
Fishell, Gord
机构
[1] NYU, Ctr Med, Skirball Inst Biomol Med, Dev Genet Program, New York, NY 10016 USA
[2] NYU, Ctr Med, Skirball Inst Biomol Med, Dept Cell Biol, New York, NY 10016 USA
基金
美国国家卫生研究院;
关键词
CGE; dorsoventral patterning; LGE; MGE; midline;
D O I
10.1093/cercor/bhk023
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Pax6 and Gli3 are dorsally expressed genes that are known to antagonize sonic hedgehog (Shh) activity. We have previously shown that dorsoventral patterning defects seen in Shh(-/-) mutants are rescued in Shh(-/-);Gli3(-/-) compound mutants. Here we investigate if the loss of Pax6 can also ameliorate defects seen in Shh(-/-) mutants. In support of this notion, we observe that the fusion of the cerebral vesicles seen in Shh(-/-) mutants is partially corrected in E12.5 Shh(-/-);Pax6(-/-) compound mutants. Investigation of pan-ventral markers such as Dlx2 also shows that, unlike Shh(-/-),; a broad domain of expression of this gene is observed in Shh(-/-);Pax6(-/-) mice. Interestingly, we observe that while the expression of ER81 in the ventral telencephalon is expanded, the expression of Ebf1 is lost. This suggests that the rescued ventral domain observed in Shh(-/-);Pax6(-/-) mice is the dorsal lateral ganglionic eminence region. With regard to dorsal telencephalic patterning, we also observe rescue of the pallial-subpallial boundary, as well as a partial rescue of the dorsal midline. Together, our findings are consistent with Pax6 function being required for aspects of Gli3-mediated telencephalic patterning.
引用
收藏
页码:I96 / I102
页数:7
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