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Publication : Zic2 promotes axonal divergence at the optic chiasm midline by EphB1-dependent and -independent mechanisms.

First Author  García-Frigola C Year  2008
Journal  Development Volume  135
Issue  10 Pages  1833-41
PubMed ID  18417618 Mgi Jnum  J:134680
Mgi Id  MGI:3789524 Doi  10.1242/dev.020693
Citation  Garcia-Frigola C, et al. (2008) Zic2 promotes axonal divergence at the optic chiasm midline by EphB1-dependent and -independent mechanisms. Development 135(10):1833-41
abstractText  Axons of retinal ganglion cells (RGCs) make a divergent choice at the optic chiasm to cross or avoid the midline in order to project to ipsilateral and contralateral targets, thereby establishing the binocular visual pathway. The zinc-finger transcription factor Zic2 and a member of the Eph family of receptor tyrosine kinases, EphB1, are both essential for proper development of the ipsilateral projection at the mammalian optic chiasm midline. Here, we demonstrate in mouse by functional experiments in vivo that Zic2 is not only required but is also sufficient to change the trajectory of RGC axons from crossed to uncrossed. In addition, our results reveal that this transcription factor regulates the expression of EphB1 in RGCs and also suggest the existence of an additional EphB1-independent pathway controlled by Zic2 that contributes to retinal axon divergence at the midline.
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