Vax2 is a homeobox gene whose expression is confined to the ventral portion of the prospective neural retina. Overexpression of this gene at early stages of development in Xenopus and in chicken embryos determines a ventralization of the retina, thus suggesting its role in the molecular pathway underlying eye development. We have generated and characterized a mouse with a targeted null mutation of the Vax2 gene. Vax2 homozygous mutant mice display incomplete closure of the optic fissure that leads to eye coloboma. This phenotype is not fully penetrant suggesting that additional factors contribute to its generation. Vax2 inactivation determines dorsalization of the expression of mid-late (EphB2 and ephrin-B2) but not early (Pax2 and Tbx5) markers of dorsal-ventral polarity in the developing retina. Finally, Vax2 mutant mice exhibit abnormal projections of ventral retinal ganglion cells. In particular, we observed the almost complete absence of ipsilaterally projecting retinal ganglion cells axons in the optic chiasm and alteration of the retinocollicular projections. All these findings indicate that Vax2 is required for the proper closure of the optic fissure, for the establishment of a physiological asymmetry on the dorsal-ventral axis of the eye and for the formation of appropriate retinocollicular connections.

Vax2 inactivation in mouse determines alteration of the eye dorsal-ventral axis, misrouting of the optic fibers and eye coloboma / A., Barbieri; G., Alfano; V., Broccoli; A., Bulfone; Marigo, Valeria; P., Bovolenta; A., Ballabio; S., Banfi. - In: EUROPEAN JOURNAL OF HUMAN GENETICS. - ISSN 1018-4813. - STAMPA. - 10:(2002), pp. 235-235. (Intervento presentato al convegno EUROPEAN HUMAN GENETICS CONFERENCE 2002 tenutosi a Strasburgo, Francia nel 25-28 Maggio 2002).

Vax2 inactivation in mouse determines alteration of the eye dorsal-ventral axis, misrouting of the optic fibers and eye coloboma

MARIGO, Valeria;
2002

Abstract

Vax2 is a homeobox gene whose expression is confined to the ventral portion of the prospective neural retina. Overexpression of this gene at early stages of development in Xenopus and in chicken embryos determines a ventralization of the retina, thus suggesting its role in the molecular pathway underlying eye development. We have generated and characterized a mouse with a targeted null mutation of the Vax2 gene. Vax2 homozygous mutant mice display incomplete closure of the optic fissure that leads to eye coloboma. This phenotype is not fully penetrant suggesting that additional factors contribute to its generation. Vax2 inactivation determines dorsalization of the expression of mid-late (EphB2 and ephrin-B2) but not early (Pax2 and Tbx5) markers of dorsal-ventral polarity in the developing retina. Finally, Vax2 mutant mice exhibit abnormal projections of ventral retinal ganglion cells. In particular, we observed the almost complete absence of ipsilaterally projecting retinal ganglion cells axons in the optic chiasm and alteration of the retinocollicular projections. All these findings indicate that Vax2 is required for the proper closure of the optic fissure, for the establishment of a physiological asymmetry on the dorsal-ventral axis of the eye and for the formation of appropriate retinocollicular connections.
2002
10
235
235
A., Barbieri; G., Alfano; V., Broccoli; A., Bulfone; Marigo, Valeria; P., Bovolenta; A., Ballabio; S., Banfi
Vax2 inactivation in mouse determines alteration of the eye dorsal-ventral axis, misrouting of the optic fibers and eye coloboma / A., Barbieri; G., Alfano; V., Broccoli; A., Bulfone; Marigo, Valeria; P., Bovolenta; A., Ballabio; S., Banfi. - In: EUROPEAN JOURNAL OF HUMAN GENETICS. - ISSN 1018-4813. - STAMPA. - 10:(2002), pp. 235-235. (Intervento presentato al convegno EUROPEAN HUMAN GENETICS CONFERENCE 2002 tenutosi a Strasburgo, Francia nel 25-28 Maggio 2002).
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/797491
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