AP-2α transcription factor is required for early morphogenesis of the lens vesicle

被引:140
作者
West-Mays, JA
Zhang, J
Nottoli, T
Hagopian-Donaldson, S
Libby, D
Strissel, KJ
Williams, T
机构
[1] New England Med Ctr, Dept Ophthalmol, Boston, MA 02111 USA
[2] Tufts Univ, Sch Med, Boston, MA 02111 USA
[3] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06511 USA
关键词
transcription factor AP-2 alpha; eye; lens; retina; Pax6;
D O I
10.1006/dbio.1998.9132
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
AP-2 transcription factors are a family of retinoic acid-responsive genes, which are involved in complex morphogenetic processes. In the current study, we determine the requirement for AP-2 alpha in early morphogenesis of the eye by examining the nature of the ocular defects in AP-2 alpha null and chimeric mice. AP-2 alpha null embryos exhibited ocular phenotypes ranging from a complete lack of eyes (anophthalmia) to defects in the developing lens involving a persistent adhesion of the lens to the overlying surface ectoderm. Two genes involved in lens development and differentiation, Pax6 and MIP26 were also misexpressed. AP-2 alpha mutants also exhibited defects in the optic cup consisting of transdifferentiation of the dorsal retinal pigmented epithelium into neural retina and the absence of a defined ganglion cell layer. Newly generated chimeric embryos consisting of a population of AP-2 alpha(-/-) and AP-2 alpha(+/+) cells exhibit ocular defects similar to those seen in the knockout embryos. Immunolocalization of AP-2 proteins (alpha, beta, and gamma) to the normal developing eye revealed both unique and overlapping expression patterns, with AP-2 alpha expressed in a number of the ocular tissues that exhibited defects in the mutants, including the developing lens where AP-2 alpha is uniquely expressed. Together these findings demonstrate a requirement for AP-2 alpha in early morphogenesis of the eye. (C) 1999 Academic Press.
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页码:46 / 62
页数:17
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