Development · 2001 · 144 citations · 36 references
Life SciencesDevelopmental BiologyGeneticsEmbryogenesisMorphogenesisOrganogenesisEye DevelopmentOcular DevelopmentOcular Developmental GeneticsOcular MorphogenesisRetinal Circuit FormationRetinal DevelopmentHomeobox Gene FunctionLoss-of-function ModelsOptic Vesicle FormationOrgan Size ControlRetinal Cell Fate DeterminationRetinal MorphogenesisTranscriptional RepressionTranscriptional Repression Mechanisms
The complete absence of eyes in the medaka fish mutation eyeless is the result of defective optic vesicle evagination. We show that the eyeless mutation is caused by an intronic insertion in the Rx3 homeobox gene resulting in a transcriptional repression of the locus that is rescued by injection of plasmid DNA containing the wild-type locus. Functional analysis reveals that Six3- and Pax6- dependent retina determination does not require Rx3. However, gain- and loss-of-function phenotypes show that Rx3 is indispensable to initiate optic vesicle evagination and to control vesicle proliferation, by that regulating organ size. Thus, Rx3 acts at a key position coupling the determination with subsequent morphogenesis and differentiation of the developing eye.
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Mouse Small eye results from mutations in a paired-like homeobox-containing gene
Robert E. Hill, Jack Favor, Brigid L.M. Hogan et al. · Nature · 1991 · 1.2K citations
The Rx homeobox gene is essential for vertebrate eye development
Peter H. Mathers, Alexander Grinberg, Kathleen Mahon et al. · Nature · 1997 · 715 citations