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1.
Ophthalmic Genet ; 20(1): 7-21, 1999 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-10415461

RESUMO

Mouse Six3 is a homeobox gene expressed almost exclusively in the developing retina, lens, hypothalamus, and pituitary. It belongs to the same family as sine oculis, a Drosophila regulatory gene that encodes a transcription factor essential for eye development. The optix gene is its closest known Drosophila homologue, with a homeodomain that is 95% identical in sequence to the Six3 protein. We have isolated the homologous human gene, SIX3, which is expressed in the adult retina and encodes a 332 amino acid protein that is 98% identical to its mouse counterpart. The SIX3 protein coding region is interrupted by a single intron located just downstream of the homeobox. A surprising feature of the SIX3 gene is a 533 nucleotide 5' untranslated region that contains long polypyrimidine tracts with 96% identity to mouse Six3. We have used in-situ hybridization to map SIX3 to 2p21-p22, a site that is syntenic with the Six3 region of mouse chromosome 17. Large heterozygous deletions associated with human holoprosencephaly type 2 have been previously mapped to 2p21, opening the possibility that SIX3 could be involved in the development of midline structures of the head. Alternatively, the expression pattern of mouse Six3 suggests that human SIX3 could be involved in disorders of eye and pituitary development.


Assuntos
Cromossomos Humanos Par 2 , Proteínas do Olho/genética , Genes Homeobox , Proteínas de Homeodomínio/genética , Proteínas do Tecido Nervoso/genética , Adulto , Sequência de Aminoácidos , Animais , Sequência de Bases , Embrião de Galinha , Mapeamento Cromossômico , Anormalidades do Olho/genética , Expressão Gênica , Humanos , Hibridização in Situ Fluorescente , Íntrons , Camundongos , Dados de Sequência Molecular , Hipófise/anormalidades , Prosencéfalo/embriologia , Retina/metabolismo , Proteína Homeobox SIX3
2.
Proc Natl Acad Sci U S A ; 95(18): 10643-8, 1998 Sep 01.
Artigo em Inglês | MEDLINE | ID: mdl-9724757

RESUMO

Vertebrate eye development begins at the gastrula stage, when a region known as the eye field acquires the capacity to generate retina and lens. Optx2, a homeobox gene of the sine oculis-Six family, is selectively expressed in this early eye field and later in the lens placode and optic vesicle. The distal and ventral portion of the optic vesicle are fated to become the retina and optic nerve, whereas the dorsal portion eventually loses its neural characteristics and activates the synthesis of melanin, forming the retinal pigment epithelium. Optx2 expression is turned off in the future pigment epithelium but remains expressed in the proliferating neuroblasts and differentiating cells of the neural retina. When an Optx2-expressing plasmid is transfected into embryonic or mature chicken pigment epithelial cells, these cells adopt a neuronal morphology and express markers characteristic of developing neural retina and photoreceptors. One explanation of these results is that Optx2 functions as a determinant of retinal precursors and that it has induced the transdifferentiation of pigment epithelium into retinal neurons and photoreceptors. We also have isolated optix, a Drosophila gene that is the closest insect homologue of Optx2 and Six3. Optix is expressed during early development of the fly head and eye primordia.


Assuntos
Regulação da Expressão Gênica no Desenvolvimento/genética , Genes Homeobox , Proteínas de Homeodomínio/genética , Epitélio Pigmentado Ocular/metabolismo , Transativadores/genética , Sequência de Aminoácidos , Animais , Sequência de Bases , Embrião de Galinha , Clonagem Molecular , DNA Complementar , Dados de Sequência Molecular , Fenótipo , Epitélio Pigmentado Ocular/embriologia , Homologia de Sequência de Aminoácidos
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