Literature DB >> 12167403

The homeobox gene Six3 is a potential regulator of anterior segment formation in the chick eye.

Yi-Wen Hsieh1, Xiang-Mei Zhang, Eddie Lin, Guillermo Oliver, Xian-Jie Yang.   

Abstract

The anterior segment of the vertebrate eye consists of highly organized and specialized ocular tissues critical for normal vision. The periocular mesenchyme, originating from the neural crest, contributes extensively to the anterior segment. During chick eye morphogenesis, the homeobox gene Six3 is expressed in a subset of periocular mesenchymal cells and in differentiating anterior segment tissues. Retrovirus-mediated misexpression of Six3 causes eye anterior segment malformation, including corneal protrusion and opacification, ciliary body and iris hypoplasia, and trabecular meshwork dysgenesis. Histological and molecular marker analyses demonstrate that Six3 misexpression disrupts the integrity of the corneal endothelium and the expression of extracellular matrix components critical for corneal transparency. Six3 misexpression also leads to a reduction of the periocular mesenchymal cell population expressing Lmx1b, Pitx2, and Pax6, transcription factors critical for eye anterior segment morphogenesis. Moreover, elevated levels of Six3 attenuate proliferation of periocular mesenchymal cells in vitro and differentiating anterior segment tissues in vivo. These results suggest that, in addition to its function in eye primordium determination, Six3 plays a role in regulating the development of the vertebrate eye anterior segment.

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Year:  2002        PMID: 12167403      PMCID: PMC7048386          DOI: 10.1006/dbio.2002.0732

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  7 in total

1.  Homozygous nonsense mutation in the FOXE3 gene as a cause of congenital primary aphakia in humans.

Authors:  Sophie Valleix; Florence Niel; Brigitte Nedelec; Marie-Paule Algros; Claire Schwartz; Bernard Delbosc; Marc Delpech; Bernadette Kantelip
Journal:  Am J Hum Genet       Date:  2006-06-08       Impact factor: 11.025

2.  Loss of Msx2 function down-regulates the FoxE3 expression and results in anterior segment dysgenesis resembling Peters anomaly.

Authors:  Jiangyue Zhao; Kirio Kawai; Hongyan Wang; Di Wu; Mingwu Wang; Zhicao Yue; Jinsong Zhang; Yi-Hsin Liu
Journal:  Am J Pathol       Date:  2012-04-13       Impact factor: 4.307

3.  Semaphorin3A/neuropilin-1 signaling acts as a molecular switch regulating neural crest migration during cornea development.

Authors:  Peter Y Lwigale; Marianne Bronner-Fraser
Journal:  Dev Biol       Date:  2009-10-13       Impact factor: 3.582

4.  Independent degeneration of photoreceptors and retinal pigment epithelium in conditional knockout mouse models of choroideremia.

Authors:  Tanya Tolmachova; Ross Anders; Magnus Abrink; Laurence Bugeon; Margaret J Dallman; Clare E Futter; José S Ramalho; Felix Tonagel; Naoyuki Tanimoto; Mathias W Seeliger; Clare Huxley; Miguel C Seabra
Journal:  J Clin Invest       Date:  2006-01-12       Impact factor: 14.808

Review 5.  Chromosome abnormalities and the genetics of congenital corneal opacification.

Authors:  A Mataftsi; L Islam; D Kelberman; J C Sowden; K K Nischal
Journal:  Mol Vis       Date:  2011-06-17       Impact factor: 2.367

Review 6.  Progenitors for the corneal endothelium and trabecular meshwork: a potential source for personalized stem cell therapy in corneal endothelial diseases and glaucoma.

Authors:  Wing Yan Yu; Carl Sheridan; Ian Grierson; Sharon Mason; Victoria Kearns; Amy Cheuk Yin Lo; David Wong
Journal:  J Biomed Biotechnol       Date:  2011-12-06

7.  Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma.

Authors:  Anthony P Khawaja; Jessica N Cooke Bailey; Nicholas J Wareham; Robert A Scott; Mark Simcoe; Robert P Igo; Yeunjoo E Song; Robert Wojciechowski; Ching-Yu Cheng; Peng T Khaw; Louis R Pasquale; Jonathan L Haines; Paul J Foster; Janey L Wiggs; Chris J Hammond; Pirro G Hysi
Journal:  Nat Genet       Date:  2018-05-21       Impact factor: 38.330

  7 in total

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