Literature DB >> 14991709

Identification of ciliary epithelial-specific genes using subtractive libraries and cDNA arrays in the avian eye.

Ryo Kubota1, Chris McGuire, Blair Dierks, Thomas A Reh.   

Abstract

The ciliary epithelium of the ciliary body is derived from the anterior rim of the developing optic cup. Several recent studies have found that developmental abnormalities in this tissue can underlie congenital glaucoma. However, there is little known about the development of the ciliary epithelium. To better understand the developmental events responsible for the specification of this domain of the optic cup, we used a subtractive library, differential screening approach along with the construction of cDNA arrays to identify genes expressed in the ciliary epithelium of the chicken. We identified many genes specifically expressed in the ciliary epithelium, including a number that had been described previously as enriched in the ciliary epithelium of other species. By analyzing the expression of these genes during eye development, we were able to correlate the onset of ciliary epithelial gene expression with a reduction in mitotic activity in this region. We propose that the mechanisms that regulate the expression of ciliary epithelial genes are linked to the reduction in proliferation that results in the epithelial monolayer in this region. Copyright 2004 Wiley-Liss, Inc.

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Year:  2004        PMID: 14991709     DOI: 10.1002/dvdy.20000

Source DB:  PubMed          Journal:  Dev Dyn        ISSN: 1058-8388            Impact factor:   3.780


  11 in total

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Authors:  Melanie R Roberts; Maya Srinivas; Douglas Forrest; Gabriella Morreale de Escobar; Thomas A Reh
Journal:  Proc Natl Acad Sci U S A       Date:  2006-04-10       Impact factor: 11.205

Review 2.  The other pigment cell: specification and development of the pigmented epithelium of the vertebrate eye.

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Journal:  Pigment Cell Res       Date:  2006-10

3.  FGF-mediated induction of ciliary body tissue in the chick eye.

Authors:  Magnus R Dias da Silva; Nicola Tiffin; Tatsuo Mima; Takashi Mikawa; Jeanette Hyer
Journal:  Dev Biol       Date:  2006-12-21       Impact factor: 3.582

4.  Combinatorial regulation of optic cup progenitor cell fate by SOX2 and PAX6.

Authors:  Danielle Matsushima; Whitney Heavner; Larysa H Pevny
Journal:  Development       Date:  2011-02       Impact factor: 6.868

5.  Patterning of the circumferential marginal zone of progenitors in the chicken retina.

Authors:  Kanika Ghai; Jennifer J Stanke; Andy J Fischer
Journal:  Brain Res       Date:  2007-02-02       Impact factor: 3.252

6.  Identification of genes expressed preferentially in the developing peripheral margin of the optic cup.

Authors:  Jeffrey M Trimarchi; Seo-Hee Cho; Constance L Cepko
Journal:  Dev Dyn       Date:  2009-09       Impact factor: 3.780

7.  Retinal and anterior eye compartments derive from a common progenitor pool in the avian optic cup.

Authors:  Sara J Venters; Paulina D Cuenca; Jeanette Hyer
Journal:  Mol Vis       Date:  2011-12-20       Impact factor: 2.367

8.  Foxg1 is required to limit the formation of ciliary margin tissue and Wnt/β-catenin signalling in the developing nasal retina of the mouse.

Authors:  Vassiliki Fotaki; Rowena Smith; Thomas Pratt; David J Price
Journal:  Dev Biol       Date:  2013-04-24       Impact factor: 3.582

9.  Central and peripheral retina arise through distinct developmental paths.

Authors:  Sara J Venters; Takashi Mikawa; Jeanette Hyer
Journal:  PLoS One       Date:  2013-04-16       Impact factor: 3.240

10.  β-Catenin inactivation is a pre-requisite for chick retina regeneration.

Authors:  Jie Zhu; Agustin Luz-Madrigal; Tracy Haynes; Julia Zavada; Amy K Burke; Katia Del Rio-Tsonis
Journal:  PLoS One       Date:  2014-07-08       Impact factor: 3.240

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