Literature DB >> 8077289

cDNA from human ocular ciliary epithelium homologous to beta ig-h3 is preferentially expressed as an extracellular protein in the corneal epithelium.

J Escribano1, N Hernando, S Ghosh, J Crabb, M Coca-Prados.   

Abstract

The non-pigmented ciliary epithelium is largely responsible for the formation of aqueous humor in the mammalian eye. To provide a basis for studies at the molecular level, a directional expression cDNA library was constructed in Uni-ZAP XR vector from poly A+ RNA of the human non-pigmented ciliary epithelial derived ODM-2 cell line. Fifty-three cDNA clones were isolated from the library and characterized by partial sequence analysis. Approximately 49% of the clones exhibited homology with known genes in the GenBank/EMBL databases. The putative identification of these clones may reflect the transcriptional activity of the ODM-2 cells in culture. One of the identified clones, ODM-42-I, was found to be specific and highly expressed in the corneal epithelium. This clone had an exact match with a recently discovered human gene, beta ig-h3 (Skonier et al., 1992, DNA Cell Biol., 11:511-522), which codes a surface recognition protein, inducible by transforming growth factor beta (TGF-beta), and containing a putative binding site (RDG) for integrins. The ODM-42-I cDNA clone displays a distinctive pattern of expression found in the human eye, expressed almost exclusively in the cornea. Further studies, using sera from a synthetic peptide to the carboxy-terminal region of ODM-42-I, reveal that the protein is heterogeneous in charge and is preferentially expressed on the extracellular surface of corneal epithelial cells, and might share immunologic properties with integrins beta 1.

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Year:  1994        PMID: 8077289     DOI: 10.1002/jcp.1041600314

Source DB:  PubMed          Journal:  J Cell Physiol        ISSN: 0021-9541            Impact factor:   6.384


  40 in total

1.  TGFBI and CHST6 gene analysis in Chinese stromal corneal dystrophies.

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Journal:  Int J Ophthalmol       Date:  2012-06-18       Impact factor: 1.779

2.  Chinese family with atypical granular corneal dystrophy type I caused by the typical R555W mutation in TGFBI.

Authors:  Su-Juan Zhao; Ya-Nan Zhu; Xing-Chao Shentu; Qi Miao
Journal:  Int J Ophthalmol       Date:  2013-08-18       Impact factor: 1.779

3.  Mutation in transforming growth factor beta induced protein associated with granular corneal dystrophy type 1 reduces the proteolytic susceptibility through local structural stabilization.

Authors:  Jarl Underhaug; Heidi Koldsø; Kasper Runager; Jakob Toudahl Nielsen; Charlotte S Sørensen; Torsten Kristensen; Daniel E Otzen; Henrik Karring; Anders Malmendal; Birgit Schiøtt; Jan J Enghild; Niels Chr Nielsen
Journal:  Biochim Biophys Acta       Date:  2013-10-12

4.  Mutation analysis of TGFBI and KRT12 in a case of concomitant keratoconus and granular corneal dystrophy.

Authors:  Xianli Du; Peng Chen; Dapeng Sun
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2017-05-31       Impact factor: 3.117

5.  Unique TGFBI protein in lattice corneal dystrophy.

Authors:  Yu-Ping Han; Austin J Sim; Smita C Vora; Andrew J W Huang
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-10-28       Impact factor: 4.799

6.  Fibril Core of Transforming Growth Factor Beta-Induced Protein (TGFBIp) Facilitates Aggregation of Corneal TGFBIp.

Authors:  Charlotte S Sørensen; Kasper Runager; Carsten Scavenius; Morten M Jensen; Nadia S Nielsen; Gunna Christiansen; Steen V Petersen; Henrik Karring; Kristian W Sanggaard; Jan J Enghild
Journal:  Biochemistry       Date:  2015-05-06       Impact factor: 3.162

7.  Differential expression and processing of transforming growth factor beta induced protein (TGFBIp) in the normal human cornea during postnatal development and aging.

Authors:  Henrik Karring; Kasper Runager; Zuzana Valnickova; Ida B Thøgersen; Torben Møller-Pedersen; Gordon K Klintworth; Jan J Enghild
Journal:  Exp Eye Res       Date:  2009-09-26       Impact factor: 3.467

8.  Different phenotypes of lattice corneal dystrophy type I in patients with 417C>T (R124C) and 1762A>G (H572R) mutations in TGFBI (BIGH3).

Authors:  Pablo Romero; Mauricio Moraga; Luisa Herrera
Journal:  Mol Vis       Date:  2010-08-13       Impact factor: 2.367

9.  Evidence against a blood derived origin for transforming growth factor beta induced protein in corneal disorders caused by mutations in the TGFBI gene.

Authors:  Henrik Karring; Zuzana Valnickova; Ida B Thøgersen; Chris J Hedegaard; Torben Møller-Pedersen; Torsten Kristensen; Gordon K Klintworth; Jan J Enghild
Journal:  Mol Vis       Date:  2007-06-27       Impact factor: 2.367

10.  A novel mutation I522N within the TGFBI gene caused lattice corneal dystrophy I.

Authors:  Chunmei Zhang; Guang Zeng; Hui Lin; Dandan Li; Liming Zhao; Nan Zhou; Yanhua Qi
Journal:  Mol Vis       Date:  2009-11-28       Impact factor: 2.367

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