The cataract-associated protein TMEM114, and TMEM235, are glycosylated transmembrane proteins that are distinct from claudin family members

Geoffrey J. Maher, Emma N. Hilton, Jill E. Urquhart, Alice E. Davidson, Helen L. Spencer, Graeme C. Black, Forbes D. Manson

    Research output: Contribution to journalArticlepeer-review

    Abstract

    A novel gene, TMEM114, was annotated as a member of the claudin gene family and was subsequently associated as a cause of autosomal dominant cataract because of a translocation in its putative promoter. Our bioinformatic and molecular analyses of TMEM114, and the closely related TMEM235, demonstrate that these proteins are more closely related to members of the voltage dependent calcium channel gamma subunit family. TMEM114 and TMEM235 differed from claudins in terms of localisation in polarised epithelial cells and by the presence of N-linked glycans. By gene expression knockdown in Xenopus tropicalis we also demonstrate a role for Tmem114 in eye development. Structured summary of protein interactions: Claudin-2 and ZO-1 colocalize by fluorescence microscopy (View interaction). ZO-1 and Tmem114 colocalize by fluorescence microscopy (View interaction). © 2011 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
    Original languageEnglish
    Pages (from-to)2187-2192
    Number of pages5
    JournalFEBS Letters
    Volume585
    Issue number14
    DOIs
    Publication statusPublished - 21 Jul 2011

    Keywords

    • CACNG
    • Cataract
    • Claudin
    • Morpholino
    • N-glycosylation

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