Mutation in HSF4 associated with early but not late-onset hereditary cataract in the Boston Terrier

Cathryn S. Mellersh, Kathryn T. Graves, Bryan McLaughlin, Rosalyn B. Ennis, Louise Pettitt, Mark Vaudin, Keith C. Barnett

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

Primary hereditary cataract (HC) is one of the most common disorders in purebred dogs and is a leading cause of blindness. Boston Terriers suffer from 2 distinct forms of HC which occur at different ages and which are different in their appearance and progression. Early-onset hereditary cataract (EHC) affects dogs within the first few months of life, is always progressive and bilateral, and results in total blindness, whereas late-onset hereditary cataract (LHC) in general affects dogs over the age of 3 and is more variable in its clinical phenotype, age of onset, progression, and the degree to which vision is impaired. A mutation in HSF4 has recently been reported in a small number of Boston Terriers affected with EHC. In this study, we analyzed 22 additional Boston Terriers affected with early-onset cataract to confirm that the HSF4 mutation is causative for this form of cataract in this breed. In addition, we analyzed 40 Boston Terriers that were either clinically clear or affected with LHC for the presence or absence of the HSF4 mutation. By also sequencing HSF4 in dogs affected with LHC, we conclude that HSF4 is not associated with the development of the late-onset form of cataract and that the 2 forms of cataract in this breed are therefore genetically discrete conditions.

Original languageEnglish
Pages (from-to)531-533
Number of pages3
JournalJournal of Heredity
Volume98
Issue number5
DOIs
StatePublished - 2007

Funding

This work was funded by the Kennel Club Charitable Trust, the Boston Terrier Club of America, and individual Boston Terrier owners.

FundersFunder number
Kennel Club Charitable Trust

    ASJC Scopus subject areas

    • Biotechnology
    • Molecular Biology
    • Genetics
    • Genetics(clinical)

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