Left-sided embryonic expression of the BCL-6 corepressor, BCOR, is required for vertebrate laterality determination

Forbes Manson, Emma N. Hilton, Forbes D C Manson, Jill E. Urquhart, Jennifer J. Johnston, Anne M. Slavotinek, Peter Hedera, Eva Lena Stattin, Ann Nordgren, Leslie G. Biesecker, Graeme C M Black

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Oculofaciocardiodental (OFCD) syndrome is an X-linked male lethal condition encompassing cardiac septal defects, as well as ocular and dental anomalies. The gene mutated in OFCD syndrome, the BCL-6 corepressor (BCOR), is part of a transcriptional repression complex whose transcriptional targets remain largely unknown. We reviewed cases of OFCD syndrome and identified patients exhibiting defective lateralization including dextrocardia, asplenia and intestinal malrotation, suggesting that BCOR is required in normal laterality determination. To study the function of BCOR, we used morpholino oligonucleotides (MOs) to knockdown expression of xtBcor in Xenopus tropicalis, thus creating an animal model for OFCD syndrome. The resulting tadpoles had cardiac and ocular features characteristic of OFCD syndrome. Reversed cardiac orientation and disorganized gut patterning were seen when MOs were injected into the left side of embryos, demonstrating a left-sided requirement for xtBcor in lateral determination in Xenopus. Ocular defects displayed no left-right bias and included anterior and posterior segment disorders such as microphthalmia and coloboma. Expression of xtPitx2c was shown to be downregulated when xtBcor was depleted. This identifies a pathway in which xtBcor is required for lateral specification, a process intrinsically linked to correct cardiac septal development. © 2007 The Author(s).
    Original languageEnglish
    Pages (from-to)1773-1782
    Number of pages9
    JournalHuman Molecular Genetics
    Volume16
    Issue number14
    DOIs
    Publication statusPublished - 15 Jul 2007

    Keywords

    • Animals
    • Body Patterning
    • Chromosomes, Human, X
    • genetics: Craniofacial Abnormalities
    • metabolism: DNA-Binding Proteins
    • genetics: Eye Diseases
    • Female
    • Gene Expression Regulation, Developmental
    • embryology: Heart
    • Humans
    • Male
    • Mutation
    • biosynthesis: Proto-Oncogene Proteins
    • biosynthesis: Repressor Proteins
    • Syndrome
    • Tissue Distribution
    • metabolism: Xenopus

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