Directly repeated sequences associated with pathogenic mitochondrial DNA deletions

D. R. Johns, S. L. Rutledge, O. C. Stine, O. Hurko

    Research output: Contribution to journalArticlepeer-review

    Abstract

    We determined the nucleotide sequences of junctional regions associated with large deletions of mitochondrial DNA found in four unrelated individuals with a phenotype of chronic progressive external ophthalmoplegia. In each patient, the deletion breakpoint occurred within a directly repeated sequence of 13-18 base pairs, present in different regions of the normal mitochondrial genome - separated by 4.5-7.7 kilobases. In two patients, the deletions were identical. When all four repeated sequences are compared, a consensus sequence of 11 nucleotides emerges, similar to putative recombination signals, suggesting the involvement of a recombinational event. Partially deleted and normal mitochondrial DNAs were found in all tissues examined, but in very different proportions, indicating that these mutations originated before the primary cell layers diverged.

    Original languageEnglish (US)
    Pages (from-to)8059-8062
    Number of pages4
    JournalProceedings of the National Academy of Sciences of the United States of America
    Volume86
    Issue number20
    StatePublished - 1989

    ASJC Scopus subject areas

    • General
    • Genetics

    Fingerprint

    Dive into the research topics of 'Directly repeated sequences associated with pathogenic mitochondrial DNA deletions'. Together they form a unique fingerprint.

    Cite this