Letter | Published:

Ha-ras hypervariable alleles in myelodysplasia

Nature volume 321, pages 8485 (01 May 1986) | Download Citation

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Abstract

The somatic mutation of one of the ras oncogenes is now considered to be a critical step in the pathogenesis of many tumours1,2. Circumstantial evidence also suggests that some individuals may be genetically predisposed to malignancy3 and a general method used to analyse such disease susceptibility is the study of restriction fragment length polymorphisms (RFLPs) at particular loci4,5. The Harvey ras (Ha-ras) locus includes a hypervariable region (HVR) which consists of a series of 28-base-pair (bp) tandem repeats 3′ to the gene6. This arrangement gives rise to alleles of a wide range of sizes, making such genetic analysis possible. A previous study reported that white blood cell DNA from cancer patients frequently showed allelic restriction fragments at the Ha-ras locus which were found only rarely in normal unaffected individuals, and it was concluded that the inheritance of such unusual alleles may be linked to a susceptibility to cancer7. As this conclusion has major implications we sought to investigate whether this association could be confirmed in patients with myelodysplasia, a common haematological malignancy reported to have the highest frequency of rare alleles7. The Ha-ras alleles were characterized in normal healthy individuals and compared with those found in patients with myelodysplasia (MDS). Our results, reported here, show that the distribution of Ha-ras alleles in myelodysplastic patients is not significantly different from that in normal individuals.

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Author information

Affiliations

  1. MRC Molecular Haematology Unit, Nuffield Department of Clinical Medicine, John Radcliffe Hospital, Headington, Oxford OX3 9DU, UK

    • S. L. Thein
    •  & J. Flint
  2. Department of Haematology, John Radcliffe Hospital, Headington, Oxford OX3 9DU, UK

    • J. S. Wainscoat
  3. Department of Haematology, Royal Victorian Hospital, Boscombe, Bournemouth BH1 4JG, UK

    • D. G. Oscier

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DOI

https://doi.org/10.1038/321084a0

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