Use of repetitive DNA for diagnosis of chromosomal rearrangements

Hum Genet. 1983;64(4):339-42. doi: 10.1007/BF00292365.

Abstract

We have used two repeated DNA fragments (3.4 and 2.1 kb) released from Y chromosome DNA by digestion with the restriction endonuclease Hae III to analyze potential Y chromosome/autosome translocations. Two female patients were studied who each had an abnormal chromosome 22 with extra quinacrine fluorescent material on the short arm. The origin of the 22p+ chromosomes was uncertain after standard cytologic examinations. Analysis of one patient's DNA with the Y-specific repeated DNA probes revealed the presence of both the 3.4 and 2.1kb Y-specific fragments. Thus, in this patient, the additional material was from the Y chromosome. Analysis of the second patient's DNA for Y-specific repeated DNA was negative, indicating that the extra chromosomal segment was not from the long arm of the Y chromosome. These two cases demonstrate that repeated DNA can distinguish between similar appearing aberrant chromosomes and may be useful in karyotypic and prenatal diagnosis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Base Sequence
  • Chromosome Banding
  • Chromosomes, Human, 21-22 and Y*
  • DNA / analysis
  • DNA Restriction Enzymes
  • Deoxyribonucleases, Type II Site-Specific*
  • Female
  • Humans
  • Karyotyping
  • Male
  • Middle Aged
  • Phenotype
  • Repetitive Sequences, Nucleic Acid*
  • Translocation, Genetic*
  • Y Chromosome*

Substances

  • DNA
  • DNA Restriction Enzymes
  • Deoxyribonucleases, Type II Site-Specific
  • GGCC-specific type II deoxyribonucleases