Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat

Cell. 1997 Feb 7;88(3):367-74. doi: 10.1016/s0092-8674(00)81875-9.

Abstract

Fragile sites are nonstaining gaps in chromosomes induced by specific tissue culture conditions. They vary both in population frequency and in the culture conditions required for induction. Folate-sensitive fragile sites are due to expansion of p(CCG)n trinucleotide repeats; however, the relationship between sequence composition and the chemistry of induction of fragile sites is unclear. To clarify this relationship, the distamycin A-sensitive fragile site FRA16B was isolated by positional cloning and found to be an expanded 33 bp AT-rich minisatellite repeat, p(ATATA TTATATATTATATCTAATAATATATC/ATA)n (consistent with DNA sequence binding preferences of chemicals that induce its cytogenetic expression). Therefore the mutation mechanism associated with trinucleotide repeats is also a property of minisatellite repeats (variable number tandem repeats).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Composition
  • Base Sequence
  • Blotting, Southern
  • Chromosome Fragile Sites
  • Chromosome Fragility*
  • Chromosomes, Human, Pair 16*
  • Cloning, Molecular
  • DNA, Satellite* / chemistry
  • Gene Amplification*
  • Humans
  • Minisatellite Repeats*
  • Molecular Sequence Data
  • Polymerase Chain Reaction
  • Polymorphism, Genetic

Substances

  • DNA, Satellite

Associated data

  • GENBANK/U85253