Identification of a neocentromere in a rearranged Y chromosome with no detectable DYZ3 centromeric sequence

Am J Med Genet. 2002 Dec 1;113(3):263-7. doi: 10.1002/ajmg.10701.

Abstract

An 18-year-old woman was evaluated because of primary amenorrhea and hypogonadism. Chromosome analysis from peripheral blood lymphocytes revealed a nonmosaic 46,X,+mar constitution. The marker was shown to be a rearranged Y chromosome consisting of an inverted duplication of the long arm: rea(Y)(qter-q11::q11-qter). Deletion mapping analysis with Y-specific STS showed that the marker lacked Yp and Y-centromeric (DYZ3) sequences, but it was positive for Yq sequences tested. Fluorescence in situ hybridization analysis with Y and X chromosome centromeric and pancentromeric probes showed no hybridization signals. The marker chromosome is present in 100% of the cells; therefore, it is mitotically stable despite the absence of DYZ3 centromeric sequence. Hybridization with CENP-A and CENP-C specific antibodies localized a neocentromere close to the breakpoint.

Publication types

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

MeSH terms

  • Adolescent
  • Amenorrhea / genetics
  • Centromere / genetics*
  • Chromosome Banding
  • Chromosomes, Human, Y / genetics*
  • Female
  • Humans
  • Hypogonadism / genetics
  • In Situ Hybridization, Fluorescence
  • Prohibitins
  • Sex Chromosome Aberrations*