Characterisation of a 161 kb deletion extending from the NBR1 to the BRCA1 genes in a French breast-ovarian cancer family

Hum Mutat. 2003 Jun;21(6):654. doi: 10.1002/humu.9148.

Abstract

A large germline deletion removing exons 1 to 22 of the BRCA1 gene has been previously detected using quantitative PCR based methods (QMPSF and real time PCR gene dosage assay) in a woman affected with breast and ovarian cancer. Here, we report its characterisation by using colour bar code on combed DNA of the BRCA1 region. The 5' boundary is located in a Alu Y sequence in NBR1 intron 18 whereas the 3' boundary is located in a Alu Sc sequence in BRCA1 intron 22. This 161 kb deletion encompassing the NBR1, PsiBRCA1, NBR2 and BRCA1 genes is the largest BRCA1 deletion reported so far. No specific phenotype was associated with the hemizygosity of these four genes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • BRCA1 Protein / genetics*
  • Base Sequence
  • Breast Neoplasms / genetics*
  • Chromosomes, Human, Pair 17 / genetics
  • DNA Mutational Analysis / methods
  • Family Health
  • Female
  • France
  • Gene Deletion*
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Molecular Sequence Data
  • Ovarian Neoplasms / genetics*
  • Proteins / genetics*

Substances

  • BRCA1 Protein
  • Intracellular Signaling Peptides and Proteins
  • NBR1 protein, human
  • Proteins

Associated data

  • OMIM/113705