New concepts to improve resolution and sensitivity of molecular cytogenetic diagnostics by multicolor fluorescence in situ hybridization

Cytometry. 2001 May 1;44(1):7-15. doi: 10.1002/1097-0320(20010501)44:1<7::aid-cyto1076>3.0.co;2-g.

Abstract

Background: Routine application of multicolor fluorescence in situ hybridization (M-FISH) technology for molecular cytogenetic diagnostics has been hampered by several technical limitations. First, when using chromosome-specific painting probes, there is a limit in cytogenetic resolution of approximately 2-3 Mb, which can mask hidden structural abnormalities that have a significant clinical effect. Second, using whole chromosome painting probes, intrachromosomal rearrangements cannot be detected and the exact localization of breakpoints is often not possible.

Methods: We suggest the use of multiplex-labeled region or locus- specific probes in combination with an optimal probe design to improve the sensitivity and resolution of the M-FISH technology. To allow the application of this assay in routine diagnostics, we developed a multipurpose image analysis system.

Results: goldFISH was applied to the study of cryptic translocations in mental retardation patients and to the study of high-resolution breakpoint mapping in non-small cell lung cancer patients. For an individual with mental retardation, who had an apparently normal karyotype by G-banding, we detected an unbalanced translocation involving chromosomes 2 and 7.

Conclusions: In combination with optimally designed probe kits, goldFISH overcomes most of the present limitations of the M-FISH technology and results in virtually 100% reliability for detecting interchromosomal and intrachromosomal rearrangements.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Automation
  • Carcinoma, Non-Small-Cell Lung / diagnosis
  • Carcinoma, Non-Small-Cell Lung / genetics*
  • Humans
  • In Situ Hybridization, Fluorescence / methods*
  • Intellectual Disability / diagnosis
  • Intellectual Disability / genetics*
  • Lung Neoplasms / diagnosis
  • Lung Neoplasms / genetics*
  • Metaphase
  • Sensitivity and Specificity
  • Translocation, Genetic