Quantitative analysis of centromeric FISH spots during the cell cycle by image cytometry.

Abstract

Two-color fluorescence in situ hybridization (FISH) with chromosome enumeration DNA probes specific to chromosomes 7, 11, 17, and 18 was applied to CAL-51 breast cancer cells to examine whether the fluorescence intensity of FISH spots was associated with cell cycle progression. The fluorescence intensity of each FISH spot was quantitatively analyzed based on the cell cycle stage determined by image cytometry at the single-cell level. The spot intensity of cells in the G2 phase was larger than that in the G0/1 phase. This increased intensity was not seen during the early and mid S phases, whereas the cells in the late S phase showed significant increases in spot intensity, reaching the same level as that observed in the G2 phase, indicating that alpha satellite DNA in the centromeric region was replicated in the late S phase. Thus, image cytometry can successfully detect small differences in the fluorescence intensities of centromeric spots of homologous chromosomes. This combinational image analysis of FISH spots and the cell cycle with cell image cytometry provides insights into new aspects of the cell cycle. This is the first report demonstrating that image cytometry can be used to analyze the fluorescence intensity of FISH signals during the cell cycle.

• Authors: Genta Amakawa, Kenzo Ikemoto, Hideaki Ito, Tomoko Furuya, Kohsuke Sasaki
• Journal: The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society (J Histochem Cytochem) Vol. 61 Issue 10 Pg. 699-705 (Oct 2013) ISSN: 1551-5044 [Electronic] United States
• PMID: 23832878 (Publication Type: Journal Article)

Topics

• Cell Cycle
• Cell Line, Tumor
• Centromere (metabolism)
• Humans
• Image Cytometry
• In Situ Hybridization, Fluorescence
• Spectrometry, Fluorescence