IMAGES IN CLINICAL HEMATOLOGY

 

Comet assay in myelodysplastic syndromes

 

 

Paulo Florentino Teixeira Neto; Ronald Feitosa Pinheiro; Romélia Pinheiro Gonçalves

Universidade Federal do Ceará - UFC, Fortaleza, CE, Brazil

Corresponding author

 

The comet assay (single-cell gel electrophoresis) has been established as a simple, rapid, flexible and sensitive method of detecting DNA damage in single cells^(1,2). Cells embedded in agarose on a microscope slide are lysed with detergent. Electrophoresis at high pH results in structures resembling comets, observed by fluorescence microscopy; the intensity of the comet tail relative to the head reflects DNA damage⁽²⁾. The lesion of each cell is quantified according to the comet tail length as class 0 (no tail) to 4 (almost all DNA in tail)⁽³⁾. Due to genetic instability of myelodysplastic syndromes, the comet assay can be useful to detect DNA lesion intensity and correlate this with cytogenetic abnormalities. Figure 1 illustrates a cell from a healthy 46-year-old control individual classified as comet class 0. Figures 2A - E illustrate cells from a 61-year-old patient with myelodysplastic syndrome (47, XY, +8) classified as comet class 0, 1 and 2.

 

 

References

1. Singh NP, McCoy MT, Tice RR, Schneider EL. A simple technique for quantitation of low levels of DNA damage in individual cells. Exp Cell Res. 1988;175(1):184-91.         [ Links ]

2. Collins AR, Dusinska M, Franklin M, Somorovská M, Petrovská H, Duthie S, et al. Comet assay in human biomonitoring studies: reliability, validation, and applications. Environ Mol Mutagen. 1997;30(2):139-46.         [ Links ]

3. Collins AR. The comet assay for DNA damage and repair: principles, applications and limitations. Mol Biotechnol. 2004;26(1):249-61.         [ Links ]

 

 

Corresponding author:
Paulo Florentino Teixeira Neto
Universidade Federal do Ceará - UFC Laboratório de Hematologia
Rua Capitão Francisco Pedro, 1210 Rodolfo Teófilo
60430-370 Fortaleza, CE, Brazil
paulimneto@gmail.com

Submitted: 4/18/2012
Accepted: 5/2/2012
Conflict-of-interest disclosure: The authors declare no competing financial interest

 

 

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