Array-comparative genomic hybridization

Array-comparative genomic hybridization (also CMA, Chromosomal microarray analysis, microarray-based comparative genomic hybridization, array CGH, a-CGH, aCGH, or virtual karyotype) is a technique to detect genomic copy number variations at a higher resolution level than chromosome-based comparative genomic hybridization (CGH).[1]

Contents

Process

DNA from a test sample and normal reference sample are labelled differentially, using different fluorophores, and hybridized to several thousand probes. The probes are derived from most of the known genes and non-coding regions of the genome, printed on a glass slide.

The fluorescence intensity of the test and of the reference DNA is then measured, to calculate the ratio between them and subsequently the copy number changes for a particular location in the genome.

Efficiency

Using this method, copy number changes at a level of 5–10 kilobases of DNA sequences can be detected. Today even high-resolution CGH (HR-CGH) arrays are accurate to detect structural variations (SV) at resolution of 200 bp [2]. This method allows one to identify new recurrent chromosome changes such as

in disease conditions such as cancer and birth defects due to chromosome aberrations.

Technical considerations

There are several requirements that are dependent on the application of aCGH:

First baby born from the procedure

In September 2009, it was reported that the first baby born after screening with this procedure using polar body biopsy analysis, was Oliver, who was born in the UK to a 41-year-old woman. Of eight eggs that had been tested from the woman, only two were found to be chromosomally normal, and one of those two was used to make the embryo that became Oliver. Prior to Oliver's birth, his mother had undergone 13 failed attempts at in vitro fertilization.[3] The procedure was overseen by CARE Fertility.

See also

References

  1. ^ Shinawi M, Cheung SW (2008). "The array CGH and its clinical applications". Drug Discov Today 13 (17–18): 760–70. doi:10.1016/j.drudis.2008.06.007. PMID 18617013. 
  2. ^ Urban, A.E., Korbel, J.O., Selzer, R., Richmond, T., Hacker, A., Popescu,G.V., Cubells, J.F., Green, R., Emanuel, B.S., Gerstein, M.B. (2006). "High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays". Proc. Natl. Acad. Sci. 103: 4534–39. 
  3. ^ First baby born from new egg-screening technique, Breitbart, September 2, 2009

External links