Applications of FISH

Fluorescent in situ hybridization (FISH) is a genetic technique used to diagnose congenital diseases such as Down's Syndrome and Edward's Syndrome. It has also been used to detect cancer and diagnose infectious diseases.

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The DNA in our cells consists of a double helix or two strands of DNA which are repeatedly wound around each other. Each strand contains a sequence of the four bases: adenine (A), guanine (G), cytosine (C), and thymine (T). Each base in a strand pairs to its complementary base on the other strand (A pairs with T, C pairs with G) using hydrogen bonding.

The high affinity with which complementary base pairs (A-T, C-G) bind to their corresponding partner is called ‘hybridization’. Hybridization forms the basis of Fluorescence In Situ Hybridisation or FISH.

In FISH, small DNA strands which have been labeled with a fluorescent probe are allowed to bind to fragments of a person’s DNA, corresponding to a particular genomic region of interest.  This is useful to assess chromosome or gene copy numbers.

If there has been a duplication, more of the probe will hybridize with the sample DNA and more fluorescence will be detected. If there has been a deletion in the genome, the probe cannot attach to its complementary region as it is absent and no fluorescence will be detected. This technique has been applied to serve diagnostic purposes in clinical medicine.

Prenatal diagnosis of chromosomal abnormalities

Prenatal diagnosis is critical to determine the health and congenital abnormalities in the unborn fetus. Common chromosomal abnormalities include Patau syndrome (presence of an extra copy of chromosome 13), Edward’s syndrome (presence of an extra copy of chromosome 18), and Down’s syndrome (presence of an extra copy of chromosome 21).

When a fluorescent DNA probe is tested against healthy regions of chromosomes 13, 18, or 21, two fluorescent signals corresponding to two chromosomes would be observed. However, in the case of gene duplication or the presence of an extra copy of a chromosome, three florescent signals would be visible. Thus, FISH has led to the easy diagnosis of congenital disorders which may not be easily evident under a microscope.

Detection of copy number variants (CNVs) in adults

Different types of FISH probes can detect different chromosomal aberrations. Probes specific to a particular gene locus can determine gene fusions, aneuploidy or an abnormal number of chromosomes, and loss of chromosomal region or whole chromosome in an adult.

FISH has a 50-fold higher resolution than the conventionally used Giemsa stain to detect genetic diseases. The Giemsa stain compares the light and dark patterns of euchromatin and heterochromatin between control and test case to detect defects; whereas FISH is based on direct visualization of specific regions of the genome. Also, it is less time-consuming than karyotyping which requires culturing of cells and subsequently arrest at the metaphase to observe the structural features of chromosomes.

Detection of cancer

FISH is widely used to detect chromosomal abnormalities associated with cancers. HER2 positive breast cancer has extra copies of the HER2 gene and FISH testing is done on breast cancer tissue removed during biopsy to detect the extra copies of the gene. Additional copies of the HER2 gene lead to more HER2 receptors in the cells and these receptors receive signals that stimulate the growth of breast cancer cells.

FISH also has higher sensitivity in detecting cancers. In the case of bladder cancer, FISH has a 50% higher sensitivity (true positive rate) than routine cytology. Chromosomal aberrations are found in 60% of acute myeloid leukemia and 65-90% of acute lymphocytic leukemia. FISH was found to more sensitive and reliable technique to diagnose acute leukemia compared to G-banding which involves staining the chromosomes with Giemsa stain to yield dark and light bands which correspond to heterochromatin and euchromatin.

Detection of infectious diseases

Phylogenetic group-specific 16S ribosomal RNA (rRNA) are used in FISH to detect infectious agents. Oligonucleotide sequences complementary to 16S rRNA (17-34 nucleotides in length) as FISH probes can be used for the analysis of microbial communities in the oral cavity and gastrointestinal flora. Both the oral cavity and intestine are heavily colonized, and FISH has been used to detect pathogens within the microbial community.

Specific oligonucleotide probes have also been designed to detect pathogens in respiratory tract infections. Similarly, FISH has also been used to detect pathogens within tissues. Genus and species-specific oligonucleotide probes have been used to identify pathogenic microorganisms in blood cultures. For example, FISH probes complementary to a specific sequence of 16s rRNA can detect malaria infection in blood samples.

Further Reading

Last Updated: Jan 19, 2022

Dr. Surat P

Written by

Dr. Surat P

Dr. Surat graduated with a Ph.D. in Cell Biology and Mechanobiology from the Tata Institute of Fundamental Research (Mumbai, India) in 2016. Prior to her Ph.D., Surat studied for a Bachelor of Science (B.Sc.) degree in Zoology, during which she was the recipient of an Indian Academy of Sciences Summer Fellowship to study the proteins involved in AIDs. She produces feature articles on a wide range of topics, such as medical ethics, data manipulation, pseudoscience and superstition, education, and human evolution. She is passionate about science communication and writes articles covering all areas of the life sciences.  

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