Fluorescence in situ hybridization

Multiplex RNA visualization in cells using ViewRNA FISH Assays
A metaphase cell positive for the bcr/abl rearrangement (associated with chronic myelogenous leukemia) using FISH. The chromosomes can be seen in blue. The chromosome that is labeled with green and red spots (upper left) is the one where the rearrangement is present.

Fluorescence in situ hybridization (FISH) is a cytogenetic technique that uses fluorescent probes that bind to only those parts of the chromosome with a high degree of sequence complementarity. It was developed by biomedical researchers in the early 1980s[1] and is used to detect and localize the presence or absence of specific DNA sequences on chromosomes. Fluorescence microscopy can be used to find out where the fluorescent probe is bound to the chromosomes. FISH is often used for finding specific features in DNA for use in genetic counseling, medicine, and species identification.[2] FISH can also be used to detect and localize specific RNA targets (mRNA, lncRNA and miRNA) in cells, circulating tumor cells, and tissue samples. In this context, it can help define the spatial-temporal patterns of gene expression within cells and tissues.

Probes – RNA and DNA

ViewRNA detection of miR-133(green) and myogenin mRNA (red) in C2C12 differentiating cells

RNA probes can be designed for any gene or any sequence within a gene for visualization of mRNA,[3][4][5] lncRNA[6][7][8] and miRNA in tissues and cells. FISH is used by examining the cellular reproduction cycle, specifically interphase of the nuclei for any chromosomal abnormalities.[9] This technique [FISH] allows the analysis of a large series of archival cases much easier to identify the pinpointed chromosome by creating a probe with an artificial chromosomal foundation that will attract similar chromosomes.[9] The hybridization signals for each probe when a nucleic abnormality is detected.[9] Each probe for the detection of mRNA and lncRNA is composed of 20 oligonucleotide pairs, each pair covering a space of 40–50 bp. For miRNA detection, the probes use proprietary chemistry for specific detection of miRNA and cover the entire miRNA sequence.

Urothelial cells marked with four different probes

Probes are often derived from fragments of DNA that were isolated, purified, and amplified for use in the Human Genome Project. The size of the human genome is so large, compared to the length that could be sequenced directly, that it was necessary to divide the genome into fragments. (In the eventual analysis, these fragments were put into order by digesting a copy of each fragment into still smaller fragments using sequence-specific endonucleases, measuring the size of each small fragment using size-exclusion chromatography, and using that information to determine where the large fragments overlapped one another.) To preserve the fragments with their individual DNA sequences, the fragments were added into a system of continually replicating bacteria populations. Clonal populations of bacteria, each population maintaining a single artificial chromosome, are stored in various laboratories around the world. The artificial chromosomes (BAC) can be grown, extracted, and labeled, in any lab. These fragments are on the order of 100 thousand base-pairs, and are the basis for most FISH probes.

Preparation and hybridization process – RNA

Cells, circulating tumor cells (CTCs), or formalin-fixed paraffin-embedded (FFPE) or frozen tissue sections are fixed, then permeabilized to allow target accessibility. FISH has also been successfully done on unfixed cells.[10] A target-specific probe, composed of 20 oligonucleotide pairs, hybridizes to the target RNA(s). Separate but compatible signal amplification systems enable the multiplex assay (up to two targets per assay). Signal amplification is achieved via a series of sequential hybridization steps. At the end of the assay the tissue samples are visualized under a fluorescence microscope.

Preparation and hybridization process – DNA

Scheme of the principle of the FISH Experiment to localize a gene in the nucleus.

First, a probe is constructed. The probe must be large enough to hybridize specifically with its target but not so large as to impede the hybridization process. The probe is tagged directly with fluorophores, with targets for antibodies or with biotin. Tagging can be done in various ways, such as nick translation, or PCR using tagged nucleotides.

Then, an interphase or metaphase chromosome preparation is produced. The chromosomes are firmly attached to a substrate, usually glass. Repetitive DNA sequences must be blocked by adding short fragments of DNA to the sample. The probe is then applied to the chromosome DNA and incubated for approximately 12 hours while hybridizing. Several wash steps remove all unhybridized or partially hybridized probes. The results are then visualized and quantified using a microscope that is capable of exciting the dye and recording images.

If the fluorescent signal is weak, amplification of the signal may be necessary in order to exceed the detection threshold of the microscope. Fluorescent signal strength depends on many factors such as probe labeling efficiency, the type of probe, and the type of dye. Fluorescently tagged antibodies or streptavidin are bound to the dye molecule. These secondary components are selected so that they have a strong signal.

Variations on probes and analysis

Interphase cells positive for a chromosomal t(9;22) rearrangement.

FISH is a very general technique. The differences between the various FISH techniques are usually due to variations in the sequence and labeling of the probes; and how they are used in combination. Probes are divided into two generic categories: cellular and acellular. In fluorescence "in situ" hybridization refers to the cellular placement of the probe.[11]

Probe size is important because longer probes hybridize less specifically than shorter probes, "a short strand of DNA or RNA (often 10–25 nucleotides) which is complementary to a given target sequence, it can be used to identify or locate the target.". The overlap defines the resolution of detectable features. For example, if the goal of an experiment is to detect the breakpoint of a translocation, then the overlap of the probes — the degree to which one DNA sequence is contained in the adjacent probes — defines the minimum window in which the breakpoint may be detected.

The mixture of probe sequences determines the type of feature the probe can detect. Probes that hybridize along an entire chromosome are used to count the number of a certain chromosome, show translocations, or identify extra-chromosomal fragments of chromatin. This is often called "whole-chromosome painting." If every possible probe is used, every chromosome, (the whole genome) would be marked fluorescently, which would not be particularly useful for determining features of individual sequences. However, it is possible to create a mixture of smaller probes that are specific to a particular region (locus) of DNA; these mixtures are used to detect deletion mutations. When combined with a specific color, a locus-specific probe mixture is used to detect very specific translocations. Special locus-specific probe mixtures are often used to count chromosomes, by binding to the centromeric regions of chromosomes, which are distinctive enough to identify each chromosome (with the exception of Chromosome 13, 14, 21, 22.)

A variety of other techniques use mixtures of differently colored probes. A range of colors in mixtures of fluorescent dyes can be detected, so each human chromosome can be identified by a characteristic color using whole-chromosome probe mixtures and a variety of ratios of colors. Although there are more chromosomes than easily distinguishable fluorescent dye colors, ratios of probe mixtures can be used to create secondary colors. Similar to comparative genomic hybridization, the probe mixture for the secondary colors is created by mixing the correct ratio of two sets of differently colored probes for the same chromosome. This technique is sometimes called M-FISH.

The same physics that make a variety of colors possible for M-FISH can be used for the detection of translocations. That is, colors that are adjacent appear to overlap; a secondary color is observed. Some assays are designed so that the secondary color will be present or absent in cases of interest. An example is the detection of BCR/ABL translocations, where the secondary color indicates disease. This variation is often called double-fusion FISH or D-FISH. In the opposite situation—where the absence of the secondary color is pathological—is illustrated by an assay used to investigate translocations where only one of the breakpoints is known or constant. Locus-specific probes are made for one side of the breakpoint and the other intact chromosome. In normal cells, the secondary color is observed, but only the primary colors are observed when the translocation occurs. This technique is sometimes called "break-apart FISH".

Single-molecule RNA FISH

Single-molecule RNA FISH, also known as Stellaris® RNA FISH,[12] is a method of detecting and quantifying mRNA and other long RNA molecules in a thin layer of tissue sample. Targets can be reliably imaged through the application of multiple short singly labeled oligonucleotide probes.[13] The binding of up to 48 fluorescent labeled oligos to a single molecule of mRNA provides sufficient fluorescence to accurately detect and localize each target mRNA in a wide-field fluorescent microscopy image. Probes not binding to the intended sequence do not achieve sufficient localized fluorescence to be distinguished from background.[14]

Single-molecule RNA FISH assays can be performed in simplex or multiplex, and can be used as a follow-up experiment to quantitative PCR, or imaged simultaneously with a fluorescent antibody assay. The technology has potential applications in cancer diagnosis,[15] neuroscience, gene expression analysis,[16] and companion diagnostics.

Fiber FISH

In an alternative technique to interphase or metaphase preparations, fiber FISH, interphase chromosomes are attached to a slide in such a way that they are stretched out in a straight line, rather than being tightly coiled, as in conventional FISH, or adopting a chromosome territory conformation, as in interphase FISH. This is accomplished by applying mechanical shear along the length of the slide, either to cells that have been fixed to the slide and then lysed, or to a solution of purified DNA. A technique known as chromosome combing is increasingly used for this purpose. The extended conformation of the chromosomes allows dramatically higher resolution – even down to a few kilobases. The preparation of fiber FISH samples, although conceptually simple, is a rather skilled art, and only specialized laboratories use the technique routinely. [Reference needed]

Q-FISH

Q-FISH combines FISH with PNAs and computer software to quantify fluorescence intensity. This technique is used routinely in telomere length research.

Flow-FISH

Flow-FISH uses flow cytometry to perform FISH automatically using per-cell fluorescence measurements.

Medical applications

Often parents of children with a developmental disability want to know more about their child's conditions before choosing to have another child. These concerns can be addressed by analysis of the parents' and child's DNA. In cases where the child's developmental disability is not understood, the cause of it can potentially be determined using FISH and cytogenetic techniques. Examples of diseases that are diagnosed using FISH include Prader-Willi syndrome, Angelman syndrome, 22q13 deletion syndrome, chronic myelogenous leukemia, acute lymphoblastic leukemia, Cri-du-chat, Velocardiofacial syndrome, and Down syndrome. FISH on sperm cells is indicated for men with an abnormal somatic or meiotic karyotype as well as those with oligozoospermia, since approximately 50% of oligozoospermic men have an increased rate of sperm chromosome abnormalities.[17] The analysis of chromosomes 21, X, and Y is enough to identify oligozoospermic individuals at risk.[17]

In medicine, FISH can be used to form a diagnosis, to evaluate prognosis, or to evaluate remission of a disease, such as cancer. Treatment can then be specifically tailored. A traditional exam involving metaphase chromosome analysis is often unable to identify features that distinguish one disease from another, due to subtle chromosomal features; FISH can elucidate these differences. FISH can also be used to detect diseased cells more easily than standard Cytogenetic methods, which require dividing cells and requires labor and time-intensive manual preparation and analysis of the slides by a technologist. FISH, on the other hand, does not require living cells and can be quantified automatically, a computer counts the fluorescent dots present. However, a trained technologist is required to distinguish subtle differences in banding patterns on bent and twisted metaphase chromosomes. FISH can be incorporated into Lab-on-a-chip microfluidic device. This technology is still in a developmental stage but, like other lab on a chip methods, it may lead to more portable diagnostic techniques.[18][19]

Species identification

FISH is often used in clinical studies. If a patient is infected with a suspected pathogen, bacteria, from the patient's tissues or fluids, are typically grown on agar to determine the identity of the pathogen. Many bacteria, however, even well-known species, do not grow well under laboratory conditions. FISH can be used to detect directly the presence of the suspect on small samples of patient's tissue.

FISH can also be used to compare the genomes of two biological species, to deduce evolutionary relationships. A similar hybridization technique is called a zoo blot. Bacterial FISH probes are often primers for the 16s rRNA region.

FISH is widely used in the field of microbial ecology, to identify microorganisms. Biofilms, for example, are composed of complex (often) multi-species bacterial organizations. Preparing DNA probes for one species and performing FISH with this probe allows one to visualize the distribution of this specific species within the biofilm. Preparing probes (in two different colors) for two species allows to visualize/study co-localization of these two species in the biofilm, and can be useful in determining the fine architecture of the biofilm.

Comparative genomic hybridization

Comparative genomic hybridization can be described as a method that uses FISH in a parallel manner with the comparison of the hybridization strength to recall any major disruptions in the duplication process of the DNA sequences in the genome of the nucleus.[20]

Virtual karyotype

Virtual karyotyping is another cost-effective, clinically available alternative to FISH panels using thousands to millions of probes on a single array to detect copy number changes, genome-wide, at unprecedented resolution. Currently, this type of analysis will only detect gains and losses of chromosomal material and will not detect balanced rearrangements, such as translocations and inversions which are hallmark aberrations seen in many types of leukemia and lymphoma.

Spectral karyotype

Spectral karyotyping is an image of colored chromosomes. Spectral karyotyping involves FISH using multiple forms of many types of probes with the result to see each chromosome labeled through its metaphase stage. This type of karyotyping is used specifically when seeking out chromosome arrangements.

See also

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Gallery

References

  1. ↑ Langer-Safer, P. R.; Levine, M.; Ward, D. C. (1982). "Immunological method for mapping genes on Drosophila polytene chromosomes". Proceedings of the National Academy of Sciences. 79 (14): 4381–5. Bibcode:1982PNAS...79.4381L. doi:10.1073/pnas.79.14.4381. PMC 346675Freely accessible. PMID 6812046.
  2. ↑ Amann, Rudolf; Fuchs, Bernhard M. (2008). "Single-cell identification in microbial communities by improved fluorescence in situ hybridization techniques". Nature Reviews Microbiology. 6 (5): 339–348. doi:10.1038/nrmicro1888.
  3. ↑ Anthony, S. J.; St. Leger, J. A.; Pugliares, K.; Ip, H. S.; Chan, J. M.; Carpenter, Z. W.; Navarrete-Macias, I.; Sanchez-Leon, M.; Saliki, J. T.; Pedersen, J.; Karesh, W.; Daszak, P.; Rabadan, R.; Rowles, T.; Lipkin, W. I. (2012). "Emergence of Fatal Avian Influenza in New England Harbor Seals". MBio. 3 (4): e00166–e00112. doi:10.1128/mBio.00166-12. PMC 3419516Freely accessible. PMID 22851656.
  4. ↑ Everitt, A. R.; Clare, S.; Pertel, T.; John, S. P.; Wash, R. S.; Smith, S. E.; Chin, C. R.; Feeley, E. M.; Sims, J. S.; Adams, D. J.; Wise, H. M.; Kane, L.; Goulding, D.; Digard, P.; Anttila, V.; Baillie, J. K.; Walsh, T. S.; Hume, D. A.; Palotie, A.; Xue, Y.; Colonna, V.; Tyler-Smith, C.; Dunning, J.; Gordon, S. B.; Everingham, K.; Dawson, H.; Hope, D.; Ramsay, P.; Walsh (Local Lead Investigator), T. S.; et al. (2012). "IFITM3 restricts the morbidity and mortality associated with influenza". Nature. 484 (7395): 519–23. Bibcode:2012Natur.484..519.. doi:10.1038/nature10921. PMID 22446628.
  5. ↑ Louzada, S.; Adega, F.; Chaves, R. (2012). "Defining the sister rat mammary tumor cell lines HH-16 cl.2/1 and HH-16.cl.4 as an in vitro cell model for Erbb2". PLoS ONE. 7 (1): e29923. Bibcode:2012PLoSO...729923L. doi:10.1371/journal.pone.0029923. PMC 3254647Freely accessible. PMID 22253826.
  6. ↑ Ting, D. T.; Lipson, D.; Paul, S.; Brannigan, B. W.; Akhavanfard, S.; Coffman, E. J.; Contino, G.; Deshpande, V.; Iafrate, A. J.; Letovsky, S.; Rivera, M. N.; Bardeesy, N.; Maheswaran, S.; Haber, D. A. (2011). "Aberrant Overexpression of Satellite Repeats in Pancreatic and Other Epithelial Cancers". Science. 331 (6017): 593–6. Bibcode:2011Sci...331..593T. doi:10.1126/science.1200801. PMC 3701432Freely accessible. PMID 21233348.
  7. ↑ Zhang, B.; Arun, G.; Mao, Y. S.; Lazar, Z.; Hung, G.; Bhattacharjee, G.; Xiao, X.; Booth, C. J.; Wu, J.; Zhang, C.; Spector, D. L. (2012). "The lncRNA Malat1 is Dispensable for Mouse Development but Its Transcription Plays a cis-Regulatory Role in the Adult". Cell Reports. 2 (1): 111–23. doi:10.1016/j.celrep.2012.06.003. PMC 3408587Freely accessible. PMID 22840402.
  8. ↑ Lee, K.; Kunkeaw, N.; Jeon, S. H.; Lee, I.; Johnson, B. H.; Kang, G. -Y.; Bang, J. Y.; Park, H. S.; Leelayuwat, C.; Lee, Y. S. (2011). "Precursor miR-886, a novel noncoding RNA repressed in cancer, associates with PKR and modulates its activity". RNA. 17 (6): 1076–89. doi:10.1261/rna.2701111. PMC 3096040Freely accessible. PMID 21518807.
  9. 1 2 3 Bernasconi, B.; Karamitopolou-Diamantiis, E.; Tornillo, L.; Lugli, A.; Di Vizio, D.; Dirnhofer, S.; Wengmann, S.; Glatz-Krieger, K.; Fend, F.; Capella, C.; Insabato, L.; Terracciano, L. M. (2008). "Chromosomal instability in gastric mucosa-associated lymphoid tissue lymphomas: A fluorescent in situ hybridization study using a tissue microarray approach". Human Pathology. 39 (4): 536–42. doi:10.1016/j.humpath.2007.08.009. PMID 18234275.
  10. ↑ Haroon, Mohamed F.; Skennerton, Connor T.; Steen, Jason A.; Lachner, Nancy; Hugenholtz, Philip & Tyson, Gene W. (2013). "Chapter One – In-Solution Fluorescence In Situ Hybridization and Fluorescence-Activated Cell Sorting for Single Cell and Population Genome Recovery". In F. DeLong Edward. Methods in Enzymology. 531. Academic Press. pp. 3–19.
  11. ↑ Camesano, Terri A.; Mello, Charlene M. (2008). ACS Symposium Series. American Chemical Society. ISBN 9780841274303.
  12. ↑ Orjalo, ArturoV. Jr.; Johansson, HansE. (2016-01-01). Feng, Yi; Zhang, Lin, eds. Stellaris® RNA Fluorescence In Situ Hybridization for the Simultaneous Detection of Immature and Mature Long Noncoding RNAs in Adherent Cells. Methods in Molecular Biology. Springer New York. pp. 119–134. doi:10.1007/978-1-4939-3378-5_10. ISBN 9781493933761.
  13. ↑ Raj, A.; Van Den Bogaard, P.; Rifkin, S. A.; Van Oudenaarden, A.; Tyagi, S. (2008). "Imaging individual mRNA molecules using multiple singly labeled probes". Nature Methods. 5 (10): 877–9. doi:10.1038/nmeth.1253. PMID 18806792.
  14. ↑ Biosearch Technologies Signs Exclusive License for Single Molecule FISH Technologies from UMDNJ. biosearchtech.com
  15. ↑ "A New Test for Recurrent Colon Cancer". Annals of Internal Medicine. 131 (11): 805. 1999. doi:10.7326/0003-4819-131-11-199912070-00024.
  16. ↑ Kosman, D.; Mizutani, C. M.; Lemons, D; Cox, W. G.; McGinnis, W; Bier, E (2004). "Multiplex Detection of RNA Expression in Drosophila Embryos". Science. 305 (5685): 846. doi:10.1126/science.1099247. PMID 15297669.
  17. 1 2 Sarrate, Z.; Vidal, F.; Blanco, J. (2010). "Role of sperm fluorescent in situ hybridization studies in infertile patients: Indications, study approach, and clinical relevance". Fertility and Sterility. 93 (6): 1892–902. doi:10.1016/j.fertnstert.2008.12.139. PMID 19254793.
  18. ↑ Kurz, C. M.; v.d. Moosdijk, S.; Thielecke, H.; Velten, T. (2011). "Towards a cellular multi-parameter analysis platform: Fluorescence in situ hybridization (FISH) on microhole-array chips". 2011 Annual International Conference of the IEEE Engineering in Medicine and Biology Society. p. 8408. doi:10.1109/IEMBS.2011.6092074. ISBN 978-1-4577-1589-1.
  19. ↑ Dill, K.; Hui Liu, R.; Grodzinski, P. (2008). Microarrays: Preparation, Microfluidics, Detection Methods, and Biological Applications. Springer. p. 323. ISBN 0387727167.
  20. ↑ "Comparative Genomic Hybridization". McGraw-Hill Dictionary of Scientific and Technical Terms. Retrieved September 19, 2013.

Further reading

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