Fluorescence In situ Hybridization: Cell-Based Genetic Diagnostic and Research Applications

被引:137
作者
Cui, Chenghua [1 ,2 ]
Shu, Wei [1 ,3 ]
Li, Peining [1 ]
机构
[1] Yale Sch Med, Dept Genet, Lab Clin Cytogenet, New Haven, CT 06510 USA
[2] Chinese Acad Med Sci, Inst Hematol & Blood Dis Hosp, Dept Pathol, Tianjin, Peoples R China
[3] Guangxi Med Univ, Dept Cell Biol & Genet, Nanning, Peoples R China
关键词
fluorescence in situ hybridization (FISH); genetic diagnosis; aneuploidy; pathogenic copy number variants (CNV); microdeletion/microduplication syndromes; Cas-9 mediated FISH (CASFISH); oligopaint-FISH; single molecule RNA FISH (smRNA-FISH); INSITU HYBRIDIZATION; PRENATAL-DIAGNOSIS; MESSENGER-RNA; GENOMIC LOCI; CANCER; CHROMOSOME; FISH; ABNORMALITIES; AMPLIFICATION; KARYOTYPE;
D O I
10.3389/fcell.2016.00089
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Fluorescence in situ hybridization (FISH) is a macromolecule recognition technology based on the complementary nature of DNA or DNA/RNA double strands. Selected DNA strands incorporated with fluorophore-coupled nucleotides can be used as probes to hybridize onto the complementary sequences in tested cells and tissues and then visualized through a fluorescence microscope or an imaging system. This technology was initially developed as a physical mapping tool to delineate genes within chromosomes. Its high analytical resolution to a single gene level and high sensitivity and specificity enabled an immediate application for genetic diagnosis of constitutional common aneuploidies, microdeletion/microduplication syndromes, and subtelomeric rearrangements. FISH tests using panels of gene-specific probes for somatic recurrent losses, gains, and translocations have been routinely applied for hematologic and solid tumors and are one of the fastest-growing areas in cancer diagnosis. FISH has also been used to detect infectious microbias and parasites like malaria in human blood cells. Recent advances in FISH technology involve various methods for improving probe labeling efficiency and the use of super resolution imaging systems for direct visualization of intra-nuclear chromosomal organization and profiling of RNA transcription in single cells. Cas9-mediated FISH (CASFISH) allowed in situ labeling of repetitive sequences and single-copy sequences without the disruption of nuclear genomic organization in fixed or living cells. Using oligopaint-FISH and super-resolution imaging enabled in situ visualization of chromosome haplotypes from differentially specified single-nucleotide polymorphism loci. Single molecule RNA FISH (smRNA-FISH) using combinatorial labeling or sequential barcoding by multiple round of hybridization were applied to measure mRNA expression of multiple genes within single cells. Research applications of these single molecule single cells DNA and RNA FISH techniques have visualized intra-nuclear genomic structure and sub-cellular transcriptional dynamics of many genes and revealed their functions in various biological processes.
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页数:11
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共 79 条
[1]  
[Anonymous], 2000, Genetics In Medicine, V2, P356, DOI DOI 10.1097/00125817-200011000-00011
[2]   Single-molecule super-resolution imaging of chromosomes and in situ haplotype visualization using Oligopaint FISH probes [J].
Beliveau, Brian J. ;
Boettiger, Alistair N. ;
Avendano, Maier S. ;
Jungmann, Ralf ;
McCole, Ruth B. ;
Joyce, Eric F. ;
Kim-Kiselak, Caroline ;
Bantignies, Frederic ;
Fonseka, Chamith Y. ;
Erceg, Jelena ;
Hannan, Mohammed A. ;
Hoang, Hien G. ;
Colognori, David ;
Lee, Jeannie T. ;
Shih, William M. ;
Yin, Peng ;
Zhuang, Xiaowei ;
Wu, Chao-ting .
NATURE COMMUNICATIONS, 2015, 6
[3]   Translocation of the IgH locus is nearly ubiquitous in multiple myeloma as detected by immuno-FISH [J].
Boersma-Vreugdenhil, GR ;
Peeters, T ;
Bast, BJEG .
BLOOD, 2003, 101 (04) :1653-1653
[4]   Quantitative gene expression analysis in Caenorhabditis elegans using single molecule RNA FISH [J].
Bolkova, Jitka ;
Lanctot, Christian .
METHODS, 2016, 98 :42-49
[5]   Localization and abundance analysis of human IncRNAs at single-cell and single-molecule resolution [J].
Cabili, Moran N. ;
Dunagin, Margaret C. ;
McClanahan, Patrick D. ;
Biaesch, Andrew ;
Padovan-Merhar, Olivia ;
Regev, Aviv ;
Rinn, John L. ;
Raj, Arjun .
GENOME BIOLOGY, 2015, 16
[6]   Design and validation of a pericentromeric BAC clone set aimed at improving diagnosis and phenotype prediction of supernumerary marker chromosomes [J].
Castronovo, Chiara ;
Valtorta, Emanuele ;
Crippa, Milena ;
Tedoldi, Sara ;
Romitti, Lorenza ;
Amione, Maria Cristina ;
Guerneri, Silvana ;
Rusconi, Daniela ;
Ballarati, Lucia ;
Milani, Donatella ;
Grosso, Enrico ;
Cavalli, Pietro ;
Giardino, Daniela ;
Bonati, Maria Teresa ;
Larizza, Lidia ;
Finelli, Palma .
MOLECULAR CYTOGENETICS, 2013, 6
[7]   Dynamic Imaging of Genomic Loci in Living Human Cells by an Optimized CRISPR/Cas System [J].
Chen, Baohui ;
Gilbert, Luke A. ;
Cimini, Beth A. ;
Schnitzbauer, Joerg ;
Zhang, Wei ;
Li, Gene-Wei ;
Park, Jason ;
Blackburn, Elizabeth H. ;
Weissman, Jonathan S. ;
Qi, Lei S. ;
Huang, Bo .
CELL, 2013, 155 (07) :1479-1491
[8]   Statistical Treatment of Fluorescence in Situ Hybridization Validation Data to Generate Normal Reference Ranges Using Excel Functions [J].
Ciolino, Allison L. ;
Tang, Mary E. ;
Bryant, Ron .
JOURNAL OF MOLECULAR DIAGNOSTICS, 2009, 11 (04) :330-333
[9]   Increased aneuploidy in spermatozoa from testicular tumour patients after chemotherapy with cisplatin, etoposide and bleomycin [J].
De Mas, P ;
Daudin, M ;
Vincent, MC ;
Bourrouillou, G ;
Calvas, P ;
Mieusset, R ;
Bujan, L .
HUMAN REPRODUCTION, 2001, 16 (06) :1204-1208
[10]   PHYLOGENETIC STAINS - RIBOSOMAL RNA-BASED PROBES FOR THE IDENTIFICATION OF SINGLE CELLS [J].
DELONG, EF ;
WICKHAM, GS ;
PACE, NR .
SCIENCE, 1989, 243 (4896) :1360-1363