A universal assay for detection of oncogenic fusion transcripts by oligo microarray analysis

BackgroundThe ability to detect neoplasia-specific fusion genes is important not only in cancer research, but also increasingly in clinical settings to ensure that correct diagnosis is made and the optimal treatment is chosen. However, the available methodologies to detect such fusions all have their distinct short-comings.ResultsWe describe a novel oligonucleotide microarray strategy whereby one can screen for all known oncogenic fusion transcripts in a single experiment. To accomplish this, we combine measurements of chimeric transcript junctions with exon-wise measurements of individual fusion partners. To demonstrate the usefulness of the approach, we designed a DNA microarray containing 68,861 oligonucleotide probes that includes oligos covering all combinations of chimeric exon-exon junctions from 275 pairs of fusion genes, as well as sets of oligos internal to all the exons of the fusion partners. Using this array, proof of principle was demonstrated by detection of known fusion genes (such as TCF3:PBX1, ETV6:RUNX1, and TMPRSS2:ERG) from all six positive controls consisting of leukemia cell lines and prostate cancer biopsies.ConclusionThis new method bears promise of an important complement to currently used diagnostic and research tools for the detection of fusion genes in neoplastic diseases.

[1]  M. Greaves,et al.  Phenotypic characterisation of a unique non-T, non-B acute lymphoblastic leukaemia cell line , 1977, Nature.

[2]  Y. Matsuo,et al.  Establishment and characterization of human B cell precursor-leukemia cell lines. , 1998, Leukemia research.

[3]  Lee T. Sam,et al.  Transcriptome Sequencing to Detect Gene Fusions in Cancer , 2009, Nature.

[4]  M. Teixeira,et al.  Recurrent fusion oncogenes in carcinomas. , 2006, Critical reviews in oncogenesis.

[5]  P. Sorensen,et al.  ETV6-NTRK3: a chimeric protein tyrosine kinase with transformation activity in multiple cell lineages. , 2005, Seminars in cancer biology.

[6]  A. Chinnaiyan,et al.  Recurrent gene fusions in prostate cancer , 2008, Nature Reviews Cancer.

[7]  Atif Shahab,et al.  Fusion transcripts and transcribed retrotransposed loci discovered through comprehensive transcriptome analysis using Paired-End diTags (PETs). , 2007, Genome research.

[8]  Martin Vingron,et al.  Mapping translocation breakpoints by next-generation sequencing. , 2008, Genome research.

[9]  R. Eeles,et al.  Detection of TMPRSS2-ERG translocations in human prostate cancer by expression profiling using GeneChip Human Exon 1.0 ST arrays. , 2008, The Journal of molecular diagnostics : JMD.

[10]  Jessica Wang-Rodriguez,et al.  A sensitive array-based assay for identifying multiple TMPRSS2:ERG fusion gene variants , 2008, Nucleic acids research.

[11]  R. Henrique,et al.  TMPRSS2-ERG gene fusion causing ERG overexpression precedes chromosome copy number changes in prostate carcinomas and paired HGPIN lesions. , 2006, Neoplasia.

[12]  A. Mirzabekov,et al.  Clinical screening of gene rearrangements in childhood leukemia by using a multiplex polymerase chain reaction-microarray approach. , 2003, Clinical cancer research : an official journal of the American Association for Cancer Research.

[13]  A. Morley,et al.  RCH-ACV: a lymphoblastic leukemia cell line with chromosome translocation 1;19 and trisomy 8. , 1986, Cancer genetics and cytogenetics.

[14]  Antony V. Cox,et al.  Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing , 2008, Nature Genetics.

[15]  J. Tchinda,et al.  Recurrent fusion of TMPRSS2 and ETS transcription factor genes in prostate cancer. , 2006, Science.

[16]  Jason E. Stewart,et al.  Minimum information about a microarray experiment (MIAME)—toward standards for microarray data , 2001, Nature Genetics.

[17]  J. Rowley,et al.  Screening and quantification of multiple chromosome translocations in human leukemia. , 2003, Clinical chemistry.

[18]  S. Varambally,et al.  Characterization of TMPRSS2:ETV5 and SLC45A3:ETV5 gene fusions in prostate cancer. , 2008, Cancer research.

[19]  F. J. Novo,et al.  TICdb: a collection of gene-mapped translocation breakpoints in cancer , 2007, BMC Genomics.

[20]  B. Johansson,et al.  Fusion genes and rearranged genes as a linear function of chromosome aberrations in cancer , 2004, Nature Genetics.

[21]  A. Mirzabekov,et al.  Identification of chromosomal translocations in leukemias by hybridization with oligonucleotide microarrays. , 2002, Haematologica.