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Oligonucleotide gap-fill ligation for mutation detection and sequencing in situ
Stockholm University, Science for Life Laboratory (SciLifeLab). Stockholm University, Faculty of Science, Department of Biochemistry and Biophysics.
Stockholm University, Science for Life Laboratory (SciLifeLab). Stockholm University, Faculty of Science, Department of Biochemistry and Biophysics.
Stockholm University, Science for Life Laboratory (SciLifeLab). Stockholm University, Faculty of Science, Department of Biochemistry and Biophysics.
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Number of Authors: 7
2015 (English)In: Nucleic Acids Research, ISSN 0305-1048, E-ISSN 1362-4962, Vol. 43, no 22, e151Article in journal (Refereed) Published
Abstract [en]

In clinical diagnostics a great need exists for targeted in situ multiplex nucleic acid analysis as the mutational status can offer guidance for effective treatment. One well-established method uses padlock probes for mutation detection and multiplex expression analysis directly in cells and tissues. Here, we use oligonucleotide gap-fill ligation to further increase specificity and to capture molecular substrates for in situ sequencing. Short oligonucleotides are joined at both ends of a padlock gap probe by two ligation events and are then locally amplified by target-primed rolling circle amplification (RCA) pre-serving spatial information. We demonstrate the specific detection of the A3243G mutation of mitochondrial DNA and we successfully characterize a single nucleotide variant in the ACTB mRNA in cells by in situ sequencing of RCA products generated by padlock gap-fill ligation. To demonstrate the clinical applicability of our assay, we show specific detection of a point mutation in the EGFR gene in fresh frozen and formalin-fixed, paraffin-embedded (FFPE) lung cancer samples and confirm the detected mutation by in situ sequencing. This approach presents several advantages over conventional padlock probes allowing simpler assay design for multiplexed mutation detection to screen for the presence of mutations in clinically relevant mutational hotspots directly in situ.

Place, publisher, year, edition, pages
2015. Vol. 43, no 22, e151
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Biological Sciences
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URN: urn:nbn:se:su:diva-128581DOI: 10.1093/nar/gkv772ISI: 000371237600003PubMedID: 26240388OAI: oai:DiVA.org:su-128581DiVA: diva2:916349
Available from: 2016-04-01 Created: 2016-03-30 Last updated: 2016-04-01Bibliographically approved

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Mezger, AnjaQian, XiaoyanNilsson, Mats
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Science for Life Laboratory (SciLifeLab)Department of Biochemistry and Biophysics
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