Melting curve analysis after T allele enrichment (MelcaTle) as a highly sensitive and reliable method for detecting the JAK2V617F mutation
Detection of the JAK2V617F mutation is essential for diagnosing patients with classical myeloproliferative neoplasms (MPNs). However, detection of the low-frequency JAK2V617F mutation is a challenging task due to the necessity of discriminating between true-positive and false-positive results. Here,...
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creator | Morishita, Soji Takahashi, Kochi Araki, Marito Hironaka, Yumi Sunami, Yoshitaka Edahiro, Yoko Tsutsui, Miyuki Ohsaka, Akimichi Tsuneda, Satoshi Komatsu, Norio |
description | Detection of the JAK2V617F mutation is essential for diagnosing patients with classical myeloproliferative neoplasms (MPNs). However, detection of the low-frequency JAK2V617F mutation is a challenging task due to the necessity of discriminating between true-positive and false-positive results. Here, we have developed a highly sensitive and accurate assay for the detection of JAK2V617F and named it melting curve analysis after T allele enrichment (MelcaTle). MelcaTle comprises three steps: 1) two cycles of JAK2V617F allele enrichment by PCR amplification followed by BsaXI digestion, 2) selective amplification of the JAK2V617F allele in the presence of a bridged nucleic acid (BNA) probe, and 3) a melting curve assay using a BODIPY-FL-labeled oligonucleotide. Using this assay, we successfully detected nearly a single copy of the JAK2V617F allele, without false-positive signals, using 10 ng of genomic DNA standard. Furthermore, MelcaTle showed no positive signals in 90 assays screening healthy individuals for JAK2V617F. When applying MelcaTle to 27 patients who were initially classified as JAK2V617F-positive on the basis of allele-specific PCR analysis and were thus suspected as having MPNs, we found that two of the patients were actually JAK2V617F-negative. A more careful clinical data analysis revealed that these two patients had developed transient erythrocytosis of unknown etiology but not polycythemia vera, a subtype of MPNs. These findings indicate that the newly developed MelcaTle assay should markedly improve the diagnosis of JAK2V617F-positive MPNs. |
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However, detection of the low-frequency JAK2V617F mutation is a challenging task due to the necessity of discriminating between true-positive and false-positive results. Here, we have developed a highly sensitive and accurate assay for the detection of JAK2V617F and named it melting curve analysis after T allele enrichment (MelcaTle). MelcaTle comprises three steps: 1) two cycles of JAK2V617F allele enrichment by PCR amplification followed by BsaXI digestion, 2) selective amplification of the JAK2V617F allele in the presence of a bridged nucleic acid (BNA) probe, and 3) a melting curve assay using a BODIPY-FL-labeled oligonucleotide. Using this assay, we successfully detected nearly a single copy of the JAK2V617F allele, without false-positive signals, using 10 ng of genomic DNA standard. Furthermore, MelcaTle showed no positive signals in 90 assays screening healthy individuals for JAK2V617F. When applying MelcaTle to 27 patients who were initially classified as JAK2V617F-positive on the basis of allele-specific PCR analysis and were thus suspected as having MPNs, we found that two of the patients were actually JAK2V617F-negative. A more careful clinical data analysis revealed that these two patients had developed transient erythrocytosis of unknown etiology but not polycythemia vera, a subtype of MPNs. These findings indicate that the newly developed MelcaTle assay should markedly improve the diagnosis of JAK2V617F-positive MPNs.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0122003</identifier><identifier>PMID: 25794279</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Alleles ; Amplification ; Assaying ; Blood cancer ; Data analysis ; Data processing ; Deoxyribonucleic acid ; DNA ; DNA Mutational Analysis - methods ; Enrichment ; Etiology ; Genetic testing ; Hematology ; Humans ; Janus Kinase 2 - genetics ; Leukemia ; Life sciences ; Medical diagnosis ; Medicine ; Melting ; Melting curve ; Methods ; Mutation ; Mutation - genetics ; Myeloproliferative Disorders - enzymology ; Myeloproliferative Disorders - genetics ; Neoplasms ; Nucleic Acid Denaturation - genetics ; Nucleic acids ; Oligonucleotides ; Patients ; Peptides ; Polycythemia ; Polycythemia vera ; Polymerase chain reaction ; Reproducibility of Results ; Stem cells ; Tumors ; University graduates</subject><ispartof>PloS one, 2015-03, Vol.10 (3), p.e0122003-e0122003</ispartof><rights>COPYRIGHT 2015 Public Library of Science</rights><rights>2015 Morishita et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 Morishita et al 2015 Morishita et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-cd86c52b49a6ccbc9ed8809256149046fddfec0669e6b7a19acfbde266d3633f3</citedby><cites>FETCH-LOGICAL-c692t-cd86c52b49a6ccbc9ed8809256149046fddfec0669e6b7a19acfbde266d3633f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4368779/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4368779/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2100,2919,23857,27915,27916,53782,53784,79361,79362</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25794279$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Eaves, Connie J</contributor><creatorcontrib>Morishita, Soji</creatorcontrib><creatorcontrib>Takahashi, Kochi</creatorcontrib><creatorcontrib>Araki, Marito</creatorcontrib><creatorcontrib>Hironaka, Yumi</creatorcontrib><creatorcontrib>Sunami, Yoshitaka</creatorcontrib><creatorcontrib>Edahiro, Yoko</creatorcontrib><creatorcontrib>Tsutsui, Miyuki</creatorcontrib><creatorcontrib>Ohsaka, Akimichi</creatorcontrib><creatorcontrib>Tsuneda, Satoshi</creatorcontrib><creatorcontrib>Komatsu, Norio</creatorcontrib><title>Melting curve analysis after T allele enrichment (MelcaTle) as a highly sensitive and reliable method for detecting the JAK2V617F mutation</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Detection of the JAK2V617F mutation is essential for diagnosing patients with classical myeloproliferative neoplasms (MPNs). 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When applying MelcaTle to 27 patients who were initially classified as JAK2V617F-positive on the basis of allele-specific PCR analysis and were thus suspected as having MPNs, we found that two of the patients were actually JAK2V617F-negative. A more careful clinical data analysis revealed that these two patients had developed transient erythrocytosis of unknown etiology but not polycythemia vera, a subtype of MPNs. These findings indicate that the newly developed MelcaTle assay should markedly improve the diagnosis of JAK2V617F-positive MPNs.</description><subject>Alleles</subject><subject>Amplification</subject><subject>Assaying</subject><subject>Blood cancer</subject><subject>Data analysis</subject><subject>Data processing</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA Mutational Analysis - methods</subject><subject>Enrichment</subject><subject>Etiology</subject><subject>Genetic testing</subject><subject>Hematology</subject><subject>Humans</subject><subject>Janus Kinase 2 - genetics</subject><subject>Leukemia</subject><subject>Life sciences</subject><subject>Medical diagnosis</subject><subject>Medicine</subject><subject>Melting</subject><subject>Melting curve</subject><subject>Methods</subject><subject>Mutation</subject><subject>Mutation - genetics</subject><subject>Myeloproliferative Disorders - enzymology</subject><subject>Myeloproliferative Disorders - genetics</subject><subject>Neoplasms</subject><subject>Nucleic Acid Denaturation - genetics</subject><subject>Nucleic acids</subject><subject>Oligonucleotides</subject><subject>Patients</subject><subject>Peptides</subject><subject>Polycythemia</subject><subject>Polycythemia vera</subject><subject>Polymerase chain reaction</subject><subject>Reproducibility of Results</subject><subject>Stem cells</subject><subject>Tumors</subject><subject>University graduates</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqNk81u1DAUhSMEoqXwBggsIaF2MUNsJ068QRpVFApFlaB0azn2zcSVE09tp6KvwFPj-WnVoC5QFomuv3OOfeObZa9xPse0wh-u3OgHaecrN8A8x4TkOX2S7WNOyYyRnD598L2XvQjhKs9LWjP2PNsjZcULUvH97M93sNEMS6RGfwNIJsfbYAKSbQSPLpC0FiwgGLxRXQ9DRIdJoeSFhSMkE4c6s-zsLQowBBPNxkMjD9bIJgl7iJ3TqHUeaYigNlmxA_R18Y1cMlydoH6MMho3vMyetdIGeLV7H2S_Tj5dHH-ZnZ1_Pj1enM0U4yTOlK6ZKklTcMmUahQHXdc5JyXDBc8L1mrdgsoZ48CaSmIuVdtoIIxpyiht6UH2duu7si6IXRuDwIwVnOZliRNxuiW0k1di5U0v_a1w0ohNwfmlkD4aZUHURc3LllW4aVhBWCV1VUItcc2gVoWuktfHXdrY9KBVaqGXdmI6XRlMJ5buRhSU1VXFk8HhzsC76xFCFL0JCqyVA7hxs29GeMnIOuvdP-jjp9tRS5kOYIbWpVy1NhWLgtC65Lhcx84fodKjoTcq3bnWpPpEcDQRJCbC77iUYwji9OeP_2fPL6fs-wdsB9LGLjg7rq9MmILFFlTeheChvW8yzsV6ZO66IdYjI3Yjk2RvHv6ge9HdjNC_EyYRhA</recordid><startdate>20150320</startdate><enddate>20150320</enddate><creator>Morishita, Soji</creator><creator>Takahashi, Kochi</creator><creator>Araki, Marito</creator><creator>Hironaka, Yumi</creator><creator>Sunami, Yoshitaka</creator><creator>Edahiro, Yoko</creator><creator>Tsutsui, Miyuki</creator><creator>Ohsaka, Akimichi</creator><creator>Tsuneda, Satoshi</creator><creator>Komatsu, Norio</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20150320</creationdate><title>Melting curve analysis after T allele enrichment (MelcaTle) as a highly sensitive and reliable method for detecting the JAK2V617F mutation</title><author>Morishita, Soji ; Takahashi, Kochi ; Araki, Marito ; Hironaka, Yumi ; Sunami, Yoshitaka ; Edahiro, Yoko ; Tsutsui, Miyuki ; Ohsaka, Akimichi ; Tsuneda, Satoshi ; Komatsu, Norio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-cd86c52b49a6ccbc9ed8809256149046fddfec0669e6b7a19acfbde266d3633f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Alleles</topic><topic>Amplification</topic><topic>Assaying</topic><topic>Blood cancer</topic><topic>Data analysis</topic><topic>Data processing</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA Mutational Analysis - methods</topic><topic>Enrichment</topic><topic>Etiology</topic><topic>Genetic testing</topic><topic>Hematology</topic><topic>Humans</topic><topic>Janus Kinase 2 - genetics</topic><topic>Leukemia</topic><topic>Life sciences</topic><topic>Medical diagnosis</topic><topic>Medicine</topic><topic>Melting</topic><topic>Melting curve</topic><topic>Methods</topic><topic>Mutation</topic><topic>Mutation - genetics</topic><topic>Myeloproliferative Disorders - enzymology</topic><topic>Myeloproliferative Disorders - genetics</topic><topic>Neoplasms</topic><topic>Nucleic Acid Denaturation - genetics</topic><topic>Nucleic acids</topic><topic>Oligonucleotides</topic><topic>Patients</topic><topic>Peptides</topic><topic>Polycythemia</topic><topic>Polycythemia vera</topic><topic>Polymerase chain reaction</topic><topic>Reproducibility of Results</topic><topic>Stem cells</topic><topic>Tumors</topic><topic>University graduates</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Morishita, Soji</creatorcontrib><creatorcontrib>Takahashi, Kochi</creatorcontrib><creatorcontrib>Araki, Marito</creatorcontrib><creatorcontrib>Hironaka, Yumi</creatorcontrib><creatorcontrib>Sunami, Yoshitaka</creatorcontrib><creatorcontrib>Edahiro, Yoko</creatorcontrib><creatorcontrib>Tsutsui, Miyuki</creatorcontrib><creatorcontrib>Ohsaka, Akimichi</creatorcontrib><creatorcontrib>Tsuneda, Satoshi</creatorcontrib><creatorcontrib>Komatsu, Norio</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Proquest Nursing & Allied Health Source</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - 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However, detection of the low-frequency JAK2V617F mutation is a challenging task due to the necessity of discriminating between true-positive and false-positive results. Here, we have developed a highly sensitive and accurate assay for the detection of JAK2V617F and named it melting curve analysis after T allele enrichment (MelcaTle). MelcaTle comprises three steps: 1) two cycles of JAK2V617F allele enrichment by PCR amplification followed by BsaXI digestion, 2) selective amplification of the JAK2V617F allele in the presence of a bridged nucleic acid (BNA) probe, and 3) a melting curve assay using a BODIPY-FL-labeled oligonucleotide. Using this assay, we successfully detected nearly a single copy of the JAK2V617F allele, without false-positive signals, using 10 ng of genomic DNA standard. Furthermore, MelcaTle showed no positive signals in 90 assays screening healthy individuals for JAK2V617F. When applying MelcaTle to 27 patients who were initially classified as JAK2V617F-positive on the basis of allele-specific PCR analysis and were thus suspected as having MPNs, we found that two of the patients were actually JAK2V617F-negative. A more careful clinical data analysis revealed that these two patients had developed transient erythrocytosis of unknown etiology but not polycythemia vera, a subtype of MPNs. These findings indicate that the newly developed MelcaTle assay should markedly improve the diagnosis of JAK2V617F-positive MPNs.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>25794279</pmid><doi>10.1371/journal.pone.0122003</doi><oa>free_for_read</oa></addata></record> |
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subjects | Alleles Amplification Assaying Blood cancer Data analysis Data processing Deoxyribonucleic acid DNA DNA Mutational Analysis - methods Enrichment Etiology Genetic testing Hematology Humans Janus Kinase 2 - genetics Leukemia Life sciences Medical diagnosis Medicine Melting Melting curve Methods Mutation Mutation - genetics Myeloproliferative Disorders - enzymology Myeloproliferative Disorders - genetics Neoplasms Nucleic Acid Denaturation - genetics Nucleic acids Oligonucleotides Patients Peptides Polycythemia Polycythemia vera Polymerase chain reaction Reproducibility of Results Stem cells Tumors University graduates |
title | Melting curve analysis after T allele enrichment (MelcaTle) as a highly sensitive and reliable method for detecting the JAK2V617F mutation |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-15T00%3A30%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Melting%20curve%20analysis%20after%20T%20allele%20enrichment%20(MelcaTle)%20as%20a%20highly%20sensitive%20and%20reliable%20method%20for%20detecting%20the%20JAK2V617F%20mutation&rft.jtitle=PloS%20one&rft.au=Morishita,%20Soji&rft.date=2015-03-20&rft.volume=10&rft.issue=3&rft.spage=e0122003&rft.epage=e0122003&rft.pages=e0122003-e0122003&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0122003&rft_dat=%3Cgale_plos_%3EA423859159%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1664930551&rft_id=info:pmid/25794279&rft_galeid=A423859159&rft_doaj_id=oai_doaj_org_article_84895f671bb64267ad75e8a186e8c4d7&rfr_iscdi=true |