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Direct Molecular Haplotyping of the IVS-8 Poly(TG) and PolyT Repeat Tracts in the Cystic Fibrosis Gene by Melting Curve Analysis of Hybridization Probes
Molecular haplotyping is a developing technology with great potential for use in clinical diagnostics. We describe a haplotyping method that uses PCR combined with hybridization probes. We designed a LightCycler assay that uses fluorescence resonance energy transfer hybridization probes to haplotype...
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Published in: | Clinical chemistry (Baltimore, Md.) Md.), 2005-09, Vol.51 (9), p.1619-1623 |
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creator | Millson, Alison Pont-Kingdon, Genevieve Page, Sam Lyon, Elaine |
description | Molecular haplotyping is a developing technology with great potential for use in clinical diagnostics. We describe a haplotyping method that uses PCR combined with hybridization probes.
We designed a LightCycler assay that uses fluorescence resonance energy transfer hybridization probes to haplotype the poly(TG) and polyT (TG-T) tract in the IVS-8 region of the CFTR gene. The reporter probe was designed as a perfect match to the TG12-5T allele.
Analysis of 132 samples revealed 9 unique derivative melting temperatures (Tms); the lowest was 42.4 degrees C and the highest was 63.6 degrees C. The lowest Tms were in the TGn-9T group, the intermediate Tms in the TGn-7T group, and the highest Tms in the TGn-5T group. Haplotype frequencies were highest (39%) for TG11-7T and lowest (0.4%) for TG13-5T.
Different combinations of polymorphisms under the reporter hybridization probe had unique and characteristic Tms. This property enables genotyping as well as determination of the phase of multiple variants under the probe, a principle we demonstrated by haplotyping the TG-T repeat tract in the IVS-8 region of the CFTR gene. |
doi_str_mv | 10.1373/clinchem.2005.052159 |
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We designed a LightCycler assay that uses fluorescence resonance energy transfer hybridization probes to haplotype the poly(TG) and polyT (TG-T) tract in the IVS-8 region of the CFTR gene. The reporter probe was designed as a perfect match to the TG12-5T allele.
Analysis of 132 samples revealed 9 unique derivative melting temperatures (Tms); the lowest was 42.4 degrees C and the highest was 63.6 degrees C. The lowest Tms were in the TGn-9T group, the intermediate Tms in the TGn-7T group, and the highest Tms in the TGn-5T group. Haplotype frequencies were highest (39%) for TG11-7T and lowest (0.4%) for TG13-5T.
Different combinations of polymorphisms under the reporter hybridization probe had unique and characteristic Tms. This property enables genotyping as well as determination of the phase of multiple variants under the probe, a principle we demonstrated by haplotyping the TG-T repeat tract in the IVS-8 region of the CFTR gene.</description><identifier>ISSN: 0009-9147</identifier><identifier>EISSN: 1530-8561</identifier><identifier>DOI: 10.1373/clinchem.2005.052159</identifier><identifier>PMID: 16020494</identifier><identifier>CODEN: CLCHAU</identifier><language>eng</language><publisher>Washington, DC: Am Assoc Clin Chem</publisher><subject>Analytical, structural and metabolic biochemistry ; Annealing ; Biological and medical sciences ; Chromosomes ; Cystic fibrosis ; Cystic Fibrosis - genetics ; Cystic Fibrosis Transmembrane Conductance Regulator - genetics ; Energy transfer ; Fluorescence Resonance Energy Transfer ; Fundamental and applied biological sciences. Psychology ; Genotype & phenotype ; Haplotypes ; Humans ; Hybridization ; Introns ; Investigative techniques, diagnostic techniques (general aspects) ; Medical sciences ; Melting ; Mutation ; Nucleic Acid Amplification Techniques ; Poly G - genetics ; Poly T - genetics ; Probes ; Proteins ; Temperature</subject><ispartof>Clinical chemistry (Baltimore, Md.), 2005-09, Vol.51 (9), p.1619-1623</ispartof><rights>2005 INIST-CNRS</rights><rights>Copyright American Association for Clinical Chemistry Sep 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c505t-2afc29f23606cf7008cc45ec0afe3041b3b7cb1ae4010690e7c67085c0550e053</citedby><cites>FETCH-LOGICAL-c505t-2afc29f23606cf7008cc45ec0afe3041b3b7cb1ae4010690e7c67085c0550e053</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17075564$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16020494$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Millson, Alison</creatorcontrib><creatorcontrib>Pont-Kingdon, Genevieve</creatorcontrib><creatorcontrib>Page, Sam</creatorcontrib><creatorcontrib>Lyon, Elaine</creatorcontrib><title>Direct Molecular Haplotyping of the IVS-8 Poly(TG) and PolyT Repeat Tracts in the Cystic Fibrosis Gene by Melting Curve Analysis of Hybridization Probes</title><title>Clinical chemistry (Baltimore, Md.)</title><addtitle>Clin Chem</addtitle><description>Molecular haplotyping is a developing technology with great potential for use in clinical diagnostics. We describe a haplotyping method that uses PCR combined with hybridization probes.
We designed a LightCycler assay that uses fluorescence resonance energy transfer hybridization probes to haplotype the poly(TG) and polyT (TG-T) tract in the IVS-8 region of the CFTR gene. The reporter probe was designed as a perfect match to the TG12-5T allele.
Analysis of 132 samples revealed 9 unique derivative melting temperatures (Tms); the lowest was 42.4 degrees C and the highest was 63.6 degrees C. The lowest Tms were in the TGn-9T group, the intermediate Tms in the TGn-7T group, and the highest Tms in the TGn-5T group. Haplotype frequencies were highest (39%) for TG11-7T and lowest (0.4%) for TG13-5T.
Different combinations of polymorphisms under the reporter hybridization probe had unique and characteristic Tms. This property enables genotyping as well as determination of the phase of multiple variants under the probe, a principle we demonstrated by haplotyping the TG-T repeat tract in the IVS-8 region of the CFTR gene.</description><subject>Analytical, structural and metabolic biochemistry</subject><subject>Annealing</subject><subject>Biological and medical sciences</subject><subject>Chromosomes</subject><subject>Cystic fibrosis</subject><subject>Cystic Fibrosis - genetics</subject><subject>Cystic Fibrosis Transmembrane Conductance Regulator - genetics</subject><subject>Energy transfer</subject><subject>Fluorescence Resonance Energy Transfer</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genotype & phenotype</subject><subject>Haplotypes</subject><subject>Humans</subject><subject>Hybridization</subject><subject>Introns</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Medical sciences</subject><subject>Melting</subject><subject>Mutation</subject><subject>Nucleic Acid Amplification Techniques</subject><subject>Poly G - genetics</subject><subject>Poly T - genetics</subject><subject>Probes</subject><subject>Proteins</subject><subject>Temperature</subject><issn>0009-9147</issn><issn>1530-8561</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNpdkV1v0zAUhiMEYmXwDxCykEBwkXKc2HF8ORXWTtrEBIVby3FPVk_Ox-yEKvwSfi7uWlSJK-vIz3mPXj1J8prCnOYi_2Scbc0Wm3kGwOfAM8rlk2RGeQ5pyQv6NJkBgEwlZeIseRHCfRyZKIvnyRktIAMm2Sz589l6NAO56Rya0WlPVrp33TD1tr0jXU2GLZKrn9_Tktx2bvqwXn4kut08DmvyDXvUA1l7bYZAbPtIL6YwWEMubeW7YANZYoukmsgNumEfuhj9LyQXrXbT_jveWE2Vtxv7Ww-2a8mt7yoML5NntXYBXx3f8-TH5Zf1YpVef11eLS6uU8OBD2mma5PJOssLKEwtAEpjGEcDusYcGK3ySpiKamRAoZCAwhQCSm6Ac0Dg-Xny_pDb--5hxDCoxgaDzukWuzEoKllGpRQRfPsfeN-NPrYIKqMMIBOURYgdIBO7B4-16r1ttJ8UBbXXpv5pU3tt6qAtrr05Zo9Vg5vT0tFTBN4dAR2MdrXXrbHhxAkQnBfs1GZr77a7qFaFRjsXY6na7XacKhlDqcz_AgAfrx0</recordid><startdate>20050901</startdate><enddate>20050901</enddate><creator>Millson, Alison</creator><creator>Pont-Kingdon, Genevieve</creator><creator>Page, Sam</creator><creator>Lyon, Elaine</creator><general>Am Assoc Clin Chem</general><general>American Association for Clinical Chemistry</general><general>Oxford University Press</general><scope>IQODW</scope><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>3V.</scope><scope>4U-</scope><scope>7QO</scope><scope>7RV</scope><scope>7TM</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>BKSAR</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>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PCBAR</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>S0X</scope></search><sort><creationdate>20050901</creationdate><title>Direct Molecular Haplotyping of the IVS-8 Poly(TG) and PolyT Repeat Tracts in the Cystic Fibrosis Gene by Melting Curve Analysis of Hybridization Probes</title><author>Millson, Alison ; Pont-Kingdon, Genevieve ; Page, Sam ; Lyon, Elaine</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c505t-2afc29f23606cf7008cc45ec0afe3041b3b7cb1ae4010690e7c67085c0550e053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Analytical, structural and metabolic biochemistry</topic><topic>Annealing</topic><topic>Biological and medical sciences</topic><topic>Chromosomes</topic><topic>Cystic fibrosis</topic><topic>Cystic Fibrosis - genetics</topic><topic>Cystic Fibrosis Transmembrane Conductance Regulator - genetics</topic><topic>Energy transfer</topic><topic>Fluorescence Resonance Energy Transfer</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genotype & phenotype</topic><topic>Haplotypes</topic><topic>Humans</topic><topic>Hybridization</topic><topic>Introns</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Medical sciences</topic><topic>Melting</topic><topic>Mutation</topic><topic>Nucleic Acid Amplification Techniques</topic><topic>Poly G - genetics</topic><topic>Poly T - genetics</topic><topic>Probes</topic><topic>Proteins</topic><topic>Temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Millson, Alison</creatorcontrib><creatorcontrib>Pont-Kingdon, Genevieve</creatorcontrib><creatorcontrib>Page, Sam</creatorcontrib><creatorcontrib>Lyon, Elaine</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>University Readers</collection><collection>Biotechnology Research Abstracts</collection><collection>Proquest Nursing & Allied Health Source</collection><collection>Nucleic Acids Abstracts</collection><collection>Toxicology Abstracts</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database (Proquest)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology 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 Database (Proquest)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Earth, Atmospheric & Aquatic Science Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central</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>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>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Science Journals</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest Earth, Atmospheric & Aquatic Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>SIRS Editorial</collection><jtitle>Clinical chemistry (Baltimore, Md.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Millson, Alison</au><au>Pont-Kingdon, Genevieve</au><au>Page, Sam</au><au>Lyon, Elaine</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Direct Molecular Haplotyping of the IVS-8 Poly(TG) and PolyT Repeat Tracts in the Cystic Fibrosis Gene by Melting Curve Analysis of Hybridization Probes</atitle><jtitle>Clinical chemistry (Baltimore, Md.)</jtitle><addtitle>Clin Chem</addtitle><date>2005-09-01</date><risdate>2005</risdate><volume>51</volume><issue>9</issue><spage>1619</spage><epage>1623</epage><pages>1619-1623</pages><issn>0009-9147</issn><eissn>1530-8561</eissn><coden>CLCHAU</coden><abstract>Molecular haplotyping is a developing technology with great potential for use in clinical diagnostics. We describe a haplotyping method that uses PCR combined with hybridization probes.
We designed a LightCycler assay that uses fluorescence resonance energy transfer hybridization probes to haplotype the poly(TG) and polyT (TG-T) tract in the IVS-8 region of the CFTR gene. The reporter probe was designed as a perfect match to the TG12-5T allele.
Analysis of 132 samples revealed 9 unique derivative melting temperatures (Tms); the lowest was 42.4 degrees C and the highest was 63.6 degrees C. The lowest Tms were in the TGn-9T group, the intermediate Tms in the TGn-7T group, and the highest Tms in the TGn-5T group. Haplotype frequencies were highest (39%) for TG11-7T and lowest (0.4%) for TG13-5T.
Different combinations of polymorphisms under the reporter hybridization probe had unique and characteristic Tms. This property enables genotyping as well as determination of the phase of multiple variants under the probe, a principle we demonstrated by haplotyping the TG-T repeat tract in the IVS-8 region of the CFTR gene.</abstract><cop>Washington, DC</cop><pub>Am Assoc Clin Chem</pub><pmid>16020494</pmid><doi>10.1373/clinchem.2005.052159</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analytical, structural and metabolic biochemistry Annealing Biological and medical sciences Chromosomes Cystic fibrosis Cystic Fibrosis - genetics Cystic Fibrosis Transmembrane Conductance Regulator - genetics Energy transfer Fluorescence Resonance Energy Transfer Fundamental and applied biological sciences. Psychology Genotype & phenotype Haplotypes Humans Hybridization Introns Investigative techniques, diagnostic techniques (general aspects) Medical sciences Melting Mutation Nucleic Acid Amplification Techniques Poly G - genetics Poly T - genetics Probes Proteins Temperature |
title | Direct Molecular Haplotyping of the IVS-8 Poly(TG) and PolyT Repeat Tracts in the Cystic Fibrosis Gene by Melting Curve Analysis of Hybridization Probes |
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