Role of TRAV locus in low caries experience

Caries is the most common chronic, multifactorial disease in the world today; and little is still known about the genetic factors influencing susceptibility. Our previous genome-wide linkage scan has identified five loci related to caries susceptibility: 5q13.3, 13q31.1, 14q11.2, 14q 24.3, and Xq27....

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Veröffentlicht in:Human genetics 2013-09, Vol.132 (9), p.1015-1025
Hauptverfasser: Briseño-Ruiz, Jessica, Shimizu, Takehiko, Deeley, Kathleen, Dizak, Piper M., Ruff, Timothy D., Faraco, Italo M., Poletta, Fernando A., Brancher, João A., Pecharki, Giovana D., Küchler, Erika C., Tannure, Patricia N., Lips, Andrea, Vieira, Thays C. S., Patir, Asli, Koruyucu, Mine, Mereb, Juan C., Resick, Judith M., Brandon, Carla A., Letra, Ariadne, Silva, Renato M., Cooper, Margaret E., Seymen, Figen, Costa, Marcelo C., Granjeiro, José M., Trevilatto, Paula C., Orioli, Iêda M., Castilla, Eduardo E., Marazita, Mary L., Vieira, Alexandre R.
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container_end_page 1025
container_issue 9
container_start_page 1015
container_title Human genetics
container_volume 132
creator Briseño-Ruiz, Jessica
Shimizu, Takehiko
Deeley, Kathleen
Dizak, Piper M.
Ruff, Timothy D.
Faraco, Italo M.
Poletta, Fernando A.
Brancher, João A.
Pecharki, Giovana D.
Küchler, Erika C.
Tannure, Patricia N.
Lips, Andrea
Vieira, Thays C. S.
Patir, Asli
Koruyucu, Mine
Mereb, Juan C.
Resick, Judith M.
Brandon, Carla A.
Letra, Ariadne
Silva, Renato M.
Cooper, Margaret E.
Seymen, Figen
Costa, Marcelo C.
Granjeiro, José M.
Trevilatto, Paula C.
Orioli, Iêda M.
Castilla, Eduardo E.
Marazita, Mary L.
Vieira, Alexandre R.
description Caries is the most common chronic, multifactorial disease in the world today; and little is still known about the genetic factors influencing susceptibility. Our previous genome-wide linkage scan has identified five loci related to caries susceptibility: 5q13.3, 13q31.1, 14q11.2, 14q 24.3, and Xq27. In the present study, we fine mapped the 14q11.2 locus to identify genetic contributors to caries susceptibility. Four hundred seventy-seven subjects from 72 pedigrees with similar cultural and behavioral habits and limited access to dental care living in the Philippines were studied. An additional 387 DNA samples from unrelated individuals were used to determine allele frequencies. For replication purposes, a total of 1,446 independent subjects from four different populations were analyzed based on their caries experience (low versus high). Forty-eight markers in 14q11.2 were genotyped using TaqMan chemistry. Transmission disequilibrium test was used to detect over transmission of alleles in the Filipino families, and Chi-square, Fisher’s exact and logistic regression were used to test for association between low caries experience and variant alleles in the replication data sets. We finally assessed the mRNA expression of TRAV4 in the saliva of 143 study subjects. In the Filipino families, statistically significant associations were found between low caries experience and markers in TRAV4 . We were able to replicate these results in the populations studied that were characteristically from underserved areas. Direct sequencing of 22 subjects carrying the associated alleles detects one missense mutation (Y30R) that is predicted to be probably damaging. Finally, we observed higher expression in children and teenagers with low caries experience, correlating with specific alleles in TRAV4. Our results suggest that TRAV4 may have a role in protecting against caries.
doi_str_mv 10.1007/s00439-013-1313-4
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S. ; Patir, Asli ; Koruyucu, Mine ; Mereb, Juan C. ; Resick, Judith M. ; Brandon, Carla A. ; Letra, Ariadne ; Silva, Renato M. ; Cooper, Margaret E. ; Seymen, Figen ; Costa, Marcelo C. ; Granjeiro, José M. ; Trevilatto, Paula C. ; Orioli, Iêda M. ; Castilla, Eduardo E. ; Marazita, Mary L. ; Vieira, Alexandre R.</creator><creatorcontrib>Briseño-Ruiz, Jessica ; Shimizu, Takehiko ; Deeley, Kathleen ; Dizak, Piper M. ; Ruff, Timothy D. ; Faraco, Italo M. ; Poletta, Fernando A. ; Brancher, João A. ; Pecharki, Giovana D. ; Küchler, Erika C. ; Tannure, Patricia N. ; Lips, Andrea ; Vieira, Thays C. S. ; Patir, Asli ; Koruyucu, Mine ; Mereb, Juan C. ; Resick, Judith M. ; Brandon, Carla A. ; Letra, Ariadne ; Silva, Renato M. ; Cooper, Margaret E. ; Seymen, Figen ; Costa, Marcelo C. ; Granjeiro, José M. ; Trevilatto, Paula C. ; Orioli, Iêda M. ; Castilla, Eduardo E. ; Marazita, Mary L. ; Vieira, Alexandre R.</creatorcontrib><description>Caries is the most common chronic, multifactorial disease in the world today; and little is still known about the genetic factors influencing susceptibility. Our previous genome-wide linkage scan has identified five loci related to caries susceptibility: 5q13.3, 13q31.1, 14q11.2, 14q 24.3, and Xq27. In the present study, we fine mapped the 14q11.2 locus to identify genetic contributors to caries susceptibility. Four hundred seventy-seven subjects from 72 pedigrees with similar cultural and behavioral habits and limited access to dental care living in the Philippines were studied. An additional 387 DNA samples from unrelated individuals were used to determine allele frequencies. For replication purposes, a total of 1,446 independent subjects from four different populations were analyzed based on their caries experience (low versus high). Forty-eight markers in 14q11.2 were genotyped using TaqMan chemistry. Transmission disequilibrium test was used to detect over transmission of alleles in the Filipino families, and Chi-square, Fisher’s exact and logistic regression were used to test for association between low caries experience and variant alleles in the replication data sets. We finally assessed the mRNA expression of TRAV4 in the saliva of 143 study subjects. In the Filipino families, statistically significant associations were found between low caries experience and markers in TRAV4 . We were able to replicate these results in the populations studied that were characteristically from underserved areas. Direct sequencing of 22 subjects carrying the associated alleles detects one missense mutation (Y30R) that is predicted to be probably damaging. Finally, we observed higher expression in children and teenagers with low caries experience, correlating with specific alleles in TRAV4. 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S.</creatorcontrib><creatorcontrib>Patir, Asli</creatorcontrib><creatorcontrib>Koruyucu, Mine</creatorcontrib><creatorcontrib>Mereb, Juan C.</creatorcontrib><creatorcontrib>Resick, Judith M.</creatorcontrib><creatorcontrib>Brandon, Carla A.</creatorcontrib><creatorcontrib>Letra, Ariadne</creatorcontrib><creatorcontrib>Silva, Renato M.</creatorcontrib><creatorcontrib>Cooper, Margaret E.</creatorcontrib><creatorcontrib>Seymen, Figen</creatorcontrib><creatorcontrib>Costa, Marcelo C.</creatorcontrib><creatorcontrib>Granjeiro, José M.</creatorcontrib><creatorcontrib>Trevilatto, Paula C.</creatorcontrib><creatorcontrib>Orioli, Iêda M.</creatorcontrib><creatorcontrib>Castilla, Eduardo E.</creatorcontrib><creatorcontrib>Marazita, Mary L.</creatorcontrib><creatorcontrib>Vieira, Alexandre R.</creatorcontrib><title>Role of TRAV locus in low caries experience</title><title>Human genetics</title><addtitle>Hum Genet</addtitle><addtitle>Hum Genet</addtitle><description>Caries is the most common chronic, multifactorial disease in the world today; and little is still known about the genetic factors influencing susceptibility. Our previous genome-wide linkage scan has identified five loci related to caries susceptibility: 5q13.3, 13q31.1, 14q11.2, 14q 24.3, and Xq27. In the present study, we fine mapped the 14q11.2 locus to identify genetic contributors to caries susceptibility. Four hundred seventy-seven subjects from 72 pedigrees with similar cultural and behavioral habits and limited access to dental care living in the Philippines were studied. An additional 387 DNA samples from unrelated individuals were used to determine allele frequencies. For replication purposes, a total of 1,446 independent subjects from four different populations were analyzed based on their caries experience (low versus high). Forty-eight markers in 14q11.2 were genotyped using TaqMan chemistry. Transmission disequilibrium test was used to detect over transmission of alleles in the Filipino families, and Chi-square, Fisher’s exact and logistic regression were used to test for association between low caries experience and variant alleles in the replication data sets. We finally assessed the mRNA expression of TRAV4 in the saliva of 143 study subjects. In the Filipino families, statistically significant associations were found between low caries experience and markers in TRAV4 . We were able to replicate these results in the populations studied that were characteristically from underserved areas. Direct sequencing of 22 subjects carrying the associated alleles detects one missense mutation (Y30R) that is predicted to be probably damaging. Finally, we observed higher expression in children and teenagers with low caries experience, correlating with specific alleles in TRAV4. Our results suggest that TRAV4 may have a role in protecting against caries.</description><subject>Base Sequence</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Chromosomes</subject><subject>Chromosomes, Human, Pair 14 - genetics</subject><subject>Dental Caries - epidemiology</subject><subject>Dental Caries - genetics</subject><subject>Dentistry</subject><subject>DNA Primers - genetics</subject><subject>Gene Frequency</subject><subject>Gene Function</subject><subject>Genes, T-Cell Receptor alpha - genetics</subject><subject>Genetic Association Studies</subject><subject>Genetic Loci - genetics</subject><subject>Genetic Predisposition to Disease - genetics</subject><subject>Genetic testing</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Human Genetics</subject><subject>Humans</subject><subject>Inheritance Patterns - genetics</subject><subject>Linkage Disequilibrium</subject><subject>Logistic Models</subject><subject>Metabolic Diseases</subject><subject>Molecular Medicine</subject><subject>Molecular Sequence Data</subject><subject>Mutation, Missense - genetics</subject><subject>Original Investigation</subject><subject>Pediatrics</subject><subject>Philippines - epidemiology</subject><subject>Saliva - metabolism</subject><subject>Sequence Analysis, DNA</subject><issn>0340-6717</issn><issn>1432-1203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqNkl9rFDEUxYModq1-AF9kwBdFpt78n3kRlqK2UCis1deQzWbWlNlkTWa0fnvvsO3SFQsSSELyuyc3h0PISwonFEC_LwCCtzVQXlOOk3hEZlRwVlMG_DGZARdQK031EXlWyjUAlS2TT8kR40pqCXJG3i1S76vUVVeL-beqT24sVYi4-VU5m4Mvlb_ZetxE55-TJ53ti39xux6Tr58-Xp2e1ReXn89P5xe1UxqGWrWglq7xVAjVaiUEWFys7KQSsOSSCtZY6ADbcbzpEGYAfMW4YEu1aig_Jh92uttxufEr5-OQbW-2OWxs_m2SDebwJobvZp1-Gq7xSapQ4M2tQE4_Rl8GswnF-b630aexGPRIAOOtbP4DZWgo-sUQff0Xep3GHNGJiQJoKaDwnlrb3psQu4QtuknUzLkQTLeaT1on_6BwrPwmuBR9F_D8oODtQQEyg78Z1nYsxZx_WRyydMe6nErJvttbR8FMwTG74BgMjpmCY6a2X933fF9xlxQE2A4oeBXXPt_7_YOqfwAI38bJ</recordid><startdate>20130901</startdate><enddate>20130901</enddate><creator>Briseño-Ruiz, Jessica</creator><creator>Shimizu, Takehiko</creator><creator>Deeley, Kathleen</creator><creator>Dizak, Piper M.</creator><creator>Ruff, Timothy D.</creator><creator>Faraco, Italo M.</creator><creator>Poletta, Fernando A.</creator><creator>Brancher, João A.</creator><creator>Pecharki, Giovana D.</creator><creator>Küchler, Erika C.</creator><creator>Tannure, Patricia N.</creator><creator>Lips, Andrea</creator><creator>Vieira, Thays C. 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S. ; Patir, Asli ; Koruyucu, Mine ; Mereb, Juan C. ; Resick, Judith M. ; Brandon, Carla A. ; Letra, Ariadne ; Silva, Renato M. ; Cooper, Margaret E. ; Seymen, Figen ; Costa, Marcelo C. ; Granjeiro, José M. ; Trevilatto, Paula C. ; Orioli, Iêda M. ; Castilla, Eduardo E. ; Marazita, Mary L. ; Vieira, Alexandre R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c670t-6906bc8e1446976440a976a5f5640b351428a0f0001c38f06b2003d2342b6d813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Base Sequence</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Chromosomes</topic><topic>Chromosomes, Human, Pair 14 - genetics</topic><topic>Dental Caries - epidemiology</topic><topic>Dental Caries - genetics</topic><topic>Dentistry</topic><topic>DNA Primers - genetics</topic><topic>Gene Frequency</topic><topic>Gene Function</topic><topic>Genes, T-Cell Receptor alpha - genetics</topic><topic>Genetic Association Studies</topic><topic>Genetic Loci - genetics</topic><topic>Genetic Predisposition to Disease - genetics</topic><topic>Genetic testing</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Human Genetics</topic><topic>Humans</topic><topic>Inheritance Patterns - genetics</topic><topic>Linkage Disequilibrium</topic><topic>Logistic Models</topic><topic>Metabolic Diseases</topic><topic>Molecular Medicine</topic><topic>Molecular Sequence Data</topic><topic>Mutation, Missense - genetics</topic><topic>Original Investigation</topic><topic>Pediatrics</topic><topic>Philippines - epidemiology</topic><topic>Saliva - metabolism</topic><topic>Sequence Analysis, DNA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Briseño-Ruiz, Jessica</creatorcontrib><creatorcontrib>Shimizu, Takehiko</creatorcontrib><creatorcontrib>Deeley, Kathleen</creatorcontrib><creatorcontrib>Dizak, Piper M.</creatorcontrib><creatorcontrib>Ruff, Timothy D.</creatorcontrib><creatorcontrib>Faraco, Italo M.</creatorcontrib><creatorcontrib>Poletta, Fernando A.</creatorcontrib><creatorcontrib>Brancher, João A.</creatorcontrib><creatorcontrib>Pecharki, Giovana D.</creatorcontrib><creatorcontrib>Küchler, Erika C.</creatorcontrib><creatorcontrib>Tannure, Patricia N.</creatorcontrib><creatorcontrib>Lips, Andrea</creatorcontrib><creatorcontrib>Vieira, Thays C. 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S.</au><au>Patir, Asli</au><au>Koruyucu, Mine</au><au>Mereb, Juan C.</au><au>Resick, Judith M.</au><au>Brandon, Carla A.</au><au>Letra, Ariadne</au><au>Silva, Renato M.</au><au>Cooper, Margaret E.</au><au>Seymen, Figen</au><au>Costa, Marcelo C.</au><au>Granjeiro, José M.</au><au>Trevilatto, Paula C.</au><au>Orioli, Iêda M.</au><au>Castilla, Eduardo E.</au><au>Marazita, Mary L.</au><au>Vieira, Alexandre R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Role of TRAV locus in low caries experience</atitle><jtitle>Human genetics</jtitle><stitle>Hum Genet</stitle><addtitle>Hum Genet</addtitle><date>2013-09-01</date><risdate>2013</risdate><volume>132</volume><issue>9</issue><spage>1015</spage><epage>1025</epage><pages>1015-1025</pages><issn>0340-6717</issn><eissn>1432-1203</eissn><abstract>Caries is the most common chronic, multifactorial disease in the world today; and little is still known about the genetic factors influencing susceptibility. Our previous genome-wide linkage scan has identified five loci related to caries susceptibility: 5q13.3, 13q31.1, 14q11.2, 14q 24.3, and Xq27. In the present study, we fine mapped the 14q11.2 locus to identify genetic contributors to caries susceptibility. Four hundred seventy-seven subjects from 72 pedigrees with similar cultural and behavioral habits and limited access to dental care living in the Philippines were studied. An additional 387 DNA samples from unrelated individuals were used to determine allele frequencies. For replication purposes, a total of 1,446 independent subjects from four different populations were analyzed based on their caries experience (low versus high). Forty-eight markers in 14q11.2 were genotyped using TaqMan chemistry. Transmission disequilibrium test was used to detect over transmission of alleles in the Filipino families, and Chi-square, Fisher’s exact and logistic regression were used to test for association between low caries experience and variant alleles in the replication data sets. We finally assessed the mRNA expression of TRAV4 in the saliva of 143 study subjects. In the Filipino families, statistically significant associations were found between low caries experience and markers in TRAV4 . We were able to replicate these results in the populations studied that were characteristically from underserved areas. Direct sequencing of 22 subjects carrying the associated alleles detects one missense mutation (Y30R) that is predicted to be probably damaging. Finally, we observed higher expression in children and teenagers with low caries experience, correlating with specific alleles in TRAV4. Our results suggest that TRAV4 may have a role in protecting against caries.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>23657505</pmid><doi>10.1007/s00439-013-1313-4</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 0340-6717
ispartof Human genetics, 2013-09, Vol.132 (9), p.1015-1025
issn 0340-6717
1432-1203
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3744616
source MEDLINE; SpringerLink Journals - AutoHoldings
subjects Base Sequence
Biomedical and Life Sciences
Biomedicine
Chromosomes
Chromosomes, Human, Pair 14 - genetics
Dental Caries - epidemiology
Dental Caries - genetics
Dentistry
DNA Primers - genetics
Gene Frequency
Gene Function
Genes, T-Cell Receptor alpha - genetics
Genetic Association Studies
Genetic Loci - genetics
Genetic Predisposition to Disease - genetics
Genetic testing
Genomes
Genomics
Human Genetics
Humans
Inheritance Patterns - genetics
Linkage Disequilibrium
Logistic Models
Metabolic Diseases
Molecular Medicine
Molecular Sequence Data
Mutation, Missense - genetics
Original Investigation
Pediatrics
Philippines - epidemiology
Saliva - metabolism
Sequence Analysis, DNA
title Role of TRAV locus in low caries experience
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