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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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 |
format | Article |
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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><identifier>ISSN: 0340-6717</identifier><identifier>EISSN: 1432-1203</identifier><identifier>DOI: 10.1007/s00439-013-1313-4</identifier><identifier>PMID: 23657505</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>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</subject><ispartof>Human genetics, 2013-09, Vol.132 (9), p.1015-1025</ispartof><rights>Springer-Verlag Berlin Heidelberg 2013</rights><rights>COPYRIGHT 2013 Springer</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c670t-6906bc8e1446976440a976a5f5640b351428a0f0001c38f06b2003d2342b6d813</citedby><cites>FETCH-LOGICAL-c670t-6906bc8e1446976440a976a5f5640b351428a0f0001c38f06b2003d2342b6d813</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00439-013-1313-4$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00439-013-1313-4$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23657505$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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. 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> |
fulltext | fulltext |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T08%3A08%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Role%20of%20TRAV%20locus%20in%20low%20caries%20experience&rft.jtitle=Human%20genetics&rft.au=Brise%C3%B1o-Ruiz,%20Jessica&rft.date=2013-09-01&rft.volume=132&rft.issue=9&rft.spage=1015&rft.epage=1025&rft.pages=1015-1025&rft.issn=0340-6717&rft.eissn=1432-1203&rft_id=info:doi/10.1007/s00439-013-1313-4&rft_dat=%3Cgale_pubme%3EA344279732%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1420091014&rft_id=info:pmid/23657505&rft_galeid=A344279732&rfr_iscdi=true |