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dc.contributor.author
Briseño Ruiz, Jessica  
dc.contributor.author
Shimizu, Takehiko  
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Deeley, Kathleen  
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Dizak, Piper M.  
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Ruff, Timothy D  
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Faraco Jr., Italo M.  
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Poletta, Fernando Adrián  
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Brancher, Joao A.  
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Pecharki, Giovana D.  
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Kuchler, Erika C  
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Tannure, Patricia N.  
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Lips, Andrea  
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Vieira, Thays C. S.  
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Patir, Asli  
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Koruyucu, Mine  
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Mereb, J. C.  
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Resick, Judith M.  
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Brandon, Carla A.  
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Letra, Ariadme  
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Silva, Renato M.  
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Cooper, Margaret E.  
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Seymen, Figen  
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Costa, Marcelo C.  
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Granjeiro, Jose M  
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Trevilatto, Paula C.  
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Orioli, Eeda M.  
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Castilla, Eduardo Enrique  
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Marazita, Mary L.  
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Vieira, Alexandre R.  
dc.date.available
2017-10-06T20:04:24Z  
dc.date.issued
2013-09  
dc.identifier.citation
Briseño Ruiz, Jessica; Shimizu, Takehiko; Deeley, Kathleen; Dizak, Piper M.; Ruff, Timothy D; et al.; Role of TRAV locus in low caries experience; Springer; Human Genetics.; 132; 9; 9-2013; 1015-1025  
dc.identifier.issn
0340-6717  
dc.identifier.uri
http://hdl.handle.net/11336/26169  
dc.description.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.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Springer  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Trav  
dc.subject.classification
Bioquímica y Biología Molecular  
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Medicina Básica  
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CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
Role of TRAV locus in low caries experience  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2017-09-28T18:13:39Z  
dc.journal.volume
132  
dc.journal.number
9  
dc.journal.pagination
1015-1025  
dc.journal.pais
Alemania  
dc.journal.ciudad
Berlin  
dc.description.fil
Fil: Briseño Ruiz, Jessica. University of Pittsburgh; Estados Unidos  
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Fil: Shimizu, Takehiko. Nihon University of Dentistry at Matsudo; Japón  
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Fil: Deeley, Kathleen. University of Pittsburgh; Estados Unidos  
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Fil: Dizak, Piper M.. University of Pittsburgh; Estados Unidos  
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Fil: Ruff, Timothy D. University of Pittsburgh; Estados Unidos  
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Fil: Faraco Jr., Italo M.. University of Pittsburgh; Estados Unidos  
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Fil: Poletta, Fernando Adrián. Centro de Educación Médica e Investigaciones Clínicas “Norberto Quirno”; Argentina. Estudio Colaborativo Latino Americano de Malformaciones Congénitas. Buenos Aires; Argentina. Instituto de investigación en Porto Alegre; Brasil. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina  
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Fil: Brancher, Joao A.. Universidade Federal do Paraná; Brasil  
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Fil: Pecharki, Giovana D.. Universidade Federal do Paraná; Brasil  
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Fil: Kuchler, Erika C. University of Pittsburgh; Estados Unidos  
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Fil: Tannure, Patricia N.. Universidade Federal do Rio de Janeiro; Brasil  
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Fil: Lips, Andrea. Universidade Federal Fluminense; Brasil  
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Fil: Vieira, Thays C. S.. Universidade Federal Fluminense; Brasil  
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Fil: Patir, Asli. Istanbul Medipol University; Turquía  
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Fil: Koruyucu, Mine. Istanbul University; Turquía  
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Fil: Mereb, J. C.. Estudio Colaborativo Latino Americano de Malformaciones Congénita; Argentina  
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Fil: Resick, Judith M.. University of Pittsburgh; Estados Unidos  
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Fil: Brandon, Carla A.. University of Pittsburgh; Estados Unidos  
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Fil: Letra, Ariadme. University of Texas Health Science Center at Houston; Estados Unidos  
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Fil: Silva, Renato M.. University of Texas Health Science Center at Houston; Estados Unidos  
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Fil: Cooper, Margaret E.. University of Pittsburgh; Estados Unidos  
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Fil: Seymen, Figen. Istanbul University; Turquía  
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Fil: Costa, Marcelo C.. Universidade Federal do Rio de Janeiro; Brasil  
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Fil: Granjeiro, Jose M. Universidade Federal Fluminense; Brasil  
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Fil: Trevilatto, Paula C.. Universidade Federal do Paraná; Brasil  
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Fil: Orioli, Eeda M.. Instituto Nacional de Metrologia, Qualidade e Tecnologia; Brasil  
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Fil: Castilla, Eduardo Enrique. Centro de Educación Médica e Investigaciones Clínicas “Norberto Quirno”; Argentina. Estudio Colaborativo Latino Americano de Malformaciones Congénitas. Buenos Aires; Argentina. Instituto de investigación en Porto Alegre; Brasil  
dc.description.fil
Fil: Marazita, Mary L.. University of Pittsburgh; Estados Unidos  
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Fil: Vieira, Alexandre R.. University of Pittsburgh; Estados Unidos  
dc.journal.title
Human Genetics.  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1007/s00439-013-1313-4  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://link.springer.com/article/10.1007/s00439-013-1313-4