TY - JOUR
T1 - Host susceptibility to periodontitis
T2 - Mapping murine genomic regions
AU - Shusterman, A.
AU - Durrant, C.
AU - Mott, R.
AU - Polak, D.
AU - Schaefer, A.
AU - Weiss, E. I.
AU - Iraqi, F. A.
AU - Houri-Haddad, Y.
N1 - Funding Information: This work was supported by the Israel Science Foundation (grant number 429/09 ).
PY - 2013/5
Y1 - 2013/5
N2 - Host susceptibility to periodontal infection is controlled by genetic factors. As a step toward identifying and cloning these factors, we generated an A/J × BALB/cJ F2 mouse resource population. A genome-wide search for Quantitative Trait Loci (QTL) associated with periodontitis was performed. We aimed to quantify the phenotypic response of the progenies to periodontitis by microCT analysis, to perform a genome-wide search for QTL associated with periodontitis, and, finally, to suggest candidate genes for periodontitis. We were able to produce 408 F2 mice. All mice were co-infected with Porphyromonas gingivalis and Fusobacterium nucleatum bacteria. Six weeks following infection, alveolar bone loss was quantified by computerized tomography (microCT) technology. We found normal distribution of the phenotype, with 2 highly significant QTL on chromosomes 5 and 3. A third significant QTL was found on chromosome 1. Candidate genes were suggested, such as Toll-like receptors (TLR) 1 and 6, chemokines, and bone-remodeling genes (enamelin, ameloblastin, and amelotin). This report shows that periodontitis in mice is a polygenic trait with highly significant mapped QTL.
AB - Host susceptibility to periodontal infection is controlled by genetic factors. As a step toward identifying and cloning these factors, we generated an A/J × BALB/cJ F2 mouse resource population. A genome-wide search for Quantitative Trait Loci (QTL) associated with periodontitis was performed. We aimed to quantify the phenotypic response of the progenies to periodontitis by microCT analysis, to perform a genome-wide search for QTL associated with periodontitis, and, finally, to suggest candidate genes for periodontitis. We were able to produce 408 F2 mice. All mice were co-infected with Porphyromonas gingivalis and Fusobacterium nucleatum bacteria. Six weeks following infection, alveolar bone loss was quantified by computerized tomography (microCT) technology. We found normal distribution of the phenotype, with 2 highly significant QTL on chromosomes 5 and 3. A third significant QTL was found on chromosome 1. Candidate genes were suggested, such as Toll-like receptors (TLR) 1 and 6, chemokines, and bone-remodeling genes (enamelin, ameloblastin, and amelotin). This report shows that periodontitis in mice is a polygenic trait with highly significant mapped QTL.
KW - alveolar bone loss
KW - animal model
KW - cone-beam computed tomography
KW - periodontal diseases
KW - quantitative trait loci
KW - single nucleotide polymorphis
UR - http://www.scopus.com/inward/record.url?scp=84876368638&partnerID=8YFLogxK
U2 - 10.1177/0022034513484039
DO - 10.1177/0022034513484039
M3 - مقالة
C2 - 23539559
SN - 0022-0345
VL - 92
SP - 438
EP - 443
JO - Journal of Dental Research
JF - Journal of Dental Research
IS - 5
ER -