Related Experiment Video
Updated: Jan 2, 2026

10:26
Inducing Apical Periodontitis in Mice
Published on: August 6, 2019
12.8K
WNT gene polymorphisms and predisposition to apical periodontitis.
Letícia Chaves de Souza1,2, Franco Cavalla2,3,4, Lorena Maili5,6
1Department of Endodontics, University of Texas Health Science Center School of Dentistry, Houston, 77054, USA.
Scientific Reports
|December 14, 2019
Summary
Genetic variations in WNT genes are linked to apical periodontitis (AP) susceptibility. Specific WNT gene polymorphisms and their expression patterns may influence the development of this dental condition.
Area of Science:
- Genetics
- Oral Biology
- Molecular Biology
Background:
- Single nucleotide polymorphisms (SNPs) in WNT genes can alter gene/protein function.
- These alterations may predispose individuals to apical periodontitis (AP).
Purpose of the Study:
- To investigate the association between SNPs in WNT3, WNT3A, WNT5A, WNT8A, WNT9B, and WNT11 genes and apical periodontitis (AP).
Main Methods:
- Case-control study comparing individuals with AP and deep caries to controls with deep caries but no AP.
- Genotyping using real-time PCR with Taqman chemistry.
- Statistical analysis with Fisher Exact tests and Bonferroni correction.
- Luciferase reporter assays and gene expression analysis in AP tissues.
Main Results:
- A trend for association between WNT3 rs9890413 genotypes and AP.
- Allelic association for WNT3A rs1745420 with AP.
- Significant association of WNT3-WNT9B-WNT3A haplotypes with AP.
- Increased transcriptional activity with the alternate G allele in WNT3A rs1745420.
- Elevated WNT3, WNT3A, and WNT5A expression in AP tissues, inversely correlated with SERPINB1, COL1A1, and TIMP1.
Conclusions:
- WNT genes play a role in modulating apical periodontitis (AP).
- Polymorphisms in WNT genes may increase susceptibility to AP.
- Gene expression patterns of WNTs and associated genes provide insights into AP pathogenesis.
Related Concept Videos
Canonical Wnt Signaling Pathway
10.3K
The gene encoding the main signaling molecules of the Wnt signaling pathways (the Wnt proteins) was discovered almost four decades ago by Nüsslein-Volhard and Wieschaus. They identified and originally named the gene "wingless" (wg) after a phenotype discovered during their landmark genetic screen in Drosophila for body pattern defects. At around the same time, another researcher named Harold Varmus found that a murine tumor virus activates the mammalian wg homolog, Int-1, which...
10.3K
Non-Canonical Wnt Signaling Pathways
8.2K
Wnt is a zygotic effect gene that is expressed during very early embryonic development. It regulates various processes in animals starting from early development through the adult stage, such as organogenesis in the embryo and maintenance of neuronal and blood stem cells. Wnt proteins can induce a wide variety of intracellular pathways depending upon the specific abilities of different Wnt ligands to form a complex with shared and cognate receptors in the presence of different co-receptors. The...
8.2K
Single Nucleotide Polymorphisms-SNPs
17.8K
A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
17.8K
Pleiotropy
43.1K
Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
43.1K
Genome-wide Association Studies-GWAS
15.2K
Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
GWAS does not require the identification of the target gene involved in...
15.2K
Pedigree Analysis
88.6K
Overview
88.6K

