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Yeast As a Chassis for Developing Functional Assays to Study Human P53
Published on: August 4, 2019
p53 codon 72 proline/arginine polymorphism and autoimmune thyroid diseases.
Rong-Hsing Chen1, Chwen-Tzuei Chang, Tzu-Yuan Wang
1Department of Internal Medicine, China Medical University Hospital, China Medical University, Taichung, Taiwan.
Journal of Clinical Laboratory Analysis
|September 23, 2008
Summary
The p53 gene
Area of Science:
- Immunogenetics
- Molecular Biology
Background:
- The p53 protein is involved in apoptosis and immunological reactions.
- Autoimmune thyroid diseases (AITD) include Hashimoto's thyroiditis (HT) and Graves' disease (GD).
- Genetic factors play a role in the development of AITD.
Purpose of the Study:
- To investigate the p53 gene's proline/arginine polymorphism at codon 72 as a potential genetic marker for AITD.
- To determine if specific p53 genotypes are associated with an increased susceptibility to HT or GD.
Main Methods:
- Polymerase chain reaction (PCR) analysis was used to screen for the p53 codon 72 (Pro72/Arg72) polymorphism.
- Genotyping was performed on 107 HT patients, 90 GD patients, and 105 normal controls.
- Statistical analysis, including odds ratios and confidence intervals, was used to compare genotype and allelic frequencies.
Main Results:
- Hashimoto's thyroiditis patients showed a significantly higher ratio of the Arg/Arg homozygous genotype (33.7%) compared to normal controls (17.1%; P=0.005).
- The odds ratio for developing HT with the Arg/Arg genotype was 2.450.
- No significant differences in genotype or allelic frequencies were observed for Graves' disease patients compared to controls.
Conclusions:
- The p53 codon 72 proline/arginine polymorphism, specifically arginine homozygosity, is associated with an increased susceptibility to Hashimoto's thyroiditis.
- This p53 polymorphism may serve as a predictive genetic marker for HT development.
- The p53 polymorphism is not significantly associated with Graves' disease susceptibility.
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