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Association between Cullin-3 Single-Nucleotide Polymorphism rs17479770 and Essential Hypertension in the Male Chinese
Jin Li1,2, Jing Hu3, Rong Sun4
1School of Bioscience and Bioengineering, South China University of Technology, Guangzhou, China.
Insights
The CUL3 gene variant rs17479770 may protect against essential hypertension (EH) in the Chinese Han population. Specifically, the TT genotype and T allele in males showed a decreased risk of developing EH.
Area of Science:
- Genetics
- Cardiovascular Disease
- Molecular Biology
Background:
- Essential hypertension (EH) affects over a billion people globally and is a complex multifactorial disease.
- While CUL3 gene mutations are linked to secondary hypertension, the role of CUL3 polymorphisms in EH remains unexplored.
- This study focuses on the Chinese Han population to investigate potential associations.
Purpose of the Study:
- To investigate the association between CUL3 gene single nucleotide polymorphisms (SNPs) rs17479770 and rs3738952 and essential hypertension (EH).
- To determine if CUL3 gene variants influence the risk of developing EH in the Chinese Han population.
Main Methods:
- A case-control study involving 520 participants (259 EH patients, 261 controls).
- Participants were matched for age, gender, BMI, and key metabolic markers (TG, TC, HbA1c).
- Polymerase Chain Reaction (PCR) and Restriction Fragment Length Polymorphism (RFLP) were used to analyze CUL3 SNPs rs17479770 and rs3738952.
Main Results:
- No significant differences in allele, genotype, or haplotype distributions were found for rs3738952 or the combined haplotype.
- The rs17479770 TT genotype was significantly associated with a reduced risk of EH in males and the overall dataset (P=0.050, P=0.042).
- A trend towards decreased EH risk was observed for the rs17479770 T allele in males (P=0.064).
Conclusions:
- The CUL3 rs17479770 variant may act as a protective factor in the development of essential hypertension.
- This specific CUL3 gene variant shows potential as a biomarker for EH risk stratification.
Background:
Hypertension, including essential and secondary hypertension, is a multifactorial disease, affecting more than one billion people worldwide. Secondary hypertension can result from mutations of cullin-3 (CUL3); however, whether polymorphisms of CUL3 are associated with essential hypertension (EH) has not been reported. Here, we investigated the association between CUL3 SNPs rs17479770 and rs3738952 and EH in the Chinese Han population.
Methods:
This case-control study investigated 520 representatives, including 259 patients with EH and 261 normotensive controls matched for age, gender, BMI, TG, TC, and HbA1c for the distribution of functional rs17479770 and rs3738952 within the CUL3 gene by using PCR and RFLP.
Results:
Our results showed that there was no significant difference in allele and genotype distribution of rs3738952 and haplotype distribution of rs17479770 and rs3738952 between the EH group and normotensive group, whereas the rs17479770 TT genotype in male and the full data set were significantly associated with the decreased risk of EH (P = 0.050, P = 0.042), and rs17479770 allele T in male was shown to have the correlation tendency of the decreased risk of EH (P = 0.064).
Conclusion:
Our data suggest that the CUL3 rs17479770 variant could be a protective factor in the pathogenesis of EH.
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