Ontology highlight
ABSTRACT: Unlabelled
Circadian clock genes are critical regulators of energy homeostasis and metabolism. However, whether variation in the circadian genes is associated with metabolic phenotypes in humans remains to be explored. In this study, we systemically genotyped 20 tag single nucleotide polymorphisms (SNPs) in 8 candidate genes involved in circadian clock, including CLOCK, BMAL1(ARNTL), PER1, PER2, CRY1, CRY2, CSNK1E,, and NOC(CCRN4L) in 1,510 non-diabetic Chinese subjects in Taipei and Yunlin populations in Taiwan. Their associations with metabolic phenotypes were analyzed. We found that genetic variation in the NOC gene, rs9684900 was associated with body mass index (BMI) (P = 0.0016, Bonferroni corrected P = 0.032). Another variant, rs135764 in the CSNK1E gene was associated with fasting glucose (P = 0.0023, Bonferroni corrected P = 0.046). These associations were consistent in both Taipei and Yunlin populations. Significant epistatic and joint effects between SNPs on BMI and related phenotypes were observed. Furthermore, NOC mRNA levels in human abdominal adipose tissue were significantly increased in obese subjects compared to non-obese controls.Conclusion
Genetic variation in the NOC gene is associated with BMI in Chinese subjects.
SUBMITTER: Chang YC
PROVIDER: S-EPMC3724939 | biostudies-literature | 2013
REPOSITORIES: biostudies-literature
Chang Yi-Cheng YC Chiu Yen-Feng YF Liu Pi-Hua PH Hee Siow Wei SW Chang Tien-Jyun TJ Jiang Yi-Der YD Lee Wei-Jei WJ Lee Po-Chu PC Kao Hui-Yi HY Hwang Juey-Jen JJ Chuang Lee-Ming LM Chuang Lee-Ming LM
PloS one 20130726 7
<h4>Unlabelled</h4>Circadian clock genes are critical regulators of energy homeostasis and metabolism. However, whether variation in the circadian genes is associated with metabolic phenotypes in humans remains to be explored. In this study, we systemically genotyped 20 tag single nucleotide polymorphisms (SNPs) in 8 candidate genes involved in circadian clock, including CLOCK, BMAL1(ARNTL), PER1, PER2, CRY1, CRY2, CSNK1E,, and NOC(CCRN4L) in 1,510 non-diabetic Chinese subjects in Taipei and Yun ...[more]