KISS1 Gene Polymorphisms in Korean Girls with Central Precocious Puberty.
10.3346/jkms.2014.29.8.1120
- Author:
Young Jun RHIE
1
;
Kee Hyoung LEE
;
Jung Min KO
;
Woo Jung LEE
;
Jung Hyun KIM
;
Ho Seong KIM
Author Information
1. Department of Pediatrics, Korea University College of Medicine, Seoul, Korea.
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
KISS1 Gene;
Kisspeptins;
G-Protein Coupled Receptor-54;
Precocious Puberty, Central
- MeSH:
Base Sequence;
Child;
Female;
Genetic Markers/genetics;
Genetic Predisposition to Disease/*epidemiology/*genetics;
Humans;
Kisspeptins/*genetics;
Molecular Sequence Data;
Point Mutation/genetics;
Polymorphism, Single Nucleotide/*genetics;
Prevalence;
Puberty, Precocious/*epidemiology/*genetics;
Reproducibility of Results;
Republic of Korea/epidemiology;
Risk Assessment;
Sensitivity and Specificity
- From:Journal of Korean Medical Science
2014;29(8):1120-1125
- CountryRepublic of Korea
- Language:English
-
Abstract:
Kisspeptin/G-protein couple receptor-54 (GPR54) system plays a key role in the activation of the gonadotropic axis at puberty. Central precocious puberty (CPP) is caused by the premature activation of hypothalamic gonadotropin-releasing hormone secretion. This study was aimed to identify KISS1 gene variations and to investigate the associations between KISS1 gene variations and CPP in Korean girls. All coding exons of KISS1 gene were sequenced in Korean girls with CPP (n = 143) and their healthy controls (n = 101). Nine polymorphisms were identified in KISS1 gene. A novel single-nucleotide polymorphism (SNP), 55648176 T/G, was identified for the first time. SNP 55648184 C/G and 55648186 -/T were detected more frequently in CPP group than in control group. SNP 55648176 T/G was detected less frequently in CPP group than in control group. Haplotype GGGC-ACCC was detected less frequently in CPP group. The genetic variations of KISS1 gene can be contributing factors of development of CPP. The association between the gene variations and CPP should be validated by further evidence obtained from large-scaled and functional studies.
