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韩国中枢性性早熟女童的KISS1基因多态性

KISS1 gene polymorphisms in Korean girls with central precocious puberty.

作者信息

Rhie Young-Jun, Lee Kee-Hyoung, Ko Jung Min, Lee Woo Jung, Kim Jung Hyun, Kim Ho-Seong

机构信息

Department of Pediatrics, Korea University College of Medicine, Seoul, Korea.

Department of Pediatrics, Seoul National University College of Medicine, Seoul, Korea.

出版信息

J Korean Med Sci. 2014 Aug;29(8):1120-5. doi: 10.3346/jkms.2014.29.8.1120. Epub 2014 Jul 30.

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.

摘要

亲吻素/G蛋白偶联受体54(GPR54)系统在青春期促性腺轴的激活中起关键作用。中枢性性早熟(CPP)是由下丘脑促性腺激素释放激素分泌过早激活引起的。本研究旨在鉴定KISS1基因变异,并调查韩国女孩中KISS1基因变异与CPP之间的关联。对患有CPP的韩国女孩(n = 143)及其健康对照(n = 101)的KISS1基因所有编码外显子进行了测序。在KISS1基因中鉴定出9种多态性。首次鉴定出一种新的单核苷酸多态性(SNP),即55648176 T/G。SNP 55648184 C/G和55648186 -/T在CPP组中的检出频率高于对照组。SNP 55648176 T/G在CPP组中的检出频率低于对照组。单倍型GGGC-ACCC在CPP组中的检出频率较低。KISS1基因的遗传变异可能是CPP发生发展的促成因素。基因变异与CPP之间的关联应通过大规模和功能性研究获得的进一步证据来验证。

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本文引用的文献

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Serum kisspeptin levels in Korean girls with central precocious puberty.
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Mutations of the KISS1 gene in disorders of puberty.
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