Gajdos Zofia Kz, Hirschhorn Joel N, Palmert Mark R
Division of Endocrinology, Children's Hospital, Department of Genetics, Harvard Medical School, Boston, Massachusetts, USA.
Curr Opin Endocrinol Diabetes Obes. 2009 Feb;16(1):16-24. doi: 10.1097/MED.0b013e328320253c.
Puberty is an important developmental stage during which reproductive capacity is attained. Genetic and environmental factors both influence the timing of puberty, which varies greatly among individuals. However, although genetic variation is known to influence the normal spectrum of pubertal timing, the specific genes involved remain unknown.
Recent genetic analyses have identified a number of genes responsible for rare disorders of pubertal timing such as hypogonadotropic hypogonadism and Kallmann syndrome. However, although the genetic basis of population variation in the timing of puberty is an active area of investigation, no genetic loci have been reproducibly associated with pubertal timing thus far.
This review provides an update of the genes implicated in disorders of puberty, discusses genes and pathways that may be involved in the timing of normal puberty, and suggests additional avenues of investigation to identify genetic regulators of puberty in the general population.
青春期是生殖能力得以实现的重要发育阶段。遗传和环境因素均会影响青春期的启动时间,个体之间差异很大。然而,尽管已知基因变异会影响青春期启动时间的正常范围,但具体涉及的基因仍不清楚。
近期的基因分析已鉴定出一些导致青春期启动罕见疾病的基因,如低促性腺激素性性腺功能减退和卡尔曼综合征。然而,尽管青春期启动时间的人群变异的遗传基础是一个活跃的研究领域,但迄今为止尚无基因位点被反复证实与青春期启动时间相关。
本综述提供了与青春期疾病相关基因的最新信息,讨论了可能参与正常青春期启动时间的基因和途径,并提出了其他调查途径,以识别普通人群中青春期的基因调节因子。