What controls the timing of puberty? An update on progress from genetic investigation

被引:55
作者
Gajdos, Zofia K. Z. [2 ,3 ,4 ]
Hirschhorn, Joel N. [2 ,3 ,4 ]
Palmert, Mark R. [1 ]
机构
[1] Hosp Sick Children, Div Endocrinol, Toronto, ON M5G 1X8, Canada
[2] Harvard Univ, Sch Med, Program Genom, Boston, MA USA
[3] Harvard Univ, Sch Med, Dept Genet, Childrens Hosp,Div Endocrinol, Boston, MA USA
[4] Broad Inst MIT & Harvard, Program Med & Populat Genet, Cambridge, MA USA
关键词
genetic regulation; genetics; hypogonadotropic hypogonadism; Kallmann syndrome; pubertal timing; puberty; GONADOTROPIN-RELEASING-HORMONE; IDIOPATHIC HYPOGONADOTROPIC HYPOGONADISM; RECEPTOR-ALPHA GENE; NATURALLY-OCCURRING MUTATIONS; CENTRAL PRECOCIOUS PUBERTY; LINKED KALLMANN-SYNDROME; QUANTITATIVE TRAIT LOCI; BREAST-CANCER RISK; CONSTITUTIONAL DELAY; COMMON VARIANTS;
D O I
10.1097/MED.0b013e328320253c
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review 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 findings 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. Summary 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.
引用
收藏
页码:16 / 24
页数:9
相关论文
共 98 条
[1]   Genetic causes of human reproductive disease [J].
Achermann, JC ;
Ozisik, G ;
Meeks, JJ ;
Jameson, JL .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (06) :2447-2454
[2]   CYP17 genetic polymorphism, breast cancer, and breast cancer risk factors [J].
Ambrosone, CB ;
Moysich, KB ;
Furberg, H ;
Freudenheim, JL ;
Bowman, ED ;
Ahmed, S ;
Graham, S ;
Vena, JE ;
Shields, PG .
BREAST CANCER RESEARCH, 2003, 5 (02) :R45-R51
[3]   A genome-wide linkage scan for age at menarche in three populations of European descent [J].
Anderson, Carl A. ;
Zhu, Gu ;
Falchi, Mario ;
van den Berg, Stephanie M. ;
Treloar, Susan A. ;
Spector, Timothy D. ;
Martin, Nicholas G. ;
Boomsma, Dorret I. ;
Visscher, Peter M. ;
Montgomery, Grant W. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2008, 93 (10) :3965-3970
[4]   Relative weight and race influence average age at menarche: Results from two nationally representative surveys of US girls studied 25 years apart [J].
Anderson, SE ;
Dallal, GE ;
Must, A .
PEDIATRICS, 2003, 111 (04) :844-850
[5]   Phenotypic variation in constitutional delay of growth and puberty: relationship to specific leptin and leptin receptor gene polymorphisms [J].
Banerjee, Indraneel ;
Trueman, Julie A. ;
Hall, Catherine M. ;
Price, David A. ;
Patel, Leena ;
Whatmore, Andrew J. ;
Hirschhorn, Joel N. ;
Read, Andrew P. ;
Palmert, Mark R. ;
Clayton, Peter E. .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2006, 155 (01) :121-126
[6]   Four naturally occurring mutations in the human GnRH receptor affect ligand binding and receptor function [J].
Bédécarrats, GY ;
Linher, KD ;
Janovick, JA ;
Beranova, M ;
Kada, F ;
Seminara, SB ;
Conn, PM ;
Kaiser, UB .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2003, 205 (1-2) :51-64
[7]   Two common naturally occurring mutations in the human gonadotropin-releasing hormone (GnRH) receptor have differential effects on gonadotropin gene expression and on GnRH-mediated signal transduction [J].
Bedecarrats, GY ;
Linher, KD ;
Kaiser, UB .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (02) :834-843
[8]   Prevalence, phenotypic spectrum, and modes of inheritance of gonadotropin-releasing hormone receptor mutations in idiopathic hypogonadotropic hypogonadism [J].
Beranova, M ;
Oliveira, LMB ;
Bédécarrats, GY ;
Schipani, E ;
Vallejo, M ;
Ammini, AC ;
Quintos, JB ;
Hall, JE ;
Martin, KA ;
Hayes, FJ ;
Pitteloud, N ;
Kaiser, UB ;
Crowley, WF ;
Seminara, SB .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (04) :1580-1588
[9]   The prevalence of gonadotropin-releasing hormone receptor mutations in a large cohort of patients with hypogonadotropic hypogonadism [J].
Bhagavath, B ;
Ozata, M ;
Ozdemir, IC ;
Bolu, E ;
Bick, DP ;
Sherins, RJ ;
Layman, LC .
FERTILITY AND STERILITY, 2005, 84 (04) :951-957
[10]   Pubertal correlates in black and white girls [J].
Biro, FM ;
Huang, B ;
Crawford, PB ;
Lucky, AW ;
Streigel-Moore, R ;
Barton, BA ;
Daniels, S .
JOURNAL OF PEDIATRICS, 2006, 148 (02) :234-240