A quantitative trait locus on chromosome 6 regulates the onset of puberty in mice

被引:22
作者
Nathan, Brandon M.
Hodges, Craig A.
Supelak, Pamela J.
Burrage, Lindsay C.
Nadeau, Joseph H.
Palmert, Mark R.
机构
[1] Univ Hosp Cleveland, Rainbow Babies & Childrens Hosp, Div Pediat Endocrinol & Metab, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Sch Med, Dept Pediat, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Sch Med, Dept Genet, Cleveland, OH 44106 USA
关键词
D O I
10.1210/en.2006-0745
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Puberty is a fundamental developmental process experienced by all reproductively competent adults, yet the specific factors that regulate variation in its timing remain elusive. Using a new approach to identifying these factors, we have performed a survey among a panel of chromosome substitution strains (for inbred strains C57BL/6J and A/J) followed by linkage analysis to map a quantitative trait locus (QTL) on the distal end of chromosome 6 that regulates pubertal timing ( as assessed by vaginal opening) in mice. The location of the QTL was then refined to a region between marker D6MIT59 and the end of the chromosome by generating and phenotyping a panel of 12 congenic strains, each with a unique and overlapping homozygous segment of the A/J chromosome on an otherwise uniform C57BL/6J genomic background. Additional characterization of the QTL indicated that the effects of the responsible gene(s) are gender specific and inherited in a codominant manner without parent-of-origin effects. These findings represent an important advancement toward identification of novel factors that regulate maturation of the hypothalamic-pituitary-gonadal axis and determine the timing of puberty.
引用
收藏
页码:5132 / 5138
页数:7
相关论文
共 58 条
[1]   The effect of a null mutation in the follicle-stimulating hormone receptor gene on mouse reproduction [J].
Abel, MH ;
Wootton, AN ;
Wilkins, V ;
Huhtaniemi, I ;
Knight, PG ;
Charlton, HM .
ENDOCRINOLOGY, 2000, 141 (05) :1795-1803
[2]   Perinatal changes in hypothalamic N-methyl-D-aspartate receptors and their relationship to gonadotropin-releasing hormone neurons [J].
Adams, MM ;
Flagg, RA ;
Gore, AC .
ENDOCRINOLOGY, 1999, 140 (05) :2288-2296
[3]   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
[4]   Dynamics of ovarian development in the FORKO immature mouse: Structural and functional implications for ovarian reserve [J].
Balla, A ;
Danilovich, N ;
Yang, YZ ;
Sairam, MR .
BIOLOGY OF REPRODUCTION, 2003, 69 (04) :1281-1293
[5]   Bench and bedside - The G protein-coupled receptor GPR54 and puberty [J].
Beier, DR ;
Dluhy, RG .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (17) :1589-1592
[6]   Chromosome substitution strains: some quantitative considerations for genome scans and fine mapping [J].
Belknap, JK .
MAMMALIAN GENOME, 2003, 14 (11) :723-732
[7]   R/qtl: QTL mapping in experimental crosses [J].
Broman, KW ;
Wu, H ;
Sen, S ;
Churchill, GA .
BIOINFORMATICS, 2003, 19 (07) :889-890
[8]  
Camden R W, 1967, ANL Rep, P228
[9]   A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction [J].
Clément, K ;
Vaisse, C ;
Lahlou, N ;
Cabrol, S ;
Pelloux, V ;
Cassuto, D ;
Gourmelen, M ;
Dina, C ;
Chambaz, J ;
Lacorte, JM ;
Basdevant, A ;
Bougneres, P ;
Lebouc, Y ;
Froguel, P ;
Guy-Grand, B .
NATURE, 1998, 392 (6674) :398-401
[10]   Parent-daughter transmission of the androgen receptor gene as an explanation of the effect of father absence on age of menarche [J].
Comings, DE ;
Muhleman, D ;
Johnson, JP ;
MacMurray, JP .
CHILD DEVELOPMENT, 2002, 73 (04) :1046-1051