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Submitted on June 6, 2006
Accepted on July 20, 2006
Division of Pediatric Endocrinology and Metabolism, Rainbow Babies and Children’s Hospital, University Hospitals of Cleveland, Cleveland, OH 44106; Department of Pediatrics, Case School of Medicine, Cleveland, OH 44106; Department of Genetics, Case School of Medicine, Cleveland, OH 44106
* To whom correspondence should be addressed. E-mail: mark.palmert{at}case.edu.
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 [CSSs for inbred strains C57BL/6J (B6) 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 B6 genomic background. Further 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.
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