A whole-genome linkage scan suggests several genomic regions potentially containing QTLs underlying the variation of stature

Am J Med Genet. 2002 Nov 15;113(1):29-39. doi: 10.1002/ajmg.10742.

Abstract

Human height is a complex trait under the control of both genetic and environment factors. In order to identify genomic regions underlying the variation of stature, we performed a whole-genome linkage analysis on a sample of 53 human pedigrees containing 1,249 sib pairs, 1,098 grandparent-grandchildren pairs, 1,993 avuncular pairs, and 1,172 first-cousin pairs. Several genomic regions were suggested by our study to be linked with human height variation. These regions include 5q31 at 144 cM from pter on chromosome 5 (with a maximum LOD score of 2.14 in multipoint linkage analyses), Xp22 at the marker DXS1060, and Xq25 at DXS1001 on the X chromosome (with LOD scores of 1.95 and 1.91, respectively, in two-point linkage analyses). Noticeably, Xp22 happens to be the very region where a newly identified gene underlying idiopathic short stature, SHOX, maps. Based on our findings, further confirmation and fine-mapping studies are to be pursued on expanded samples and/or with denser markers for eventual identification of major functional genes involved in human height variation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Body Height / genetics*
  • Chromosome Mapping*
  • Chromosomes, Human, Pair 5*
  • Chromosomes, Human, X
  • Female
  • Genetic Variation*
  • Genome, Human*
  • Humans
  • Lod Score
  • Male
  • Pedigree
  • Quantitative Trait Loci*
  • Sex Characteristics