In:
American Journal of Human Biology, Wiley, Vol. 25, No. 6 ( 2013-11), p. 743-750
Abstract:
There is phenotypic overlap between Brachydactyly Type D (BDD) and Brachydactyly Type E (BDE) that suggests a possible common underlying etiology. We seek to understand the genetic underpinnings of, and relationship between, these skeletal anomalies. Methods The Jirel ethnic group of eastern Nepal participates in various genetic epidemiologic studies, including those in which hand‐wrist radiographs have been taken to examine skeletal development. Nearly 2,130 individuals (969 males; 1,161 females) were phenotyped for BDD/BDE. Of these, 1,722 individuals (773 males; 949 females) were genotyped for 371 STR markers spanning the autosomal genome. Variance components‐based linkage analysis was used to conduct a genome‐wide linkage scan for QTL influencing the BDD/BDE phenotype. Results BDD was present in 3.55%, and BDE was present in 0.39%, of the study sample. Because of the phenotypic overlap between two traits, affecteds of either type were considered as affected by a single combined phenotype (BDD/BDE) having a prevalence of 3.94%. The additive genetic heritability of BDD/BDE was highly significant ( h 2 ± SE = 0.89 ± 0.13; P = 1.7 × 10 −11 ). Significant linkage of BDD/BDE was found to markers on chromosome 7p21‐7p14 (peak LOD score = 3.74 at 7p15 between markers D7S493 and D7S516). Conclusions Possible positional candidate genes in the one‐lod support interval of this QTL include TWIST and the HOXA1‐A13 cluster. This is the first study to report significant linkage results for BDD/BDE using a large extended pedigree, and the first to suggest that mutations in TWIST and/or the HOXA1‐A13 cluster may contribute to these specific skeletal anomalies. Am. J. Hum. Biol. 25:743–750, 2013. © 2013 Wiley Periodicals, Inc.
Type of Medium:
Online Resource
ISSN:
1042-0533
,
1520-6300
Language:
English
Publisher:
Wiley
Publication Date:
2013
detail.hit.zdb_id:
2001218-4
SSG:
12
