IBD sharing around the PPARG locus is not increased in dizygotic twins or their mothers


Autoria(s): Duffy, David; Montgomery, Grant; Treloar, Susan; Birley, Andrew; Kirk, Katherine; Boomsma, Dorret; Beem, Leo; de Geus, Eco; Slagboom, Eline; Knighton, Joharna; Reed, Peter; Martin, Nicholas
Data(s)

01/01/2001

Resumo

We observe no evidence of linkage to the region around the PPARG locus in several samples of DZ twins who have been genotyped at multiple markers on chromosome 3 (Fig. 1). Among 199 Australian DZ twins ascertained for a history of wheezing2, mean identity by descent (IBD) sharing at the position of PPARG is 0.463 (99% bootstrapped confidence interval=0.412−0.516). We obtained a similar result with 232 pairs of Australian adolescent DZ twins taking part in a longitudinal study of naevus development3 (0.444, 0.390−0.499), and a set of 125 Australian adult DZ twin pairs assessed for anxiety4 (0.508, 0.435−0.580). A Dutch scan of 160 DZ twin pairs5 obtained slightly more encouraging results (0.553, 0.482−0.587, peak maximum lod score (MLS)=0.57). Pooling all these samples gives 0.477 (0.454−0.512) at the position of PPARG. The test for heterogeneity of sharing between studies was not significant (P=0.10). In the combined dataset, the peak IBD sharing (MLS=0.70) is 50 cM closer to the centromere than PPARG. Finally, in a sample of 203 Australian and New Zealand sister pairs where each had given birth to DZ twins6, sharing across the region is also not increased (0.433). We do not replicate linkage in the populations we study to survival of a twin pregnancy or polyovulation.

Identificador

http://espace.library.uq.edu.au/view/UQ:58545

Idioma(s)

eng

Publicador

Nature American Inc

Palavras-Chave #Genetics & Heredity #CX #321011 Medical Genetics #730107 Inherited diseases (incl. gene therapy)
Tipo

Journal Article