Linkage relationships between a major gene for catechol-O-methyltransferase activity and 25 polymorphic marker systems

A. F. Wilson, R. C. Elston, R. M. Siervogel, Richard M Weinshilboum, L. J. Ward

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

Segregation analysis has provided evidence suggesting the existence of a major gene for catechol-o-methyltransferase (COMT) activity in man. Five large families (4 Caucasian, 1 black), with a total of 1,189 individuals, were ascertained as part of a genetic study of blood pressure. Erythrocyte COMT activity and status at 25 polymorphic genetic marker loci were determined on more than 518 individuals in these pedigrees. Genetic linkage analysis of COMT with each of the 25 marker foci was performed in two ways: 1) using parameter estimates from segregation analysis of untransformed COMT activity, and 2) using parameter estimates from segregation analysis of the power transformation of the COMT activity that maximized the likelihood of the genetic hypothesis in each family. Tight and close linkage were excluded at 21 and 15 loci, respectively. A lod score of 1.27 at θ = 0.1 was found between the loci for COMT activity and phosphogluconate dehydrogenase (PGD). Transformation of the data had little effect on the outcome of the linkage analysis.

Original languageEnglish (US)
Pages (from-to)525-532
Number of pages8
JournalAmerican Journal of Medical Genetics
Volume19
Issue number3
DOIs
StatePublished - 1984

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Catechol O-Methyltransferase
Genes
Phosphogluconate Dehydrogenase
Lod Score
Genetic Linkage
Genetic Loci
Pedigree
Genetic Markers
Erythrocytes
Blood Pressure

ASJC Scopus subject areas

  • Genetics(clinical)

Cite this

Linkage relationships between a major gene for catechol-O-methyltransferase activity and 25 polymorphic marker systems. / Wilson, A. F.; Elston, R. C.; Siervogel, R. M.; Weinshilboum, Richard M; Ward, L. J.

In: American Journal of Medical Genetics, Vol. 19, No. 3, 1984, p. 525-532.

Research output: Contribution to journalArticle

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