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 language | English (US) |
|---|---|
| Pages (from-to) | 525-532 |
| Number of pages | 8 |
| Journal | American Journal of Medical Genetics |
| Volume | 19 |
| Issue number | 3 |
| DOIs | |
| State | Published - 1984 |
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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 journal › Article
}
TY - JOUR
T1 - Linkage relationships between a major gene for catechol-O-methyltransferase activity and 25 polymorphic marker systems
AU - Wilson, A. F.
AU - Elston, R. C.
AU - Siervogel, R. M.
AU - Weinshilboum, Richard M
AU - Ward, L. J.
PY - 1984
Y1 - 1984
N2 - 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.
AB - 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.
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U2 - 10.1002/ajmg.1320190314
DO - 10.1002/ajmg.1320190314
M3 - Article
VL - 19
SP - 525
EP - 532
JO - American Journal of Medical Genetics, Part A
JF - American Journal of Medical Genetics, Part A
SN - 0148-7299
IS - 3
ER -