Literature DB >> 6951409

Segregation and linkage studies of plasma dopamine-beta-hydroxylase (DBH), erythrocyte catechol-O-methyltransferase (COMT), and platelet monoamine oxidase (MAO): possible linkage between the ABO locus and a gene controlling DBH activity.

L R Goldin, E S Gershon, C R Lake, D L Murphy, M McGinniss, R S Sparkes.   

Abstract

Measurements of dopamine-beta-hydroxylase (DBH), catechol-O-methyltransferase (COMT), and monoamine oxidase (MAO) along with 27 polymorphic marker phenotypes were available for 162 patients with major affective disorders and 1,125 of their relatives. Levels of enzymes were previously found not to be associated with illness. Pedigree analysis methods for quantitative traits are used to test single-gene hypotheses for segregation of DBH in 32 families with 411 individuals. COMT in 30 families with 351 individuals, and MAO in 50 families with 309 individuals. The familial distribution of both DBH and COMT are consistent with two codominant alleles at the same locus that account for 56% and 59% of the total variance, respectively. MAO activity cannot be shown to be segregating as a single major gene, but a purely nongenetic hypothesis is also rejected. A possible linkage of a locus for DBH to the ABO locus is indicated by a maximum lod score of 1.82 at 0% and 10% recombination fractions for males and females, respectively. A lod score of 0.61 at 0% recombination for a similar analysis in a single large pedigree was reported by Elston et al., making the combined lod score for the two studies equal to 2.32 at 0% recombination.

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Year:  1982        PMID: 6951409      PMCID: PMC1685293     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  22 in total

1.  Inheritance of very low serum dopamine-beta-hydroxylase activity.

Authors:  R M Weinshilboum; H G Schorott; F A Raymond; W H Weidman; L R Elveback
Journal:  Am J Hum Genet       Date:  1975-09       Impact factor: 11.025

2.  Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.

Authors:  J Ott
Journal:  Am J Hum Genet       Date:  1974-09       Impact factor: 11.025

3.  Salivary and pancreatic amylase: electrophoretic characterizations and genetic studies.

Authors:  A D Merritt; M L Rivas; D Bixler; R Newell
Journal:  Am J Hum Genet       Date:  1973-09       Impact factor: 11.025

4.  Studies on blood and urine glucose in Seminole Indians: indications for segregation of a major gene.

Authors:  R C Elston; K K Namboodiri; H V Nino; W S Pollitzer
Journal:  Am J Hum Genet       Date:  1974-01       Impact factor: 11.025

5.  Genetic control of platelet and plasma monoamine oxidase activity.

Authors:  A Nies; D S Robinson; K R Lamborn; R P Lampert
Journal:  Arch Gen Psychiatry       Date:  1973-06

6.  A general model for the genetic analysis of pedigree data.

Authors:  R C Elston; J Stewart
Journal:  Hum Hered       Date:  1971       Impact factor: 0.444

7.  Some observations upon a new inhibitor of monoamine oxidase in brain tissue.

Authors:  J P Johnston
Journal:  Biochem Pharmacol       Date:  1968-07       Impact factor: 5.858

8.  A sensitive enzymatic assay for dopamine- -hydroxylase.

Authors:  P B Molinoff; R Weinshilboum; J Axelrod
Journal:  J Pharmacol Exp Ther       Date:  1971-09       Impact factor: 4.030

9.  Erythrocyte soluble catechol-O-methyl transferase activity in primary affective disorder. A clinical and genetic study.

Authors:  E S Gershon; W Z Jonas
Journal:  Arch Gen Psychiatry       Date:  1975-11

10.  Study of the genetic transmission of hypercholesterolemia and hypertriglyceridemia in a 195 member kindred.

Authors:  R C Elston; K K Namboodiri; C J Glueck; R Fallat; R Tsang; V Leuba
Journal:  Ann Hum Genet       Date:  1975-07       Impact factor: 1.670

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  16 in total

Review 1.  Linkage analysis in the next-generation sequencing era.

Authors:  Joan E Bailey-Wilson; Alexander F Wilson
Journal:  Hum Hered       Date:  2011-12-23       Impact factor: 0.444

2.  Sample-size guidelines for linkage analysis of a dominant locus for a quantitative trait by the method of lod scores.

Authors:  M Boehnke
Journal:  Am J Hum Genet       Date:  1990-08       Impact factor: 11.025

3.  The catecholamine biosynthetic enzyme dopamine β-hydroxylase (DBH): first genome-wide search positions trait-determining variants acting additively in the proximal promoter.

Authors:  Maja Mustapic; Adam X Maihofer; Manjula Mahata; Yuqing Chen; Dewleen G Baker; Daniel T O'Connor; Caroline M Nievergelt
Journal:  Hum Mol Genet       Date:  2014-06-30       Impact factor: 6.150

4.  Platelet monoamine oxidase (MAO) activity: evidence for a single major locus.

Authors:  J Rice; P McGuffin; L R Goldin; E G Shaskan; E S Gershon
Journal:  Am J Hum Genet       Date:  1984-01       Impact factor: 11.025

Review 5.  Human genetics of plasma dopamine beta-hydroxylase activity: applications to research in psychiatry and neurology.

Authors:  J F Cubells; C P Zabetian
Journal:  Psychopharmacology (Berl)       Date:  2004-04-16       Impact factor: 4.530

6.  The structure of linkage disequilibrium at the DBH locus strongly influences the magnitude of association between diallelic markers and plasma dopamine beta-hydroxylase activity.

Authors:  Cyrus P Zabetian; Sarah G Buxbaum; Robert C Elston; Michael D Köhnke; George M Anderson; Joel Gelernter; Joseph F Cubells
Journal:  Am J Hum Genet       Date:  2003-04-30       Impact factor: 11.025

7.  Catechol-O-methyltransferase: a method for autoradiographic visualization of isozymes in cellogel.

Authors:  C Brahe; N Crosti; P Meera Khan; A Serra
Journal:  Biochem Genet       Date:  1984-02       Impact factor: 1.890

8.  Study on DBH genetic polymorphisms and plasma activity in attention deficit hyperactivity disorder patients from Eastern India.

Authors:  Nipa Bhaduri; Kanyakumarika Sarkar; Swagata Sinha; Anindita Chattopadhyay; Kanchan Mukhopadhyay
Journal:  Cell Mol Neurobiol       Date:  2009-09-16       Impact factor: 5.046

9.  Linkage of a gene regulating dopamine-beta-hydroxylase activity and the ABO blood group locus.

Authors:  A F Wilson; R C Elston; R M Siervogel; L D Tran
Journal:  Am J Hum Genet       Date:  1988-01       Impact factor: 11.025

10.  Assignment of the catechol-O-methyltransferase gene to human chromosome 22 in somatic cell hybrids.

Authors:  C Brahe; P Bannetta; P Meera Khan; F Arwert; A Serra
Journal:  Hum Genet       Date:  1986-11       Impact factor: 4.132

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