Two-locus admixture linkage analysis of bipolar and unipolar affective disorder supports the presence of susceptibility loci on chromosomes 11p15 and 21q22

Following a report of a linkage study that yielded evidence for a susceptibility locus for bipolar affective disorder on the long arm of chromosome 21, we studied 23 multiply affected pedigrees collected from Iceland and the UK, using the markers PFKL, D21S171, and D21S49. Counting only bipolar case...

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Published in:Genomics
Main Authors: Smyth, C, Kalsi, G, Curtis, D, Brynjolfsson, J, ONeill, J, Rifkin, L, Moloney, E, Murphy, P, Petursson, H, Gurling, H
Format: Article in Journal/Newspaper
Language:English
Published: 1997
Subjects:
Online Access:https://kclpure.kcl.ac.uk/portal/en/publications/twolocus-admixture-linkage-analysis-of-bipolar-and-unipolar-affective-disorder-supports-the-presence-of-susceptibility-loci-on-chromosomes-11p15-and-21q22(55e2ed76-cae2-4d26-a515-ddebe8e55ba4).html
https://doi.org/10.1006/geno.1996.4486
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spelling ftkingscollondon:oai:pure.atira.dk:publications/55e2ed76-cae2-4d26-a515-ddebe8e55ba4 2023-05-15T16:50:55+02:00 Two-locus admixture linkage analysis of bipolar and unipolar affective disorder supports the presence of susceptibility loci on chromosomes 11p15 and 21q22 Smyth, C Kalsi, G Curtis, D Brynjolfsson, J ONeill, J Rifkin, L Moloney, E Murphy, P Petursson, H Gurling, H 1997-02-01 https://kclpure.kcl.ac.uk/portal/en/publications/twolocus-admixture-linkage-analysis-of-bipolar-and-unipolar-affective-disorder-supports-the-presence-of-susceptibility-loci-on-chromosomes-11p15-and-21q22(55e2ed76-cae2-4d26-a515-ddebe8e55ba4).html https://doi.org/10.1006/geno.1996.4486 eng eng info:eu-repo/semantics/restrictedAccess Smyth , C , Kalsi , G , Curtis , D , Brynjolfsson , J , ONeill , J , Rifkin , L , Moloney , E , Murphy , P , Petursson , H & Gurling , H 1997 , ' Two-locus admixture linkage analysis of bipolar and unipolar affective disorder supports the presence of susceptibility loci on chromosomes 11p15 and 21q22 ' , Genomics , vol. 39 , no. 3 , pp. 271-278 . https://doi.org/10.1006/geno.1996.4486 FAMILY DNA MARKERS PEDIGREES COMPLEX SEGREGATION ANALYSIS MANIC-DEPRESSIVE ILLNESS GENETIC-LINKAGE COLOR-BLINDNESS TYROSINE-HYDROXYLASE POLYMORPHISMS HETEROGENEITY X-CHROMOSOME article 1997 ftkingscollondon https://doi.org/10.1006/geno.1996.4486 2022-10-14T10:16:39Z Following a report of a linkage study that yielded evidence for a susceptibility locus for bipolar affective disorder on the long arm of chromosome 21, we studied 23 multiply affected pedigrees collected from Iceland and the UK, using the markers PFKL, D21S171, and D21S49. Counting only bipolar cases as affected, a two-point LOD of 1.28 was obtained using D21S171 (theta = 0.01, alpha = 0.35), with three Icelandic families producing LODs of 0.63, 0.62, and 1.74 (all at theta = 0.0). Affected sib pair analysis demonstrated increased allele sharing at D21S171 (P = 0.001) when unipolar cases were also considered affected. The same set of pedigrees had previously been typed for a tyrosine hydroxylase gene (TH) polymorphism at 11p15 and had shown some moderate evidence for linkage. When information from TH and the 21q markers was combined in a two-locus admixture analysis, an overall admixture LOD of 3.87 was obtained using the bipolar affection model. Thus the data are compatible with the hypothesis that a locus at or near TH influences susceptibility in some pedigrees, while a locus near D21S171 is active in others. Similar analyses in other datasets should be carried out to confirm or refute our tentative finding. (C) 1997 Academic Press. Article in Journal/Newspaper Iceland King's College, London: Research Portal Long Arm ENVELOPE(-55.648,-55.648,49.517,49.517) Genomics 39 3 271 278
institution Open Polar
collection King's College, London: Research Portal
op_collection_id ftkingscollondon
language English
topic FAMILY
DNA MARKERS
PEDIGREES
COMPLEX SEGREGATION ANALYSIS
MANIC-DEPRESSIVE ILLNESS
GENETIC-LINKAGE
COLOR-BLINDNESS
TYROSINE-HYDROXYLASE POLYMORPHISMS
HETEROGENEITY
X-CHROMOSOME
spellingShingle FAMILY
DNA MARKERS
PEDIGREES
COMPLEX SEGREGATION ANALYSIS
MANIC-DEPRESSIVE ILLNESS
GENETIC-LINKAGE
COLOR-BLINDNESS
TYROSINE-HYDROXYLASE POLYMORPHISMS
HETEROGENEITY
X-CHROMOSOME
Smyth, C
Kalsi, G
Curtis, D
Brynjolfsson, J
ONeill, J
Rifkin, L
Moloney, E
Murphy, P
Petursson, H
Gurling, H
Two-locus admixture linkage analysis of bipolar and unipolar affective disorder supports the presence of susceptibility loci on chromosomes 11p15 and 21q22
topic_facet FAMILY
DNA MARKERS
PEDIGREES
COMPLEX SEGREGATION ANALYSIS
MANIC-DEPRESSIVE ILLNESS
GENETIC-LINKAGE
COLOR-BLINDNESS
TYROSINE-HYDROXYLASE POLYMORPHISMS
HETEROGENEITY
X-CHROMOSOME
description Following a report of a linkage study that yielded evidence for a susceptibility locus for bipolar affective disorder on the long arm of chromosome 21, we studied 23 multiply affected pedigrees collected from Iceland and the UK, using the markers PFKL, D21S171, and D21S49. Counting only bipolar cases as affected, a two-point LOD of 1.28 was obtained using D21S171 (theta = 0.01, alpha = 0.35), with three Icelandic families producing LODs of 0.63, 0.62, and 1.74 (all at theta = 0.0). Affected sib pair analysis demonstrated increased allele sharing at D21S171 (P = 0.001) when unipolar cases were also considered affected. The same set of pedigrees had previously been typed for a tyrosine hydroxylase gene (TH) polymorphism at 11p15 and had shown some moderate evidence for linkage. When information from TH and the 21q markers was combined in a two-locus admixture analysis, an overall admixture LOD of 3.87 was obtained using the bipolar affection model. Thus the data are compatible with the hypothesis that a locus at or near TH influences susceptibility in some pedigrees, while a locus near D21S171 is active in others. Similar analyses in other datasets should be carried out to confirm or refute our tentative finding. (C) 1997 Academic Press.
format Article in Journal/Newspaper
author Smyth, C
Kalsi, G
Curtis, D
Brynjolfsson, J
ONeill, J
Rifkin, L
Moloney, E
Murphy, P
Petursson, H
Gurling, H
author_facet Smyth, C
Kalsi, G
Curtis, D
Brynjolfsson, J
ONeill, J
Rifkin, L
Moloney, E
Murphy, P
Petursson, H
Gurling, H
author_sort Smyth, C
title Two-locus admixture linkage analysis of bipolar and unipolar affective disorder supports the presence of susceptibility loci on chromosomes 11p15 and 21q22
title_short Two-locus admixture linkage analysis of bipolar and unipolar affective disorder supports the presence of susceptibility loci on chromosomes 11p15 and 21q22
title_full Two-locus admixture linkage analysis of bipolar and unipolar affective disorder supports the presence of susceptibility loci on chromosomes 11p15 and 21q22
title_fullStr Two-locus admixture linkage analysis of bipolar and unipolar affective disorder supports the presence of susceptibility loci on chromosomes 11p15 and 21q22
title_full_unstemmed Two-locus admixture linkage analysis of bipolar and unipolar affective disorder supports the presence of susceptibility loci on chromosomes 11p15 and 21q22
title_sort two-locus admixture linkage analysis of bipolar and unipolar affective disorder supports the presence of susceptibility loci on chromosomes 11p15 and 21q22
publishDate 1997
url https://kclpure.kcl.ac.uk/portal/en/publications/twolocus-admixture-linkage-analysis-of-bipolar-and-unipolar-affective-disorder-supports-the-presence-of-susceptibility-loci-on-chromosomes-11p15-and-21q22(55e2ed76-cae2-4d26-a515-ddebe8e55ba4).html
https://doi.org/10.1006/geno.1996.4486
long_lat ENVELOPE(-55.648,-55.648,49.517,49.517)
geographic Long Arm
geographic_facet Long Arm
genre Iceland
genre_facet Iceland
op_source Smyth , C , Kalsi , G , Curtis , D , Brynjolfsson , J , ONeill , J , Rifkin , L , Moloney , E , Murphy , P , Petursson , H & Gurling , H 1997 , ' Two-locus admixture linkage analysis of bipolar and unipolar affective disorder supports the presence of susceptibility loci on chromosomes 11p15 and 21q22 ' , Genomics , vol. 39 , no. 3 , pp. 271-278 . https://doi.org/10.1006/geno.1996.4486
op_rights info:eu-repo/semantics/restrictedAccess
op_doi https://doi.org/10.1006/geno.1996.4486
container_title Genomics
container_volume 39
container_issue 3
container_start_page 271
op_container_end_page 278
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