Loading…
Common 5' -globin RFLP haplotypes harbour a surprising level of ancestral sequence mosaicism
Blocks of linkage disequilibrium (LD) in the human genome represent segments of ancestral chromosomes. To investigate the relationship between LD and genealogy, we analysed diversity associated with restriction fragment length polymorphism (RFLP) haplotypes of the 5[variant prime] β-globin gene comp...
Saved in:
Published in: | Human genetics 2003-07, Vol.113 (2), p.123 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | |
container_issue | 2 |
container_start_page | 123 |
container_title | Human genetics |
container_volume | 113 |
creator | Webster, Matthew T Clegg, John B Harding, Rosalind M |
description | Blocks of linkage disequilibrium (LD) in the human genome represent segments of ancestral chromosomes. To investigate the relationship between LD and genealogy, we analysed diversity associated with restriction fragment length polymorphism (RFLP) haplotypes of the 5[variant prime] β-globin gene complex. Genealogical analyses were based on sequence alleles that spanned a 12.2-kb interval, covering 3.1 kb around the ψβ gene and 6.2 kb of the δ-globin gene and its 5[variant prime] flanking sequence known as the R/T region. Diversity was sampled from a Kenyan Luo population where recent malarial selection has contributed to substantial LD. A single common sequence allele spanning the 12.2-kb interval exclusively identified the ancestral chromosome bearing the "Bantu" βs (sickle-cell) RFLP haplotype. Other common 5[variant prime] RFLP haplotypes comprised interspersed segments from multiple ancestral chromosomes. Nucleotide diversity was similar between ψβ and R/T-δ-globin but was non-uniformly distributed within the R/T-δ-globin region. High diversity associated with the 5[variant prime] R/T identified two ancestral lineages that probably date back more than 2 million years. Within this genealogy, variation has been introduced into the 3[variant prime] R/T by gene conversion from other ancestral chromosomes. Diversity in δ-globin was found to lead through parts of the main genealogy but to coalesce in a more recent ancestor. The well-known recombination hotspot is clearly restricted to the region 3[variant prime] of δ-globin. Our analyses show that, whereas one common haplotype in a block of high LD represents a long segment from a single ancestral chromosome, others are mosaics of short segments from multiple ancestors related in genealogies of unsuspected complexity. |
doi_str_mv | 10.1007/s00439-003-0954-0 |
format | article |
fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_journals_215520308</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A791238686</galeid><sourcerecordid>A791238686</sourcerecordid><originalsourceid>FETCH-LOGICAL-g898-cd11f63e0fd96fb8706867320de03f9e47f89f5d0d78a8357089dc5b5d837f33</originalsourceid><addsrcrecordid>eNpVj8FKxDAQhoMouK4-gLegB_EQnTRNkxyXxdWFBWXXo1DSJqld2qY2rejbG1gPepoZ-Jj_-xG6pHBHAcR9AEiZIgCMgOIpgSM0oylLCE2AHaMZsBRIJqg4RWch7AEoVwmfobelb1vfYX6DSdX4ou7wdrV5we-6b_z43dsQ16Hw04A1DtPQD3Wouwo39tM22Dusu9KGcdANDvZjsvHCrQ-6LuvQnqMTp5tgL37nHO1WD6_LJ7J5flwvFxtSSSVJaSh1GbPgjMpcIQVkMhMsAWOBOWVT4aRy3IARUkvGBUhlSl5wI5lwjM3R1eFrP_hoEMZ8H3W7GJgnlPPYH2SErg9QpRub153z0bls61DmC6FowmQMjdTtP6r03Wi_xkpPIeTr3fYv-wPNsm1g</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>215520308</pqid></control><display><type>article</type><title>Common 5' -globin RFLP haplotypes harbour a surprising level of ancestral sequence mosaicism</title><source>Springer Nature</source><creator>Webster, Matthew T ; Clegg, John B ; Harding, Rosalind M</creator><creatorcontrib>Webster, Matthew T ; Clegg, John B ; Harding, Rosalind M</creatorcontrib><description>Blocks of linkage disequilibrium (LD) in the human genome represent segments of ancestral chromosomes. To investigate the relationship between LD and genealogy, we analysed diversity associated with restriction fragment length polymorphism (RFLP) haplotypes of the 5[variant prime] β-globin gene complex. Genealogical analyses were based on sequence alleles that spanned a 12.2-kb interval, covering 3.1 kb around the ψβ gene and 6.2 kb of the δ-globin gene and its 5[variant prime] flanking sequence known as the R/T region. Diversity was sampled from a Kenyan Luo population where recent malarial selection has contributed to substantial LD. A single common sequence allele spanning the 12.2-kb interval exclusively identified the ancestral chromosome bearing the "Bantu" βs (sickle-cell) RFLP haplotype. Other common 5[variant prime] RFLP haplotypes comprised interspersed segments from multiple ancestral chromosomes. Nucleotide diversity was similar between ψβ and R/T-δ-globin but was non-uniformly distributed within the R/T-δ-globin region. High diversity associated with the 5[variant prime] R/T identified two ancestral lineages that probably date back more than 2 million years. Within this genealogy, variation has been introduced into the 3[variant prime] R/T by gene conversion from other ancestral chromosomes. Diversity in δ-globin was found to lead through parts of the main genealogy but to coalesce in a more recent ancestor. The well-known recombination hotspot is clearly restricted to the region 3[variant prime] of δ-globin. Our analyses show that, whereas one common haplotype in a block of high LD represents a long segment from a single ancestral chromosome, others are mosaics of short segments from multiple ancestors related in genealogies of unsuspected complexity.</description><identifier>ISSN: 0340-6717</identifier><identifier>EISSN: 1432-1203</identifier><identifier>DOI: 10.1007/s00439-003-0954-0</identifier><language>eng</language><publisher>Heidelberg: Springer</publisher><subject>Analysis ; Ethylenediaminetetraacetic acid ; Genes ; Genetic aspects ; Genetic polymorphisms ; Genomes ; Genomics</subject><ispartof>Human genetics, 2003-07, Vol.113 (2), p.123</ispartof><rights>COPYRIGHT 2003 Springer</rights><rights>Springer-Verlag 2003</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Webster, Matthew T</creatorcontrib><creatorcontrib>Clegg, John B</creatorcontrib><creatorcontrib>Harding, Rosalind M</creatorcontrib><title>Common 5' -globin RFLP haplotypes harbour a surprising level of ancestral sequence mosaicism</title><title>Human genetics</title><description>Blocks of linkage disequilibrium (LD) in the human genome represent segments of ancestral chromosomes. To investigate the relationship between LD and genealogy, we analysed diversity associated with restriction fragment length polymorphism (RFLP) haplotypes of the 5[variant prime] β-globin gene complex. Genealogical analyses were based on sequence alleles that spanned a 12.2-kb interval, covering 3.1 kb around the ψβ gene and 6.2 kb of the δ-globin gene and its 5[variant prime] flanking sequence known as the R/T region. Diversity was sampled from a Kenyan Luo population where recent malarial selection has contributed to substantial LD. A single common sequence allele spanning the 12.2-kb interval exclusively identified the ancestral chromosome bearing the "Bantu" βs (sickle-cell) RFLP haplotype. Other common 5[variant prime] RFLP haplotypes comprised interspersed segments from multiple ancestral chromosomes. Nucleotide diversity was similar between ψβ and R/T-δ-globin but was non-uniformly distributed within the R/T-δ-globin region. High diversity associated with the 5[variant prime] R/T identified two ancestral lineages that probably date back more than 2 million years. Within this genealogy, variation has been introduced into the 3[variant prime] R/T by gene conversion from other ancestral chromosomes. Diversity in δ-globin was found to lead through parts of the main genealogy but to coalesce in a more recent ancestor. The well-known recombination hotspot is clearly restricted to the region 3[variant prime] of δ-globin. Our analyses show that, whereas one common haplotype in a block of high LD represents a long segment from a single ancestral chromosome, others are mosaics of short segments from multiple ancestors related in genealogies of unsuspected complexity.</description><subject>Analysis</subject><subject>Ethylenediaminetetraacetic acid</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genetic polymorphisms</subject><subject>Genomes</subject><subject>Genomics</subject><issn>0340-6717</issn><issn>1432-1203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNpVj8FKxDAQhoMouK4-gLegB_EQnTRNkxyXxdWFBWXXo1DSJqld2qY2rejbG1gPepoZ-Jj_-xG6pHBHAcR9AEiZIgCMgOIpgSM0oylLCE2AHaMZsBRIJqg4RWch7AEoVwmfobelb1vfYX6DSdX4ou7wdrV5we-6b_z43dsQ16Hw04A1DtPQD3Wouwo39tM22Dusu9KGcdANDvZjsvHCrQ-6LuvQnqMTp5tgL37nHO1WD6_LJ7J5flwvFxtSSSVJaSh1GbPgjMpcIQVkMhMsAWOBOWVT4aRy3IARUkvGBUhlSl5wI5lwjM3R1eFrP_hoEMZ8H3W7GJgnlPPYH2SErg9QpRub153z0bls61DmC6FowmQMjdTtP6r03Wi_xkpPIeTr3fYv-wPNsm1g</recordid><startdate>20030701</startdate><enddate>20030701</enddate><creator>Webster, Matthew T</creator><creator>Clegg, John B</creator><creator>Harding, Rosalind M</creator><general>Springer</general><general>Springer Nature B.V</general><scope>ISR</scope><scope>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope></search><sort><creationdate>20030701</creationdate><title>Common 5' -globin RFLP haplotypes harbour a surprising level of ancestral sequence mosaicism</title><author>Webster, Matthew T ; Clegg, John B ; Harding, Rosalind M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g898-cd11f63e0fd96fb8706867320de03f9e47f89f5d0d78a8357089dc5b5d837f33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Analysis</topic><topic>Ethylenediaminetetraacetic acid</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Genetic polymorphisms</topic><topic>Genomes</topic><topic>Genomics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Webster, Matthew T</creatorcontrib><creatorcontrib>Clegg, John B</creatorcontrib><creatorcontrib>Harding, Rosalind M</creatorcontrib><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><jtitle>Human genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Webster, Matthew T</au><au>Clegg, John B</au><au>Harding, Rosalind M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Common 5' -globin RFLP haplotypes harbour a surprising level of ancestral sequence mosaicism</atitle><jtitle>Human genetics</jtitle><date>2003-07-01</date><risdate>2003</risdate><volume>113</volume><issue>2</issue><spage>123</spage><pages>123-</pages><issn>0340-6717</issn><eissn>1432-1203</eissn><abstract>Blocks of linkage disequilibrium (LD) in the human genome represent segments of ancestral chromosomes. To investigate the relationship between LD and genealogy, we analysed diversity associated with restriction fragment length polymorphism (RFLP) haplotypes of the 5[variant prime] β-globin gene complex. Genealogical analyses were based on sequence alleles that spanned a 12.2-kb interval, covering 3.1 kb around the ψβ gene and 6.2 kb of the δ-globin gene and its 5[variant prime] flanking sequence known as the R/T region. Diversity was sampled from a Kenyan Luo population where recent malarial selection has contributed to substantial LD. A single common sequence allele spanning the 12.2-kb interval exclusively identified the ancestral chromosome bearing the "Bantu" βs (sickle-cell) RFLP haplotype. Other common 5[variant prime] RFLP haplotypes comprised interspersed segments from multiple ancestral chromosomes. Nucleotide diversity was similar between ψβ and R/T-δ-globin but was non-uniformly distributed within the R/T-δ-globin region. High diversity associated with the 5[variant prime] R/T identified two ancestral lineages that probably date back more than 2 million years. Within this genealogy, variation has been introduced into the 3[variant prime] R/T by gene conversion from other ancestral chromosomes. Diversity in δ-globin was found to lead through parts of the main genealogy but to coalesce in a more recent ancestor. The well-known recombination hotspot is clearly restricted to the region 3[variant prime] of δ-globin. Our analyses show that, whereas one common haplotype in a block of high LD represents a long segment from a single ancestral chromosome, others are mosaics of short segments from multiple ancestors related in genealogies of unsuspected complexity.</abstract><cop>Heidelberg</cop><pub>Springer</pub><doi>10.1007/s00439-003-0954-0</doi><tpages>17</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0340-6717 |
ispartof | Human genetics, 2003-07, Vol.113 (2), p.123 |
issn | 0340-6717 1432-1203 |
language | eng |
recordid | cdi_proquest_journals_215520308 |
source | Springer Nature |
subjects | Analysis Ethylenediaminetetraacetic acid Genes Genetic aspects Genetic polymorphisms Genomes Genomics |
title | Common 5' -globin RFLP haplotypes harbour a surprising level of ancestral sequence mosaicism |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T16%3A57%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Common%205'%20-globin%20RFLP%20haplotypes%20harbour%20a%20surprising%20level%20of%20ancestral%20sequence%20mosaicism&rft.jtitle=Human%20genetics&rft.au=Webster,%20Matthew%20T&rft.date=2003-07-01&rft.volume=113&rft.issue=2&rft.spage=123&rft.pages=123-&rft.issn=0340-6717&rft.eissn=1432-1203&rft_id=info:doi/10.1007/s00439-003-0954-0&rft_dat=%3Cgale_proqu%3EA791238686%3C/gale_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-g898-cd11f63e0fd96fb8706867320de03f9e47f89f5d0d78a8357089dc5b5d837f33%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=215520308&rft_id=info:pmid/&rft_galeid=A791238686&rfr_iscdi=true |