Apparent intrachromosomal exchange on the human Y chromosome explained by population history
The human Y chromosome displays an unusual content of repetitive sequences. Y-chromosomal repeats are potential targets for intrachromosomal recombination, which is thought to be involved in a number of Y-associated defects, such as male infertility. Such rearrangements could potentially be investig...
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Veröffentlicht in: | European journal of human genetics : EJHG 2003-04, Vol.11 (4), p.304-314 |
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creator | Kittler, Ralf Erler, Axel Brauer, Silke Stoneking, Mark Kayser, Manfred |
description | The human Y chromosome displays an unusual content of repetitive sequences. Y-chromosomal repeats are potential targets for intrachromosomal recombination, which is thought to be involved in a number of Y-associated defects, such as male infertility. Such rearrangements could potentially be investigated by the use of highly polymorphic DNA markers located within the repeat units, such as microsatellites. Here we analyse the two copies of the Y-chromosomal microsatellite DYS385, which we identified and localized to an ∼190 kb duplicated and inverted fragment at Yq11.223. We found a highly significant correlation (
r
=0.853,
P
0.05) between the allele frequency distributions at both copies of the Y-STR in a German population sample (
n
=70). Such nearly identical allele frequency distribution between two copies of a duplicated highly polymorphic microsatellite cannot be explained by the independent mutational process that creates microsatellite alleles. Instead, this might be interpreted as evidence for a reciprocal intrachromosomal exchange process between the duplicated fragments. However, more detailed analyses using additional human populations as well as additional Y chromosome markers revealed that this phenomenon is highly population-specific and disappears completely when Y-STR diversity is analysed in association with two Y-SNP haplogroups. We found that the diversity of the two DYS385 loci (and other Y-STRs) is highly depending on the haplogroup background, and that equal proportions of both haplogroups in the German sample explains the nearly identical allele frequency distributions at the two DYS385 loci. Thus, we demonstrate here that allele frequency distributions at duplicate loci that are suggestive of intrachromosomal recombination can be explained solely by population history. |
doi_str_mv | 10.1038/sj.ejhg.5200960 |
format | Article |
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r
=0.853,
P
<0.001) and a nonsignificant difference in a
χ
2
-test (
χ
2
=15.45,
P
>0.05) between the allele frequency distributions at both copies of the Y-STR in a German population sample (
n
=70). Such nearly identical allele frequency distribution between two copies of a duplicated highly polymorphic microsatellite cannot be explained by the independent mutational process that creates microsatellite alleles. Instead, this might be interpreted as evidence for a reciprocal intrachromosomal exchange process between the duplicated fragments. However, more detailed analyses using additional human populations as well as additional Y chromosome markers revealed that this phenomenon is highly population-specific and disappears completely when Y-STR diversity is analysed in association with two Y-SNP haplogroups. We found that the diversity of the two DYS385 loci (and other Y-STRs) is highly depending on the haplogroup background, and that equal proportions of both haplogroups in the German sample explains the nearly identical allele frequency distributions at the two DYS385 loci. Thus, we demonstrate here that allele frequency distributions at duplicate loci that are suggestive of intrachromosomal recombination can be explained solely by population history.</description><identifier>ISSN: 1018-4813</identifier><identifier>EISSN: 1476-5438</identifier><identifier>DOI: 10.1038/sj.ejhg.5200960</identifier><identifier>PMID: 12700604</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Bioinformatics ; Biological and medical sciences ; Biomedical and Life Sciences ; Biomedicine ; Chromosome Mapping ; Chromosomes, Human, Y - genetics ; Cytogenetics ; DNA Primers ; Gene Expression ; Gene Frequency ; General aspects. Genetic counseling ; Genetic Variation ; Genetics, Population ; Germany ; Human Genetics ; Humans ; Medical genetics ; Medical sciences ; Microsatellite Repeats ; Polymorphism, Single Nucleotide ; Recombination, Genetic - genetics ; Repetitive Sequences, Nucleic Acid - genetics</subject><ispartof>European journal of human genetics : EJHG, 2003-04, Vol.11 (4), p.304-314</ispartof><rights>Springer Nature Switzerland AG 2003</rights><rights>2003 INIST-CNRS</rights><rights>Copyright Nature Publishing Group Apr 2003</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c529t-7eb7cd3e09c86ec353496e30043a9e19d6a273a9bdbf8b2632cea568b51d54103</citedby><cites>FETCH-LOGICAL-c529t-7eb7cd3e09c86ec353496e30043a9e19d6a273a9bdbf8b2632cea568b51d54103</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/sj.ejhg.5200960$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/sj.ejhg.5200960$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14710918$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12700604$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kittler, Ralf</creatorcontrib><creatorcontrib>Erler, Axel</creatorcontrib><creatorcontrib>Brauer, Silke</creatorcontrib><creatorcontrib>Stoneking, Mark</creatorcontrib><creatorcontrib>Kayser, Manfred</creatorcontrib><title>Apparent intrachromosomal exchange on the human Y chromosome explained by population history</title><title>European journal of human genetics : EJHG</title><addtitle>Eur J Hum Genet</addtitle><addtitle>Eur J Hum Genet</addtitle><description>The human Y chromosome displays an unusual content of repetitive sequences. Y-chromosomal repeats are potential targets for intrachromosomal recombination, which is thought to be involved in a number of Y-associated defects, such as male infertility. Such rearrangements could potentially be investigated by the use of highly polymorphic DNA markers located within the repeat units, such as microsatellites. Here we analyse the two copies of the Y-chromosomal microsatellite DYS385, which we identified and localized to an ∼190 kb duplicated and inverted fragment at Yq11.223. We found a highly significant correlation (
r
=0.853,
P
<0.001) and a nonsignificant difference in a
χ
2
-test (
χ
2
=15.45,
P
>0.05) between the allele frequency distributions at both copies of the Y-STR in a German population sample (
n
=70). Such nearly identical allele frequency distribution between two copies of a duplicated highly polymorphic microsatellite cannot be explained by the independent mutational process that creates microsatellite alleles. Instead, this might be interpreted as evidence for a reciprocal intrachromosomal exchange process between the duplicated fragments. However, more detailed analyses using additional human populations as well as additional Y chromosome markers revealed that this phenomenon is highly population-specific and disappears completely when Y-STR diversity is analysed in association with two Y-SNP haplogroups. We found that the diversity of the two DYS385 loci (and other Y-STRs) is highly depending on the haplogroup background, and that equal proportions of both haplogroups in the German sample explains the nearly identical allele frequency distributions at the two DYS385 loci. Thus, we demonstrate here that allele frequency distributions at duplicate loci that are suggestive of intrachromosomal recombination can be explained solely by population history.</description><subject>Bioinformatics</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Chromosome Mapping</subject><subject>Chromosomes, Human, Y - genetics</subject><subject>Cytogenetics</subject><subject>DNA Primers</subject><subject>Gene Expression</subject><subject>Gene Frequency</subject><subject>General aspects. Genetic counseling</subject><subject>Genetic Variation</subject><subject>Genetics, Population</subject><subject>Germany</subject><subject>Human Genetics</subject><subject>Humans</subject><subject>Medical genetics</subject><subject>Medical sciences</subject><subject>Microsatellite Repeats</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Recombination, Genetic - genetics</subject><subject>Repetitive Sequences, Nucleic Acid - genetics</subject><issn>1018-4813</issn><issn>1476-5438</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqF0cuL1TAUB-AgivPQtTsJgrPrnZOkTdLlMPiCATe6EISQpudOW9qkJi3M_e_N5RYvCOIqB86Xk8ePkDcMdgyEvk3DDofucVdxgFrCM3LJSiWLqhT6ea6B6aLUTFyQq5QGgNxU7CW5YFwBSCgvyc-7ebYR_UJ7v0TruhimkMJkR4pPrrP-EWnwdOmQdutkPf1B_xjMZB5t77GlzYHOYV5Hu_SZd31aQjy8Ii_2dkz4eluvyfePH77dfy4evn76cn_3ULiK10uhsFGuFQi10xKdqERZSxQApbA1srqVlqtcNm2z1w2Xgju0ldRNxdqqzP9wTW5Oc-cYfq2YFjP1yeE4Wo9hTUYJzjjLc_8HmdZ1pWuR4bu_4BDW6PMjDGdKSwHyiG5PyMWQUsS9mWM_2XgwDMwxHpMGc4zHbPHkHW-3sWszYXv2Wx4ZvN-ATc6O-2i969PZlYpBzXR2cHIpt3JG8Xy_f539G8ZIqew</recordid><startdate>20030401</startdate><enddate>20030401</enddate><creator>Kittler, Ralf</creator><creator>Erler, Axel</creator><creator>Brauer, Silke</creator><creator>Stoneking, Mark</creator><creator>Kayser, Manfred</creator><general>Springer International Publishing</general><general>Nature Publishing</general><general>Nature Publishing Group</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</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>RC3</scope><scope>7X8</scope></search><sort><creationdate>20030401</creationdate><title>Apparent intrachromosomal exchange on the human Y chromosome explained by population history</title><author>Kittler, Ralf ; Erler, Axel ; Brauer, Silke ; Stoneking, Mark ; Kayser, Manfred</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c529t-7eb7cd3e09c86ec353496e30043a9e19d6a273a9bdbf8b2632cea568b51d54103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Bioinformatics</topic><topic>Biological and medical sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Chromosome Mapping</topic><topic>Chromosomes, Human, Y - genetics</topic><topic>Cytogenetics</topic><topic>DNA Primers</topic><topic>Gene Expression</topic><topic>Gene Frequency</topic><topic>General aspects. Genetic counseling</topic><topic>Genetic Variation</topic><topic>Genetics, Population</topic><topic>Germany</topic><topic>Human Genetics</topic><topic>Humans</topic><topic>Medical genetics</topic><topic>Medical sciences</topic><topic>Microsatellite Repeats</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Recombination, Genetic - genetics</topic><topic>Repetitive Sequences, Nucleic Acid - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kittler, Ralf</creatorcontrib><creatorcontrib>Erler, Axel</creatorcontrib><creatorcontrib>Brauer, Silke</creatorcontrib><creatorcontrib>Stoneking, Mark</creatorcontrib><creatorcontrib>Kayser, Manfred</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</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>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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</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>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of human genetics : EJHG</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kittler, Ralf</au><au>Erler, Axel</au><au>Brauer, Silke</au><au>Stoneking, Mark</au><au>Kayser, Manfred</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Apparent intrachromosomal exchange on the human Y chromosome explained by population history</atitle><jtitle>European journal of human genetics : EJHG</jtitle><stitle>Eur J Hum Genet</stitle><addtitle>Eur J Hum Genet</addtitle><date>2003-04-01</date><risdate>2003</risdate><volume>11</volume><issue>4</issue><spage>304</spage><epage>314</epage><pages>304-314</pages><issn>1018-4813</issn><eissn>1476-5438</eissn><abstract>The human Y chromosome displays an unusual content of repetitive sequences. Y-chromosomal repeats are potential targets for intrachromosomal recombination, which is thought to be involved in a number of Y-associated defects, such as male infertility. Such rearrangements could potentially be investigated by the use of highly polymorphic DNA markers located within the repeat units, such as microsatellites. Here we analyse the two copies of the Y-chromosomal microsatellite DYS385, which we identified and localized to an ∼190 kb duplicated and inverted fragment at Yq11.223. We found a highly significant correlation (
r
=0.853,
P
<0.001) and a nonsignificant difference in a
χ
2
-test (
χ
2
=15.45,
P
>0.05) between the allele frequency distributions at both copies of the Y-STR in a German population sample (
n
=70). Such nearly identical allele frequency distribution between two copies of a duplicated highly polymorphic microsatellite cannot be explained by the independent mutational process that creates microsatellite alleles. Instead, this might be interpreted as evidence for a reciprocal intrachromosomal exchange process between the duplicated fragments. However, more detailed analyses using additional human populations as well as additional Y chromosome markers revealed that this phenomenon is highly population-specific and disappears completely when Y-STR diversity is analysed in association with two Y-SNP haplogroups. We found that the diversity of the two DYS385 loci (and other Y-STRs) is highly depending on the haplogroup background, and that equal proportions of both haplogroups in the German sample explains the nearly identical allele frequency distributions at the two DYS385 loci. Thus, we demonstrate here that allele frequency distributions at duplicate loci that are suggestive of intrachromosomal recombination can be explained solely by population history.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>12700604</pmid><doi>10.1038/sj.ejhg.5200960</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Bioinformatics Biological and medical sciences Biomedical and Life Sciences Biomedicine Chromosome Mapping Chromosomes, Human, Y - genetics Cytogenetics DNA Primers Gene Expression Gene Frequency General aspects. Genetic counseling Genetic Variation Genetics, Population Germany Human Genetics Humans Medical genetics Medical sciences Microsatellite Repeats Polymorphism, Single Nucleotide Recombination, Genetic - genetics Repetitive Sequences, Nucleic Acid - genetics |
title | Apparent intrachromosomal exchange on the human Y chromosome explained by population history |
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