The Diversity Profile of TP53 Is Influenced by Positive Selection on the Immediately Upstream Locus WDR79
Background/Aim:TP53 is an efficient central node in a signal transduction network that responds to minimize cancer. However, over 50% of tumors show some mutation in TP53. Thus, one might argue that this single central node network lacks robustness. Therefore, we wanted to investigate if natural sel...
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Veröffentlicht in: | Human heredity 2010-01, Vol.69 (1), p.34-44 |
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creator | Alonso, Santos Izagirre, Neskuts López, Saioa Smith-Zubiaga, Isabel Hervella, Montse Boyano, María Dolores Arroyo-Berdugo, Yoana Gardeazabal, Jesús Díaz-Ramón, José Luís Díez, Ana Sánchez Careaga, Jesus María de la Rúa, Concepción |
description | Background/Aim:TP53 is an efficient central node in a signal transduction network that responds to minimize cancer. However, over 50% of tumors show some mutation in TP53. Thus, one might argue that this single central node network lacks robustness. Therefore, we wanted to investigate if natural selection has played a role in shaping the genomic region containing TP53. Methods: We have analyzed the HapMap data for evidence of selection using F ST pairwise comparisons and the extended haplotype homozygosity test on a 200-kb region encompassing TP53. We have also resequenced 4 kb upstream TP53 in Europeans (including melanoma patients), Asians, Australian Aborigines and Africans. Results: Genetic hitchhiking by a linked, positively selected allele at the nearby gene WDR79 may be partly responsible for the sequence diversity profile of TP53. It can help explain why the TP53 Arg72 allele is the major allele in Europeans even when the alternative allele, 72Pro, has been reported to offer an increased longevity after disease. Conclusions: Despite the important role of TP53, a complex interplay with other evolutionary forces, which are extrinsic to TP53 function, may have driven the genetic diversity pattern of this locus, and, as a consequence, its structure and function. |
doi_str_mv | 10.1159/000243152 |
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However, over 50% of tumors show some mutation in TP53. Thus, one might argue that this single central node network lacks robustness. Therefore, we wanted to investigate if natural selection has played a role in shaping the genomic region containing TP53. Methods: We have analyzed the HapMap data for evidence of selection using F ST pairwise comparisons and the extended haplotype homozygosity test on a 200-kb region encompassing TP53. We have also resequenced 4 kb upstream TP53 in Europeans (including melanoma patients), Asians, Australian Aborigines and Africans. Results: Genetic hitchhiking by a linked, positively selected allele at the nearby gene WDR79 may be partly responsible for the sequence diversity profile of TP53. It can help explain why the TP53 Arg72 allele is the major allele in Europeans even when the alternative allele, 72Pro, has been reported to offer an increased longevity after disease. Conclusions: Despite the important role of TP53, a complex interplay with other evolutionary forces, which are extrinsic to TP53 function, may have driven the genetic diversity pattern of this locus, and, as a consequence, its structure and function.</description><identifier>ISSN: 0001-5652</identifier><identifier>ISSN: 1423-0062</identifier><identifier>EISSN: 1423-0062</identifier><identifier>DOI: 10.1159/000243152</identifier><identifier>PMID: 19797907</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Alleles ; Asian People - genetics ; Black People - genetics ; Gene Frequency ; Genetic diversity ; Genetic Predisposition to Disease - ethnology ; Genetic Predisposition to Disease - genetics ; Genetic Variation ; Genomics ; Genotype ; Genotype & phenotype ; Haplotypes ; Humans ; Melanoma - ethnology ; Melanoma - genetics ; Molecular Chaperones ; Mutation ; Original Paper ; Polymorphism, Single Nucleotide ; Proteins - genetics ; Selection, Genetic ; Telomerase ; Tumor Suppressor Protein p53 - genetics ; White People - genetics</subject><ispartof>Human heredity, 2010-01, Vol.69 (1), p.34-44</ispartof><rights>2009 S. Karger AG</rights><rights>2009 S. Karger AG, Basel</rights><rights>Copyright 2009 S. Karger AG, Basel.</rights><rights>Copyright (c) 2009 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-2b4b94d55ab119d6d7d201f8a061b75b9ead11802173ed1272aaf1c94797e26d3</citedby><cites>FETCH-LOGICAL-c448t-2b4b94d55ab119d6d7d201f8a061b75b9ead11802173ed1272aaf1c94797e26d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/48506838$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/48506838$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,799,2423,27901,27902,57992,58225</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19797907$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Alonso, Santos</creatorcontrib><creatorcontrib>Izagirre, Neskuts</creatorcontrib><creatorcontrib>López, Saioa</creatorcontrib><creatorcontrib>Smith-Zubiaga, Isabel</creatorcontrib><creatorcontrib>Hervella, Montse</creatorcontrib><creatorcontrib>Boyano, María Dolores</creatorcontrib><creatorcontrib>Arroyo-Berdugo, Yoana</creatorcontrib><creatorcontrib>Gardeazabal, Jesús</creatorcontrib><creatorcontrib>Díaz-Ramón, José Luís</creatorcontrib><creatorcontrib>Díez, Ana Sánchez</creatorcontrib><creatorcontrib>Careaga, Jesus María</creatorcontrib><creatorcontrib>de la Rúa, Concepción</creatorcontrib><title>The Diversity Profile of TP53 Is Influenced by Positive Selection on the Immediately Upstream Locus WDR79</title><title>Human heredity</title><addtitle>Hum Hered</addtitle><description>Background/Aim:TP53 is an efficient central node in a signal transduction network that responds to minimize cancer. However, over 50% of tumors show some mutation in TP53. Thus, one might argue that this single central node network lacks robustness. Therefore, we wanted to investigate if natural selection has played a role in shaping the genomic region containing TP53. Methods: We have analyzed the HapMap data for evidence of selection using F ST pairwise comparisons and the extended haplotype homozygosity test on a 200-kb region encompassing TP53. We have also resequenced 4 kb upstream TP53 in Europeans (including melanoma patients), Asians, Australian Aborigines and Africans. Results: Genetic hitchhiking by a linked, positively selected allele at the nearby gene WDR79 may be partly responsible for the sequence diversity profile of TP53. It can help explain why the TP53 Arg72 allele is the major allele in Europeans even when the alternative allele, 72Pro, has been reported to offer an increased longevity after disease. Conclusions: Despite the important role of TP53, a complex interplay with other evolutionary forces, which are extrinsic to TP53 function, may have driven the genetic diversity pattern of this locus, and, as a consequence, its structure and function.</description><subject>Alleles</subject><subject>Asian People - genetics</subject><subject>Black People - genetics</subject><subject>Gene Frequency</subject><subject>Genetic diversity</subject><subject>Genetic Predisposition to Disease - ethnology</subject><subject>Genetic Predisposition to Disease - genetics</subject><subject>Genetic Variation</subject><subject>Genomics</subject><subject>Genotype</subject><subject>Genotype & phenotype</subject><subject>Haplotypes</subject><subject>Humans</subject><subject>Melanoma - ethnology</subject><subject>Melanoma - genetics</subject><subject>Molecular Chaperones</subject><subject>Mutation</subject><subject>Original Paper</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Proteins - genetics</subject><subject>Selection, Genetic</subject><subject>Telomerase</subject><subject>Tumor Suppressor Protein p53 - genetics</subject><subject>White People - genetics</subject><issn>0001-5652</issn><issn>1423-0062</issn><issn>1423-0062</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp90VGL1DAQAOAgirfe-eC7SlBQ7qGaSZqmfZS783ZhwUP38LGkzVS7ts1e0gr77x3psgdymARCki8DM8PYCxAfAHTxUQghUwVaPmILSKVKhMjkY7age0h0puUJexbjlo65MOopO4HC0BRmwdrNT-SX7W8MsR33_Cb4pu2Q-4ZvbrTiq8hXQ9NNONToeEXAkyPOv2GH9dj6gdMaKciq79G1dsRuz293cQxoe7729RT598uvpjhjTxrbRXx-2E_Z7eerzcUyWX-5Xl18Wid1muZjIqu0KlKnta0ACpc546SAJrcig8roqkDrAHIhwSh0II20toG6SCkjlJlTp-z9HHcX_N2EcSz7NtbYdXZAP8XSqBRkRmUj-e6_UoKEXOaC4Jt_4NZPYaAsSkmjUJmUhM5nVAcfY8Cm3IW2t2Ffgij_tqk8tons60PAqaKq3ctDXwi8nMEvG35gOILj_7cPPi-XV7Mod64h9WpW2zj6e5TmWmS5ytUfTqGobQ</recordid><startdate>20100101</startdate><enddate>20100101</enddate><creator>Alonso, Santos</creator><creator>Izagirre, Neskuts</creator><creator>López, Saioa</creator><creator>Smith-Zubiaga, Isabel</creator><creator>Hervella, Montse</creator><creator>Boyano, María Dolores</creator><creator>Arroyo-Berdugo, Yoana</creator><creator>Gardeazabal, Jesús</creator><creator>Díaz-Ramón, José Luís</creator><creator>Díez, Ana Sánchez</creator><creator>Careaga, Jesus María</creator><creator>de la Rúa, Concepción</creator><general>S. 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genetics</topic><topic>Black People - genetics</topic><topic>Gene Frequency</topic><topic>Genetic diversity</topic><topic>Genetic Predisposition to Disease - ethnology</topic><topic>Genetic Predisposition to Disease - genetics</topic><topic>Genetic Variation</topic><topic>Genomics</topic><topic>Genotype</topic><topic>Genotype & phenotype</topic><topic>Haplotypes</topic><topic>Humans</topic><topic>Melanoma - ethnology</topic><topic>Melanoma - genetics</topic><topic>Molecular Chaperones</topic><topic>Mutation</topic><topic>Original Paper</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Proteins - genetics</topic><topic>Selection, Genetic</topic><topic>Telomerase</topic><topic>Tumor Suppressor Protein p53 - genetics</topic><topic>White People - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alonso, Santos</creatorcontrib><creatorcontrib>Izagirre, Neskuts</creatorcontrib><creatorcontrib>López, Saioa</creatorcontrib><creatorcontrib>Smith-Zubiaga, Isabel</creatorcontrib><creatorcontrib>Hervella, Montse</creatorcontrib><creatorcontrib>Boyano, María Dolores</creatorcontrib><creatorcontrib>Arroyo-Berdugo, Yoana</creatorcontrib><creatorcontrib>Gardeazabal, Jesús</creatorcontrib><creatorcontrib>Díaz-Ramón, José Luís</creatorcontrib><creatorcontrib>Díez, Ana Sánchez</creatorcontrib><creatorcontrib>Careaga, Jesus María</creatorcontrib><creatorcontrib>de la Rúa, Concepción</creatorcontrib><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>Science 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>Research Library (Alumni Edition)</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 (ProQuest)</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>Research Library Prep</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>Research Library</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</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>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Human heredity</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alonso, Santos</au><au>Izagirre, Neskuts</au><au>López, Saioa</au><au>Smith-Zubiaga, Isabel</au><au>Hervella, Montse</au><au>Boyano, María Dolores</au><au>Arroyo-Berdugo, Yoana</au><au>Gardeazabal, Jesús</au><au>Díaz-Ramón, José Luís</au><au>Díez, Ana Sánchez</au><au>Careaga, Jesus María</au><au>de la Rúa, Concepción</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Diversity Profile of TP53 Is Influenced by Positive Selection on the Immediately Upstream Locus WDR79</atitle><jtitle>Human heredity</jtitle><addtitle>Hum Hered</addtitle><date>2010-01-01</date><risdate>2010</risdate><volume>69</volume><issue>1</issue><spage>34</spage><epage>44</epage><pages>34-44</pages><issn>0001-5652</issn><issn>1423-0062</issn><eissn>1423-0062</eissn><abstract>Background/Aim:TP53 is an efficient central node in a signal transduction network that responds to minimize cancer. However, over 50% of tumors show some mutation in TP53. Thus, one might argue that this single central node network lacks robustness. Therefore, we wanted to investigate if natural selection has played a role in shaping the genomic region containing TP53. Methods: We have analyzed the HapMap data for evidence of selection using F ST pairwise comparisons and the extended haplotype homozygosity test on a 200-kb region encompassing TP53. We have also resequenced 4 kb upstream TP53 in Europeans (including melanoma patients), Asians, Australian Aborigines and Africans. Results: Genetic hitchhiking by a linked, positively selected allele at the nearby gene WDR79 may be partly responsible for the sequence diversity profile of TP53. It can help explain why the TP53 Arg72 allele is the major allele in Europeans even when the alternative allele, 72Pro, has been reported to offer an increased longevity after disease. Conclusions: Despite the important role of TP53, a complex interplay with other evolutionary forces, which are extrinsic to TP53 function, may have driven the genetic diversity pattern of this locus, and, as a consequence, its structure and function.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>19797907</pmid><doi>10.1159/000243152</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alleles Asian People - genetics Black People - genetics Gene Frequency Genetic diversity Genetic Predisposition to Disease - ethnology Genetic Predisposition to Disease - genetics Genetic Variation Genomics Genotype Genotype & phenotype Haplotypes Humans Melanoma - ethnology Melanoma - genetics Molecular Chaperones Mutation Original Paper Polymorphism, Single Nucleotide Proteins - genetics Selection, Genetic Telomerase Tumor Suppressor Protein p53 - genetics White People - genetics |
title | The Diversity Profile of TP53 Is Influenced by Positive Selection on the Immediately Upstream Locus WDR79 |
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