Fixation dynamics of beneficial alleles in prokaryotic polyploid chromosomes and plasmids
Abstract Theoretical population genetics has been mostly developed for sexually reproducing diploid and for monoploid (haploid) organisms, focusing on eukaryotes. The evolution of bacteria and archaea is often studied by models for the allele dynamics in monoploid populations. However, many prokaryo...
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Veröffentlicht in: | Genetics (Austin) 2022-09, Vol.222 (2) |
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creator | Santer, Mario Kupczok, Anne Dagan, Tal Uecker, Hildegard |
description | Abstract
Theoretical population genetics has been mostly developed for sexually reproducing diploid and for monoploid (haploid) organisms, focusing on eukaryotes. The evolution of bacteria and archaea is often studied by models for the allele dynamics in monoploid populations. However, many prokaryotic organisms harbor multicopy replicons—chromosomes and plasmids—and theory for the allele dynamics in populations of polyploid prokaryotes remains lacking. Here, we present a population genetics model for replicons with multiple copies in the cell. Using this model, we characterize the fixation process of a dominant beneficial mutation at 2 levels: the phenotype and the genotype. Our results show that depending on the mode of replication and segregation, the fixation of the mutant phenotype may precede genotypic fixation by many generations; we term this time interval the heterozygosity window. We furthermore derive concise analytical expressions for the occurrence and length of the heterozygosity window, showing that it emerges if the copy number is high and selection strong. Within the heterozygosity window, the population is phenotypically adapted, while both alleles persist in the population. Replicon ploidy thus allows for the maintenance of genetic variation following phenotypic adaptation and consequently for reversibility in adaptation to fluctuating environmental conditions. |
doi_str_mv | 10.1093/genetics/iyac121 |
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Theoretical population genetics has been mostly developed for sexually reproducing diploid and for monoploid (haploid) organisms, focusing on eukaryotes. The evolution of bacteria and archaea is often studied by models for the allele dynamics in monoploid populations. However, many prokaryotic organisms harbor multicopy replicons—chromosomes and plasmids—and theory for the allele dynamics in populations of polyploid prokaryotes remains lacking. Here, we present a population genetics model for replicons with multiple copies in the cell. Using this model, we characterize the fixation process of a dominant beneficial mutation at 2 levels: the phenotype and the genotype. Our results show that depending on the mode of replication and segregation, the fixation of the mutant phenotype may precede genotypic fixation by many generations; we term this time interval the heterozygosity window. We furthermore derive concise analytical expressions for the occurrence and length of the heterozygosity window, showing that it emerges if the copy number is high and selection strong. Within the heterozygosity window, the population is phenotypically adapted, while both alleles persist in the population. Replicon ploidy thus allows for the maintenance of genetic variation following phenotypic adaptation and consequently for reversibility in adaptation to fluctuating environmental conditions.</description><identifier>ISSN: 1943-2631</identifier><identifier>ISSN: 0016-6731</identifier><identifier>EISSN: 1943-2631</identifier><identifier>DOI: 10.1093/genetics/iyac121</identifier><identifier>PMID: 35959975</identifier><language>eng</language><publisher>Bethesda: Oxford University Press</publisher><subject>Adaptation ; Alleles ; Archaea ; Chromosomes ; Copy number ; Diploids ; Environmental conditions ; Eukaryotes ; Fixation ; Genetic diversity ; Genetics ; Genotypes ; Heterozygosity ; Investigation ; Mathematical analysis ; Mutation ; Phenotypes ; Phenotypic variations ; Plasmids ; Ploidy ; Polyploidy ; Population genetics ; Populations ; Prokaryotes ; Reproduction (biology)</subject><ispartof>Genetics (Austin), 2022-09, Vol.222 (2)</ispartof><rights>The Author(s) 2022. Published by Oxford University Press on behalf of Genetics Society of America. 2022</rights><rights>The Author(s) 2022. Published by Oxford University Press on behalf of Genetics Society of America.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c367t-dba5aa89654d5d322e5e9e70a290b7bd31f6c096fdefb9c97b6032526bf04df3</citedby><cites>FETCH-LOGICAL-c367t-dba5aa89654d5d322e5e9e70a290b7bd31f6c096fdefb9c97b6032526bf04df3</cites><orcidid>0000-0001-5237-1899 ; 0000-0002-9042-192X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,1578,27901,27902</link.rule.ids></links><search><contributor>Weinreich, D</contributor><creatorcontrib>Santer, Mario</creatorcontrib><creatorcontrib>Kupczok, Anne</creatorcontrib><creatorcontrib>Dagan, Tal</creatorcontrib><creatorcontrib>Uecker, Hildegard</creatorcontrib><title>Fixation dynamics of beneficial alleles in prokaryotic polyploid chromosomes and plasmids</title><title>Genetics (Austin)</title><description>Abstract
Theoretical population genetics has been mostly developed for sexually reproducing diploid and for monoploid (haploid) organisms, focusing on eukaryotes. The evolution of bacteria and archaea is often studied by models for the allele dynamics in monoploid populations. However, many prokaryotic organisms harbor multicopy replicons—chromosomes and plasmids—and theory for the allele dynamics in populations of polyploid prokaryotes remains lacking. Here, we present a population genetics model for replicons with multiple copies in the cell. Using this model, we characterize the fixation process of a dominant beneficial mutation at 2 levels: the phenotype and the genotype. Our results show that depending on the mode of replication and segregation, the fixation of the mutant phenotype may precede genotypic fixation by many generations; we term this time interval the heterozygosity window. We furthermore derive concise analytical expressions for the occurrence and length of the heterozygosity window, showing that it emerges if the copy number is high and selection strong. Within the heterozygosity window, the population is phenotypically adapted, while both alleles persist in the population. Replicon ploidy thus allows for the maintenance of genetic variation following phenotypic adaptation and consequently for reversibility in adaptation to fluctuating environmental conditions.</description><subject>Adaptation</subject><subject>Alleles</subject><subject>Archaea</subject><subject>Chromosomes</subject><subject>Copy number</subject><subject>Diploids</subject><subject>Environmental conditions</subject><subject>Eukaryotes</subject><subject>Fixation</subject><subject>Genetic diversity</subject><subject>Genetics</subject><subject>Genotypes</subject><subject>Heterozygosity</subject><subject>Investigation</subject><subject>Mathematical analysis</subject><subject>Mutation</subject><subject>Phenotypes</subject><subject>Phenotypic variations</subject><subject>Plasmids</subject><subject>Ploidy</subject><subject>Polyploidy</subject><subject>Population genetics</subject><subject>Populations</subject><subject>Prokaryotes</subject><subject>Reproduction (biology)</subject><issn>1943-2631</issn><issn>0016-6731</issn><issn>1943-2631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><recordid>eNqFkbtLBDEQh4MovnvLgI0gp3lsdi-NIIcvEGyusQrZPDSaTdZkV7z_3hx3itpYZSDffDPDD4AjjM4w4vT8yQQzOJXP3UIqTPAG2MW8ohNSU7z5o94Bezm_IIRqzqbbYIcyzjhv2C54vHYfcnAxQL0IsisuGC1si9c65aSH0nvjTYYuwD7FV5kWsUyEffSL3kenoXpOsYs5dgWSQcPey9w5nQ_AlpU-m8P1uw_m11fz2e3k_uHmbnZ5P1G0boaJbiWTcsprVmmmKSGGGW4aJAlHbdNqim2tEK-tNrblijdtjShhpG4tqrSl--Bipe3HtjNamTAk6UWfXFd2FVE68fsnuGfxFN8FLw7UkCI4WQtSfBtNHkTnsjLey2DimAVpEMFTgmlV0OM_6EscUyjXFYpQhKqGLYVoRakUc07Gfi-DkVjGJr5iE-vYSsvpqiWO_f_0J0Xlnuc</recordid><startdate>20220930</startdate><enddate>20220930</enddate><creator>Santer, Mario</creator><creator>Kupczok, Anne</creator><creator>Dagan, Tal</creator><creator>Uecker, Hildegard</creator><general>Oxford University Press</general><general>Genetics Society of America</general><scope>TOX</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>4T-</scope><scope>4U-</scope><scope>7QP</scope><scope>7SS</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-5237-1899</orcidid><orcidid>https://orcid.org/0000-0002-9042-192X</orcidid></search><sort><creationdate>20220930</creationdate><title>Fixation dynamics of beneficial alleles in prokaryotic polyploid chromosomes and plasmids</title><author>Santer, Mario ; Kupczok, Anne ; Dagan, Tal ; Uecker, Hildegard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c367t-dba5aa89654d5d322e5e9e70a290b7bd31f6c096fdefb9c97b6032526bf04df3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adaptation</topic><topic>Alleles</topic><topic>Archaea</topic><topic>Chromosomes</topic><topic>Copy number</topic><topic>Diploids</topic><topic>Environmental conditions</topic><topic>Eukaryotes</topic><topic>Fixation</topic><topic>Genetic diversity</topic><topic>Genetics</topic><topic>Genotypes</topic><topic>Heterozygosity</topic><topic>Investigation</topic><topic>Mathematical analysis</topic><topic>Mutation</topic><topic>Phenotypes</topic><topic>Phenotypic variations</topic><topic>Plasmids</topic><topic>Ploidy</topic><topic>Polyploidy</topic><topic>Population genetics</topic><topic>Populations</topic><topic>Prokaryotes</topic><topic>Reproduction (biology)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Santer, Mario</creatorcontrib><creatorcontrib>Kupczok, Anne</creatorcontrib><creatorcontrib>Dagan, Tal</creatorcontrib><creatorcontrib>Uecker, Hildegard</creatorcontrib><collection>Oxford Journals Open Access Collection</collection><collection>CrossRef</collection><collection>Docstoc</collection><collection>University Readers</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Genetics (Austin)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Santer, Mario</au><au>Kupczok, Anne</au><au>Dagan, Tal</au><au>Uecker, Hildegard</au><au>Weinreich, D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fixation dynamics of beneficial alleles in prokaryotic polyploid chromosomes and plasmids</atitle><jtitle>Genetics (Austin)</jtitle><date>2022-09-30</date><risdate>2022</risdate><volume>222</volume><issue>2</issue><issn>1943-2631</issn><issn>0016-6731</issn><eissn>1943-2631</eissn><abstract>Abstract
Theoretical population genetics has been mostly developed for sexually reproducing diploid and for monoploid (haploid) organisms, focusing on eukaryotes. The evolution of bacteria and archaea is often studied by models for the allele dynamics in monoploid populations. However, many prokaryotic organisms harbor multicopy replicons—chromosomes and plasmids—and theory for the allele dynamics in populations of polyploid prokaryotes remains lacking. Here, we present a population genetics model for replicons with multiple copies in the cell. Using this model, we characterize the fixation process of a dominant beneficial mutation at 2 levels: the phenotype and the genotype. Our results show that depending on the mode of replication and segregation, the fixation of the mutant phenotype may precede genotypic fixation by many generations; we term this time interval the heterozygosity window. We furthermore derive concise analytical expressions for the occurrence and length of the heterozygosity window, showing that it emerges if the copy number is high and selection strong. Within the heterozygosity window, the population is phenotypically adapted, while both alleles persist in the population. Replicon ploidy thus allows for the maintenance of genetic variation following phenotypic adaptation and consequently for reversibility in adaptation to fluctuating environmental conditions.</abstract><cop>Bethesda</cop><pub>Oxford University Press</pub><pmid>35959975</pmid><doi>10.1093/genetics/iyac121</doi><orcidid>https://orcid.org/0000-0001-5237-1899</orcidid><orcidid>https://orcid.org/0000-0002-9042-192X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adaptation Alleles Archaea Chromosomes Copy number Diploids Environmental conditions Eukaryotes Fixation Genetic diversity Genetics Genotypes Heterozygosity Investigation Mathematical analysis Mutation Phenotypes Phenotypic variations Plasmids Ploidy Polyploidy Population genetics Populations Prokaryotes Reproduction (biology) |
title | Fixation dynamics of beneficial alleles in prokaryotic polyploid chromosomes and plasmids |
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