Theoretical population genetics of mating-type linked haplo-lethal alleles
The anther-smut fungus Ustilago violacea normally produces haploid sporidia of two mating types, and conjugation between them is thought to be a prerequisite for infection of the host plant Silene alba. However, some natural populations contain high frequencies of individuals with mating-type bias,...
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Veröffentlicht in: | International journal of plant sciences 1998-03, Vol.159 (2), p.192-198 |
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description | The anther-smut fungus Ustilago violacea normally produces haploid sporidia of two mating types, and conjugation between them is thought to be a prerequisite for infection of the host plant Silene alba. However, some natural populations contain high frequencies of individuals with mating-type bias, from which sporidia of only one mating type, usually A1, can be isolated. Such populations show no reduction in fungal transmission rate. The bias is most readily interpreted as caused by the presence of deleterious recessive alleles, "haplo-lethals," that are linked to mating type. Haplo-lethals may persist in a heterozygous state if, during teliospore germination, there is premature conjugation among the immediate products of meiosis, i.e., intratetrad selfing, whereby the free-living haploid stage is bypassed We develop a theoretical model that shows how such alleles may spread if they provide a compensatory advantage in the diploid or dikaryotic phase, for example, through increased disease transmission. There is a limited range of conditions under which such haplo-lethal alleles may be maintained in a stable polymorphism, but if intratetrad selfing is high and/or they have substantial advantage in the dikaryotic phase, haplo-lethal alleles linked to mating type can spread to fixation. The occurrence of populations with a high degree of mating-type bias is therefore readily explained. Haplo-lethal alleles unlinked to mating type are much less likely to spread. In U violacea, mating type shows first-division segregation; under such situations, haplo-lethal alleles may also readily spread if they are linked to another centromere. |
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However, some natural populations contain high frequencies of individuals with mating-type bias, from which sporidia of only one mating type, usually A1, can be isolated. Such populations show no reduction in fungal transmission rate. The bias is most readily interpreted as caused by the presence of deleterious recessive alleles, "haplo-lethals," that are linked to mating type. Haplo-lethals may persist in a heterozygous state if, during teliospore germination, there is premature conjugation among the immediate products of meiosis, i.e., intratetrad selfing, whereby the free-living haploid stage is bypassed We develop a theoretical model that shows how such alleles may spread if they provide a compensatory advantage in the diploid or dikaryotic phase, for example, through increased disease transmission. There is a limited range of conditions under which such haplo-lethal alleles may be maintained in a stable polymorphism, but if intratetrad selfing is high and/or they have substantial advantage in the dikaryotic phase, haplo-lethal alleles linked to mating type can spread to fixation. The occurrence of populations with a high degree of mating-type bias is therefore readily explained. Haplo-lethal alleles unlinked to mating type are much less likely to spread. In U violacea, mating type shows first-division segregation; under such situations, haplo-lethal alleles may also readily spread if they are linked to another centromere.</description><identifier>ISSN: 1058-5893</identifier><identifier>EISSN: 1537-5315</identifier><identifier>DOI: 10.1086/297538</identifier><language>eng</language><publisher>Chicago: The University of Chicago Press</publisher><subject>AGENT PATHOGENE ; Alleles ; Anthers ; AUTOFECONDATION FORCEE ; AUTOFECUNDACION ; Bacteria ; Centromeres ; COMPATIBILITY ; DISEASE TRANSMISSION ; ENFERMEDADES FUNGOSAS ; ESPORAS ; ESPORAS FUNGICAS ; Flowers & plants ; FUNGAL DISEASES ; FUNGAL SPORES ; Fungi ; GENE ; GENE LETAL ; GENES ; GENES LETALES ; GENETICA DE POBLACIONES ; Genetics ; GENETIQUE DES POPULATIONS ; Genotypes ; GERMINACION ; GERMINATION ; HAPLOIDIA ; HAPLOIDIE ; HAPLOIDY ; HETEROCIGOTOS ; HETEROZYGOSITY ; HETEROZYGOTE ; HETEROZYGOTES ; INFECCION ; INFECTION ; Invited Contributions in Honor of Edward D. Garber, Editor ; LETHAL GENES ; MALADIE FONGIQUE ; MATHEMATICAL MODELS ; MODELE MATHEMATIQUE ; MODELOS MATEMATICOS ; NATURAL SELECTION ; ORGANISMOS PATOGENOS ; PATHOGENS ; Plant reproduction ; Plants ; POPULATION GENETICS ; Recursion ; SELECCION NATURAL ; SELECTION NATURELLE ; SELFING ; SILENE PRATENSIS ; SPORE ; SPORE FONGIQUE ; SPORES ; Teliospores ; TRANSMISION DE ENFERMEDADES ; TRANSMISSION DES MALADIES ; USTILAGO VIOLACEA ; Zygotes</subject><ispartof>International journal of plant sciences, 1998-03, Vol.159 (2), p.192-198</ispartof><rights>Copyright 1998 University of Chicago</rights><rights>Copyright University of Chicago, acting through its Press Mar 1998</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c291t-e463a70b7580ec0d11c464b5da5212eaee0963d077fdcb3a268a7c62a4b945c13</citedby><cites>FETCH-LOGICAL-c291t-e463a70b7580ec0d11c464b5da5212eaee0963d077fdcb3a268a7c62a4b945c13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/2475081$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/2475081$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>315,782,786,805,27933,27934,58026,58259</link.rule.ids></links><search><creatorcontrib>Antonovics, J</creatorcontrib><creatorcontrib>O'Keefe, K</creatorcontrib><creatorcontrib>Hood, M.E</creatorcontrib><title>Theoretical population genetics of mating-type linked haplo-lethal alleles</title><title>International journal of plant sciences</title><description>The anther-smut fungus Ustilago violacea normally produces haploid sporidia of two mating types, and conjugation between them is thought to be a prerequisite for infection of the host plant Silene alba. However, some natural populations contain high frequencies of individuals with mating-type bias, from which sporidia of only one mating type, usually A1, can be isolated. Such populations show no reduction in fungal transmission rate. The bias is most readily interpreted as caused by the presence of deleterious recessive alleles, "haplo-lethals," that are linked to mating type. Haplo-lethals may persist in a heterozygous state if, during teliospore germination, there is premature conjugation among the immediate products of meiosis, i.e., intratetrad selfing, whereby the free-living haploid stage is bypassed We develop a theoretical model that shows how such alleles may spread if they provide a compensatory advantage in the diploid or dikaryotic phase, for example, through increased disease transmission. There is a limited range of conditions under which such haplo-lethal alleles may be maintained in a stable polymorphism, but if intratetrad selfing is high and/or they have substantial advantage in the dikaryotic phase, haplo-lethal alleles linked to mating type can spread to fixation. The occurrence of populations with a high degree of mating-type bias is therefore readily explained. Haplo-lethal alleles unlinked to mating type are much less likely to spread. In U violacea, mating type shows first-division segregation; under such situations, haplo-lethal alleles may also readily spread if they are linked to another centromere.</description><subject>AGENT PATHOGENE</subject><subject>Alleles</subject><subject>Anthers</subject><subject>AUTOFECONDATION FORCEE</subject><subject>AUTOFECUNDACION</subject><subject>Bacteria</subject><subject>Centromeres</subject><subject>COMPATIBILITY</subject><subject>DISEASE TRANSMISSION</subject><subject>ENFERMEDADES FUNGOSAS</subject><subject>ESPORAS</subject><subject>ESPORAS FUNGICAS</subject><subject>Flowers & plants</subject><subject>FUNGAL DISEASES</subject><subject>FUNGAL SPORES</subject><subject>Fungi</subject><subject>GENE</subject><subject>GENE LETAL</subject><subject>GENES</subject><subject>GENES LETALES</subject><subject>GENETICA DE POBLACIONES</subject><subject>Genetics</subject><subject>GENETIQUE DES POPULATIONS</subject><subject>Genotypes</subject><subject>GERMINACION</subject><subject>GERMINATION</subject><subject>HAPLOIDIA</subject><subject>HAPLOIDIE</subject><subject>HAPLOIDY</subject><subject>HETEROCIGOTOS</subject><subject>HETEROZYGOSITY</subject><subject>HETEROZYGOTE</subject><subject>HETEROZYGOTES</subject><subject>INFECCION</subject><subject>INFECTION</subject><subject>Invited Contributions in Honor of Edward D. Garber, Editor</subject><subject>LETHAL GENES</subject><subject>MALADIE FONGIQUE</subject><subject>MATHEMATICAL MODELS</subject><subject>MODELE MATHEMATIQUE</subject><subject>MODELOS MATEMATICOS</subject><subject>NATURAL SELECTION</subject><subject>ORGANISMOS PATOGENOS</subject><subject>PATHOGENS</subject><subject>Plant reproduction</subject><subject>Plants</subject><subject>POPULATION GENETICS</subject><subject>Recursion</subject><subject>SELECCION NATURAL</subject><subject>SELECTION NATURELLE</subject><subject>SELFING</subject><subject>SILENE PRATENSIS</subject><subject>SPORE</subject><subject>SPORE FONGIQUE</subject><subject>SPORES</subject><subject>Teliospores</subject><subject>TRANSMISION DE ENFERMEDADES</subject><subject>TRANSMISSION DES MALADIES</subject><subject>USTILAGO VIOLACEA</subject><subject>Zygotes</subject><issn>1058-5893</issn><issn>1537-5315</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNo9kEtPwzAQhC0EEqXALwAp4sAt4GdsH1HFU5U40J4tx9m0KW4c7OTQf0-qIE67mvl2RxqErgl-IFgVj1RLwdQJmhHBZC4YEafjjoXKhdLsHF2ktMMYa0H1DH2sthAi9I2zPutCN3jbN6HNNtAexZSFOtuPUrvJ-0MHmW_ab6iyre18yD302_HMeg8e0iU6q61PcPU352j98rxavOXLz9f3xdMyd1STPgdeMCtxKYXC4HBFiOMFL0VlBSUULADWBauwlHXlSmZpoax0BbW81Fw4wubobvrbxfAzQOrNLgyxHSMNlVxRqjgdofsJcjGkFKE2XWz2Nh4MweZYk5lqGsGbCdylPsR_inIpsDqG3U52bYOxm9gks_4iWkssKeGY_QIgx2uQ</recordid><startdate>19980301</startdate><enddate>19980301</enddate><creator>Antonovics, J</creator><creator>O'Keefe, K</creator><creator>Hood, M.E</creator><general>The University of Chicago Press</general><general>University of Chicago, acting through its Press</general><scope>FBQ</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SN</scope><scope>7ST</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope></search><sort><creationdate>19980301</creationdate><title>Theoretical population genetics of mating-type linked haplo-lethal alleles</title><author>Antonovics, J ; O'Keefe, K ; Hood, M.E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c291t-e463a70b7580ec0d11c464b5da5212eaee0963d077fdcb3a268a7c62a4b945c13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>AGENT PATHOGENE</topic><topic>Alleles</topic><topic>Anthers</topic><topic>AUTOFECONDATION FORCEE</topic><topic>AUTOFECUNDACION</topic><topic>Bacteria</topic><topic>Centromeres</topic><topic>COMPATIBILITY</topic><topic>DISEASE TRANSMISSION</topic><topic>ENFERMEDADES FUNGOSAS</topic><topic>ESPORAS</topic><topic>ESPORAS FUNGICAS</topic><topic>Flowers & plants</topic><topic>FUNGAL DISEASES</topic><topic>FUNGAL SPORES</topic><topic>Fungi</topic><topic>GENE</topic><topic>GENE LETAL</topic><topic>GENES</topic><topic>GENES LETALES</topic><topic>GENETICA DE POBLACIONES</topic><topic>Genetics</topic><topic>GENETIQUE DES POPULATIONS</topic><topic>Genotypes</topic><topic>GERMINACION</topic><topic>GERMINATION</topic><topic>HAPLOIDIA</topic><topic>HAPLOIDIE</topic><topic>HAPLOIDY</topic><topic>HETEROCIGOTOS</topic><topic>HETEROZYGOSITY</topic><topic>HETEROZYGOTE</topic><topic>HETEROZYGOTES</topic><topic>INFECCION</topic><topic>INFECTION</topic><topic>Invited Contributions in Honor of Edward D. Garber, Editor</topic><topic>LETHAL GENES</topic><topic>MALADIE FONGIQUE</topic><topic>MATHEMATICAL MODELS</topic><topic>MODELE MATHEMATIQUE</topic><topic>MODELOS MATEMATICOS</topic><topic>NATURAL SELECTION</topic><topic>ORGANISMOS PATOGENOS</topic><topic>PATHOGENS</topic><topic>Plant reproduction</topic><topic>Plants</topic><topic>POPULATION GENETICS</topic><topic>Recursion</topic><topic>SELECCION NATURAL</topic><topic>SELECTION NATURELLE</topic><topic>SELFING</topic><topic>SILENE PRATENSIS</topic><topic>SPORE</topic><topic>SPORE FONGIQUE</topic><topic>SPORES</topic><topic>Teliospores</topic><topic>TRANSMISION DE ENFERMEDADES</topic><topic>TRANSMISSION DES MALADIES</topic><topic>USTILAGO VIOLACEA</topic><topic>Zygotes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Antonovics, J</creatorcontrib><creatorcontrib>O'Keefe, K</creatorcontrib><creatorcontrib>Hood, M.E</creatorcontrib><collection>AGRIS</collection><collection>CrossRef</collection><collection>Ecology Abstracts</collection><collection>Environment Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><jtitle>International journal of plant sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Antonovics, J</au><au>O'Keefe, K</au><au>Hood, M.E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Theoretical population genetics of mating-type linked haplo-lethal alleles</atitle><jtitle>International journal of plant sciences</jtitle><date>1998-03-01</date><risdate>1998</risdate><volume>159</volume><issue>2</issue><spage>192</spage><epage>198</epage><pages>192-198</pages><issn>1058-5893</issn><eissn>1537-5315</eissn><abstract>The anther-smut fungus Ustilago violacea normally produces haploid sporidia of two mating types, and conjugation between them is thought to be a prerequisite for infection of the host plant Silene alba. However, some natural populations contain high frequencies of individuals with mating-type bias, from which sporidia of only one mating type, usually A1, can be isolated. Such populations show no reduction in fungal transmission rate. The bias is most readily interpreted as caused by the presence of deleterious recessive alleles, "haplo-lethals," that are linked to mating type. Haplo-lethals may persist in a heterozygous state if, during teliospore germination, there is premature conjugation among the immediate products of meiosis, i.e., intratetrad selfing, whereby the free-living haploid stage is bypassed We develop a theoretical model that shows how such alleles may spread if they provide a compensatory advantage in the diploid or dikaryotic phase, for example, through increased disease transmission. There is a limited range of conditions under which such haplo-lethal alleles may be maintained in a stable polymorphism, but if intratetrad selfing is high and/or they have substantial advantage in the dikaryotic phase, haplo-lethal alleles linked to mating type can spread to fixation. The occurrence of populations with a high degree of mating-type bias is therefore readily explained. Haplo-lethal alleles unlinked to mating type are much less likely to spread. In U violacea, mating type shows first-division segregation; under such situations, haplo-lethal alleles may also readily spread if they are linked to another centromere.</abstract><cop>Chicago</cop><pub>The University of Chicago Press</pub><doi>10.1086/297538</doi><tpages>7</tpages></addata></record> |
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ispartof | International journal of plant sciences, 1998-03, Vol.159 (2), p.192-198 |
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source | JSTOR Archive Collection A-Z Listing |
subjects | AGENT PATHOGENE Alleles Anthers AUTOFECONDATION FORCEE AUTOFECUNDACION Bacteria Centromeres COMPATIBILITY DISEASE TRANSMISSION ENFERMEDADES FUNGOSAS ESPORAS ESPORAS FUNGICAS Flowers & plants FUNGAL DISEASES FUNGAL SPORES Fungi GENE GENE LETAL GENES GENES LETALES GENETICA DE POBLACIONES Genetics GENETIQUE DES POPULATIONS Genotypes GERMINACION GERMINATION HAPLOIDIA HAPLOIDIE HAPLOIDY HETEROCIGOTOS HETEROZYGOSITY HETEROZYGOTE HETEROZYGOTES INFECCION INFECTION Invited Contributions in Honor of Edward D. Garber, Editor LETHAL GENES MALADIE FONGIQUE MATHEMATICAL MODELS MODELE MATHEMATIQUE MODELOS MATEMATICOS NATURAL SELECTION ORGANISMOS PATOGENOS PATHOGENS Plant reproduction Plants POPULATION GENETICS Recursion SELECCION NATURAL SELECTION NATURELLE SELFING SILENE PRATENSIS SPORE SPORE FONGIQUE SPORES Teliospores TRANSMISION DE ENFERMEDADES TRANSMISSION DES MALADIES USTILAGO VIOLACEA Zygotes |
title | Theoretical population genetics of mating-type linked haplo-lethal alleles |
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