Consequences of whole genome duplication for 2n pollen performance
The vegetative cell of the angiosperm male gametophyte (pollen) functions as a free-living, single-celled organism that both produces and transports sperm to egg. Whole-genome duplication (WGD) should have strong effects on pollen because of the haploid to diploid transition and because of both gene...
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description | The vegetative cell of the angiosperm male gametophyte (pollen) functions as a free-living, single-celled organism that both produces and transports sperm to egg. Whole-genome duplication (WGD) should have strong effects on pollen because of the haploid to diploid transition and because of both genetic and epigenetic effects on cell-level phenotypes. To disentangle historical effects of WGD on pollen performance, studies can compare
1n
pollen from diploids to neo-
2n
pollen from diploids and synthetic autotetraploids to older
2n
pollen from established neo-autotetraploids. WGD doubles both gene number and bulk nuclear DNA mass, and a substantial proportion of diploid and autotetraploid heterozygosity can be transmitted to
2n
pollen. Relative to
1n
pollen,
2n
pollen can exhibit heterosis due to higher gene dosage, higher heterozygosity and new allelic interactions. Doubled genome size also has consequences for gene regulation and expression as well as epigenetic effects on cell architecture. Pollen volume doubling is a universal effect of WGD, whereas an increase in aperture number is common among taxa with simultaneous microsporogenesis and pored apertures, mostly eudicots. WGD instantly affects numerous evolved compromises among mature pollen functional traits and these are rapidly shaped by highly diverse tissue interactions and pollen competitive environments in the early post-WGD generations.
2n
pollen phenotypes generally incur higher performance costs, and the degree to which these are met or evolve by scaling up provisioning and metabolic vigor needs further study. |
doi_str_mv | 10.1007/s00497-021-00426-z |
format | Article |
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1n
pollen from diploids to neo-
2n
pollen from diploids and synthetic autotetraploids to older
2n
pollen from established neo-autotetraploids. WGD doubles both gene number and bulk nuclear DNA mass, and a substantial proportion of diploid and autotetraploid heterozygosity can be transmitted to
2n
pollen. Relative to
1n
pollen,
2n
pollen can exhibit heterosis due to higher gene dosage, higher heterozygosity and new allelic interactions. Doubled genome size also has consequences for gene regulation and expression as well as epigenetic effects on cell architecture. Pollen volume doubling is a universal effect of WGD, whereas an increase in aperture number is common among taxa with simultaneous microsporogenesis and pored apertures, mostly eudicots. WGD instantly affects numerous evolved compromises among mature pollen functional traits and these are rapidly shaped by highly diverse tissue interactions and pollen competitive environments in the early post-WGD generations.
2n
pollen phenotypes generally incur higher performance costs, and the degree to which these are met or evolve by scaling up provisioning and metabolic vigor needs further study.</description><identifier>ISSN: 2194-7953</identifier><identifier>EISSN: 2194-7961</identifier><identifier>DOI: 10.1007/s00497-021-00426-z</identifier><identifier>PMID: 34302535</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Agriculture ; Apertures ; Autotetraploid ; Biomedical and Life Sciences ; Cell Biology ; Diploids ; Diploidy ; Epigenetic inheritance ; Epigenetics ; Evolution of Plant Reproduction ; Gene dosage ; Gene Duplication ; Gene expression ; Gene regulation ; Genomes ; Genomics ; Heterosis ; Heterozygosity ; Humans ; Life Sciences ; Magnoliopsida - genetics ; Phenotypes ; Plant Sciences ; Pollen ; Pollen - genetics ; Polyploidy ; Provisioning ; Reproduction (copying) ; Review</subject><ispartof>Plant reproduction, 2021-12, Vol.34 (4), p.321-334</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021</rights><rights>2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.</rights><rights>COPYRIGHT 2021 Springer</rights><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-98f8f7f9d1d79a6454a27c63ff5bcc64334ce0d353916dbbf62b4b3a938a95943</citedby><cites>FETCH-LOGICAL-c448t-98f8f7f9d1d79a6454a27c63ff5bcc64334ce0d353916dbbf62b4b3a938a95943</cites><orcidid>0000-0002-1206-5667</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00497-021-00426-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00497-021-00426-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27923,27924,41487,42556,51318</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34302535$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Williams, Joseph H.</creatorcontrib><title>Consequences of whole genome duplication for 2n pollen performance</title><title>Plant reproduction</title><addtitle>Plant Reprod</addtitle><addtitle>Plant Reprod</addtitle><description>The vegetative cell of the angiosperm male gametophyte (pollen) functions as a free-living, single-celled organism that both produces and transports sperm to egg. Whole-genome duplication (WGD) should have strong effects on pollen because of the haploid to diploid transition and because of both genetic and epigenetic effects on cell-level phenotypes. To disentangle historical effects of WGD on pollen performance, studies can compare
1n
pollen from diploids to neo-
2n
pollen from diploids and synthetic autotetraploids to older
2n
pollen from established neo-autotetraploids. WGD doubles both gene number and bulk nuclear DNA mass, and a substantial proportion of diploid and autotetraploid heterozygosity can be transmitted to
2n
pollen. Relative to
1n
pollen,
2n
pollen can exhibit heterosis due to higher gene dosage, higher heterozygosity and new allelic interactions. Doubled genome size also has consequences for gene regulation and expression as well as epigenetic effects on cell architecture. Pollen volume doubling is a universal effect of WGD, whereas an increase in aperture number is common among taxa with simultaneous microsporogenesis and pored apertures, mostly eudicots. WGD instantly affects numerous evolved compromises among mature pollen functional traits and these are rapidly shaped by highly diverse tissue interactions and pollen competitive environments in the early post-WGD generations.
2n
pollen phenotypes generally incur higher performance costs, and the degree to which these are met or evolve by scaling up provisioning and metabolic vigor needs further study.</description><subject>Agriculture</subject><subject>Apertures</subject><subject>Autotetraploid</subject><subject>Biomedical and Life Sciences</subject><subject>Cell Biology</subject><subject>Diploids</subject><subject>Diploidy</subject><subject>Epigenetic inheritance</subject><subject>Epigenetics</subject><subject>Evolution of Plant Reproduction</subject><subject>Gene dosage</subject><subject>Gene Duplication</subject><subject>Gene expression</subject><subject>Gene regulation</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Heterosis</subject><subject>Heterozygosity</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Magnoliopsida - genetics</subject><subject>Phenotypes</subject><subject>Plant Sciences</subject><subject>Pollen</subject><subject>Pollen - genetics</subject><subject>Polyploidy</subject><subject>Provisioning</subject><subject>Reproduction (copying)</subject><subject>Review</subject><issn>2194-7953</issn><issn>2194-7961</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kUtv1TAQhS0EolXpH2CBIrGBRYrfjpflikelSkg81pbjjC-pEvtiJyr01zOQUlQWyIsZjb9zNKNDyFNGzxil5lWlVFrTUs5a7Lhubx6QY86sbI3V7OFdr8QROa31ilLKqGCKysfkSEhBuRLqmLze5VTh2wopQG1ybK6_5gmaPaQ8QzOsh2kMfhlzamIuDU_NIU8TYIGCg9mj7Al5FP1U4fS2npAvb9983r1vLz-8u9idX7ZBym5pbRe7aKId2GCs11JJz03QIkbVh6ClEDIAHYQSlumh76PmveyFt6LzVlkpTsiLzfdQMi5cFzePNcA0-QR5rY4rpRgTaIzo83_Qq7yWhNshZbkxmiuN1NlG7f0EbkwxL8UHfAPMY8gJ4ojzc90xbphVDAUv7wmQWeD7svdrre7i08f7LN_YUHKtBaI7lHH25Ydj1P1K0G0JOkzQ_U7Q3aDo2e3eaz_DcCf5kxcCYgMqfqU9lL-H_cf2J4SdpBg</recordid><startdate>20211201</startdate><enddate>20211201</enddate><creator>Williams, Joseph H.</creator><general>Springer Berlin Heidelberg</general><general>Springer</general><general>Springer Nature B.V</general><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>ISR</scope><scope>3V.</scope><scope>7X2</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M0K</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-1206-5667</orcidid></search><sort><creationdate>20211201</creationdate><title>Consequences of whole genome duplication for 2n pollen performance</title><author>Williams, Joseph H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-98f8f7f9d1d79a6454a27c63ff5bcc64334ce0d353916dbbf62b4b3a938a95943</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Agriculture</topic><topic>Apertures</topic><topic>Autotetraploid</topic><topic>Biomedical and Life Sciences</topic><topic>Cell Biology</topic><topic>Diploids</topic><topic>Diploidy</topic><topic>Epigenetic inheritance</topic><topic>Epigenetics</topic><topic>Evolution of Plant Reproduction</topic><topic>Gene dosage</topic><topic>Gene Duplication</topic><topic>Gene expression</topic><topic>Gene regulation</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Heterosis</topic><topic>Heterozygosity</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>Magnoliopsida - genetics</topic><topic>Phenotypes</topic><topic>Plant Sciences</topic><topic>Pollen</topic><topic>Pollen - genetics</topic><topic>Polyploidy</topic><topic>Provisioning</topic><topic>Reproduction (copying)</topic><topic>Review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Williams, Joseph H.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Agricultural Science Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</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>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>Plant reproduction</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Williams, Joseph H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Consequences of whole genome duplication for 2n pollen performance</atitle><jtitle>Plant reproduction</jtitle><stitle>Plant Reprod</stitle><addtitle>Plant Reprod</addtitle><date>2021-12-01</date><risdate>2021</risdate><volume>34</volume><issue>4</issue><spage>321</spage><epage>334</epage><pages>321-334</pages><issn>2194-7953</issn><eissn>2194-7961</eissn><abstract>The vegetative cell of the angiosperm male gametophyte (pollen) functions as a free-living, single-celled organism that both produces and transports sperm to egg. Whole-genome duplication (WGD) should have strong effects on pollen because of the haploid to diploid transition and because of both genetic and epigenetic effects on cell-level phenotypes. To disentangle historical effects of WGD on pollen performance, studies can compare
1n
pollen from diploids to neo-
2n
pollen from diploids and synthetic autotetraploids to older
2n
pollen from established neo-autotetraploids. WGD doubles both gene number and bulk nuclear DNA mass, and a substantial proportion of diploid and autotetraploid heterozygosity can be transmitted to
2n
pollen. Relative to
1n
pollen,
2n
pollen can exhibit heterosis due to higher gene dosage, higher heterozygosity and new allelic interactions. Doubled genome size also has consequences for gene regulation and expression as well as epigenetic effects on cell architecture. Pollen volume doubling is a universal effect of WGD, whereas an increase in aperture number is common among taxa with simultaneous microsporogenesis and pored apertures, mostly eudicots. WGD instantly affects numerous evolved compromises among mature pollen functional traits and these are rapidly shaped by highly diverse tissue interactions and pollen competitive environments in the early post-WGD generations.
2n
pollen phenotypes generally incur higher performance costs, and the degree to which these are met or evolve by scaling up provisioning and metabolic vigor needs further study.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>34302535</pmid><doi>10.1007/s00497-021-00426-z</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-1206-5667</orcidid></addata></record> |
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subjects | Agriculture Apertures Autotetraploid Biomedical and Life Sciences Cell Biology Diploids Diploidy Epigenetic inheritance Epigenetics Evolution of Plant Reproduction Gene dosage Gene Duplication Gene expression Gene regulation Genomes Genomics Heterosis Heterozygosity Humans Life Sciences Magnoliopsida - genetics Phenotypes Plant Sciences Pollen Pollen - genetics Polyploidy Provisioning Reproduction (copying) Review |
title | Consequences of whole genome duplication for 2n pollen performance |
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