perspective on the evolution of germ-cell development and germinal mosaics of deleterious mutations

In many animals a small number of primordial germ cells (PGCs) are set aside early in development, mitosis and mitochondrial DNA syntheses are arrested, transcription is stopped or reduced, and the PGCs migrate later to the emerging gonads and become germ cells. What could be the evolutionary advant...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Genetica 2015-10, Vol.143 (5), p.563-569
Hauptverfasser: Woodruff, Ronny C, Balinski, Michael A, Bouzat, Juan L
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 569
container_issue 5
container_start_page 563
container_title Genetica
container_volume 143
creator Woodruff, Ronny C
Balinski, Michael A
Bouzat, Juan L
description In many animals a small number of primordial germ cells (PGCs) are set aside early in development, mitosis and mitochondrial DNA syntheses are arrested, transcription is stopped or reduced, and the PGCs migrate later to the emerging gonads and become germ cells. What could be the evolutionary advantage of sequestering non-dividing PGCs early in development? A commonly cited advantage is a reduction in the number of new deleterious mutations that would occur if there were additional divisions in PGCs early in development. We would like to add to this advantage the fact that these additional mutations in PGCs give rise to germinal mosaics (i.e., premeiotic clusters of mutation) in multiple progeny of the same individual, thus having a larger detrimental effect on the evolutionary fitness of their carriers. Here, we reviewed published studies providing evidence that germinal mosaics of deleterious mutant alleles are not rare, occur for all types of genetic damage, and have been observed in all tested organisms and in nature. We propose the hypothesis that PGC sequestration during early animal development may have evolved in part in response to selection for preventing the occurrence of premeiotic clusters of deleterious mutant alleles, and describe a series of predictions that would allow the assessment of the potential role of germinal mosaics on the evolution of PGC sequestration.
doi_str_mv 10.1007/s10709-015-9854-1
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1722183101</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3797944811</sourcerecordid><originalsourceid>FETCH-LOGICAL-c451t-a201763f362f45851e894dff8d2e3e72029efc0d26e2e9855244209af3270dae3</originalsourceid><addsrcrecordid>eNqNks1O3TAQhS1UVG6hD9BNidRNN4YZO7aTZYX6JyGxaFlbJhnToCRO7eRKvD0OgarqAnVlWfPN8Zk5ZuwdwhkCmPOEYKDmgIrXlSo5HrAdKiO5rpR5xXYAqLk2YI7Ym5TuAKA2un7NjoRGlBLkjjUTxTRRM3d7KsJYzL-ooH3ol7nLt-CLW4oDb6jvi5b21IdpoHEu3Ng-VrrR9cUQkuuatNIt9TRT7MKSimGZ3aqSTtihd32it0_nMbv-8vnnxTd-efX1-8WnS96UCmfuBKDR0kstfKkqhVTVZet91QqSZASImnwDrdAkKM-rRFkKqJ2XwkDrSB6zj5vuFMPvhdJshy6t1t1I2ZBFIwRWEgH_A82rAqOkzOiHf9C7sMQ890YpVArLTOFGNTGkFMnbKXaDi_cWwa5h2S0sm8Oya1h2NfH-SXm5Gaj90_GcTgbEBqRcGvO-_3r6BdXTrcm7YN1t7JK9_pFXq_NvkEIrLR8Au4Knww</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1709515514</pqid></control><display><type>article</type><title>perspective on the evolution of germ-cell development and germinal mosaics of deleterious mutations</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>Woodruff, Ronny C ; Balinski, Michael A ; Bouzat, Juan L</creator><creatorcontrib>Woodruff, Ronny C ; Balinski, Michael A ; Bouzat, Juan L</creatorcontrib><description>In many animals a small number of primordial germ cells (PGCs) are set aside early in development, mitosis and mitochondrial DNA syntheses are arrested, transcription is stopped or reduced, and the PGCs migrate later to the emerging gonads and become germ cells. What could be the evolutionary advantage of sequestering non-dividing PGCs early in development? A commonly cited advantage is a reduction in the number of new deleterious mutations that would occur if there were additional divisions in PGCs early in development. We would like to add to this advantage the fact that these additional mutations in PGCs give rise to germinal mosaics (i.e., premeiotic clusters of mutation) in multiple progeny of the same individual, thus having a larger detrimental effect on the evolutionary fitness of their carriers. Here, we reviewed published studies providing evidence that germinal mosaics of deleterious mutant alleles are not rare, occur for all types of genetic damage, and have been observed in all tested organisms and in nature. We propose the hypothesis that PGC sequestration during early animal development may have evolved in part in response to selection for preventing the occurrence of premeiotic clusters of deleterious mutant alleles, and describe a series of predictions that would allow the assessment of the potential role of germinal mosaics on the evolution of PGC sequestration.</description><identifier>ISSN: 0016-6707</identifier><identifier>EISSN: 1573-6857</identifier><identifier>DOI: 10.1007/s10709-015-9854-1</identifier><identifier>PMID: 26113303</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>alleles ; animal development ; Animal Genetics and Genomics ; Animals ; Biological Evolution ; Biomedical and Life Sciences ; Chromosome aberrations ; early development ; evolution ; Evolutionary Biology ; germ cells ; Germ Cells - growth &amp; development ; Germ Cells - physiology ; Germ-Line Mutation ; Gonads ; Gonads - embryology ; Gonads - growth &amp; development ; Human Genetics ; Humans ; Life Sciences ; Microbial Genetics and Genomics ; Mitochondrial DNA ; mitosis ; mutants ; Mutation ; Plant Genetics and Genomics ; prediction ; progeny ; selection response</subject><ispartof>Genetica, 2015-10, Vol.143 (5), p.563-569</ispartof><rights>Springer International Publishing Switzerland 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c451t-a201763f362f45851e894dff8d2e3e72029efc0d26e2e9855244209af3270dae3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10709-015-9854-1$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10709-015-9854-1$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26113303$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Woodruff, Ronny C</creatorcontrib><creatorcontrib>Balinski, Michael A</creatorcontrib><creatorcontrib>Bouzat, Juan L</creatorcontrib><title>perspective on the evolution of germ-cell development and germinal mosaics of deleterious mutations</title><title>Genetica</title><addtitle>Genetica</addtitle><addtitle>Genetica</addtitle><description>In many animals a small number of primordial germ cells (PGCs) are set aside early in development, mitosis and mitochondrial DNA syntheses are arrested, transcription is stopped or reduced, and the PGCs migrate later to the emerging gonads and become germ cells. What could be the evolutionary advantage of sequestering non-dividing PGCs early in development? A commonly cited advantage is a reduction in the number of new deleterious mutations that would occur if there were additional divisions in PGCs early in development. We would like to add to this advantage the fact that these additional mutations in PGCs give rise to germinal mosaics (i.e., premeiotic clusters of mutation) in multiple progeny of the same individual, thus having a larger detrimental effect on the evolutionary fitness of their carriers. Here, we reviewed published studies providing evidence that germinal mosaics of deleterious mutant alleles are not rare, occur for all types of genetic damage, and have been observed in all tested organisms and in nature. We propose the hypothesis that PGC sequestration during early animal development may have evolved in part in response to selection for preventing the occurrence of premeiotic clusters of deleterious mutant alleles, and describe a series of predictions that would allow the assessment of the potential role of germinal mosaics on the evolution of PGC sequestration.</description><subject>alleles</subject><subject>animal development</subject><subject>Animal Genetics and Genomics</subject><subject>Animals</subject><subject>Biological Evolution</subject><subject>Biomedical and Life Sciences</subject><subject>Chromosome aberrations</subject><subject>early development</subject><subject>evolution</subject><subject>Evolutionary Biology</subject><subject>germ cells</subject><subject>Germ Cells - growth &amp; development</subject><subject>Germ Cells - physiology</subject><subject>Germ-Line Mutation</subject><subject>Gonads</subject><subject>Gonads - embryology</subject><subject>Gonads - growth &amp; development</subject><subject>Human Genetics</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Microbial Genetics and Genomics</subject><subject>Mitochondrial DNA</subject><subject>mitosis</subject><subject>mutants</subject><subject>Mutation</subject><subject>Plant Genetics and Genomics</subject><subject>prediction</subject><subject>progeny</subject><subject>selection response</subject><issn>0016-6707</issn><issn>1573-6857</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNks1O3TAQhS1UVG6hD9BNidRNN4YZO7aTZYX6JyGxaFlbJhnToCRO7eRKvD0OgarqAnVlWfPN8Zk5ZuwdwhkCmPOEYKDmgIrXlSo5HrAdKiO5rpR5xXYAqLk2YI7Ym5TuAKA2un7NjoRGlBLkjjUTxTRRM3d7KsJYzL-ooH3ol7nLt-CLW4oDb6jvi5b21IdpoHEu3Ng-VrrR9cUQkuuatNIt9TRT7MKSimGZ3aqSTtihd32it0_nMbv-8vnnxTd-efX1-8WnS96UCmfuBKDR0kstfKkqhVTVZet91QqSZASImnwDrdAkKM-rRFkKqJ2XwkDrSB6zj5vuFMPvhdJshy6t1t1I2ZBFIwRWEgH_A82rAqOkzOiHf9C7sMQ890YpVArLTOFGNTGkFMnbKXaDi_cWwa5h2S0sm8Oya1h2NfH-SXm5Gaj90_GcTgbEBqRcGvO-_3r6BdXTrcm7YN1t7JK9_pFXq_NvkEIrLR8Au4Knww</recordid><startdate>20151001</startdate><enddate>20151001</enddate><creator>Woodruff, Ronny C</creator><creator>Balinski, Michael A</creator><creator>Bouzat, Juan L</creator><general>Springer International Publishing</general><general>Springer Nature B.V</general><scope>FBQ</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>7QL</scope><scope>7SN</scope><scope>7SS</scope><scope>7T7</scope><scope>7TK</scope><scope>7U9</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>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</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>20151001</creationdate><title>perspective on the evolution of germ-cell development and germinal mosaics of deleterious mutations</title><author>Woodruff, Ronny C ; Balinski, Michael A ; Bouzat, Juan L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c451t-a201763f362f45851e894dff8d2e3e72029efc0d26e2e9855244209af3270dae3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>alleles</topic><topic>animal development</topic><topic>Animal Genetics and Genomics</topic><topic>Animals</topic><topic>Biological Evolution</topic><topic>Biomedical and Life Sciences</topic><topic>Chromosome aberrations</topic><topic>early development</topic><topic>evolution</topic><topic>Evolutionary Biology</topic><topic>germ cells</topic><topic>Germ Cells - growth &amp; development</topic><topic>Germ Cells - physiology</topic><topic>Germ-Line Mutation</topic><topic>Gonads</topic><topic>Gonads - embryology</topic><topic>Gonads - growth &amp; development</topic><topic>Human Genetics</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>Microbial Genetics and Genomics</topic><topic>Mitochondrial DNA</topic><topic>mitosis</topic><topic>mutants</topic><topic>Mutation</topic><topic>Plant Genetics and Genomics</topic><topic>prediction</topic><topic>progeny</topic><topic>selection response</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Woodruff, Ronny C</creatorcontrib><creatorcontrib>Balinski, Michael A</creatorcontrib><creatorcontrib>Bouzat, Juan L</creatorcontrib><collection>AGRIS</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>Bacteriology Abstracts (Microbiology B)</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health &amp; 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 One Sustainability</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>Environmental Sciences and Pollution Management</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>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</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>Genetica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Woodruff, Ronny C</au><au>Balinski, Michael A</au><au>Bouzat, Juan L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>perspective on the evolution of germ-cell development and germinal mosaics of deleterious mutations</atitle><jtitle>Genetica</jtitle><stitle>Genetica</stitle><addtitle>Genetica</addtitle><date>2015-10-01</date><risdate>2015</risdate><volume>143</volume><issue>5</issue><spage>563</spage><epage>569</epage><pages>563-569</pages><issn>0016-6707</issn><eissn>1573-6857</eissn><abstract>In many animals a small number of primordial germ cells (PGCs) are set aside early in development, mitosis and mitochondrial DNA syntheses are arrested, transcription is stopped or reduced, and the PGCs migrate later to the emerging gonads and become germ cells. What could be the evolutionary advantage of sequestering non-dividing PGCs early in development? A commonly cited advantage is a reduction in the number of new deleterious mutations that would occur if there were additional divisions in PGCs early in development. We would like to add to this advantage the fact that these additional mutations in PGCs give rise to germinal mosaics (i.e., premeiotic clusters of mutation) in multiple progeny of the same individual, thus having a larger detrimental effect on the evolutionary fitness of their carriers. Here, we reviewed published studies providing evidence that germinal mosaics of deleterious mutant alleles are not rare, occur for all types of genetic damage, and have been observed in all tested organisms and in nature. We propose the hypothesis that PGC sequestration during early animal development may have evolved in part in response to selection for preventing the occurrence of premeiotic clusters of deleterious mutant alleles, and describe a series of predictions that would allow the assessment of the potential role of germinal mosaics on the evolution of PGC sequestration.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>26113303</pmid><doi>10.1007/s10709-015-9854-1</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0016-6707
ispartof Genetica, 2015-10, Vol.143 (5), p.563-569
issn 0016-6707
1573-6857
language eng
recordid cdi_proquest_miscellaneous_1722183101
source MEDLINE; SpringerLink Journals - AutoHoldings
subjects alleles
animal development
Animal Genetics and Genomics
Animals
Biological Evolution
Biomedical and Life Sciences
Chromosome aberrations
early development
evolution
Evolutionary Biology
germ cells
Germ Cells - growth & development
Germ Cells - physiology
Germ-Line Mutation
Gonads
Gonads - embryology
Gonads - growth & development
Human Genetics
Humans
Life Sciences
Microbial Genetics and Genomics
Mitochondrial DNA
mitosis
mutants
Mutation
Plant Genetics and Genomics
prediction
progeny
selection response
title perspective on the evolution of germ-cell development and germinal mosaics of deleterious mutations
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T01%3A06%3A51IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=perspective%20on%20the%20evolution%20of%20germ-cell%20development%20and%20germinal%20mosaics%20of%20deleterious%20mutations&rft.jtitle=Genetica&rft.au=Woodruff,%20Ronny%20C&rft.date=2015-10-01&rft.volume=143&rft.issue=5&rft.spage=563&rft.epage=569&rft.pages=563-569&rft.issn=0016-6707&rft.eissn=1573-6857&rft_id=info:doi/10.1007/s10709-015-9854-1&rft_dat=%3Cproquest_cross%3E3797944811%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1709515514&rft_id=info:pmid/26113303&rfr_iscdi=true