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Adaptive plasticity and epigenetic variation in response to warming in an Alpine plant
Environmentally induced phenotypic plasticity may be a critical component of response to changing environments. We examined local differentiation and adaptive phenotypic plasticity in response to elevated temperature in half‐sib lines collected across an elevation gradient for the alpine herb, Wahle...
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Published in: | Ecology and evolution 2015-02, Vol.5 (3), p.634-647 |
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description | Environmentally induced phenotypic plasticity may be a critical component of response to changing environments. We examined local differentiation and adaptive phenotypic plasticity in response to elevated temperature in half‐sib lines collected across an elevation gradient for the alpine herb, Wahlenbergia ceracea. Using Amplified Fragment Length Polymorphism (AFLP), we found low but significant genetic differentiation between low‐ and high‐elevation seedlings, and seedlings originating from low elevations grew faster and showed stronger temperature responses (more plasticity) than those from medium and high elevations. Furthermore, plasticity was more often adaptive for plants of low‐elevation origin and maladaptive for plants of high elevation. With methylation sensitive‐AFLP (MS‐AFLP), we revealed an increase in epigenetic variation in response to temperature in low‐elevation seedlings. Although we did not find significant direct correlations between MS‐AFLP loci and phenotypes, our results demonstrate that adaptive plasticity in temperature response to warming varies over fine spatial scales and suggest the involvement of epigenetic mechanisms in this response.
Our work presents an exciting fusion of research on epigenetics (DNA methylation in particular) and adaptive phenotypic plasticity. The relationship between epigenetic mechanisms and phenotypic plasticity has been the subject of increasing speculation in ecological studies. Our results demonstrate that adaptive plasticity in temperature response of an alpine herb varies over remarkably fine geographic scales and indicates the involvement of epigenetic mechanisms in this response. |
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Our work presents an exciting fusion of research on epigenetics (DNA methylation in particular) and adaptive phenotypic plasticity. The relationship between epigenetic mechanisms and phenotypic plasticity has been the subject of increasing speculation in ecological studies. Our results demonstrate that adaptive plasticity in temperature response of an alpine herb varies over remarkably fine geographic scales and indicates the involvement of epigenetic mechanisms in this response.</description><identifier>ISSN: 2045-7758</identifier><identifier>EISSN: 2045-7758</identifier><identifier>DOI: 10.1002/ece3.1329</identifier><identifier>PMID: 25691987</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>Adaptive plasticity ; alpine plants ; Amplified fragment length polymorphism ; Changing environments ; Climate change ; Critical components ; Deoxyribonucleic acid ; Differentiation ; DNA ; DNA methylation ; Elevation ; Epigenetics ; Gene polymorphism ; Generalized linear models ; global warming ; High temperature ; National parks ; Original Research ; Phenotypes ; Phenotypic plasticity ; Plant introductions ; Plastic properties ; Plasticity ; Polymorphism ; Seedlings ; Seeds ; Temperature effects</subject><ispartof>Ecology and evolution, 2015-02, Vol.5 (3), p.634-647</ispartof><rights>2015 The Authors. published by John Wiley & Sons Ltd.</rights><rights>2015. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 The Authors. published by John Wiley & Sons Ltd. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5799-945f94461c0e8213757779301e9fb10285118579dbaccc58afced71b2ecdb43</citedby><cites>FETCH-LOGICAL-c5799-945f94461c0e8213757779301e9fb10285118579dbaccc58afced71b2ecdb43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2290773392/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2290773392?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,11562,25753,27924,27925,37012,44590,46052,46476,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25691987$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nicotra, Adrienne B.</creatorcontrib><creatorcontrib>Segal, Deborah L.</creatorcontrib><creatorcontrib>Hoyle, Gemma L.</creatorcontrib><creatorcontrib>Schrey, Aaron W.</creatorcontrib><creatorcontrib>Verhoeven, Koen J. F.</creatorcontrib><creatorcontrib>Richards, Christina L.</creatorcontrib><title>Adaptive plasticity and epigenetic variation in response to warming in an Alpine plant</title><title>Ecology and evolution</title><addtitle>Ecol Evol</addtitle><description>Environmentally induced phenotypic plasticity may be a critical component of response to changing environments. We examined local differentiation and adaptive phenotypic plasticity in response to elevated temperature in half‐sib lines collected across an elevation gradient for the alpine herb, Wahlenbergia ceracea. Using Amplified Fragment Length Polymorphism (AFLP), we found low but significant genetic differentiation between low‐ and high‐elevation seedlings, and seedlings originating from low elevations grew faster and showed stronger temperature responses (more plasticity) than those from medium and high elevations. Furthermore, plasticity was more often adaptive for plants of low‐elevation origin and maladaptive for plants of high elevation. With methylation sensitive‐AFLP (MS‐AFLP), we revealed an increase in epigenetic variation in response to temperature in low‐elevation seedlings. Although we did not find significant direct correlations between MS‐AFLP loci and phenotypes, our results demonstrate that adaptive plasticity in temperature response to warming varies over fine spatial scales and suggest the involvement of epigenetic mechanisms in this response.
Our work presents an exciting fusion of research on epigenetics (DNA methylation in particular) and adaptive phenotypic plasticity. The relationship between epigenetic mechanisms and phenotypic plasticity has been the subject of increasing speculation in ecological studies. Our results demonstrate that adaptive plasticity in temperature response of an alpine herb varies over remarkably fine geographic scales and indicates the involvement of epigenetic mechanisms in this response.</description><subject>Adaptive plasticity</subject><subject>alpine plants</subject><subject>Amplified fragment length polymorphism</subject><subject>Changing environments</subject><subject>Climate change</subject><subject>Critical components</subject><subject>Deoxyribonucleic acid</subject><subject>Differentiation</subject><subject>DNA</subject><subject>DNA methylation</subject><subject>Elevation</subject><subject>Epigenetics</subject><subject>Gene polymorphism</subject><subject>Generalized linear models</subject><subject>global warming</subject><subject>High temperature</subject><subject>National parks</subject><subject>Original Research</subject><subject>Phenotypes</subject><subject>Phenotypic plasticity</subject><subject>Plant introductions</subject><subject>Plastic properties</subject><subject>Plasticity</subject><subject>Polymorphism</subject><subject>Seedlings</subject><subject>Seeds</subject><subject>Temperature effects</subject><issn>2045-7758</issn><issn>2045-7758</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><recordid>eNp1kctKAzEUhoMottQufAEJuHIxbS4zzWQjlFIvUHChuA2ZzJmaMs2MybSlb-_0YqkLs0k4-fjO4fwI3VIyoISwIRjgA8qZvEBdRuIkEiJJL8_eHdQPYUHaMyIsJuIadVgyklSmoos-x7muG7sGXJc6NNbYZou1yzHUdg4O2gpea291YyuHrcMeQl25ALip8Eb7pXXzXVk7PC5r6_Ye19ygq0KXAfrHu4fen6Yfk5do9vb8OhnPIpMIKSMZJ4WM4xE1BFJGuUiEEJITCrLIKGFpQmnaknmmjTFJqgsDuaAZA5NnMe-hx4O1XmVLyA24xutS1d4utd-qSlv198fZLzWv1irmLBWjtBXcHwW--l5BaNSiWnnXTqwYk0QIziVrqYcDZXwVgofi1IEStctA7TJQuwxa9u58pBP5u_EWGB6AjS1h-79JTSdTvlf-AGg_kT4</recordid><startdate>201502</startdate><enddate>201502</enddate><creator>Nicotra, Adrienne B.</creator><creator>Segal, Deborah L.</creator><creator>Hoyle, Gemma L.</creator><creator>Schrey, Aaron W.</creator><creator>Verhoeven, Koen J. F.</creator><creator>Richards, Christina L.</creator><general>John Wiley & Sons, Inc</general><general>BlackWell Publishing Ltd</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7X2</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</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>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M0K</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>SOI</scope><scope>5PM</scope></search><sort><creationdate>201502</creationdate><title>Adaptive plasticity and epigenetic variation in response to warming in an Alpine plant</title><author>Nicotra, Adrienne B. ; Segal, Deborah L. ; Hoyle, Gemma L. ; Schrey, Aaron W. ; Verhoeven, Koen J. F. ; Richards, Christina L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5799-945f94461c0e8213757779301e9fb10285118579dbaccc58afced71b2ecdb43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adaptive plasticity</topic><topic>alpine plants</topic><topic>Amplified fragment length polymorphism</topic><topic>Changing environments</topic><topic>Climate change</topic><topic>Critical components</topic><topic>Deoxyribonucleic acid</topic><topic>Differentiation</topic><topic>DNA</topic><topic>DNA methylation</topic><topic>Elevation</topic><topic>Epigenetics</topic><topic>Gene polymorphism</topic><topic>Generalized linear models</topic><topic>global warming</topic><topic>High temperature</topic><topic>National parks</topic><topic>Original Research</topic><topic>Phenotypes</topic><topic>Phenotypic plasticity</topic><topic>Plant introductions</topic><topic>Plastic properties</topic><topic>Plasticity</topic><topic>Polymorphism</topic><topic>Seedlings</topic><topic>Seeds</topic><topic>Temperature effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nicotra, Adrienne B.</creatorcontrib><creatorcontrib>Segal, Deborah L.</creatorcontrib><creatorcontrib>Hoyle, Gemma L.</creatorcontrib><creatorcontrib>Schrey, Aaron W.</creatorcontrib><creatorcontrib>Verhoeven, Koen J. 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F.</au><au>Richards, Christina L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adaptive plasticity and epigenetic variation in response to warming in an Alpine plant</atitle><jtitle>Ecology and evolution</jtitle><addtitle>Ecol Evol</addtitle><date>2015-02</date><risdate>2015</risdate><volume>5</volume><issue>3</issue><spage>634</spage><epage>647</epage><pages>634-647</pages><issn>2045-7758</issn><eissn>2045-7758</eissn><abstract>Environmentally induced phenotypic plasticity may be a critical component of response to changing environments. We examined local differentiation and adaptive phenotypic plasticity in response to elevated temperature in half‐sib lines collected across an elevation gradient for the alpine herb, Wahlenbergia ceracea. Using Amplified Fragment Length Polymorphism (AFLP), we found low but significant genetic differentiation between low‐ and high‐elevation seedlings, and seedlings originating from low elevations grew faster and showed stronger temperature responses (more plasticity) than those from medium and high elevations. Furthermore, plasticity was more often adaptive for plants of low‐elevation origin and maladaptive for plants of high elevation. With methylation sensitive‐AFLP (MS‐AFLP), we revealed an increase in epigenetic variation in response to temperature in low‐elevation seedlings. Although we did not find significant direct correlations between MS‐AFLP loci and phenotypes, our results demonstrate that adaptive plasticity in temperature response to warming varies over fine spatial scales and suggest the involvement of epigenetic mechanisms in this response.
Our work presents an exciting fusion of research on epigenetics (DNA methylation in particular) and adaptive phenotypic plasticity. The relationship between epigenetic mechanisms and phenotypic plasticity has been the subject of increasing speculation in ecological studies. Our results demonstrate that adaptive plasticity in temperature response of an alpine herb varies over remarkably fine geographic scales and indicates the involvement of epigenetic mechanisms in this response.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>25691987</pmid><doi>10.1002/ece3.1329</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adaptive plasticity alpine plants Amplified fragment length polymorphism Changing environments Climate change Critical components Deoxyribonucleic acid Differentiation DNA DNA methylation Elevation Epigenetics Gene polymorphism Generalized linear models global warming High temperature National parks Original Research Phenotypes Phenotypic plasticity Plant introductions Plastic properties Plasticity Polymorphism Seedlings Seeds Temperature effects |
title | Adaptive plasticity and epigenetic variation in response to warming in an Alpine plant |
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