Order-level fern plastome phylogenomics: new insights from Hymenophyllales
Premise of the Study Filmy ferns (Hymenophyllales) are a highly specialized lineage, having mesophyll one‐cell layer thick and inhabiting particularly shaded and humid environments. The phylogenetic placement of Hymenophyllales has been inconclusive, and while over 87 whole fern plastomes have been...
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Veröffentlicht in: | American journal of botany 2018-09, Vol.105 (9), p.1545-1555 |
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creator | Kuo, Li-Yaung Qi, Xinping Ma, Hong Li, Fay-Wei |
description | Premise of the Study
Filmy ferns (Hymenophyllales) are a highly specialized lineage, having mesophyll one‐cell layer thick and inhabiting particularly shaded and humid environments. The phylogenetic placement of Hymenophyllales has been inconclusive, and while over 87 whole fern plastomes have been published, none was from Hymenophyllales. To better understand the evolutionary history of filmy ferns, we sequenced the first complete plastome for this order.
Methods
We compiled a phylogenomic plastome data set encompassing all 11 fern orders, and reconstructed phylogenies using different data types (nucleotides, codons, and amino acids) and partition schemes (codon positions and loci). To infer the evolution of fern plastome organization, we coded plastome features, including inversions, inverted repeat boundary shifts, gene losses, and tRNA anticodon sequences as characters, and reconstructed the ancestral states for these characters.
Key Results
We discovered a suite of novel, Hymenophyllales‐specific plastome structures that likely resulted from repeated expansions and contractions of the inverted repeat regions. Our phylogenetic analyses reveal that Hymenophyllales is highly supported as either sister to Gleicheniales or to Gleicheniales + the remaining non‐Osmundales leptosporangiates, depending on the data type and partition scheme.
Conclusions
Although our analyses could not confidently resolve the phylogenetic position of Hymenophyalles, the results here highlight the danger of drawing conclusions from “all‐in” phylogenomic data set without exploring potential inconsistencies in the data. Finally, our first order‐level reconstruction of fern plastome structural evolution provides a useful framework for future plastome research. |
doi_str_mv | 10.1002/ajb2.1152 |
format | Article |
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Filmy ferns (Hymenophyllales) are a highly specialized lineage, having mesophyll one‐cell layer thick and inhabiting particularly shaded and humid environments. The phylogenetic placement of Hymenophyllales has been inconclusive, and while over 87 whole fern plastomes have been published, none was from Hymenophyllales. To better understand the evolutionary history of filmy ferns, we sequenced the first complete plastome for this order.
Methods
We compiled a phylogenomic plastome data set encompassing all 11 fern orders, and reconstructed phylogenies using different data types (nucleotides, codons, and amino acids) and partition schemes (codon positions and loci). To infer the evolution of fern plastome organization, we coded plastome features, including inversions, inverted repeat boundary shifts, gene losses, and tRNA anticodon sequences as characters, and reconstructed the ancestral states for these characters.
Key Results
We discovered a suite of novel, Hymenophyllales‐specific plastome structures that likely resulted from repeated expansions and contractions of the inverted repeat regions. Our phylogenetic analyses reveal that Hymenophyllales is highly supported as either sister to Gleicheniales or to Gleicheniales + the remaining non‐Osmundales leptosporangiates, depending on the data type and partition scheme.
Conclusions
Although our analyses could not confidently resolve the phylogenetic position of Hymenophyalles, the results here highlight the danger of drawing conclusions from “all‐in” phylogenomic data set without exploring potential inconsistencies in the data. Finally, our first order‐level reconstruction of fern plastome structural evolution provides a useful framework for future plastome research.</description><identifier>ISSN: 0002-9122</identifier><identifier>EISSN: 1537-2197</identifier><identifier>DOI: 10.1002/ajb2.1152</identifier><identifier>PMID: 30168575</identifier><language>eng</language><publisher>United States: John Wiley and Sons, Inc</publisher><subject>Amino acids ; Codons ; Evolution ; Ferns ; Gene sequencing ; Hazards ; Humidity ; Hymenophyllum ; Inversions ; Inverted repeat ; Mesophyll ; Nucleotides ; Partitions ; phylogenetic conflict ; Phylogenetics ; Phylogeny ; plastome organization ; Plastomes ; RESEARCH ARTICLE ; Ribonucleic acid ; RNA ; Trichomanoideae ; tRNA</subject><ispartof>American journal of botany, 2018-09, Vol.105 (9), p.1545-1555</ispartof><rights>2018 Botanical Society of America</rights><rights>2018 Botanical Society of America.</rights><rights>Copyright Botanical Society of America, Inc. Sep 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4762-70936eb0b1f7290c016c806a962a5d9b5f901ce1e575aed99a80d3c1c1a645833</citedby><cites>FETCH-LOGICAL-c4762-70936eb0b1f7290c016c806a962a5d9b5f901ce1e575aed99a80d3c1c1a645833</cites><orcidid>0000-0002-3388-3757 ; 0000-0002-0076-0152</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/26617121$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/26617121$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,799,1411,1427,27903,27904,45553,45554,46388,46812,57996,58229</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30168575$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kuo, Li-Yaung</creatorcontrib><creatorcontrib>Qi, Xinping</creatorcontrib><creatorcontrib>Ma, Hong</creatorcontrib><creatorcontrib>Li, Fay-Wei</creatorcontrib><title>Order-level fern plastome phylogenomics: new insights from Hymenophyllales</title><title>American journal of botany</title><addtitle>Am J Bot</addtitle><description>Premise of the Study
Filmy ferns (Hymenophyllales) are a highly specialized lineage, having mesophyll one‐cell layer thick and inhabiting particularly shaded and humid environments. The phylogenetic placement of Hymenophyllales has been inconclusive, and while over 87 whole fern plastomes have been published, none was from Hymenophyllales. To better understand the evolutionary history of filmy ferns, we sequenced the first complete plastome for this order.
Methods
We compiled a phylogenomic plastome data set encompassing all 11 fern orders, and reconstructed phylogenies using different data types (nucleotides, codons, and amino acids) and partition schemes (codon positions and loci). To infer the evolution of fern plastome organization, we coded plastome features, including inversions, inverted repeat boundary shifts, gene losses, and tRNA anticodon sequences as characters, and reconstructed the ancestral states for these characters.
Key Results
We discovered a suite of novel, Hymenophyllales‐specific plastome structures that likely resulted from repeated expansions and contractions of the inverted repeat regions. Our phylogenetic analyses reveal that Hymenophyllales is highly supported as either sister to Gleicheniales or to Gleicheniales + the remaining non‐Osmundales leptosporangiates, depending on the data type and partition scheme.
Conclusions
Although our analyses could not confidently resolve the phylogenetic position of Hymenophyalles, the results here highlight the danger of drawing conclusions from “all‐in” phylogenomic data set without exploring potential inconsistencies in the data. Finally, our first order‐level reconstruction of fern plastome structural evolution provides a useful framework for future plastome research.</description><subject>Amino acids</subject><subject>Codons</subject><subject>Evolution</subject><subject>Ferns</subject><subject>Gene sequencing</subject><subject>Hazards</subject><subject>Humidity</subject><subject>Hymenophyllum</subject><subject>Inversions</subject><subject>Inverted repeat</subject><subject>Mesophyll</subject><subject>Nucleotides</subject><subject>Partitions</subject><subject>phylogenetic conflict</subject><subject>Phylogenetics</subject><subject>Phylogeny</subject><subject>plastome organization</subject><subject>Plastomes</subject><subject>RESEARCH ARTICLE</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>Trichomanoideae</subject><subject>tRNA</subject><issn>0002-9122</issn><issn>1537-2197</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kE1Lw0AQhhdRbK0e_AFKwYN6SLsz-djssRY_KfSi57DZTDQhH3W3Ufrv3ZLag-BpGOaZd4aHsXPgE-Acp6pMcQIQ4gEbQugLD0GKQzbkbuhJQBywE2tL18pA4jEb-ByiOBThkF0vTUbGq-iLqnFOphmvKmXXbU3j1cemat-paetC21N2lKvK0tmujtjbw_3r_MlbLB-f57OFpwMRoSe49CNKeQq5QMm1u6NjHikZoQozmYa55KAJyB1XlEmpYp75GjSoKAhj3x-xmz53ZdrPjuw6qQurqapUQ21nEwQhEdDH2KFXf9Cy7UzjvnOUjxjEAgNH3faUNq21hvJkZYpamU0CPNnaS7b2kq09x17uEru0pmxP_upywLQHvouKNv8nJbOXO9xFXvQbpZNq9hsYRSDAvfkDUut_QA</recordid><startdate>201809</startdate><enddate>201809</enddate><creator>Kuo, Li-Yaung</creator><creator>Qi, Xinping</creator><creator>Ma, Hong</creator><creator>Li, Fay-Wei</creator><general>John Wiley and Sons, Inc</general><general>Botanical Society of America, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-3388-3757</orcidid><orcidid>https://orcid.org/0000-0002-0076-0152</orcidid></search><sort><creationdate>201809</creationdate><title>Order-level fern plastome phylogenomics</title><author>Kuo, Li-Yaung ; Qi, Xinping ; Ma, Hong ; Li, Fay-Wei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4762-70936eb0b1f7290c016c806a962a5d9b5f901ce1e575aed99a80d3c1c1a645833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Amino acids</topic><topic>Codons</topic><topic>Evolution</topic><topic>Ferns</topic><topic>Gene sequencing</topic><topic>Hazards</topic><topic>Humidity</topic><topic>Hymenophyllum</topic><topic>Inversions</topic><topic>Inverted repeat</topic><topic>Mesophyll</topic><topic>Nucleotides</topic><topic>Partitions</topic><topic>phylogenetic conflict</topic><topic>Phylogenetics</topic><topic>Phylogeny</topic><topic>plastome organization</topic><topic>Plastomes</topic><topic>RESEARCH ARTICLE</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>Trichomanoideae</topic><topic>tRNA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kuo, Li-Yaung</creatorcontrib><creatorcontrib>Qi, Xinping</creatorcontrib><creatorcontrib>Ma, Hong</creatorcontrib><creatorcontrib>Li, Fay-Wei</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of botany</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kuo, Li-Yaung</au><au>Qi, Xinping</au><au>Ma, Hong</au><au>Li, Fay-Wei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Order-level fern plastome phylogenomics: new insights from Hymenophyllales</atitle><jtitle>American journal of botany</jtitle><addtitle>Am J Bot</addtitle><date>2018-09</date><risdate>2018</risdate><volume>105</volume><issue>9</issue><spage>1545</spage><epage>1555</epage><pages>1545-1555</pages><issn>0002-9122</issn><eissn>1537-2197</eissn><abstract>Premise of the Study
Filmy ferns (Hymenophyllales) are a highly specialized lineage, having mesophyll one‐cell layer thick and inhabiting particularly shaded and humid environments. The phylogenetic placement of Hymenophyllales has been inconclusive, and while over 87 whole fern plastomes have been published, none was from Hymenophyllales. To better understand the evolutionary history of filmy ferns, we sequenced the first complete plastome for this order.
Methods
We compiled a phylogenomic plastome data set encompassing all 11 fern orders, and reconstructed phylogenies using different data types (nucleotides, codons, and amino acids) and partition schemes (codon positions and loci). To infer the evolution of fern plastome organization, we coded plastome features, including inversions, inverted repeat boundary shifts, gene losses, and tRNA anticodon sequences as characters, and reconstructed the ancestral states for these characters.
Key Results
We discovered a suite of novel, Hymenophyllales‐specific plastome structures that likely resulted from repeated expansions and contractions of the inverted repeat regions. Our phylogenetic analyses reveal that Hymenophyllales is highly supported as either sister to Gleicheniales or to Gleicheniales + the remaining non‐Osmundales leptosporangiates, depending on the data type and partition scheme.
Conclusions
Although our analyses could not confidently resolve the phylogenetic position of Hymenophyalles, the results here highlight the danger of drawing conclusions from “all‐in” phylogenomic data set without exploring potential inconsistencies in the data. Finally, our first order‐level reconstruction of fern plastome structural evolution provides a useful framework for future plastome research.</abstract><cop>United States</cop><pub>John Wiley and Sons, Inc</pub><pmid>30168575</pmid><doi>10.1002/ajb2.1152</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-3388-3757</orcidid><orcidid>https://orcid.org/0000-0002-0076-0152</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Amino acids Codons Evolution Ferns Gene sequencing Hazards Humidity Hymenophyllum Inversions Inverted repeat Mesophyll Nucleotides Partitions phylogenetic conflict Phylogenetics Phylogeny plastome organization Plastomes RESEARCH ARTICLE Ribonucleic acid RNA Trichomanoideae tRNA |
title | Order-level fern plastome phylogenomics: new insights from Hymenophyllales |
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