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Comparative and phylogenetic analyses of Loranthaceae plastomes provide insights into the evolutionary trajectories of plastome degradation in hemiparasitic plants
The lifestyle transition from autotrophy to heterotrophy often leads to extensive degradation of plastomes in parasitic plants, while the evolutionary trajectories of plastome degradation associated with parasitism in hemiparasitic plants remain poorly understood. In this study, phylogeny-oriented c...
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Published in: | BMC plant biology 2024-05, Vol.24 (1), p.406-406, Article 406 |
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description | The lifestyle transition from autotrophy to heterotrophy often leads to extensive degradation of plastomes in parasitic plants, while the evolutionary trajectories of plastome degradation associated with parasitism in hemiparasitic plants remain poorly understood. In this study, phylogeny-oriented comparative analyses were conducted to investigate whether obligate Loranthaceae stem-parasites experienced higher degrees of plastome degradation than closely related facultative root-parasites and to explore the potential evolutionary events that triggered the 'domino effect' in plastome degradation of hemiparasitic plants.
Through phylogeny-oriented comparative analyses, the results indicate that Loranthaceae hemiparasites have undergone varying degrees of plastome degradation as they evolved towards a heterotrophic lifestyle. Compared to closely related facultative root-parasites, all obligate stem-parasites exhibited an elevated degree plastome degradation, characterized by increased downsizing, gene loss, and pseudogenization, thereby providing empirical evidence supporting the theoretical expectation that evolution from facultative parasitism to obligate parasitism may result in a higher degree of plastome degradation in hemiparasites. Along with infra-familial divergence in Loranthaceae, several lineage-specific gene loss/pseudogenization events occurred at deep nodes, whereas further independent gene loss/pseudogenization events were observed in shallow branches.
The findings suggest that in addition to the increasing levels of nutritional reliance on host plants, cladogenesis can be considered as another pivotal evolutionary event triggering the 'domino effect' in plastome degradation of hemiparasitic plants. These findings provide new insights into the evolutionary trajectory of plastome degradation in hemiparasitic plants. |
doi_str_mv | 10.1186/s12870-024-05094-5 |
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Through phylogeny-oriented comparative analyses, the results indicate that Loranthaceae hemiparasites have undergone varying degrees of plastome degradation as they evolved towards a heterotrophic lifestyle. Compared to closely related facultative root-parasites, all obligate stem-parasites exhibited an elevated degree plastome degradation, characterized by increased downsizing, gene loss, and pseudogenization, thereby providing empirical evidence supporting the theoretical expectation that evolution from facultative parasitism to obligate parasitism may result in a higher degree of plastome degradation in hemiparasites. Along with infra-familial divergence in Loranthaceae, several lineage-specific gene loss/pseudogenization events occurred at deep nodes, whereas further independent gene loss/pseudogenization events were observed in shallow branches.
The findings suggest that in addition to the increasing levels of nutritional reliance on host plants, cladogenesis can be considered as another pivotal evolutionary event triggering the 'domino effect' in plastome degradation of hemiparasitic plants. These findings provide new insights into the evolutionary trajectory of plastome degradation in hemiparasitic plants.</description><identifier>ISSN: 1471-2229</identifier><identifier>EISSN: 1471-2229</identifier><identifier>DOI: 10.1186/s12870-024-05094-5</identifier><identifier>PMID: 38750463</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Autotrophy ; Biological Evolution ; Biotechnology industry ; Botanical research ; Chloroplasts ; Comparative analysis ; Degradation ; Downsizing ; Evolution ; Evolution, Molecular ; Facultative parasitism ; Gene loss ; Gene mutations ; Genes ; Genetic aspects ; Genetic testing ; Genomes ; Heterotrophy ; Host plants ; Identification and classification ; Lifestyles ; Loranthaceae ; Loranthaceae - genetics ; Loranthaceae - physiology ; Mistletoe ; Natural history ; Nutrients ; Obligate parasitism ; Parasites ; Parasitic plants ; Parasitism ; Phylogenetics ; Phylogeny ; Physiological aspects ; Plant genetics ; Plants ; Plastids ; Plastids - genetics ; Plastome degradation ; Plastomes ; Proteins ; Pseudogenization ; Stems</subject><ispartof>BMC plant biology, 2024-05, Vol.24 (1), p.406-406, Article 406</ispartof><rights>2024. The Author(s).</rights><rights>COPYRIGHT 2024 BioMed Central Ltd.</rights><rights>2024. This work is licensed 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>The Author(s) 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c549t-1ebe764056432ab4f2b9d35f1c6e69d7990690e374647f8f8a32e3a10271a2b93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11097404/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3066881581?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38750463$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tang, Lilei</creatorcontrib><creatorcontrib>Wang, Tinglu</creatorcontrib><creatorcontrib>Hou, Luxiao</creatorcontrib><creatorcontrib>Zhang, Guangfei</creatorcontrib><creatorcontrib>Deng, Min</creatorcontrib><creatorcontrib>Guo, Xiaorong</creatorcontrib><creatorcontrib>Ji, Yunheng</creatorcontrib><title>Comparative and phylogenetic analyses of Loranthaceae plastomes provide insights into the evolutionary trajectories of plastome degradation in hemiparasitic plants</title><title>BMC plant biology</title><addtitle>BMC Plant Biol</addtitle><description>The lifestyle transition from autotrophy to heterotrophy often leads to extensive degradation of plastomes in parasitic plants, while the evolutionary trajectories of plastome degradation associated with parasitism in hemiparasitic plants remain poorly understood. In this study, phylogeny-oriented comparative analyses were conducted to investigate whether obligate Loranthaceae stem-parasites experienced higher degrees of plastome degradation than closely related facultative root-parasites and to explore the potential evolutionary events that triggered the 'domino effect' in plastome degradation of hemiparasitic plants.
Through phylogeny-oriented comparative analyses, the results indicate that Loranthaceae hemiparasites have undergone varying degrees of plastome degradation as they evolved towards a heterotrophic lifestyle. Compared to closely related facultative root-parasites, all obligate stem-parasites exhibited an elevated degree plastome degradation, characterized by increased downsizing, gene loss, and pseudogenization, thereby providing empirical evidence supporting the theoretical expectation that evolution from facultative parasitism to obligate parasitism may result in a higher degree of plastome degradation in hemiparasites. Along with infra-familial divergence in Loranthaceae, several lineage-specific gene loss/pseudogenization events occurred at deep nodes, whereas further independent gene loss/pseudogenization events were observed in shallow branches.
The findings suggest that in addition to the increasing levels of nutritional reliance on host plants, cladogenesis can be considered as another pivotal evolutionary event triggering the 'domino effect' in plastome degradation of hemiparasitic plants. These findings provide new insights into the evolutionary trajectory of plastome degradation in hemiparasitic plants.</description><subject>Autotrophy</subject><subject>Biological Evolution</subject><subject>Biotechnology industry</subject><subject>Botanical research</subject><subject>Chloroplasts</subject><subject>Comparative analysis</subject><subject>Degradation</subject><subject>Downsizing</subject><subject>Evolution</subject><subject>Evolution, Molecular</subject><subject>Facultative parasitism</subject><subject>Gene loss</subject><subject>Gene mutations</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genetic testing</subject><subject>Genomes</subject><subject>Heterotrophy</subject><subject>Host plants</subject><subject>Identification and classification</subject><subject>Lifestyles</subject><subject>Loranthaceae</subject><subject>Loranthaceae - genetics</subject><subject>Loranthaceae - physiology</subject><subject>Mistletoe</subject><subject>Natural history</subject><subject>Nutrients</subject><subject>Obligate parasitism</subject><subject>Parasites</subject><subject>Parasitic plants</subject><subject>Parasitism</subject><subject>Phylogenetics</subject><subject>Phylogeny</subject><subject>Physiological aspects</subject><subject>Plant genetics</subject><subject>Plants</subject><subject>Plastids</subject><subject>Plastids - genetics</subject><subject>Plastome degradation</subject><subject>Plastomes</subject><subject>Proteins</subject><subject>Pseudogenization</subject><subject>Stems</subject><issn>1471-2229</issn><issn>1471-2229</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkstu1DAUhiMEoqXwAixQJDawSPEtvqxQNeIy0khIXNaWk5wkHiVxsJ0RfR5eFKfTlg5CWcQ6_v7fx8d_lr3E6BJjyd8FTKRABSKsQCVSrCgfZeeYCVwQQtTjB-uz7FkIe4SwkEw9zc6oFCVinJ5nvzdunI030R4gN1OTz_314DqYINo6FcxwHSDkrs13zpsp9qYGA_k8mBDdmHZm7w62gdxOwXZ9DGkRXR57yOHghiVaNxl_nUdv9lBH5-3R7c4gb6DzpjErl6R5D6Nd-wl2PT9RUwzPsyetGQK8uP1fZD8-fvi--Vzsvnzabq52RV0yFQsMFQjOUMkZJaZiLalUQ8sW1xy4aoRSiCsEVDDORCtbaSgBajAiApvE0otse_RtnNnr2dsxda6dsfqm4HynjU9tDaCTbSWUbCqDgXGMVYtRa1jLiVQYiTp5vT96zUs1QlPDlCYwnJie7ky21507aIyREgyx5PDm1sG7nwuEqEcbahjSSMAtQVNUllLREomEvv4H3bvFp7dbKc6lxKXEf6nOpBvYqXXp4Ho11VdCMUQkoyt1-R8qfU16mdpN0NpUPxG8PREkJsKv2JklBL399vWUJUe29i4ED-39QDDSa6b1MdM6ZVrfZFqXSfTq4SjvJXchpn8AGrb0BA</recordid><startdate>20240516</startdate><enddate>20240516</enddate><creator>Tang, Lilei</creator><creator>Wang, Tinglu</creator><creator>Hou, Luxiao</creator><creator>Zhang, Guangfei</creator><creator>Deng, Min</creator><creator>Guo, Xiaorong</creator><creator>Ji, Yunheng</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</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>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</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>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20240516</creationdate><title>Comparative and phylogenetic analyses of Loranthaceae plastomes provide insights into the evolutionary trajectories of plastome degradation in hemiparasitic plants</title><author>Tang, Lilei ; Wang, Tinglu ; Hou, Luxiao ; Zhang, Guangfei ; Deng, Min ; Guo, Xiaorong ; Ji, Yunheng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c549t-1ebe764056432ab4f2b9d35f1c6e69d7990690e374647f8f8a32e3a10271a2b93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Autotrophy</topic><topic>Biological Evolution</topic><topic>Biotechnology industry</topic><topic>Botanical research</topic><topic>Chloroplasts</topic><topic>Comparative analysis</topic><topic>Degradation</topic><topic>Downsizing</topic><topic>Evolution</topic><topic>Evolution, Molecular</topic><topic>Facultative parasitism</topic><topic>Gene loss</topic><topic>Gene mutations</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Genetic testing</topic><topic>Genomes</topic><topic>Heterotrophy</topic><topic>Host plants</topic><topic>Identification and classification</topic><topic>Lifestyles</topic><topic>Loranthaceae</topic><topic>Loranthaceae - 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In this study, phylogeny-oriented comparative analyses were conducted to investigate whether obligate Loranthaceae stem-parasites experienced higher degrees of plastome degradation than closely related facultative root-parasites and to explore the potential evolutionary events that triggered the 'domino effect' in plastome degradation of hemiparasitic plants.
Through phylogeny-oriented comparative analyses, the results indicate that Loranthaceae hemiparasites have undergone varying degrees of plastome degradation as they evolved towards a heterotrophic lifestyle. Compared to closely related facultative root-parasites, all obligate stem-parasites exhibited an elevated degree plastome degradation, characterized by increased downsizing, gene loss, and pseudogenization, thereby providing empirical evidence supporting the theoretical expectation that evolution from facultative parasitism to obligate parasitism may result in a higher degree of plastome degradation in hemiparasites. Along with infra-familial divergence in Loranthaceae, several lineage-specific gene loss/pseudogenization events occurred at deep nodes, whereas further independent gene loss/pseudogenization events were observed in shallow branches.
The findings suggest that in addition to the increasing levels of nutritional reliance on host plants, cladogenesis can be considered as another pivotal evolutionary event triggering the 'domino effect' in plastome degradation of hemiparasitic plants. These findings provide new insights into the evolutionary trajectory of plastome degradation in hemiparasitic plants.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>38750463</pmid><doi>10.1186/s12870-024-05094-5</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Autotrophy Biological Evolution Biotechnology industry Botanical research Chloroplasts Comparative analysis Degradation Downsizing Evolution Evolution, Molecular Facultative parasitism Gene loss Gene mutations Genes Genetic aspects Genetic testing Genomes Heterotrophy Host plants Identification and classification Lifestyles Loranthaceae Loranthaceae - genetics Loranthaceae - physiology Mistletoe Natural history Nutrients Obligate parasitism Parasites Parasitic plants Parasitism Phylogenetics Phylogeny Physiological aspects Plant genetics Plants Plastids Plastids - genetics Plastome degradation Plastomes Proteins Pseudogenization Stems |
title | Comparative and phylogenetic analyses of Loranthaceae plastomes provide insights into the evolutionary trajectories of plastome degradation in hemiparasitic plants |
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