Search for evolutionary roots of land plant arabinogalactan‐proteins in charophytes: presence of a rhamnogalactan‐protein in Spirogyra pratensis (Zygnematophyceae)
SUMMARY Charophyte green algae (CGA) are assigned to be the closest relatives of land plants and therefore enlighten processes in the colonization of terrestrial habitats. For the transition from water to land, plants needed significant physiological and structural changes, as well as with regard to...
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Veröffentlicht in: | The Plant journal : for cell and molecular biology 2022-02, Vol.109 (3), p.568-584 |
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creator | Pfeifer, Lukas Utermöhlen, Jon Happ, Kathrin Permann, Charlotte Holzinger, Andreas Schwartzenberg, Klaus Classen, Birgit |
description | SUMMARY
Charophyte green algae (CGA) are assigned to be the closest relatives of land plants and therefore enlighten processes in the colonization of terrestrial habitats. For the transition from water to land, plants needed significant physiological and structural changes, as well as with regard to cell wall composition. Sequential extraction of cell walls of Nitellopsis obtusa (Charophyceae) and Spirogyra pratensis (Zygnematophyceae) offered a comparative overview on cell wall composition of late branching CGA. Because arabinogalactan‐proteins (AGPs) are considered common for all land plant cell walls, we were interested in whether these special glycoproteins are present in CGA. Therefore, we investigated both species with regard to characteristic features of AGPs. In the cell wall of Nitellopsis, no hydroxyproline was present and no AGP was precipitable with the β‐glucosyl Yariv’s reagent (βGlcY). By contrast, βGlcY precipitation of the water‐soluble cell wall fraction of Spirogyra yielded a glycoprotein fraction rich in hydroxyproline, indicating the presence of AGPs. Putative AGPs in the cell walls of non‐conjugating Spirogyra filaments, especially in the area of transverse walls, were detected by staining with βGlcY. Labelling increased strongly in generative growth stages, especially during zygospore development. Investigations of the fine structure of the glycan part of βGlcY‐precipitated molecules revealed that the galactan backbone resembled that of AGPs with 1,3‐ 1,6‐ and 1,3,6‐linked Galp moieties. Araf was present only in small amounts and the terminating sugars consisted predominantly of pyranosidic terminal and 1,3‐linked rhamnose residues. We introduce the term ‘rhamnogalactan‐protein’ for this special AGP‐modification present in S. pratensis.
Significance Statement
Approximately 500 million years ago, land plants evolved in the streptophyte lineage, which required severe changes in cell wall composition, as well as with regard to arabinogalactan‐proteins (AGPs), which are signaling glycoproteins in all land plants. Our investigations on Nitellopsis (Charophyceae) and Spirogyra (Zygnematophyceae) help to determine the evolutionary origin of AGPs in algae and reveal that only Spirogyra contains molecules comparable to land plant AGPs, which possess unique structural modifications, namely rhamnose instead of arabinose (rhamnogalactan‐proteins). |
doi_str_mv | 10.1111/tpj.15577 |
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Charophyte green algae (CGA) are assigned to be the closest relatives of land plants and therefore enlighten processes in the colonization of terrestrial habitats. For the transition from water to land, plants needed significant physiological and structural changes, as well as with regard to cell wall composition. Sequential extraction of cell walls of Nitellopsis obtusa (Charophyceae) and Spirogyra pratensis (Zygnematophyceae) offered a comparative overview on cell wall composition of late branching CGA. Because arabinogalactan‐proteins (AGPs) are considered common for all land plant cell walls, we were interested in whether these special glycoproteins are present in CGA. Therefore, we investigated both species with regard to characteristic features of AGPs. In the cell wall of Nitellopsis, no hydroxyproline was present and no AGP was precipitable with the β‐glucosyl Yariv’s reagent (βGlcY). By contrast, βGlcY precipitation of the water‐soluble cell wall fraction of Spirogyra yielded a glycoprotein fraction rich in hydroxyproline, indicating the presence of AGPs. Putative AGPs in the cell walls of non‐conjugating Spirogyra filaments, especially in the area of transverse walls, were detected by staining with βGlcY. Labelling increased strongly in generative growth stages, especially during zygospore development. Investigations of the fine structure of the glycan part of βGlcY‐precipitated molecules revealed that the galactan backbone resembled that of AGPs with 1,3‐ 1,6‐ and 1,3,6‐linked Galp moieties. Araf was present only in small amounts and the terminating sugars consisted predominantly of pyranosidic terminal and 1,3‐linked rhamnose residues. We introduce the term ‘rhamnogalactan‐protein’ for this special AGP‐modification present in S. pratensis.
Significance Statement
Approximately 500 million years ago, land plants evolved in the streptophyte lineage, which required severe changes in cell wall composition, as well as with regard to arabinogalactan‐proteins (AGPs), which are signaling glycoproteins in all land plants. Our investigations on Nitellopsis (Charophyceae) and Spirogyra (Zygnematophyceae) help to determine the evolutionary origin of AGPs in algae and reveal that only Spirogyra contains molecules comparable to land plant AGPs, which possess unique structural modifications, namely rhamnose instead of arabinose (rhamnogalactan‐proteins).</description><identifier>ISSN: 0960-7412</identifier><identifier>EISSN: 1365-313X</identifier><identifier>DOI: 10.1111/tpj.15577</identifier><identifier>PMID: 34767672</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Algae ; Aquatic plants ; Arabinogalactan ; arabinogalactan‐proteins ; Biological Evolution ; cell wall ; Cell Wall - chemistry ; Cell walls ; Charophyceae ; Charophyceae - chemistry ; Charophyceae - genetics ; charophyte algae ; Chemical precipitation ; Composition ; Embryophyta - chemistry ; Filaments ; Fine structure ; Galactans - chemistry ; Galactans - genetics ; Glycan ; Glycoproteins ; Hydroxyproline ; Labeling ; Mucoproteins - chemistry ; Mucoproteins - genetics ; Nitellopsis obtuse ; plant evolution ; Plant Proteins - chemistry ; Plant Proteins - genetics ; polysaccharides ; Proteins ; Reagents ; Rhamnose ; Spirogyra ; Spirogyra - chemistry ; Spirogyra - genetics ; Spirogyra pratensis ; Sugar ; terrestrialization ; Ultrastructure ; Yariv’s reagent ; Zygnematophyceae</subject><ispartof>The Plant journal : for cell and molecular biology, 2022-02, Vol.109 (3), p.568-584</ispartof><rights>2021 The Authors. published by Society for Experimental Biology and John Wiley & Sons Ltd.</rights><rights>2021 The Authors. The Plant Journal published by Society for Experimental Biology and John Wiley & Sons Ltd.</rights><rights>2021. This article 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><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5097-b6fe9e052de1b05f9efeea577e40da7723c978e114d74e9c81568fd9396a09b23</citedby><cites>FETCH-LOGICAL-c5097-b6fe9e052de1b05f9efeea577e40da7723c978e114d74e9c81568fd9396a09b23</cites><orcidid>0000-0003-1452-801X ; 0000-0002-7076-4597 ; 0000-0003-0276-6053 ; 0000-0002-7745-3978</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Ftpj.15577$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Ftpj.15577$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34767672$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pfeifer, Lukas</creatorcontrib><creatorcontrib>Utermöhlen, Jon</creatorcontrib><creatorcontrib>Happ, Kathrin</creatorcontrib><creatorcontrib>Permann, Charlotte</creatorcontrib><creatorcontrib>Holzinger, Andreas</creatorcontrib><creatorcontrib>Schwartzenberg, Klaus</creatorcontrib><creatorcontrib>Classen, Birgit</creatorcontrib><title>Search for evolutionary roots of land plant arabinogalactan‐proteins in charophytes: presence of a rhamnogalactan‐protein in Spirogyra pratensis (Zygnematophyceae)</title><title>The Plant journal : for cell and molecular biology</title><addtitle>Plant J</addtitle><description>SUMMARY
Charophyte green algae (CGA) are assigned to be the closest relatives of land plants and therefore enlighten processes in the colonization of terrestrial habitats. For the transition from water to land, plants needed significant physiological and structural changes, as well as with regard to cell wall composition. Sequential extraction of cell walls of Nitellopsis obtusa (Charophyceae) and Spirogyra pratensis (Zygnematophyceae) offered a comparative overview on cell wall composition of late branching CGA. Because arabinogalactan‐proteins (AGPs) are considered common for all land plant cell walls, we were interested in whether these special glycoproteins are present in CGA. Therefore, we investigated both species with regard to characteristic features of AGPs. In the cell wall of Nitellopsis, no hydroxyproline was present and no AGP was precipitable with the β‐glucosyl Yariv’s reagent (βGlcY). By contrast, βGlcY precipitation of the water‐soluble cell wall fraction of Spirogyra yielded a glycoprotein fraction rich in hydroxyproline, indicating the presence of AGPs. Putative AGPs in the cell walls of non‐conjugating Spirogyra filaments, especially in the area of transverse walls, were detected by staining with βGlcY. Labelling increased strongly in generative growth stages, especially during zygospore development. Investigations of the fine structure of the glycan part of βGlcY‐precipitated molecules revealed that the galactan backbone resembled that of AGPs with 1,3‐ 1,6‐ and 1,3,6‐linked Galp moieties. Araf was present only in small amounts and the terminating sugars consisted predominantly of pyranosidic terminal and 1,3‐linked rhamnose residues. We introduce the term ‘rhamnogalactan‐protein’ for this special AGP‐modification present in S. pratensis.
Significance Statement
Approximately 500 million years ago, land plants evolved in the streptophyte lineage, which required severe changes in cell wall composition, as well as with regard to arabinogalactan‐proteins (AGPs), which are signaling glycoproteins in all land plants. Our investigations on Nitellopsis (Charophyceae) and Spirogyra (Zygnematophyceae) help to determine the evolutionary origin of AGPs in algae and reveal that only Spirogyra contains molecules comparable to land plant AGPs, which possess unique structural modifications, namely rhamnose instead of arabinose (rhamnogalactan‐proteins).</description><subject>Algae</subject><subject>Aquatic plants</subject><subject>Arabinogalactan</subject><subject>arabinogalactan‐proteins</subject><subject>Biological Evolution</subject><subject>cell wall</subject><subject>Cell Wall - chemistry</subject><subject>Cell walls</subject><subject>Charophyceae</subject><subject>Charophyceae - chemistry</subject><subject>Charophyceae - genetics</subject><subject>charophyte algae</subject><subject>Chemical precipitation</subject><subject>Composition</subject><subject>Embryophyta - chemistry</subject><subject>Filaments</subject><subject>Fine structure</subject><subject>Galactans - chemistry</subject><subject>Galactans - genetics</subject><subject>Glycan</subject><subject>Glycoproteins</subject><subject>Hydroxyproline</subject><subject>Labeling</subject><subject>Mucoproteins - chemistry</subject><subject>Mucoproteins - genetics</subject><subject>Nitellopsis obtuse</subject><subject>plant evolution</subject><subject>Plant Proteins - chemistry</subject><subject>Plant Proteins - genetics</subject><subject>polysaccharides</subject><subject>Proteins</subject><subject>Reagents</subject><subject>Rhamnose</subject><subject>Spirogyra</subject><subject>Spirogyra - chemistry</subject><subject>Spirogyra - genetics</subject><subject>Spirogyra pratensis</subject><subject>Sugar</subject><subject>terrestrialization</subject><subject>Ultrastructure</subject><subject>Yariv’s reagent</subject><subject>Zygnematophyceae</subject><issn>0960-7412</issn><issn>1365-313X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>EIF</sourceid><recordid>eNp1kd9qFDEUhwdR7Fq98AUk4E17MW2SmSQbLwQp_qWg0AriTTibObOTZTYZk2xl73wE38L38knMurWoaALJRb7zcXJ-VfWQ0RNW1mmeVidMCKVuVTPWSFE3rPlwu5pRLWmtWsYPqnsprShlqpHt3eqgaZUsm8-qbxcI0Q6kD5HgVRg32QUPcUtiCDmR0JMRfEemcmYCERbOhyWMYDP471--TjFkdD4R54kdIIZp2GZMT8gUMaG3uDMAiQOs_1W3K7uYXAzLbYRSAxl9cokcfdwuPa4h73wWAY_vV3d6GBM-uL4Pq_cvnl-evarP3758ffbsvLaCalUvZI8aqeAdsgUVvcYeEcpksKUdKMUbq9UcGWs71aK2cybkvO90oyVQveDNYfV07502izV2Fn2OMJopunWZigngzJ8v3g1mGa6MkowLNi-Co2tBDJ82mLJZu2RxLAPEsEmGC61azWUjCvr4L3QVNtGX7xkueSOkVkIW6nhP2RhSitjfNMOo2cVvSvzmZ_yFffR79zfkr7wLcLoHPrsRt_83mct3b_bKH2EGwbM</recordid><startdate>202202</startdate><enddate>202202</enddate><creator>Pfeifer, Lukas</creator><creator>Utermöhlen, Jon</creator><creator>Happ, Kathrin</creator><creator>Permann, Charlotte</creator><creator>Holzinger, Andreas</creator><creator>Schwartzenberg, Klaus</creator><creator>Classen, Birgit</creator><general>Blackwell Publishing Ltd</general><scope>24P</scope><scope>WIN</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>7QO</scope><scope>7QP</scope><scope>7QR</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1452-801X</orcidid><orcidid>https://orcid.org/0000-0002-7076-4597</orcidid><orcidid>https://orcid.org/0000-0003-0276-6053</orcidid><orcidid>https://orcid.org/0000-0002-7745-3978</orcidid></search><sort><creationdate>202202</creationdate><title>Search for evolutionary roots of land plant arabinogalactan‐proteins in charophytes: presence of a rhamnogalactan‐protein in Spirogyra pratensis (Zygnematophyceae)</title><author>Pfeifer, Lukas ; Utermöhlen, Jon ; Happ, Kathrin ; Permann, Charlotte ; Holzinger, Andreas ; Schwartzenberg, Klaus ; Classen, Birgit</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5097-b6fe9e052de1b05f9efeea577e40da7723c978e114d74e9c81568fd9396a09b23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Algae</topic><topic>Aquatic plants</topic><topic>Arabinogalactan</topic><topic>arabinogalactan‐proteins</topic><topic>Biological Evolution</topic><topic>cell wall</topic><topic>Cell Wall - chemistry</topic><topic>Cell walls</topic><topic>Charophyceae</topic><topic>Charophyceae - chemistry</topic><topic>Charophyceae - genetics</topic><topic>charophyte algae</topic><topic>Chemical precipitation</topic><topic>Composition</topic><topic>Embryophyta - chemistry</topic><topic>Filaments</topic><topic>Fine structure</topic><topic>Galactans - chemistry</topic><topic>Galactans - genetics</topic><topic>Glycan</topic><topic>Glycoproteins</topic><topic>Hydroxyproline</topic><topic>Labeling</topic><topic>Mucoproteins - chemistry</topic><topic>Mucoproteins - genetics</topic><topic>Nitellopsis obtuse</topic><topic>plant evolution</topic><topic>Plant Proteins - chemistry</topic><topic>Plant Proteins - genetics</topic><topic>polysaccharides</topic><topic>Proteins</topic><topic>Reagents</topic><topic>Rhamnose</topic><topic>Spirogyra</topic><topic>Spirogyra - chemistry</topic><topic>Spirogyra - genetics</topic><topic>Spirogyra pratensis</topic><topic>Sugar</topic><topic>terrestrialization</topic><topic>Ultrastructure</topic><topic>Yariv’s reagent</topic><topic>Zygnematophyceae</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pfeifer, Lukas</creatorcontrib><creatorcontrib>Utermöhlen, Jon</creatorcontrib><creatorcontrib>Happ, Kathrin</creatorcontrib><creatorcontrib>Permann, Charlotte</creatorcontrib><creatorcontrib>Holzinger, Andreas</creatorcontrib><creatorcontrib>Schwartzenberg, Klaus</creatorcontrib><creatorcontrib>Classen, Birgit</creatorcontrib><collection>Wiley-Blackwell Open Access Titles</collection><collection>Wiley Free Content</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Plant journal : for cell and molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pfeifer, Lukas</au><au>Utermöhlen, Jon</au><au>Happ, Kathrin</au><au>Permann, Charlotte</au><au>Holzinger, Andreas</au><au>Schwartzenberg, Klaus</au><au>Classen, Birgit</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Search for evolutionary roots of land plant arabinogalactan‐proteins in charophytes: presence of a rhamnogalactan‐protein in Spirogyra pratensis (Zygnematophyceae)</atitle><jtitle>The Plant journal : for cell and molecular biology</jtitle><addtitle>Plant J</addtitle><date>2022-02</date><risdate>2022</risdate><volume>109</volume><issue>3</issue><spage>568</spage><epage>584</epage><pages>568-584</pages><issn>0960-7412</issn><eissn>1365-313X</eissn><abstract>SUMMARY
Charophyte green algae (CGA) are assigned to be the closest relatives of land plants and therefore enlighten processes in the colonization of terrestrial habitats. For the transition from water to land, plants needed significant physiological and structural changes, as well as with regard to cell wall composition. Sequential extraction of cell walls of Nitellopsis obtusa (Charophyceae) and Spirogyra pratensis (Zygnematophyceae) offered a comparative overview on cell wall composition of late branching CGA. Because arabinogalactan‐proteins (AGPs) are considered common for all land plant cell walls, we were interested in whether these special glycoproteins are present in CGA. Therefore, we investigated both species with regard to characteristic features of AGPs. In the cell wall of Nitellopsis, no hydroxyproline was present and no AGP was precipitable with the β‐glucosyl Yariv’s reagent (βGlcY). By contrast, βGlcY precipitation of the water‐soluble cell wall fraction of Spirogyra yielded a glycoprotein fraction rich in hydroxyproline, indicating the presence of AGPs. Putative AGPs in the cell walls of non‐conjugating Spirogyra filaments, especially in the area of transverse walls, were detected by staining with βGlcY. Labelling increased strongly in generative growth stages, especially during zygospore development. Investigations of the fine structure of the glycan part of βGlcY‐precipitated molecules revealed that the galactan backbone resembled that of AGPs with 1,3‐ 1,6‐ and 1,3,6‐linked Galp moieties. Araf was present only in small amounts and the terminating sugars consisted predominantly of pyranosidic terminal and 1,3‐linked rhamnose residues. We introduce the term ‘rhamnogalactan‐protein’ for this special AGP‐modification present in S. pratensis.
Significance Statement
Approximately 500 million years ago, land plants evolved in the streptophyte lineage, which required severe changes in cell wall composition, as well as with regard to arabinogalactan‐proteins (AGPs), which are signaling glycoproteins in all land plants. Our investigations on Nitellopsis (Charophyceae) and Spirogyra (Zygnematophyceae) help to determine the evolutionary origin of AGPs in algae and reveal that only Spirogyra contains molecules comparable to land plant AGPs, which possess unique structural modifications, namely rhamnose instead of arabinose (rhamnogalactan‐proteins).</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>34767672</pmid><doi>10.1111/tpj.15577</doi><tpages>584</tpages><orcidid>https://orcid.org/0000-0003-1452-801X</orcidid><orcidid>https://orcid.org/0000-0002-7076-4597</orcidid><orcidid>https://orcid.org/0000-0003-0276-6053</orcidid><orcidid>https://orcid.org/0000-0002-7745-3978</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Algae Aquatic plants Arabinogalactan arabinogalactan‐proteins Biological Evolution cell wall Cell Wall - chemistry Cell walls Charophyceae Charophyceae - chemistry Charophyceae - genetics charophyte algae Chemical precipitation Composition Embryophyta - chemistry Filaments Fine structure Galactans - chemistry Galactans - genetics Glycan Glycoproteins Hydroxyproline Labeling Mucoproteins - chemistry Mucoproteins - genetics Nitellopsis obtuse plant evolution Plant Proteins - chemistry Plant Proteins - genetics polysaccharides Proteins Reagents Rhamnose Spirogyra Spirogyra - chemistry Spirogyra - genetics Spirogyra pratensis Sugar terrestrialization Ultrastructure Yariv’s reagent Zygnematophyceae |
title | Search for evolutionary roots of land plant arabinogalactan‐proteins in charophytes: presence of a rhamnogalactan‐protein in Spirogyra pratensis (Zygnematophyceae) |
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