Expression of a luteoviral movement protein in transgenic plants leads to carbohydrate accumulation and reduced photosynthetic capacity in source leaves
Summary Elucidating the role of viral genes in transgenic plants revealed that the movement protein (MP) from tobacco mosaic virus is responsible for altered carbohydrate allocation in tobacco and potato plants. To study whether this is a general feature of viral MPs, the movement protein MP17 of po...
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Veröffentlicht in: | The Plant journal : for cell and molecular biology 1997-11, Vol.12 (5), p.1045-1056 |
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creator | Herbers, Karin Tacke, Eckhardt Hazirezaei, Mohammad Krause, Klaus‐Peter Melzer, Michael Rohde, Wolfgang Sonnewald, Uwe |
description | Summary
Elucidating the role of viral genes in transgenic plants revealed that the movement protein (MP) from tobacco mosaic virus is responsible for altered carbohydrate allocation in tobacco and potato plants. To study whether this is a general feature of viral MPs, the movement protein MP17 of potato leafroll virus (PLRV), a phloem‐restricted luteovirus, was constitutively expressed in tobacco plants. Transgenic lines were strongly reduced in height and developed bleached and sometimes even necrotic areas on their source leaves. Levels of soluble sugars and starch were significantly increased in source leaves. Yet, in leaf laminae the hexose—phosphate content was unaltered and ATP reduced to only a small extent, indicating that these leaves were able to maintain homeostatic conditions by compartmentalization of soluble sugars, probably in the vacuole. On the contrary, midribs contained lower levels of soluble sugars, ATP, hexose—phosphates and UDP‐glucose supporting the concept of limited uptake and catabolism of sucrose in the phloem. The accumulation of carbohydrates led to a decreased photosynthetic capacity and carboxylation efficiency of ribulose‐1,5‐bisphosphate carboxylase/oxygenase (rubisco) probably owing to decreased expression of photosynthetic proteins. In parallel, levels of pathogenesis‐related proteins were elevated which may be the reason for the obtained limited resistance against the unrelated potato virus Y (PVY)N in the transgenic tobacco plants. Ultrathin sections of affected leaves harvested from 2‐week‐old plants revealed plasmodesmal alterations in the phloem tissue while plasmodesmata between mesophyll cells were indistinguishable from wild‐type. These data favour the phloem tissue to be the primary site of PLRV MP17 action in altering carbohydrate metabolism. |
doi_str_mv | 10.1046/j.1365-313X.1997.12051045.x |
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Elucidating the role of viral genes in transgenic plants revealed that the movement protein (MP) from tobacco mosaic virus is responsible for altered carbohydrate allocation in tobacco and potato plants. To study whether this is a general feature of viral MPs, the movement protein MP17 of potato leafroll virus (PLRV), a phloem‐restricted luteovirus, was constitutively expressed in tobacco plants. Transgenic lines were strongly reduced in height and developed bleached and sometimes even necrotic areas on their source leaves. Levels of soluble sugars and starch were significantly increased in source leaves. Yet, in leaf laminae the hexose—phosphate content was unaltered and ATP reduced to only a small extent, indicating that these leaves were able to maintain homeostatic conditions by compartmentalization of soluble sugars, probably in the vacuole. On the contrary, midribs contained lower levels of soluble sugars, ATP, hexose—phosphates and UDP‐glucose supporting the concept of limited uptake and catabolism of sucrose in the phloem. The accumulation of carbohydrates led to a decreased photosynthetic capacity and carboxylation efficiency of ribulose‐1,5‐bisphosphate carboxylase/oxygenase (rubisco) probably owing to decreased expression of photosynthetic proteins. In parallel, levels of pathogenesis‐related proteins were elevated which may be the reason for the obtained limited resistance against the unrelated potato virus Y (PVY)N in the transgenic tobacco plants. Ultrathin sections of affected leaves harvested from 2‐week‐old plants revealed plasmodesmal alterations in the phloem tissue while plasmodesmata between mesophyll cells were indistinguishable from wild‐type. These data favour the phloem tissue to be the primary site of PLRV MP17 action in altering carbohydrate metabolism.</description><identifier>ISSN: 0960-7412</identifier><identifier>EISSN: 1365-313X</identifier><identifier>DOI: 10.1046/j.1365-313X.1997.12051045.x</identifier><identifier>PMID: 9418046</identifier><language>eng</language><publisher>Osney Mead, Oxford OX2 0EL, UK: Blackwell Science Ltd</publisher><subject>Biological and medical sciences ; Carbohydrate Metabolism ; Fundamental and applied biological sciences. Psychology ; Light ; Luteovirus - genetics ; Luteovirus - physiology ; Nicotiana - physiology ; Nicotiana - ultrastructure ; Nicotiana - virology ; Photosynthesis - physiology ; Phytopathology. Animal pests. Plant and forest protection ; Plant Leaves ; Plant Viral Movement Proteins ; Plant viruses and viroids ; Plants, Genetically Modified ; Plants, Toxic ; Potyvirus - genetics ; Potyvirus - physiology ; Recombinant Fusion Proteins - biosynthesis ; Systematics. Structure, properties and multiplication. Genetics ; Tobacco Mosaic Virus - physiology ; Transcription, Genetic ; Viral Proteins - biosynthesis</subject><ispartof>The Plant journal : for cell and molecular biology, 1997-11, Vol.12 (5), p.1045-1056</ispartof><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4375-131c8d0ca84b5aa2cf9a09776272c9562cc23752ca4c49a08b63ea535c6271223</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1046%2Fj.1365-313X.1997.12051045.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1046%2Fj.1365-313X.1997.12051045.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2110924$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9418046$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Herbers, Karin</creatorcontrib><creatorcontrib>Tacke, Eckhardt</creatorcontrib><creatorcontrib>Hazirezaei, Mohammad</creatorcontrib><creatorcontrib>Krause, Klaus‐Peter</creatorcontrib><creatorcontrib>Melzer, Michael</creatorcontrib><creatorcontrib>Rohde, Wolfgang</creatorcontrib><creatorcontrib>Sonnewald, Uwe</creatorcontrib><title>Expression of a luteoviral movement protein in transgenic plants leads to carbohydrate accumulation and reduced photosynthetic capacity in source leaves</title><title>The Plant journal : for cell and molecular biology</title><addtitle>Plant J</addtitle><description>Summary
Elucidating the role of viral genes in transgenic plants revealed that the movement protein (MP) from tobacco mosaic virus is responsible for altered carbohydrate allocation in tobacco and potato plants. To study whether this is a general feature of viral MPs, the movement protein MP17 of potato leafroll virus (PLRV), a phloem‐restricted luteovirus, was constitutively expressed in tobacco plants. Transgenic lines were strongly reduced in height and developed bleached and sometimes even necrotic areas on their source leaves. Levels of soluble sugars and starch were significantly increased in source leaves. Yet, in leaf laminae the hexose—phosphate content was unaltered and ATP reduced to only a small extent, indicating that these leaves were able to maintain homeostatic conditions by compartmentalization of soluble sugars, probably in the vacuole. On the contrary, midribs contained lower levels of soluble sugars, ATP, hexose—phosphates and UDP‐glucose supporting the concept of limited uptake and catabolism of sucrose in the phloem. The accumulation of carbohydrates led to a decreased photosynthetic capacity and carboxylation efficiency of ribulose‐1,5‐bisphosphate carboxylase/oxygenase (rubisco) probably owing to decreased expression of photosynthetic proteins. In parallel, levels of pathogenesis‐related proteins were elevated which may be the reason for the obtained limited resistance against the unrelated potato virus Y (PVY)N in the transgenic tobacco plants. Ultrathin sections of affected leaves harvested from 2‐week‐old plants revealed plasmodesmal alterations in the phloem tissue while plasmodesmata between mesophyll cells were indistinguishable from wild‐type. These data favour the phloem tissue to be the primary site of PLRV MP17 action in altering carbohydrate metabolism.</description><subject>Biological and medical sciences</subject><subject>Carbohydrate Metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Light</subject><subject>Luteovirus - genetics</subject><subject>Luteovirus - physiology</subject><subject>Nicotiana - physiology</subject><subject>Nicotiana - ultrastructure</subject><subject>Nicotiana - virology</subject><subject>Photosynthesis - physiology</subject><subject>Phytopathology. Animal pests. Plant and forest protection</subject><subject>Plant Leaves</subject><subject>Plant Viral Movement Proteins</subject><subject>Plant viruses and viroids</subject><subject>Plants, Genetically Modified</subject><subject>Plants, Toxic</subject><subject>Potyvirus - genetics</subject><subject>Potyvirus - physiology</subject><subject>Recombinant Fusion Proteins - biosynthesis</subject><subject>Systematics. Structure, properties and multiplication. Genetics</subject><subject>Tobacco Mosaic Virus - physiology</subject><subject>Transcription, Genetic</subject><subject>Viral Proteins - biosynthesis</subject><issn>0960-7412</issn><issn>1365-313X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkd2O0zAQhS0EWsrCIyBZAnGX4J_EacQVWpY_rQQXi8SdNZ1MaaokDrZTmjfhcXHUbu-RLFnW-eZ4Zg5jr6TIpSjM230utSkzLfXPXNZ1lUslyqSU-fERW120x2wlaiOyqpDqKXsWwl4IWWlTXLGrupDrZLVif2-Po6cQWjdwt-XAuymSO7QeOt67A_U0RD56F6kdeDrRwxB-0dAiHzsYYuAdQRN4dBzBb9xubjxE4oA49VMHcTGGoeGemgmp4ePORRfmIe4oJhOEEbCN8-Id3OSRFsMDhefsyRa6QC_O9zX78fH2_uZzdvft05eb93cZFroqM6klrhuBsC42JYDCbQ2iriqjKoV1aRSiSpxCKLBI0npjNEGpS0yEVEpfszcn3zTk74lCtH0bkLo0HLkpWGm0NkYXCXx3AtG7EDxt7ejbHvxspbBLLnZvl93bZfd2ycU-5GKPqfrl-Ztp01NzqT0HkfTXZx0CQrdNa8Y2XDAlpajV0sSHE_an7Wj-nw7s_fevDy_9D9-Grow</recordid><startdate>199711</startdate><enddate>199711</enddate><creator>Herbers, Karin</creator><creator>Tacke, Eckhardt</creator><creator>Hazirezaei, Mohammad</creator><creator>Krause, Klaus‐Peter</creator><creator>Melzer, Michael</creator><creator>Rohde, Wolfgang</creator><creator>Sonnewald, Uwe</creator><general>Blackwell Science Ltd</general><general>Blackwell Science</general><scope>IQODW</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>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>199711</creationdate><title>Expression of a luteoviral movement protein in transgenic plants leads to carbohydrate accumulation and reduced photosynthetic capacity in source leaves</title><author>Herbers, Karin ; Tacke, Eckhardt ; Hazirezaei, Mohammad ; Krause, Klaus‐Peter ; Melzer, Michael ; Rohde, Wolfgang ; Sonnewald, Uwe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4375-131c8d0ca84b5aa2cf9a09776272c9562cc23752ca4c49a08b63ea535c6271223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Biological and medical sciences</topic><topic>Carbohydrate Metabolism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Light</topic><topic>Luteovirus - genetics</topic><topic>Luteovirus - physiology</topic><topic>Nicotiana - physiology</topic><topic>Nicotiana - ultrastructure</topic><topic>Nicotiana - virology</topic><topic>Photosynthesis - physiology</topic><topic>Phytopathology. Animal pests. Plant and forest protection</topic><topic>Plant Leaves</topic><topic>Plant Viral Movement Proteins</topic><topic>Plant viruses and viroids</topic><topic>Plants, Genetically Modified</topic><topic>Plants, Toxic</topic><topic>Potyvirus - genetics</topic><topic>Potyvirus - physiology</topic><topic>Recombinant Fusion Proteins - biosynthesis</topic><topic>Systematics. Structure, properties and multiplication. Genetics</topic><topic>Tobacco Mosaic Virus - physiology</topic><topic>Transcription, Genetic</topic><topic>Viral Proteins - biosynthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Herbers, Karin</creatorcontrib><creatorcontrib>Tacke, Eckhardt</creatorcontrib><creatorcontrib>Hazirezaei, Mohammad</creatorcontrib><creatorcontrib>Krause, Klaus‐Peter</creatorcontrib><creatorcontrib>Melzer, Michael</creatorcontrib><creatorcontrib>Rohde, Wolfgang</creatorcontrib><creatorcontrib>Sonnewald, Uwe</creatorcontrib><collection>Pascal-Francis</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>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>The Plant journal : for cell and molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Herbers, Karin</au><au>Tacke, Eckhardt</au><au>Hazirezaei, Mohammad</au><au>Krause, Klaus‐Peter</au><au>Melzer, Michael</au><au>Rohde, Wolfgang</au><au>Sonnewald, Uwe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of a luteoviral movement protein in transgenic plants leads to carbohydrate accumulation and reduced photosynthetic capacity in source leaves</atitle><jtitle>The Plant journal : for cell and molecular biology</jtitle><addtitle>Plant J</addtitle><date>1997-11</date><risdate>1997</risdate><volume>12</volume><issue>5</issue><spage>1045</spage><epage>1056</epage><pages>1045-1056</pages><issn>0960-7412</issn><eissn>1365-313X</eissn><abstract>Summary
Elucidating the role of viral genes in transgenic plants revealed that the movement protein (MP) from tobacco mosaic virus is responsible for altered carbohydrate allocation in tobacco and potato plants. To study whether this is a general feature of viral MPs, the movement protein MP17 of potato leafroll virus (PLRV), a phloem‐restricted luteovirus, was constitutively expressed in tobacco plants. Transgenic lines were strongly reduced in height and developed bleached and sometimes even necrotic areas on their source leaves. Levels of soluble sugars and starch were significantly increased in source leaves. Yet, in leaf laminae the hexose—phosphate content was unaltered and ATP reduced to only a small extent, indicating that these leaves were able to maintain homeostatic conditions by compartmentalization of soluble sugars, probably in the vacuole. On the contrary, midribs contained lower levels of soluble sugars, ATP, hexose—phosphates and UDP‐glucose supporting the concept of limited uptake and catabolism of sucrose in the phloem. The accumulation of carbohydrates led to a decreased photosynthetic capacity and carboxylation efficiency of ribulose‐1,5‐bisphosphate carboxylase/oxygenase (rubisco) probably owing to decreased expression of photosynthetic proteins. In parallel, levels of pathogenesis‐related proteins were elevated which may be the reason for the obtained limited resistance against the unrelated potato virus Y (PVY)N in the transgenic tobacco plants. Ultrathin sections of affected leaves harvested from 2‐week‐old plants revealed plasmodesmal alterations in the phloem tissue while plasmodesmata between mesophyll cells were indistinguishable from wild‐type. These data favour the phloem tissue to be the primary site of PLRV MP17 action in altering carbohydrate metabolism.</abstract><cop>Osney Mead, Oxford OX2 0EL, UK</cop><pub>Blackwell Science Ltd</pub><pmid>9418046</pmid><doi>10.1046/j.1365-313X.1997.12051045.x</doi><tpages>12</tpages></addata></record> |
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subjects | Biological and medical sciences Carbohydrate Metabolism Fundamental and applied biological sciences. Psychology Light Luteovirus - genetics Luteovirus - physiology Nicotiana - physiology Nicotiana - ultrastructure Nicotiana - virology Photosynthesis - physiology Phytopathology. Animal pests. Plant and forest protection Plant Leaves Plant Viral Movement Proteins Plant viruses and viroids Plants, Genetically Modified Plants, Toxic Potyvirus - genetics Potyvirus - physiology Recombinant Fusion Proteins - biosynthesis Systematics. Structure, properties and multiplication. Genetics Tobacco Mosaic Virus - physiology Transcription, Genetic Viral Proteins - biosynthesis |
title | Expression of a luteoviral movement protein in transgenic plants leads to carbohydrate accumulation and reduced photosynthetic capacity in source leaves |
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