GUN4 protein plays a regulatory role in tetrapyrrole biosynthesis and chloroplast‐to‐nucleus signalling in Chlamydomonas reinhardtii
The GENOMES UNCOUPLED 4 (GUN4) protein is found only in aerobic photosynthetic organisms. We investigated the role of GUN4 in metabolic activities of the Mg branch of the tetrapyrrole biosynthesis pathway and the plastid signal‐mediated changes of nuclear gene expression in Chlamydomonas reinhardtii...
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Veröffentlicht in: | The Plant journal : for cell and molecular biology 2014-07, Vol.79 (2), p.285-298 |
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description | The GENOMES UNCOUPLED 4 (GUN4) protein is found only in aerobic photosynthetic organisms. We investigated the role of GUN4 in metabolic activities of the Mg branch of the tetrapyrrole biosynthesis pathway and the plastid signal‐mediated changes of nuclear gene expression in Chlamydomonas reinhardtii. In light, gun4 accumulates only 40% of the wild‐type chlorophyll level. Light‐ or dark‐grown gun4 mutant accumulates high levels of protoporphyrin IX (Proto), and displays increased sensitivity to moderate light intensities. Despite the photooxidative stress, gun4 fails to downregulate mRNA levels of the tetrapyrrole biosynthesis and the photosynthesis‐associated nuclear genes (PhANGs). In contrast, upon illumination, the Proto‐accumulating and light‐sensitive chlD–1 mutant displays the expected downregulation of the same nuclear genes. Although chlD–1 and the wild type have similar GUN4 transcript levels, the GUN4 protein in chlD–1 is hardly detectable. Overexpression of GUN4 in chlD–1 modifies the downregulation of nuclear gene expression, but also increases light tolerance. Therefore, GUN4 is proposed to function in ‘shielding’ Proto, and most likely MgProto, by reducing reactivity with O₂. Furthermore, GUN4 seems to be involved in sensing elevated levels of these photoreactive tetrapyrrole intermediates, and contributing to ¹O₂‐mediated retrograde signalling, originating from chlorophyll biosynthesis. |
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We investigated the role of GUN4 in metabolic activities of the Mg branch of the tetrapyrrole biosynthesis pathway and the plastid signal‐mediated changes of nuclear gene expression in Chlamydomonas reinhardtii. In light, gun4 accumulates only 40% of the wild‐type chlorophyll level. Light‐ or dark‐grown gun4 mutant accumulates high levels of protoporphyrin IX (Proto), and displays increased sensitivity to moderate light intensities. Despite the photooxidative stress, gun4 fails to downregulate mRNA levels of the tetrapyrrole biosynthesis and the photosynthesis‐associated nuclear genes (PhANGs). In contrast, upon illumination, the Proto‐accumulating and light‐sensitive chlD–1 mutant displays the expected downregulation of the same nuclear genes. Although chlD–1 and the wild type have similar GUN4 transcript levels, the GUN4 protein in chlD–1 is hardly detectable. Overexpression of GUN4 in chlD–1 modifies the downregulation of nuclear gene expression, but also increases light tolerance. Therefore, GUN4 is proposed to function in ‘shielding’ Proto, and most likely MgProto, by reducing reactivity with O₂. Furthermore, GUN4 seems to be involved in sensing elevated levels of these photoreactive tetrapyrrole intermediates, and contributing to ¹O₂‐mediated retrograde signalling, originating from chlorophyll biosynthesis.</description><identifier>ISSN: 0960-7412</identifier><identifier>EISSN: 1365-313X</identifier><identifier>DOI: 10.1111/tpj.12560</identifier><identifier>PMID: 24861705</identifier><language>eng</language><publisher>England: Blackwell Science</publisher><subject>autotrophs ; Biosynthesis ; Botany ; Cell Nucleus - metabolism ; Chlamydomonas reinhardtii ; Chlamydomonas reinhardtii - metabolism ; Chlorophyll ; Chloroplasts ; Chloroplasts - metabolism ; Gene expression ; gene expression regulation ; genes ; Genomics ; GUN4 ; light intensity ; lighting ; magnesium ; messenger RNA ; Mg chelatase ; mutants ; oxygen ; Proteins ; Protoporphyrins - metabolism ; protoporphyrin IX ; retrograde signalling ; Signal Transduction - physiology ; singlet oxygen ; tetrapyrrole biosynthesis pathway ; Tetrapyrroles - biosynthesis</subject><ispartof>The Plant journal : for cell and molecular biology, 2014-07, Vol.79 (2), p.285-298</ispartof><rights>2014 The Authors The Plant Journal © 2014 John Wiley & Sons Ltd</rights><rights>2014 The Authors The Plant Journal © 2014 John Wiley & Sons Ltd.</rights><rights>Copyright © 2014 John Wiley & Sons Ltd and the Society for Experimental Biology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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.12560$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Ftpj.12560$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24861705$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Brzezowski, Pawel</creatorcontrib><creatorcontrib>Schlicke, Hagen</creatorcontrib><creatorcontrib>Richter, Andreas</creatorcontrib><creatorcontrib>Dent, Rachel M</creatorcontrib><creatorcontrib>Niyogi, Krishna K</creatorcontrib><creatorcontrib>Grimm, Bernhard</creatorcontrib><title>GUN4 protein plays a regulatory role in tetrapyrrole biosynthesis and chloroplast‐to‐nucleus signalling in Chlamydomonas reinhardtii</title><title>The Plant journal : for cell and molecular biology</title><addtitle>Plant J</addtitle><description>The GENOMES UNCOUPLED 4 (GUN4) protein is found only in aerobic photosynthetic organisms. We investigated the role of GUN4 in metabolic activities of the Mg branch of the tetrapyrrole biosynthesis pathway and the plastid signal‐mediated changes of nuclear gene expression in Chlamydomonas reinhardtii. In light, gun4 accumulates only 40% of the wild‐type chlorophyll level. Light‐ or dark‐grown gun4 mutant accumulates high levels of protoporphyrin IX (Proto), and displays increased sensitivity to moderate light intensities. Despite the photooxidative stress, gun4 fails to downregulate mRNA levels of the tetrapyrrole biosynthesis and the photosynthesis‐associated nuclear genes (PhANGs). In contrast, upon illumination, the Proto‐accumulating and light‐sensitive chlD–1 mutant displays the expected downregulation of the same nuclear genes. Although chlD–1 and the wild type have similar GUN4 transcript levels, the GUN4 protein in chlD–1 is hardly detectable. Overexpression of GUN4 in chlD–1 modifies the downregulation of nuclear gene expression, but also increases light tolerance. Therefore, GUN4 is proposed to function in ‘shielding’ Proto, and most likely MgProto, by reducing reactivity with O₂. Furthermore, GUN4 seems to be involved in sensing elevated levels of these photoreactive tetrapyrrole intermediates, and contributing to ¹O₂‐mediated retrograde signalling, originating from chlorophyll biosynthesis.</description><subject>autotrophs</subject><subject>Biosynthesis</subject><subject>Botany</subject><subject>Cell Nucleus - metabolism</subject><subject>Chlamydomonas reinhardtii</subject><subject>Chlamydomonas reinhardtii - metabolism</subject><subject>Chlorophyll</subject><subject>Chloroplasts</subject><subject>Chloroplasts - metabolism</subject><subject>Gene expression</subject><subject>gene expression regulation</subject><subject>genes</subject><subject>Genomics</subject><subject>GUN4</subject><subject>light intensity</subject><subject>lighting</subject><subject>magnesium</subject><subject>messenger RNA</subject><subject>Mg chelatase</subject><subject>mutants</subject><subject>oxygen</subject><subject>Proteins</subject><subject>Protoporphyrins - metabolism</subject><subject>protoporphyrin IX</subject><subject>retrograde signalling</subject><subject>Signal Transduction - physiology</subject><subject>singlet oxygen</subject><subject>tetrapyrrole biosynthesis pathway</subject><subject>Tetrapyrroles - biosynthesis</subject><issn>0960-7412</issn><issn>1365-313X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1u1DAUhS1ERYfCgheASGzYpPVvklmiERRQVZDoSOwsJ76Z8cixg-0IZddll33GPgmemcKCFbbka-t-51pHB6FXBJ-TvC7SuDsnVFT4CVoQVomSEfbjKVrgZYXLmhN6ip7HuMOY1Kziz9Ap5U1FaiwW6O5yfc2LMfgExhWjVXMsVBFgM1mVfJiL4C0UuZUgBTXO4fBujY-zS1uIJuNOF93W-uCzPKaH2_vk8-GmzsIUi2g2Tllr3GY_ZrW1api1H7xTMf9j3FYFnYx5gU56ZSO8fKxnaP3xw83qU3n19fLz6v1V2XNOcEmzA13TnnDOK9VqYAAgehBdJxSoZddpoWvC2pYSzaimTVVnfNn0UIuuJ-wMvTvOzZ5_ThCTHEzswFrlwE9REiFItd_0P1BeC4Z53WT07T_ozk8h-z5QjDeM4j31-pGa2gG0HIMZVJjlnzgycHEEfhkL898-wXKfs8w5y0PO8ubbl8MlK94cFb3yUm2CiXL9nWIiMMa5kIb9BvXPqBU</recordid><startdate>201407</startdate><enddate>201407</enddate><creator>Brzezowski, Pawel</creator><creator>Schlicke, Hagen</creator><creator>Richter, Andreas</creator><creator>Dent, Rachel M</creator><creator>Niyogi, Krishna K</creator><creator>Grimm, Bernhard</creator><general>Blackwell Science</general><general>Blackwell Publishing Ltd</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</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></search><sort><creationdate>201407</creationdate><title>GUN4 protein plays a regulatory role in tetrapyrrole biosynthesis and chloroplast‐to‐nucleus signalling in Chlamydomonas reinhardtii</title><author>Brzezowski, Pawel ; Schlicke, Hagen ; Richter, Andreas ; Dent, Rachel M ; Niyogi, Krishna K ; Grimm, Bernhard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-f4410-2736d72f14446abde3eee5fe5cc5aea9ccd5d713bb21d32d286772f98fe75cf13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>autotrophs</topic><topic>Biosynthesis</topic><topic>Botany</topic><topic>Cell Nucleus - metabolism</topic><topic>Chlamydomonas reinhardtii</topic><topic>Chlamydomonas reinhardtii - metabolism</topic><topic>Chlorophyll</topic><topic>Chloroplasts</topic><topic>Chloroplasts - metabolism</topic><topic>Gene expression</topic><topic>gene expression regulation</topic><topic>genes</topic><topic>Genomics</topic><topic>GUN4</topic><topic>light intensity</topic><topic>lighting</topic><topic>magnesium</topic><topic>messenger RNA</topic><topic>Mg chelatase</topic><topic>mutants</topic><topic>oxygen</topic><topic>Proteins</topic><topic>Protoporphyrins - metabolism</topic><topic>protoporphyrin IX</topic><topic>retrograde signalling</topic><topic>Signal Transduction - physiology</topic><topic>singlet oxygen</topic><topic>tetrapyrrole biosynthesis pathway</topic><topic>Tetrapyrroles - biosynthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brzezowski, Pawel</creatorcontrib><creatorcontrib>Schlicke, Hagen</creatorcontrib><creatorcontrib>Richter, Andreas</creatorcontrib><creatorcontrib>Dent, Rachel M</creatorcontrib><creatorcontrib>Niyogi, Krishna K</creatorcontrib><creatorcontrib>Grimm, Bernhard</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</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><jtitle>The Plant journal : for cell and molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brzezowski, Pawel</au><au>Schlicke, Hagen</au><au>Richter, Andreas</au><au>Dent, Rachel M</au><au>Niyogi, Krishna K</au><au>Grimm, Bernhard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>GUN4 protein plays a regulatory role in tetrapyrrole biosynthesis and chloroplast‐to‐nucleus signalling in Chlamydomonas reinhardtii</atitle><jtitle>The Plant journal : for cell and molecular biology</jtitle><addtitle>Plant J</addtitle><date>2014-07</date><risdate>2014</risdate><volume>79</volume><issue>2</issue><spage>285</spage><epage>298</epage><pages>285-298</pages><issn>0960-7412</issn><eissn>1365-313X</eissn><abstract>The GENOMES UNCOUPLED 4 (GUN4) protein is found only in aerobic photosynthetic organisms. We investigated the role of GUN4 in metabolic activities of the Mg branch of the tetrapyrrole biosynthesis pathway and the plastid signal‐mediated changes of nuclear gene expression in Chlamydomonas reinhardtii. In light, gun4 accumulates only 40% of the wild‐type chlorophyll level. Light‐ or dark‐grown gun4 mutant accumulates high levels of protoporphyrin IX (Proto), and displays increased sensitivity to moderate light intensities. Despite the photooxidative stress, gun4 fails to downregulate mRNA levels of the tetrapyrrole biosynthesis and the photosynthesis‐associated nuclear genes (PhANGs). In contrast, upon illumination, the Proto‐accumulating and light‐sensitive chlD–1 mutant displays the expected downregulation of the same nuclear genes. Although chlD–1 and the wild type have similar GUN4 transcript levels, the GUN4 protein in chlD–1 is hardly detectable. Overexpression of GUN4 in chlD–1 modifies the downregulation of nuclear gene expression, but also increases light tolerance. Therefore, GUN4 is proposed to function in ‘shielding’ Proto, and most likely MgProto, by reducing reactivity with O₂. Furthermore, GUN4 seems to be involved in sensing elevated levels of these photoreactive tetrapyrrole intermediates, and contributing to ¹O₂‐mediated retrograde signalling, originating from chlorophyll biosynthesis.</abstract><cop>England</cop><pub>Blackwell Science</pub><pmid>24861705</pmid><doi>10.1111/tpj.12560</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | autotrophs Biosynthesis Botany Cell Nucleus - metabolism Chlamydomonas reinhardtii Chlamydomonas reinhardtii - metabolism Chlorophyll Chloroplasts Chloroplasts - metabolism Gene expression gene expression regulation genes Genomics GUN4 light intensity lighting magnesium messenger RNA Mg chelatase mutants oxygen Proteins Protoporphyrins - metabolism protoporphyrin IX retrograde signalling Signal Transduction - physiology singlet oxygen tetrapyrrole biosynthesis pathway Tetrapyrroles - biosynthesis |
title | GUN4 protein plays a regulatory role in tetrapyrrole biosynthesis and chloroplast‐to‐nucleus signalling in Chlamydomonas reinhardtii |
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