Isolation of cDNAs for R2R3-MYB, bHLH and WDR transcriptional regulators and identification of c and ca mutations conferring white flowers in the Japanese morning glory [Ipomoea nil]
The transcriptional regulators for anthocyanin biosynthesis include members of proteins containing an R2R3-MYb domain, a bHLH (basic helix-loop-helix) domain and conserved WD40 repeats (WDRS). Spacial and temporal expression of the structural genes encoding the enzymes for anthocyanin biosynthesis i...
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description | The transcriptional regulators for anthocyanin biosynthesis include members of proteins containing an R2R3-MYb domain, a bHLH (basic helix-loop-helix) domain and conserved WD40 repeats (WDRS). Spacial and temporal expression of the structural genes encoding the enzymes for anthocyanin biosynthesis is thought to be determined by combinations of the R2R3-MYB, bHLH and WDR factors and their interactions. While the wild-type Japanese morning glory (Ipomoea nil) exhibits blue flowers with colored stems and dark-brown seeds, the c mutants display white flowers with red stems and colored seeds, and the ca mutants exhibit white flowers with green stems and ivory seeds. Here, we characterize the tissue-specific expression of three MYB genes, three bHLH genes and two WDR genes in I. nil. We also show that the recessive c-1 and ca alleles are frameshift mutations caused by a 2 bp deletion and 7 bp insertions in the genes for the R2R3-MYB and WDR transcriptional regulators designated as InMYB1 and InWDR1, respectively. In addition to defects in flower, stem and seed pigmentations, the ca mutants were found to show reduced trichome formation in seeds but to produce leaf and stem trichomes and root hairs normally. Except for the gene for chalcone synthase E in the ca mutant, all structural genes tested were coordinately reduced in both c-1 and ca mutant flower limbs. However, slight but significant expression of the genes for chalcone synthase D, chalcone isomerase and flavanone 3-hydroxylase in the pathway for flavonol biosynthesis was detectable in c-1 and ca mutants, whereas no such residual expression could be observed in other genes involved in the later anthocyanin biosynthesis pathway. The biological roles of the C-1 and Ca genes in I. nil epidermal traits and their evolutionary implications are also discussed. |
doi_str_mv | 10.1093/pcp/pcj012 |
format | Article |
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Spacial and temporal expression of the structural genes encoding the enzymes for anthocyanin biosynthesis is thought to be determined by combinations of the R2R3-MYB, bHLH and WDR factors and their interactions. While the wild-type Japanese morning glory (Ipomoea nil) exhibits blue flowers with colored stems and dark-brown seeds, the c mutants display white flowers with red stems and colored seeds, and the ca mutants exhibit white flowers with green stems and ivory seeds. Here, we characterize the tissue-specific expression of three MYB genes, three bHLH genes and two WDR genes in I. nil. We also show that the recessive c-1 and ca alleles are frameshift mutations caused by a 2 bp deletion and 7 bp insertions in the genes for the R2R3-MYB and WDR transcriptional regulators designated as InMYB1 and InWDR1, respectively. In addition to defects in flower, stem and seed pigmentations, the ca mutants were found to show reduced trichome formation in seeds but to produce leaf and stem trichomes and root hairs normally. Except for the gene for chalcone synthase E in the ca mutant, all structural genes tested were coordinately reduced in both c-1 and ca mutant flower limbs. However, slight but significant expression of the genes for chalcone synthase D, chalcone isomerase and flavanone 3-hydroxylase in the pathway for flavonol biosynthesis was detectable in c-1 and ca mutants, whereas no such residual expression could be observed in other genes involved in the later anthocyanin biosynthesis pathway. The biological roles of the C-1 and Ca genes in I. nil epidermal traits and their evolutionary implications are also discussed.</description><identifier>ISSN: 0032-0781</identifier><identifier>EISSN: 1471-9053</identifier><identifier>DOI: 10.1093/pcp/pcj012</identifier><identifier>PMID: 16446312</identifier><language>eng</language><publisher>Japan: Oxford University Press</publisher><subject>3GGT ; 3GT ; Acyltransferases - genetics ; Acyltransferases - physiology ; Alleles ; Amino Acid Sequence ; ANS ; ANTHOCYANE ; anthocyanidin synthase ; Anthocyanin biosynthesis ; ANTHOCYANINS ; Anthocyanins - biosynthesis ; ANTOCIANINAS ; Base Sequence ; Basic Helix-Loop-Helix Transcription Factors - chemistry ; Basic Helix-Loop-Helix Transcription Factors - genetics ; basic helix–loop–helix ; before flower opening ; BFO ; bHLH ; BIOSINTESIS ; BIOSYNTHESE ; BIOSYNTHESIS ; chalcone isomerase ; chalcone synthase ; CHI ; CHS ; DFR ; dihydroflavonol 4-reductase ; DNA, Complementary - isolation & purification ; DNA, Plant - genetics ; DNA, Plant - isolation & purification ; early biosynthetic gene ; EBG ; EST ; expressed sequence tag ; F3H ; F3′H ; flavanone 3-hydroxylase ; flavonoid 3′-hydroxylase ; Flower and seed pigmentation ; Flowers - genetics ; GENE ; Gene Expression Regulation, Enzymologic ; Gene Expression Regulation, Plant ; GENES ; Genes, Plant ; Genes, Recessive ; glutathione S-transferase ; GST ; HBA ; Heavenly Blue anthocyanin ; Intramolecular Lyases - genetics ; Intramolecular Lyases - physiology ; Ipomoea - genetics ; Ipomoea nil ; late biosynthetic gene ; LBG ; Mixed Function Oxygenases - genetics ; Mixed Function Oxygenases - physiology ; Molecular Sequence Data ; Mutation ; Na+/H+ exchanger ; NHX ; PHARBITIS NIL ; PIGMENTACION ; PIGMENTATION ; Pigmentation - genetics ; reverse transcription–PCR ; RT–PCR ; Seeds ; Transcription Factors - chemistry ; Transcription Factors - genetics ; Transcriptional regulator genes ; TRICHOME ; Trichome formation ; TRICHOMES ; TRICOMAS ; UDP-glucose:anthocyanidin 3-O-glucose-2′′-O-glucosyltransferase ; UDP-glucose:flavonoid 3-O-glucosyltransferase ; untranslated region ; UTR ; WD40 repeat ; WDR</subject><ispartof>Plant and cell physiology, 2006-04, Vol.47 (4), p.457-470</ispartof><rights>Copyright Oxford University Press(England) Apr 2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c494t-f0928fd6d4080b87a6bf6befbdff01576ae9b8b9603711485eb805b742b4ce223</citedby><cites>FETCH-LOGICAL-c494t-f0928fd6d4080b87a6bf6befbdff01576ae9b8b9603711485eb805b742b4ce223</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16446312$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Morita, Y.(National Inst. for Basic Biology, Okazaki, Aichi (Japan))</creatorcontrib><creatorcontrib>Saitoh, M</creatorcontrib><creatorcontrib>Hoshino, A</creatorcontrib><creatorcontrib>Nitasaka, E</creatorcontrib><creatorcontrib>Iida, S</creatorcontrib><title>Isolation of cDNAs for R2R3-MYB, bHLH and WDR transcriptional regulators and identification of c and ca mutations conferring white flowers in the Japanese morning glory [Ipomoea nil]</title><title>Plant and cell physiology</title><addtitle>Plant Cell Physiol</addtitle><description>The transcriptional regulators for anthocyanin biosynthesis include members of proteins containing an R2R3-MYb domain, a bHLH (basic helix-loop-helix) domain and conserved WD40 repeats (WDRS). Spacial and temporal expression of the structural genes encoding the enzymes for anthocyanin biosynthesis is thought to be determined by combinations of the R2R3-MYB, bHLH and WDR factors and their interactions. While the wild-type Japanese morning glory (Ipomoea nil) exhibits blue flowers with colored stems and dark-brown seeds, the c mutants display white flowers with red stems and colored seeds, and the ca mutants exhibit white flowers with green stems and ivory seeds. Here, we characterize the tissue-specific expression of three MYB genes, three bHLH genes and two WDR genes in I. nil. We also show that the recessive c-1 and ca alleles are frameshift mutations caused by a 2 bp deletion and 7 bp insertions in the genes for the R2R3-MYB and WDR transcriptional regulators designated as InMYB1 and InWDR1, respectively. In addition to defects in flower, stem and seed pigmentations, the ca mutants were found to show reduced trichome formation in seeds but to produce leaf and stem trichomes and root hairs normally. Except for the gene for chalcone synthase E in the ca mutant, all structural genes tested were coordinately reduced in both c-1 and ca mutant flower limbs. However, slight but significant expression of the genes for chalcone synthase D, chalcone isomerase and flavanone 3-hydroxylase in the pathway for flavonol biosynthesis was detectable in c-1 and ca mutants, whereas no such residual expression could be observed in other genes involved in the later anthocyanin biosynthesis pathway. The biological roles of the C-1 and Ca genes in I. nil epidermal traits and their evolutionary implications are also discussed.</description><subject>3GGT</subject><subject>3GT</subject><subject>Acyltransferases - genetics</subject><subject>Acyltransferases - physiology</subject><subject>Alleles</subject><subject>Amino Acid Sequence</subject><subject>ANS</subject><subject>ANTHOCYANE</subject><subject>anthocyanidin synthase</subject><subject>Anthocyanin biosynthesis</subject><subject>ANTHOCYANINS</subject><subject>Anthocyanins - biosynthesis</subject><subject>ANTOCIANINAS</subject><subject>Base Sequence</subject><subject>Basic Helix-Loop-Helix Transcription Factors - chemistry</subject><subject>Basic Helix-Loop-Helix Transcription Factors - genetics</subject><subject>basic helix–loop–helix</subject><subject>before flower opening</subject><subject>BFO</subject><subject>bHLH</subject><subject>BIOSINTESIS</subject><subject>BIOSYNTHESE</subject><subject>BIOSYNTHESIS</subject><subject>chalcone isomerase</subject><subject>chalcone synthase</subject><subject>CHI</subject><subject>CHS</subject><subject>DFR</subject><subject>dihydroflavonol 4-reductase</subject><subject>DNA, Complementary - isolation & purification</subject><subject>DNA, Plant - genetics</subject><subject>DNA, Plant - isolation & purification</subject><subject>early biosynthetic gene</subject><subject>EBG</subject><subject>EST</subject><subject>expressed sequence tag</subject><subject>F3H</subject><subject>F3′H</subject><subject>flavanone 3-hydroxylase</subject><subject>flavonoid 3′-hydroxylase</subject><subject>Flower and seed pigmentation</subject><subject>Flowers - genetics</subject><subject>GENE</subject><subject>Gene Expression Regulation, Enzymologic</subject><subject>Gene Expression Regulation, Plant</subject><subject>GENES</subject><subject>Genes, Plant</subject><subject>Genes, Recessive</subject><subject>glutathione S-transferase</subject><subject>GST</subject><subject>HBA</subject><subject>Heavenly Blue anthocyanin</subject><subject>Intramolecular Lyases - genetics</subject><subject>Intramolecular Lyases - physiology</subject><subject>Ipomoea - genetics</subject><subject>Ipomoea nil</subject><subject>late biosynthetic gene</subject><subject>LBG</subject><subject>Mixed Function Oxygenases - genetics</subject><subject>Mixed Function Oxygenases - physiology</subject><subject>Molecular Sequence Data</subject><subject>Mutation</subject><subject>Na+/H+ exchanger</subject><subject>NHX</subject><subject>PHARBITIS NIL</subject><subject>PIGMENTACION</subject><subject>PIGMENTATION</subject><subject>Pigmentation - genetics</subject><subject>reverse transcription–PCR</subject><subject>RT–PCR</subject><subject>Seeds</subject><subject>Transcription Factors - chemistry</subject><subject>Transcription Factors - genetics</subject><subject>Transcriptional regulator genes</subject><subject>TRICHOME</subject><subject>Trichome formation</subject><subject>TRICHOMES</subject><subject>TRICOMAS</subject><subject>UDP-glucose:anthocyanidin 3-O-glucose-2′′-O-glucosyltransferase</subject><subject>UDP-glucose:flavonoid 3-O-glucosyltransferase</subject><subject>untranslated region</subject><subject>UTR</subject><subject>WD40 repeat</subject><subject>WDR</subject><issn>0032-0781</issn><issn>1471-9053</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkktv1DAUhSMEotPChj3I6qILROA6TpxkWaZAZhgeGoF4CVm2Y089JHGwE5X-MX4fnsmISmxYWLauv3t0dM-NogcYnmIoybNe9uFsASe3ohlOcxyXkJHb0QyAJDHkBT6Kjr3fAoQ3gbvREaZpSglOZtHvhbcNH4ztkNVIXrw990hbh9bJmsRvvjx_gkS1qhDvavTpYo0Gxzsvnel3HbxBTm3G0G6d3yOmVt1gtJE3ivu65Kgdh33RI2k7rZwz3QZdXZpBId3YKxUUTIeGS4WWvOed8gq11nU7atNYd42-LXrbWsVRZ5rv96I7mjde3T_cJ9HHly8-zKt49e7VYn6-imVapkOsoUwKXdM6hQJEkXMqNBVKi1prwFlOuSpFIUoKJMc4LTIlCshEniYilSpJyEl0Nun2zv4clR9Ya7xUTRMc2tEzmpdAKSX_BXEe5EMSATz9B9za0YVZepYES0AAigA9niDprPdOadY703J3zTCwXeYsZM6mzAP86KA4ilbVN-gh5ADEE2D8oH79_efuR_BP8oxVn7-yeVkt83T1mmWBfzjxmlvGN854tnyfhOXZ7Q8Q8gc43sEh</recordid><startdate>20060401</startdate><enddate>20060401</enddate><creator>Morita, Y.(National Inst. for Basic Biology, Okazaki, Aichi (Japan))</creator><creator>Saitoh, M</creator><creator>Hoshino, A</creator><creator>Nitasaka, E</creator><creator>Iida, S</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>FBQ</scope><scope>BSCLL</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>7QL</scope><scope>7QO</scope><scope>7QP</scope><scope>7T5</scope><scope>7T7</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20060401</creationdate><title>Isolation of cDNAs for R2R3-MYB, bHLH and WDR transcriptional regulators and identification of c and ca mutations conferring white flowers in the Japanese morning glory [Ipomoea nil]</title><author>Morita, Y.(National Inst. for Basic Biology, Okazaki, Aichi (Japan)) ; Saitoh, M ; Hoshino, A ; Nitasaka, E ; Iida, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c494t-f0928fd6d4080b87a6bf6befbdff01576ae9b8b9603711485eb805b742b4ce223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>3GGT</topic><topic>3GT</topic><topic>Acyltransferases - genetics</topic><topic>Acyltransferases - physiology</topic><topic>Alleles</topic><topic>Amino Acid Sequence</topic><topic>ANS</topic><topic>ANTHOCYANE</topic><topic>anthocyanidin synthase</topic><topic>Anthocyanin biosynthesis</topic><topic>ANTHOCYANINS</topic><topic>Anthocyanins - biosynthesis</topic><topic>ANTOCIANINAS</topic><topic>Base Sequence</topic><topic>Basic Helix-Loop-Helix Transcription Factors - chemistry</topic><topic>Basic Helix-Loop-Helix Transcription Factors - genetics</topic><topic>basic helix–loop–helix</topic><topic>before flower opening</topic><topic>BFO</topic><topic>bHLH</topic><topic>BIOSINTESIS</topic><topic>BIOSYNTHESE</topic><topic>BIOSYNTHESIS</topic><topic>chalcone isomerase</topic><topic>chalcone synthase</topic><topic>CHI</topic><topic>CHS</topic><topic>DFR</topic><topic>dihydroflavonol 4-reductase</topic><topic>DNA, Complementary - isolation & purification</topic><topic>DNA, Plant - genetics</topic><topic>DNA, Plant - isolation & purification</topic><topic>early biosynthetic gene</topic><topic>EBG</topic><topic>EST</topic><topic>expressed sequence tag</topic><topic>F3H</topic><topic>F3′H</topic><topic>flavanone 3-hydroxylase</topic><topic>flavonoid 3′-hydroxylase</topic><topic>Flower and seed pigmentation</topic><topic>Flowers - genetics</topic><topic>GENE</topic><topic>Gene Expression Regulation, Enzymologic</topic><topic>Gene Expression Regulation, Plant</topic><topic>GENES</topic><topic>Genes, Plant</topic><topic>Genes, Recessive</topic><topic>glutathione S-transferase</topic><topic>GST</topic><topic>HBA</topic><topic>Heavenly Blue anthocyanin</topic><topic>Intramolecular Lyases - genetics</topic><topic>Intramolecular Lyases - physiology</topic><topic>Ipomoea - genetics</topic><topic>Ipomoea nil</topic><topic>late biosynthetic gene</topic><topic>LBG</topic><topic>Mixed Function Oxygenases - genetics</topic><topic>Mixed Function Oxygenases - physiology</topic><topic>Molecular Sequence Data</topic><topic>Mutation</topic><topic>Na+/H+ exchanger</topic><topic>NHX</topic><topic>PHARBITIS NIL</topic><topic>PIGMENTACION</topic><topic>PIGMENTATION</topic><topic>Pigmentation - genetics</topic><topic>reverse transcription–PCR</topic><topic>RT–PCR</topic><topic>Seeds</topic><topic>Transcription Factors - chemistry</topic><topic>Transcription Factors - genetics</topic><topic>Transcriptional regulator genes</topic><topic>TRICHOME</topic><topic>Trichome formation</topic><topic>TRICHOMES</topic><topic>TRICOMAS</topic><topic>UDP-glucose:anthocyanidin 3-O-glucose-2′′-O-glucosyltransferase</topic><topic>UDP-glucose:flavonoid 3-O-glucosyltransferase</topic><topic>untranslated region</topic><topic>UTR</topic><topic>WD40 repeat</topic><topic>WDR</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Morita, Y.(National Inst. for Basic Biology, Okazaki, Aichi (Japan))</creatorcontrib><creatorcontrib>Saitoh, M</creatorcontrib><creatorcontrib>Hoshino, A</creatorcontrib><creatorcontrib>Nitasaka, E</creatorcontrib><creatorcontrib>Iida, S</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids 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>ProQuest Health & Medical Complete (Alumni)</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>Plant and cell physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Morita, Y.(National Inst. for Basic Biology, Okazaki, Aichi (Japan))</au><au>Saitoh, M</au><au>Hoshino, A</au><au>Nitasaka, E</au><au>Iida, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Isolation of cDNAs for R2R3-MYB, bHLH and WDR transcriptional regulators and identification of c and ca mutations conferring white flowers in the Japanese morning glory [Ipomoea nil]</atitle><jtitle>Plant and cell physiology</jtitle><addtitle>Plant Cell Physiol</addtitle><date>2006-04-01</date><risdate>2006</risdate><volume>47</volume><issue>4</issue><spage>457</spage><epage>470</epage><pages>457-470</pages><issn>0032-0781</issn><eissn>1471-9053</eissn><abstract>The transcriptional regulators for anthocyanin biosynthesis include members of proteins containing an R2R3-MYb domain, a bHLH (basic helix-loop-helix) domain and conserved WD40 repeats (WDRS). Spacial and temporal expression of the structural genes encoding the enzymes for anthocyanin biosynthesis is thought to be determined by combinations of the R2R3-MYB, bHLH and WDR factors and their interactions. While the wild-type Japanese morning glory (Ipomoea nil) exhibits blue flowers with colored stems and dark-brown seeds, the c mutants display white flowers with red stems and colored seeds, and the ca mutants exhibit white flowers with green stems and ivory seeds. Here, we characterize the tissue-specific expression of three MYB genes, three bHLH genes and two WDR genes in I. nil. We also show that the recessive c-1 and ca alleles are frameshift mutations caused by a 2 bp deletion and 7 bp insertions in the genes for the R2R3-MYB and WDR transcriptional regulators designated as InMYB1 and InWDR1, respectively. In addition to defects in flower, stem and seed pigmentations, the ca mutants were found to show reduced trichome formation in seeds but to produce leaf and stem trichomes and root hairs normally. Except for the gene for chalcone synthase E in the ca mutant, all structural genes tested were coordinately reduced in both c-1 and ca mutant flower limbs. However, slight but significant expression of the genes for chalcone synthase D, chalcone isomerase and flavanone 3-hydroxylase in the pathway for flavonol biosynthesis was detectable in c-1 and ca mutants, whereas no such residual expression could be observed in other genes involved in the later anthocyanin biosynthesis pathway. The biological roles of the C-1 and Ca genes in I. nil epidermal traits and their evolutionary implications are also discussed.</abstract><cop>Japan</cop><pub>Oxford University Press</pub><pmid>16446312</pmid><doi>10.1093/pcp/pcj012</doi><tpages>14</tpages></addata></record> |
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ispartof | Plant and cell physiology, 2006-04, Vol.47 (4), p.457-470 |
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source | MEDLINE; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals |
subjects | 3GGT 3GT Acyltransferases - genetics Acyltransferases - physiology Alleles Amino Acid Sequence ANS ANTHOCYANE anthocyanidin synthase Anthocyanin biosynthesis ANTHOCYANINS Anthocyanins - biosynthesis ANTOCIANINAS Base Sequence Basic Helix-Loop-Helix Transcription Factors - chemistry Basic Helix-Loop-Helix Transcription Factors - genetics basic helix–loop–helix before flower opening BFO bHLH BIOSINTESIS BIOSYNTHESE BIOSYNTHESIS chalcone isomerase chalcone synthase CHI CHS DFR dihydroflavonol 4-reductase DNA, Complementary - isolation & purification DNA, Plant - genetics DNA, Plant - isolation & purification early biosynthetic gene EBG EST expressed sequence tag F3H F3′H flavanone 3-hydroxylase flavonoid 3′-hydroxylase Flower and seed pigmentation Flowers - genetics GENE Gene Expression Regulation, Enzymologic Gene Expression Regulation, Plant GENES Genes, Plant Genes, Recessive glutathione S-transferase GST HBA Heavenly Blue anthocyanin Intramolecular Lyases - genetics Intramolecular Lyases - physiology Ipomoea - genetics Ipomoea nil late biosynthetic gene LBG Mixed Function Oxygenases - genetics Mixed Function Oxygenases - physiology Molecular Sequence Data Mutation Na+/H+ exchanger NHX PHARBITIS NIL PIGMENTACION PIGMENTATION Pigmentation - genetics reverse transcription–PCR RT–PCR Seeds Transcription Factors - chemistry Transcription Factors - genetics Transcriptional regulator genes TRICHOME Trichome formation TRICHOMES TRICOMAS UDP-glucose:anthocyanidin 3-O-glucose-2′′-O-glucosyltransferase UDP-glucose:flavonoid 3-O-glucosyltransferase untranslated region UTR WD40 repeat WDR |
title | Isolation of cDNAs for R2R3-MYB, bHLH and WDR transcriptional regulators and identification of c and ca mutations conferring white flowers in the Japanese morning glory [Ipomoea nil] |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T09%3A36%3A31IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Isolation%20of%20cDNAs%20for%20R2R3-MYB,%20bHLH%20and%20WDR%20transcriptional%20regulators%20and%20identification%20of%20c%20and%20ca%20mutations%20conferring%20white%20flowers%20in%20the%20Japanese%20morning%20glory%20%5BIpomoea%20nil%5D&rft.jtitle=Plant%20and%20cell%20physiology&rft.au=Morita,%20Y.(National%20Inst.%20for%20Basic%20Biology,%20Okazaki,%20Aichi%20(Japan))&rft.date=2006-04-01&rft.volume=47&rft.issue=4&rft.spage=457&rft.epage=470&rft.pages=457-470&rft.issn=0032-0781&rft.eissn=1471-9053&rft_id=info:doi/10.1093/pcp/pcj012&rft_dat=%3Cproquest_cross%3E1029556201%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=201503008&rft_id=info:pmid/16446312&rfr_iscdi=true |