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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Veröffentlicht in:Plant and cell physiology 2006-04, Vol.47 (4), p.457-470
Hauptverfasser: Morita, Y.(National Inst. for Basic Biology, Okazaki, Aichi (Japan)), Saitoh, M, Hoshino, A, Nitasaka, E, Iida, S
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3GT
ANS
BFO
CHI
CHS
DFR
EBG
EST
F3H
GST
HBA
LBG
NHX
UTR
WDR
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container_issue 4
container_start_page 457
container_title Plant and cell physiology
container_volume 47
creator Morita, Y.(National Inst. for Basic Biology, Okazaki, Aichi (Japan))
Saitoh, M
Hoshino, A
Nitasaka, E
Iida, S
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
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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. 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purification</subject><subject>DNA, Plant - genetics</subject><subject>DNA, Plant - isolation &amp; 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 &amp; purification</topic><topic>DNA, Plant - genetics</topic><topic>DNA, Plant - isolation &amp; 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 &amp; 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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.</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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language eng
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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]
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