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Tomato locus entire
Locus details | Download GMOD XML | Note to Editors | Annotation guidelines |
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Locus | Solyc04g076850 |
Locus name | entire |
Symbol | e |
Gene activity | transcriptional repressor of auxin signaling |
Description | IAA9 is involved in tomato fruit development and leaf morphogenesis. The IAA9 protein is exclusively localized to the nucleus, supporting the putative transcriptional regulatory function. |
Chromosome | 4 |
Arm | long |
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![]() ![]() | [Associate registry name] |
This locus is associated with registry name: Auxin Induced
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![]() ![]() | unprocessed genomic sequence region underlying this gene |
>Solyc04g076850.2 SL2.50ch04:61761281..61765464
GATTATTAGAGTGATCTGTAATTGTGATGTCTCCGCCGCTCCTTGGTGTTGGGGAGGAGGAGGGCCAGAGTAATGTAACT
CTACTGGCTTCTTCAACTTCCTTAGGAAGCATATGCATAAAAGGATCAGCTCTTAAAGAGCGAAACTATATGGGTCTATC
TGATTGTTCGTCGGTGGACAGCTGTAATATTTCCACCTCATCAGAGGACAATAATGGGTGTGGATTAAATCTCAAGGCAA
CGGAGCTCAGGCTCGGTCTACCTGGATCTCAGTCTCCCGAAAGAGGTGAGGAGACTTGCCCTGTGAGCTCGACAAAGGTT
GATGAGAAGCTGCTCTTCCCCTTGCACCCTTCCAAAGATACTGCTTTCTCGGTATCGCAGAAAACAGTAGTTAGTGGCAA
CAAACGAGGATTTTCAGACGCTATGGATGGATTCTCAGAGGTGAACTATCATTTCTTTAATAAGGTTACTCATTTTTTGG
TAAAGCTGCAATTGAAGTTACATAATCTATCCTACAGGGGAAGTTTCTGTCGAATTCCGGTGTGAAAGCAGGTGATACAA
AGGAGACCTCACGTGTGCAACCACCTAAAATGAAAGATGCTAATACTCAGAGTACAGTTCCAGAGAGGCCTTCTGCTGTG
AATGATGCCTCAAACCGTGCGGGCAGTGGTGCCCCTGCTACAAAGTGAGTATCTCCCCACTAGGAGTAAGAAGTGTGATA
TTTGGATAATGATTGTACAAAATGTCTAATCTGTATCTTGGATTAATTTTAGGGCACAGGTTGTTGGTTGGCCACCCATT
CGATCTTTTAGAAAGAACACTCTAGCCTCTGCCTCGAAGAATAACGAAGAGGTTGACGGAAAAGCTGGCTCACCAGCTCT
TTTTATTAAGGTCAGCATGGATGGTGCTCCCTATTTGAGGAAAGTGGACCTCAGAACCTGTTCTGCATACCAGGAGCTAT
CTTCTGCTCTTGAAAAAATGTTCAGCTGTTTTACAATAGGTTAGCTATTTTGGAGCCTTTAGTAGCTCATAATTTCATTG
ATTGGATTAAAATAGTAAGATACATGTTCATGATTTTTCCATTGCCCTAGTTACTGCTACTTCCTTGTTATGACAGGTCA
ATATGGATCTCATGGAGCTCCTGGGAAGGATATGTTAAGTGAGAGCAAATTGAAGGATTTGCTTCATGGATCTGAGTATG
TCCTCACTTACGAAGATAAGGATGGGGACTGGATGCTTGTCGGTGATGTCCCCTGGGAGTAAGCTCTTGCTAATTCAACT
CCTTTTTCTTTTCTTCCCGTTTAGCACTGTTTGGTATAGTTTACTACATTTTCGGCCAACCTATTTCTTGGTTGTATGCT
TTTTCCATTGAGATAAAAAGAAGAATATAGTGCACGTGGTGTGGATTTAGTAGTAAATGTGGACTTGGTGCAACTGATAG
TAAATACAACTCATCTTCAGATTCAGAAATAAAATTAGACTAGTCAGTCCTCATCTTAAGGAAGTTAAACAAGTTCTTGT
ATAACTGCAAGCTTAGAGAGCAATGATGCTCTAGTAAGTCCTAAATTAAAGTGGAAATCTCAAACCTGACCCATAATTAG
GTTCTCTGAATTGAGAAGCCTTGCCATGCAGTAAGAGTTCAGGTAGGTTTGGCCTTGTGTTACAAGGAAGATCTTTTTTT
TTTGATTGATAGAGCTTTTAAGGAGATTGATTATAATGAAGTCTGATTGAATTAATAAATCAGCAAGTTAATTTTGAGGG
CCATCATTACTACTTACCATTTTAGAAAACTCATGGCTCATTTTGTATGTGTATAATGCTATGTATGAAAATATTTGCCA
TGGTTAAGCATGTAGTCAGGATTTTTATCAATCAAGATTCATGCTGCCTTCAGTTATGGATTATAATTTCTTATCTCTAG
CATGAATAGAAAAACCAATAATAATCTGATTTTTTGATAATGCCAAAGGATTAAGGGATGATAAACGTAACTAGAAGAAT
TTGGTATCATTGTTGGTTTGACACTCAACTAGGATTCAATGATATTGCTAGTGTGTGTTAGATAGCGATTGCGCTGCTTT
GGGAAAAAATGCCTAATAATCCGTGTGACATTCAACTCTTGCTTCACATGTGTCCCATTGTTAGTGGTGCTATTCCATGT
AATTTGCACAGCTTGATTCAGGGAGTTAGTCCTCTTTCTGTCTCTCTCTAGTTCGCTTTATCTCCCTTCTTTTTTGTTCT
TTTGCAATGATGAATCTGGTGGTCTACTATAACAATGGTAGACCTGAACATATTGTTTTCTTGAATCTGTTCTCTCTTGG
ACCATATAAAAATACCAGTAGTACATTTATTAAGGGCTGTTCTTTGCAAGTTCTAATATCTTAGGTTCAGACTTGTAATA
AATTTTATTGAATGTAGTTTCTGTTTGATTGTTTGTATATTTGACGATGACCATGCTTTTAATTCCTAATATTTTCATGT
TGTAGGATGTTTATCGATACTTGCAAAAGGTTGAGGATCATGAAAGGTTCAGATGCCATTGGCCTGGGTGAGTATCTCTT
GTTGAGCCTTAGACCTCTTCATTCACACAATCAAAATGAAAAACGGAAAGAAAGACCGTCTCCTCCTTCATCTCCCCCGA
CCTTGTTCTTAGGGCTTGTACTTCTGTTTTTGTATTTTGACATGCATAACCATTTGGCGAGAGATGTGGGGCTTGCTCAA
GTGGTTCAGCACCTCCACCATCAACTGGTAGGTTGAGGTTTAGAGTTCGAGTCATGCTGGAGTGTTAGTGGGAATACTAG
TGATCTTCCGGGAGGGTAGAAAAAAAGGGGAAAAACAACTACTTGGTGATAAATAGAAATATACAAACTGTAACGCAGAA
TTATCTGGTTTCAACATTTGATTTCTGTGAATCTTGATTACTTTCTATGATTTGAAACAAAACTTCCTTGCAAGTTTCAT
ATTTAAAAGATATTATTGAAGAAATAATTAGAAGTCATGAAATGCTGGTTTAGGAATTCTCCCACCCAGCTGTTCGTCAT
GAAAGTTCTCTGAATTACCGTGATGCATTTTTTCAAGTAGCGTTAAGTATTAGAGAATTGCTTGCCTGACAGAACTACAT
TTGTTATGGATCTGGCCTCATTTTATTATTTGTCAAGCGGCAATAGAAAGATTTAGGACATCAAGGTAGGCTAGGCATCT
TGAAATGGTGGTGGTAGGTTCATTTGCATTGTAGGACACACCTGCATCTGTGAGAGATGAGGATGGAGAGTGAAGGAGAA
TGGTTAATGTAGTCCCAAAACCGAAAGGAAACGAGCTATAAGTTATTGTAAATCTATGGGCAGTGTTATGCAGTTATTGC
TGTTTTAAACATGTGAGTTAGTCAGCTTTATCTCATTATAAAAGGGCAAAGGGGATAACAAACTCAGCTGTTATAATTTC
CGCAAAAGTTCTGTTACCCAATAATGCATTTCCATATGCTGATTTGTGTGCAGACTTCGGATAGGTCTTTTATTAATCTG
TAAGTGTGTTTAGTCTATGGTAATGCAACTCTAGTTTAATTTTTGGTATTGGTTGCAACATTTCAACGACCAACTCCTGC
TCCTAAGGTATGAATGATTACCTACGAAACGGAAACATGTTACAATTCCACTAACTTCTGTGCATTTTTATGTGCAGCCC
CAAGGGCTATGGAAAAGTGTCGGAGCAGAAATTAGCCTATCTACACATGATTAAAGCTATCCATCCAGCATTTCTAGTAG
GCGAGGAAGACACAAAAACGGGTGAAGAGCTCATAAACTTGAATCCTTTTTAAAGGCATGAACAGTATAGCTGGTTGTTG
GTCTTGGATAGCTCAGCATGGGTAGATGCTTTACCTGATTACGACATGGTGTTCTTTTATATTTGCGTAATATATGTCCT
CTTTTAAGTTTTTTTTATCATGTCTATTTAAAAAACCGTTTGATATTGGAGTTTGTCTGCAAACTAATGTGTGTTGTGTA
CTGAGAGCTCTTCTAGAGGTAATTTAGTAATGTTCTAAGTGTATTTGCTTGTTTAAGTTCCCTTAAGTGTGTACTTTAGA
CCCAACGTTTGTCGTTTGATTAAGTATGCGTGTGCACTTCAGAAATTGTTATTACTGTATGAATAAATGTGTCCTCCACA
TTTTTCATCGGGTTGTAGTTATCG
GATTATTAGAGTGATCTGTAATTGTGATGTCTCCGCCGCTCCTTGGTGTTGGGGAGGAGGAGGGCCAGAGTAATGTAACT
CTACTGGCTTCTTCAACTTCCTTAGGAAGCATATGCATAAAAGGATCAGCTCTTAAAGAGCGAAACTATATGGGTCTATC
TGATTGTTCGTCGGTGGACAGCTGTAATATTTCCACCTCATCAGAGGACAATAATGGGTGTGGATTAAATCTCAAGGCAA
CGGAGCTCAGGCTCGGTCTACCTGGATCTCAGTCTCCCGAAAGAGGTGAGGAGACTTGCCCTGTGAGCTCGACAAAGGTT
GATGAGAAGCTGCTCTTCCCCTTGCACCCTTCCAAAGATACTGCTTTCTCGGTATCGCAGAAAACAGTAGTTAGTGGCAA
CAAACGAGGATTTTCAGACGCTATGGATGGATTCTCAGAGGTGAACTATCATTTCTTTAATAAGGTTACTCATTTTTTGG
TAAAGCTGCAATTGAAGTTACATAATCTATCCTACAGGGGAAGTTTCTGTCGAATTCCGGTGTGAAAGCAGGTGATACAA
AGGAGACCTCACGTGTGCAACCACCTAAAATGAAAGATGCTAATACTCAGAGTACAGTTCCAGAGAGGCCTTCTGCTGTG
AATGATGCCTCAAACCGTGCGGGCAGTGGTGCCCCTGCTACAAAGTGAGTATCTCCCCACTAGGAGTAAGAAGTGTGATA
TTTGGATAATGATTGTACAAAATGTCTAATCTGTATCTTGGATTAATTTTAGGGCACAGGTTGTTGGTTGGCCACCCATT
CGATCTTTTAGAAAGAACACTCTAGCCTCTGCCTCGAAGAATAACGAAGAGGTTGACGGAAAAGCTGGCTCACCAGCTCT
TTTTATTAAGGTCAGCATGGATGGTGCTCCCTATTTGAGGAAAGTGGACCTCAGAACCTGTTCTGCATACCAGGAGCTAT
CTTCTGCTCTTGAAAAAATGTTCAGCTGTTTTACAATAGGTTAGCTATTTTGGAGCCTTTAGTAGCTCATAATTTCATTG
ATTGGATTAAAATAGTAAGATACATGTTCATGATTTTTCCATTGCCCTAGTTACTGCTACTTCCTTGTTATGACAGGTCA
ATATGGATCTCATGGAGCTCCTGGGAAGGATATGTTAAGTGAGAGCAAATTGAAGGATTTGCTTCATGGATCTGAGTATG
TCCTCACTTACGAAGATAAGGATGGGGACTGGATGCTTGTCGGTGATGTCCCCTGGGAGTAAGCTCTTGCTAATTCAACT
CCTTTTTCTTTTCTTCCCGTTTAGCACTGTTTGGTATAGTTTACTACATTTTCGGCCAACCTATTTCTTGGTTGTATGCT
TTTTCCATTGAGATAAAAAGAAGAATATAGTGCACGTGGTGTGGATTTAGTAGTAAATGTGGACTTGGTGCAACTGATAG
TAAATACAACTCATCTTCAGATTCAGAAATAAAATTAGACTAGTCAGTCCTCATCTTAAGGAAGTTAAACAAGTTCTTGT
ATAACTGCAAGCTTAGAGAGCAATGATGCTCTAGTAAGTCCTAAATTAAAGTGGAAATCTCAAACCTGACCCATAATTAG
GTTCTCTGAATTGAGAAGCCTTGCCATGCAGTAAGAGTTCAGGTAGGTTTGGCCTTGTGTTACAAGGAAGATCTTTTTTT
TTTGATTGATAGAGCTTTTAAGGAGATTGATTATAATGAAGTCTGATTGAATTAATAAATCAGCAAGTTAATTTTGAGGG
CCATCATTACTACTTACCATTTTAGAAAACTCATGGCTCATTTTGTATGTGTATAATGCTATGTATGAAAATATTTGCCA
TGGTTAAGCATGTAGTCAGGATTTTTATCAATCAAGATTCATGCTGCCTTCAGTTATGGATTATAATTTCTTATCTCTAG
CATGAATAGAAAAACCAATAATAATCTGATTTTTTGATAATGCCAAAGGATTAAGGGATGATAAACGTAACTAGAAGAAT
TTGGTATCATTGTTGGTTTGACACTCAACTAGGATTCAATGATATTGCTAGTGTGTGTTAGATAGCGATTGCGCTGCTTT
GGGAAAAAATGCCTAATAATCCGTGTGACATTCAACTCTTGCTTCACATGTGTCCCATTGTTAGTGGTGCTATTCCATGT
AATTTGCACAGCTTGATTCAGGGAGTTAGTCCTCTTTCTGTCTCTCTCTAGTTCGCTTTATCTCCCTTCTTTTTTGTTCT
TTTGCAATGATGAATCTGGTGGTCTACTATAACAATGGTAGACCTGAACATATTGTTTTCTTGAATCTGTTCTCTCTTGG
ACCATATAAAAATACCAGTAGTACATTTATTAAGGGCTGTTCTTTGCAAGTTCTAATATCTTAGGTTCAGACTTGTAATA
AATTTTATTGAATGTAGTTTCTGTTTGATTGTTTGTATATTTGACGATGACCATGCTTTTAATTCCTAATATTTTCATGT
TGTAGGATGTTTATCGATACTTGCAAAAGGTTGAGGATCATGAAAGGTTCAGATGCCATTGGCCTGGGTGAGTATCTCTT
GTTGAGCCTTAGACCTCTTCATTCACACAATCAAAATGAAAAACGGAAAGAAAGACCGTCTCCTCCTTCATCTCCCCCGA
CCTTGTTCTTAGGGCTTGTACTTCTGTTTTTGTATTTTGACATGCATAACCATTTGGCGAGAGATGTGGGGCTTGCTCAA
GTGGTTCAGCACCTCCACCATCAACTGGTAGGTTGAGGTTTAGAGTTCGAGTCATGCTGGAGTGTTAGTGGGAATACTAG
TGATCTTCCGGGAGGGTAGAAAAAAAGGGGAAAAACAACTACTTGGTGATAAATAGAAATATACAAACTGTAACGCAGAA
TTATCTGGTTTCAACATTTGATTTCTGTGAATCTTGATTACTTTCTATGATTTGAAACAAAACTTCCTTGCAAGTTTCAT
ATTTAAAAGATATTATTGAAGAAATAATTAGAAGTCATGAAATGCTGGTTTAGGAATTCTCCCACCCAGCTGTTCGTCAT
GAAAGTTCTCTGAATTACCGTGATGCATTTTTTCAAGTAGCGTTAAGTATTAGAGAATTGCTTGCCTGACAGAACTACAT
TTGTTATGGATCTGGCCTCATTTTATTATTTGTCAAGCGGCAATAGAAAGATTTAGGACATCAAGGTAGGCTAGGCATCT
TGAAATGGTGGTGGTAGGTTCATTTGCATTGTAGGACACACCTGCATCTGTGAGAGATGAGGATGGAGAGTGAAGGAGAA
TGGTTAATGTAGTCCCAAAACCGAAAGGAAACGAGCTATAAGTTATTGTAAATCTATGGGCAGTGTTATGCAGTTATTGC
TGTTTTAAACATGTGAGTTAGTCAGCTTTATCTCATTATAAAAGGGCAAAGGGGATAACAAACTCAGCTGTTATAATTTC
CGCAAAAGTTCTGTTACCCAATAATGCATTTCCATATGCTGATTTGTGTGCAGACTTCGGATAGGTCTTTTATTAATCTG
TAAGTGTGTTTAGTCTATGGTAATGCAACTCTAGTTTAATTTTTGGTATTGGTTGCAACATTTCAACGACCAACTCCTGC
TCCTAAGGTATGAATGATTACCTACGAAACGGAAACATGTTACAATTCCACTAACTTCTGTGCATTTTTATGTGCAGCCC
CAAGGGCTATGGAAAAGTGTCGGAGCAGAAATTAGCCTATCTACACATGATTAAAGCTATCCATCCAGCATTTCTAGTAG
GCGAGGAAGACACAAAAACGGGTGAAGAGCTCATAAACTTGAATCCTTTTTAAAGGCATGAACAGTATAGCTGGTTGTTG
GTCTTGGATAGCTCAGCATGGGTAGATGCTTTACCTGATTACGACATGGTGTTCTTTTATATTTGCGTAATATATGTCCT
CTTTTAAGTTTTTTTTATCATGTCTATTTAAAAAACCGTTTGATATTGGAGTTTGTCTGCAAACTAATGTGTGTTGTGTA
CTGAGAGCTCTTCTAGAGGTAATTTAGTAATGTTCTAAGTGTATTTGCTTGTTTAAGTTCCCTTAAGTGTGTACTTTAGA
CCCAACGTTTGTCGTTTGATTAAGTATGCGTGTGCACTTCAGAAATTGTTATTACTGTATGAATAAATGTGTCCTCCACA
TTTTTCATCGGGTTGTAGTTATCG
Download sequence region |
Get flanking sequences on SL2.50ch04
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![]() ![]() | terms associated with this mRNA |
![]() ![]() | spliced cDNA sequence, including UTRs |
>Solyc04g076850.2.1 Auxin responsive protein (AHRD V1 *-*- D9IQE6_CATRO); contains Interpro domain(s) IPR003311 AUX/IAA protein
GATTATTAGAGTGATCTGTAATTGTGATGTCTCCGCCGCTCCTTGGTGTTGGGGAGGAGGAGGGCCAGAGTAATGTAACT
CTACTGGCTTCTTCAACTTCCTTAGGAAGCATATGCATAAAAGGATCAGCTCTTAAAGAGCGAAACTATATGGGTCTATC
TGATTGTTCGTCGGTGGACAGCTGTAATATTTCCACCTCATCAGAGGACAATAATGGGTGTGGATTAAATCTCAAGGCAA
CGGAGCTCAGGCTCGGTCTACCTGGATCTCAGTCTCCCGAAAGAGGTGAGGAGACTTGCCCTGTGAGCTCGACAAAGGTT
GATGAGAAGCTGCTCTTCCCCTTGCACCCTTCCAAAGATACTGCTTTCTCGGTATCGCAGAAAACAGTAGTTAGTGGCAA
CAAACGAGGATTTTCAGACGCTATGGATGGATTCTCAGAGGGGAAGTTTCTGTCGAATTCCGGTGTGAAAGCAGGTGATA
CAAAGGAGACCTCACGTGTGCAACCACCTAAAATGAAAGATGCTAATACTCAGAGTACAGTTCCAGAGAGGCCTTCTGCT
GTGAATGATGCCTCAAACCGTGCGGGCAGTGGTGCCCCTGCTACAAAGGCACAGGTTGTTGGTTGGCCACCCATTCGATC
TTTTAGAAAGAACACTCTAGCCTCTGCCTCGAAGAATAACGAAGAGGTTGACGGAAAAGCTGGCTCACCAGCTCTTTTTA
TTAAGGTCAGCATGGATGGTGCTCCCTATTTGAGGAAAGTGGACCTCAGAACCTGTTCTGCATACCAGGAGCTATCTTCT
GCTCTTGAAAAAATGTTCAGCTGTTTTACAATAGGTCAATATGGATCTCATGGAGCTCCTGGGAAGGATATGTTAAGTGA
GAGCAAATTGAAGGATTTGCTTCATGGATCTGAGTATGTCCTCACTTACGAAGATAAGGATGGGGACTGGATGCTTGTCG
GTGATGTCCCCTGGGAGATGTTTATCGATACTTGCAAAAGGTTGAGGATCATGAAAGGTTCAGATGCCATTGGCCTGGCC
CCAAGGGCTATGGAAAAGTGTCGGAGCAGAAATTAGCCTATCTACACATGATTAAAGCTATCCATCCAGCATTTCTAGTA
GGCGAGGAAGACACAAAAACGGGTGAAGAGCTCATAAACTTGAATCCTTTTTAAAGGCATGAACAGTATAGCTGGTTGTT
GGTCTTGGATAGCTCAGCATGGGTAGATGCTTTACCTGATTACGACATGGTGTTCTTTTATATTTGCGTAATATATGTCC
TCTTTTAAGTTTTTTTTATCATGTCTATTTAAAAAACCGTTTGATATTGGAGTTTGTCTGCAAACTAATGTGTGTTGTGT
ACTGAGAGCTCTTCTAGAGGTAATTTAGTAATGTTCTAAGTGTATTTGCTTGTTTAAGTTCCCTTAAGTGTGTACTTTAG
ACCCAACGTTTGTCGTTTGATTAAGTATGCGTGTGCACTTCAGAAATTGTTATTACTGTATGAATAAATGTGTCCTCCAC
ATTTTTCATCGGGTTGTAGTTATCG
GATTATTAGAGTGATCTGTAATTGTGATGTCTCCGCCGCTCCTTGGTGTTGGGGAGGAGGAGGGCCAGAGTAATGTAACT
CTACTGGCTTCTTCAACTTCCTTAGGAAGCATATGCATAAAAGGATCAGCTCTTAAAGAGCGAAACTATATGGGTCTATC
TGATTGTTCGTCGGTGGACAGCTGTAATATTTCCACCTCATCAGAGGACAATAATGGGTGTGGATTAAATCTCAAGGCAA
CGGAGCTCAGGCTCGGTCTACCTGGATCTCAGTCTCCCGAAAGAGGTGAGGAGACTTGCCCTGTGAGCTCGACAAAGGTT
GATGAGAAGCTGCTCTTCCCCTTGCACCCTTCCAAAGATACTGCTTTCTCGGTATCGCAGAAAACAGTAGTTAGTGGCAA
CAAACGAGGATTTTCAGACGCTATGGATGGATTCTCAGAGGGGAAGTTTCTGTCGAATTCCGGTGTGAAAGCAGGTGATA
CAAAGGAGACCTCACGTGTGCAACCACCTAAAATGAAAGATGCTAATACTCAGAGTACAGTTCCAGAGAGGCCTTCTGCT
GTGAATGATGCCTCAAACCGTGCGGGCAGTGGTGCCCCTGCTACAAAGGCACAGGTTGTTGGTTGGCCACCCATTCGATC
TTTTAGAAAGAACACTCTAGCCTCTGCCTCGAAGAATAACGAAGAGGTTGACGGAAAAGCTGGCTCACCAGCTCTTTTTA
TTAAGGTCAGCATGGATGGTGCTCCCTATTTGAGGAAAGTGGACCTCAGAACCTGTTCTGCATACCAGGAGCTATCTTCT
GCTCTTGAAAAAATGTTCAGCTGTTTTACAATAGGTCAATATGGATCTCATGGAGCTCCTGGGAAGGATATGTTAAGTGA
GAGCAAATTGAAGGATTTGCTTCATGGATCTGAGTATGTCCTCACTTACGAAGATAAGGATGGGGACTGGATGCTTGTCG
GTGATGTCCCCTGGGAGATGTTTATCGATACTTGCAAAAGGTTGAGGATCATGAAAGGTTCAGATGCCATTGGCCTGGCC
CCAAGGGCTATGGAAAAGTGTCGGAGCAGAAATTAGCCTATCTACACATGATTAAAGCTATCCATCCAGCATTTCTAGTA
GGCGAGGAAGACACAAAAACGGGTGAAGAGCTCATAAACTTGAATCCTTTTTAAAGGCATGAACAGTATAGCTGGTTGTT
GGTCTTGGATAGCTCAGCATGGGTAGATGCTTTACCTGATTACGACATGGTGTTCTTTTATATTTGCGTAATATATGTCC
TCTTTTAAGTTTTTTTTATCATGTCTATTTAAAAAACCGTTTGATATTGGAGTTTGTCTGCAAACTAATGTGTGTTGTGT
ACTGAGAGCTCTTCTAGAGGTAATTTAGTAATGTTCTAAGTGTATTTGCTTGTTTAAGTTCCCTTAAGTGTGTACTTTAG
ACCCAACGTTTGTCGTTTGATTAAGTATGCGTGTGCACTTCAGAAATTGTTATTACTGTATGAATAAATGTGTCCTCCAC
ATTTTTCATCGGGTTGTAGTTATCG
![]() ![]() | translated polypeptide sequence |
>Solyc04g076850.2.1 Auxin responsive protein (AHRD V1 *-*- D9IQE6_CATRO); contains Interpro domain(s) IPR003311 AUX/IAA protein
MSPPLLGVGEEEGQSNVTLLASSTSLGSICIKGSALKERNYMGLSDCSSVDSCNISTSSEDNNGCGLNLKATELRLGLPG
SQSPERGEETCPVSSTKVDEKLLFPLHPSKDTAFSVSQKTVVSGNKRGFSDAMDGFSEGKFLSNSGVKAGDTKETSRVQP
PKMKDANTQSTVPERPSAVNDASNRAGSGAPATKAQVVGWPPIRSFRKNTLASASKNNEEVDGKAGSPALFIKVSMDGAP
YLRKVDLRTCSAYQELSSALEKMFSCFTIGQYGSHGAPGKDMLSESKLKDLLHGSEYVLTYEDKDGDWMLVGDVPWEMFI
DTCKRLRIMKGSDAIGLAPRAMEKCRSRN*
MSPPLLGVGEEEGQSNVTLLASSTSLGSICIKGSALKERNYMGLSDCSSVDSCNISTSSEDNNGCGLNLKATELRLGLPG
SQSPERGEETCPVSSTKVDEKLLFPLHPSKDTAFSVSQKTVVSGNKRGFSDAMDGFSEGKFLSNSGVKAGDTKETSRVQP
PKMKDANTQSTVPERPSAVNDASNRAGSGAPATKAQVVGWPPIRSFRKNTLASASKNNEEVDGKAGSPALFIKVSMDGAP
YLRKVDLRTCSAYQELSSALEKMFSCFTIGQYGSHGAPGKDMLSESKLKDLLHGSEYVLTYEDKDGDWMLVGDVPWEMFI
DTCKRLRIMKGSDAIGLAPRAMEKCRSRN*
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![]() ![]() | [Associate new unigene] |
Unigene ID:
SGN-U568849 Tomato 200607 -- build 2 -- 104 members [Remove] [Blast]
SGN-U580151 Tomato 200607 -- build 2 -- 6 members [Remove] [Blast]
SGN-U593905 Tomato 200607 -- build 2 -- 1 members [Remove] [Blast]
SGN-U580151 Tomato 200607 -- build 2 -- 6 members [Remove] [Blast]
SGN-U593905 Tomato 200607 -- build 2 -- 1 members [Remove] [Blast]
![]() ![]() | [Associate new genbank sequence] |
AF022015 Lycopersicon esculentum auxin-regulated IAA4 (IAA4) mRNA, partial cds.
AF022020 Lycopersicon esculentum auxin-regulated IAA9 (IAA9) mRNA, partial cds.
BT013567 Lycopersicon esculentum clone 132305F, mRNA sequence.
AJ937282 Lycopersicon esculentum partial mRNA for Aux/IAA protein (iaa9 gene).
AJ249996 Lycopersicon esculentum partial mRNA for auxin-responsive protein (ctd1 gene).
DQ115325 Lycopersicon esculentum AUX/IAA protein (IAA4) mRNA, complete cds.
AF022020 Lycopersicon esculentum auxin-regulated IAA9 (IAA9) mRNA, partial cds.
BT013567 Lycopersicon esculentum clone 132305F, mRNA sequence.
AJ937282 Lycopersicon esculentum partial mRNA for Aux/IAA protein (iaa9 gene).
AJ249996 Lycopersicon esculentum partial mRNA for auxin-responsive protein (ctd1 gene).
DQ115325 Lycopersicon esculentum AUX/IAA protein (IAA4) mRNA, complete cds.
Other genome matches | None |
![]() ![]() | [Associate publication] [Matching publications] |
The diageotropica mutation alters auxin induction of a subset of the Aux/IAA gene family in tomato.
Plant molecular biology (2000)
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The diageotropica (dgt) mutation has been proposed to affect either auxin perception or responsiveness in tomato plants. It has previously been demonstrated that the expression of one member of the Aux/IAA family of auxin-regulated genes is reduced in dgt plants. Here, we report the cloning of ten new members of the tomato Aux/IAA family by PCR amplification based on conserved protein domains. All of the gene family members except one (LelAA7) are expressed in etiolated tomato seedlings, although they demonstrate tissue specificity (e.g. increased expression in hypocotyls vs. roots) within the seedling. The wild-type auxin-response characteristics of the expression of these tomato LelAA genes are similar to those previously described for Aux/IAA family members in Arabidopsis. In dgt seedlings, auxin stimulation of gene expression was reduced in only a subset of LelAA genes (LelAA5, 8, 10, and 11), with the greatest reduction associated with those genes with the strongest wild-type response to auxin. The remaining LelAA genes tested exhibited essentially the same induction levels in response to the hormone in both dgt and wild-type hypocotyls. These results confirm that dgt plants can perceive auxin and suggest that a specific step in early auxin signal transduction is disrupted by the dgt mutation.
Nebenführ, A. White, TJ. Lomax, TL.
Plant molecular biology.
2000.
44(1).
73-84.
Changes in gene expression during programmed cell death in tomato cell suspensions.
Plant molecular biology (2001)
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To identify genes involved in plant programmed cell death (PCD), changes in gene expression during PCD in a model system of suspension-cultured tomato cells were studied. In this system, cell death is triggered by treatment with camptothecin, an inhibitor of topoisomerase 1. Cell death was accompanied by internucleosomal DNA degradation, indicating that the cell death process shares similarities with apoptosis in animals. Tomato homologues of DAD1 and HSR203, two genes that have been implicated in PCD, were isolated. During camptothecin-induced PCD tomato DAD1 mRNA levels roughly halve, while tomato HSR203 mRNA levels increase 5-fold. A differential display approach was used to identify novel genes that show changes in expression levels during camptothecin-induced PCD. This resulted in isolation of two up-regulated (CTU1 and CTU2) and four down-regulated (CTD1, CTD2, CTD4, and CTD5) cDNA clones. CTU1 shows high homology to various gluthatione S-transferases, whereas CTU2 is as yet unidentified. CTD1 is highly similar to Aux/IAA early-auxin-responsive genes. CTD2 corresponds to the tomato RSI-I gene, CTD4 is an unknown clone, and CTD5 shows limited homology with a proline-rich protein from maize. Addition of the calcium channel blocker lanthanum chloride prevented camptothecin-induced cell death. The effect of lanthanum chloride on camptothecin-induced gene expression was studied to discriminate between putative cell death genes and general stress genes. The possible role of the various predicted gene products in plant PCD is discussed.
Hoeberichts, FA. Orzaez, D. van der Plas, LH. Woltering, EJ.
Plant molecular biology.
2001.
45(6).
641-54.
Control of ethylene-mediated processes in tomato at the level of receptors.
Journal of experimental botany (2002)
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The plant hormone ethylene controls many aspects of development and response to the environment. In tomato, ethylene is an essential component of flower senescence, organ abscission, adventitious root initiation, and fruit ripening. Responses to ethylene are also critical for aspects of biotic and abiotic stress responses. Clearly, much of the control of these events occurs at the level of hormone synthesis. However, it is becoming apparent that levels of the ethylene receptors are also highly regulated. The tomato ethylene receptors are encoded by a family of six genes. Levels of expression of these genes are spatially and temporally controlled throughout development. Further, a subset of the receptor genes respond to external stimuli. Genetic and biochemical evidence supports a model in which the ethylene receptors act as negative regulators of downstream responses; in the absence of ethylene, receptors actively suppress expression of ethylene responsive genes. Consistent with this model, a reduction in the overall level of receptor increases ethylene responsiveness of a tissue while higher expression of receptor decreases ethylene sensitivity. Evidence to support this model will be presented.
Klee, HJ.
Journal of experimental botany.
2002.
53(377).
2057-63.
The tomato Aux/IAA transcription factor IAA9 is involved in fruit development and leaf morphogenesis.
The Plant cell (2005)
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Auxin/indole-3-acetic acid (Aux/IAA) proteins are transcriptional regulators that mediate many aspects of plant responses to auxin. While functions of most Aux/IAAs have been defined mainly by gain-of-function mutant alleles in Arabidopsis thaliana, phenotypes associated with loss-of-function mutations have been scarce and subtle. We report here that the downregulation of IAA9, a tomato (Solanum lycopersicum) gene from a distinct subfamily of Aux/IAA genes, results in a pleiotropic phenotype, consistent with its ubiquitous expression pattern. IAA9-inhibited lines have simple leaves instead of wild-type compound leaves, and fruit development is triggered before fertilization, giving rise to parthenocarpy. This indicates that IAA9 is a key mediator of leaf morphogenesis and fruit set. In addition, antisense plants displayed auxin-related growth alterations, including enhanced hypocotyl/stem elongation, increased leaf vascularization, and reduced apical dominance. Auxin dose-response assays revealed that IAA9 downregulated lines were hypersensitive to auxin, although the only early auxin-responsive gene that was found to be upregulated in the antisense lines was IAA3. The activity of the IAA3 promoter was stimulated in the IAA9 antisense genetic background, indicating that IAA9 acts in planta as a transcriptional repressor of auxin signaling. While no mutation in any member of subfamily IV has been reported to date, the phenotypes associated with the downregulation of IAA9 reveal distinct and novel roles for members of the Aux/IAA gene family.
Wang, H. Jones, B. Li, Z. Frasse, P. Delalande, C. Regad, F. Chaabouni, S. Latché, A. Pech, Jean. Bouzayen, M.
The Plant cell.
2005.
17(10).
2676-92.
A single-base deletion mutation in SlIAA9 gene causes tomato (Solanum lycopersicum) entire mutant.
Journal of plant research (2007)
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The entire (e) locus of tomato (Solanum lycopersicum L.) controls leaf morphology. Dominant E and recessive e allele of the locus produce pinnate compound and complex reduced leaves. Previous research had indicated that SlIAA9, an Aux/IAA gene, was involved in tomato leaf morphology. Down-regulation of SlIAA9 gene by antisense transgenic method decreased the leaf complex of tomato and converted tomato compound leaves to simple leaves. The leaf morphology of these transgenic lines was similar with leaf morphology of tomato entire mutant. In this paper, we report that a single-base deletion mutation in the coding region of SlIAA9 gene results in tomato entire mutant phenotypes.
Zhang, Junhong. Chen, Rugang. Xiao, Jinhua. Qian, Chunjian. Wang, Taotao. Li, Hanxia. Ouyang, Bo. Ye, Zhibiao.
Journal of plant research.
2007.
120(6).
671-8.
Auxin patterns Solanum lycopersicum leaf morphogenesis.
Development (Cambridge, England) (2009)
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One of the most striking aspects of plant diversity is variation in leaf shape. Much of this diversity is achieved by the modulation of leaf blade dissection to form lobes or leaflets. Here, we show that the phytohormone auxin is a crucial signal regulating the partitioned outgrowth necessary to develop a dissected leaf. In developing leaves, the asymmetric distribution of auxin, driven by active transport, delineates the initiation of lobes and leaflets and specifies differential laminar outgrowth. Furthermore, homologous members of the AUX/indole-3-acetic acid (IAA) gene family mediate the action of auxin in determining leaf shape by repressing outgrowth in areas of low auxin concentration during both simple and compound leaf development. These results provide molecular evidence that leaflets initiate in a process reminiscent of organogenesis at the shoot apical meristem, but that compound and simple leaves regulate marginal growth through an evolutionarily conserved mechanism, thus shedding light on the homology of compound and simple leaves.
Koenig, D. Bayer, E. Kang, J. Kuhlemeier, C. Sinha, N.
Development (Cambridge, England).
2009.
136(17).
2997-3006.
Genome-wide analysis of Aux/IAA gene family in Solanaceae species using tomato as a model.
Molecular genetics and genomics : MGG (2012)
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Auxin plays key roles in a wide variety of plant activities, including embryo development, leaf formation, phototropism, fruit development and root initiation and development. Auxin/indoleacetic acid (Aux/IAA) genes, encoding short-lived nuclear proteins, are key regulators in the auxin transduction pathway. But how they work is still unknown. In order to conduct a systematic analysis of this gene family in Solanaceae species, a genome-wide search for the homologues of auxin response genes was carried out. Here, 26 and 27 non redundant AUX/IAAs were identified in tomato and potato, respectively. Using tomato as a model, a comprehensive overview of SlIAA gene family is presented, including the gene structures, phylogeny, chromosome locations, conserved motifs and cis-elements in promoter sequences. A phylogenetic tree generated from alignments of the predicted protein sequences of 31 OsIAAs, 29 AtIAAs, 31 ZmIAAs, and 26 SlIAAs revealed that these IAAs were clustered into three major groups and ten subgroups. Among them, seven subgroups were present in both monocot and dicot species, which indicated that the major functional diversification within the IAA family predated the monocot/dicot divergence. In contrast, group C and some other subgroups seemed to be species-specific. Quantitative real-time PCR (qRT-PCR) analysis showed that 19 of the 26 SlIAA genes could be detected in all tomato organs/tissues, however, seven of them were specifically expressed in some of tomato tissues. The transcript abundance of 17 SlIAA genes were increased within a few hours when the seedlings were treated with exogenous IAA. However, those of other six SlIAAs were decreased. The results of stress treatments showed that most SIIAA family genes responded to at least one of the three stress treatments, however, they exhibited diverse expression levels under different abiotic stress conditions in tomato seedlings. SlIAA20, SlIAA21 and SlIAA22 were not significantly influenced by stress treatments even though at least one stress-related cis-element was identified in their promoter regions. In conclusion, our comparative analysis provides an insight into the evolution and expression patterns in various tissues and in response to auxin or stresses of the Aux/IAA family members in tomato, which will provide a very useful reference for cloning and functional analysis of each member of AUX/IAA gene family in Solanaceae crops.
Wu, J. Peng, Z. Liu, S. He, Y. Cheng, L. Kong, F. Wang, J. Lu, G.
Molecular genetics and genomics : MGG.
2012.
().
.
Genome-wide identification, functional analysis and expression profiling of the Aux/IAA gene family in tomato.
Plant & cell physiology (2012)
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Auxin is a central hormone that exerts pleiotropic effects on plant growth including the development of roots, shoots, flowers and fruit. The perception and signaling of the plant hormone auxin rely on the cooperative action of several components, among which auxin/indole-3-acetic acid (Aux/IAA) proteins play a pivotal role. In this study, we identified and comprehensively analyzed the entire Aux/IAA gene family in tomato (Solanum lycopersicum), a reference species for Solanaceae plants, and the model plant for fleshy fruit development. Functional characterization using a dedicated single cell system revealed that tomato Aux/IAA proteins function as active repressors of auxin-dependent gene transcription, with, however, different Aux/IAA members displaying varying levels of repression. Phylogenetic analysis indicated that the Aux/IAA gene family is slightly contracted in tomato compared with Arabidopsis, with a lower representation of non-canonical proteins. Sl-IAA genes display distinctive expression pattern in different tomato organs and tissues, and some of them display differential responses to auxin and ethylene, suggesting that Aux/IAAs may play a role in linking both hormone signaling pathways. The data presented here shed more light on Sl-IAA genes and provides new leads towards the elucidation of their function during plant development and in mediating hormone cross-talk.
Audran-Delalande, C. Bassa, C. Mila, I. Regad, F. Zouine, M. Bouzayen, M.
Plant & cell physiology.
2012.
53(4).
659-72.
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- Genomic details
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- AT1G51690.1 mRNA feature details
- AT1G51690.1 polypeptide feature details
- AT1G51690.2 mRNA feature details
- AT1G51690.2 polypeptide feature details
- AT1G51690.3 mRNA feature details
- AT1G51690.3 polypeptide feature details
- AT5G06290.1 mRNA feature details
- AT5G06290.1 polypeptide feature details
- AT5G65670.1 mRNA feature details
- AT5G65670.1 polypeptide feature details
- AT5G65670.2 mRNA feature details
- AT5G65670.2 polypeptide feature details
- AT5G43700.1 mRNA feature details
- AT5G43700.1 polypeptide feature details
- Solyc04g076850.2 gene feature details
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