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Tomato locus eukaryotic translation initiation factor 4E
Locus details | Download GMOD XML | Note to Editors | Annotation guidelines |
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eukaryotic translation initiation factor 4E is on PhyloGenes
TomDelDB genotype frequencies in tomato populations. chromosome SL2.50ch03, position: 590360
Please cite Razifard et al.
TomDelDB genotype frequencies in tomato populations. chromosome SL2.50ch03, position: 592089
Please cite Razifard et al.
TomDelDB genotype frequencies in tomato populations. chromosome SL2.50ch03, position: 592090
Please cite Razifard et al.
Registry name: | None | [Associate registry name] |
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![]() ![]() | unprocessed genomic sequence region underlying this gene |
>Solyc03g005870.2 SL2.50ch03:590058..593520
AGTGCTCCACAGTCCACAGAGCAGCAAAAATGGCAGCAGCTGAAATGGAGAGAACGATGTCGTTTGATGCAGCTGAGAAGTTGAAGGCCGCCGATGGAGGAGGAGGAGAGGTAGACGATGAACTTGAAGAAGGTGAAATTGTTGAAGAATCAAATGATACGGCATCGTATTTAGGGAAAGAAATCACAGTGAAGCATCCATTGGAGCATTCATGGACTTTTTGGTTTGATAACCCTACCACTAAATCTCGACAAACTGCTTGGGGAAGCTCACTTCGAAATGTCTACACTTTCTCCACTGTTGAAGATTTTTGGGGGTAAGTTTTTTTTTTTCCTCTTTCAAATTGGTGATAGTGTAGTGTAAGGGAAAACAGGGAGTGGATTGCAAGGTGGGGAATCGAATCCTCGAGAAAGTTTAGATAGTCAATTAATTGAGCTACTGAGATTCCTCGGATTTTTTAAAAAAAATAAATTGGGGATAGAGGAAGAGGAAATGGGGGAGACTTTTATAAGGTTATACCGTTGTTAACAAGGTGAAATTTTAGGTAGTTAATCAATTGAGCTACTAAGATTCTTTAGATACGATTTTCGTAAGCTCAAATTGGAAAATAAAAAATTAGATTATTACTAAGGAGCTGAAGAAATTCAGAAATGAGTTACCTTTTGAGCCAGCAGAACCAGTTAAGTTGAGATTTCATTGATTTTAGCTTGTTTTTAATGTTGGTTGTGAATTATGGGGTTTTATTATAATGTTCCAACAATTTTGTTGGTGTTGTAGGACTTTTTTGATTTAGCGTTTTGAATGTGTTCTGATTATCTGCCTTCACATAGGTGATATTGAGGTAAAAATGGCATCTTGATTGATTTTGCTCTCATAATTGTTAGATTTTCTTCTTGTACATTTTGCAGTTTTTAGTTAACTTGCCAAGGTGTTTAGTGGATGCACAATATGCGGTATTACTACGGAATGTCTGAATTGGTTTGAGCTTTAGTTTACCCAAGCTGTATTAGTAATTGCACATTGCTTTGTCCTTTTTTAGTTAGTACTTTCCTTAAAACTGGAATTTTGATCTCTTGGTTACTTGCCAATTTAAATTTTAGTTCATGGATCGGATTCAATGAATAGATATATGCTCTTTGGTGGTGGGAGGACAAGGATAGATAAATTAAACTCGGTAAGGAGAGAAAGTGCAGAATGAATGGAAGTTGAGACATTTTGGAGTATGGGGTGAAGAATGACCTGTGAAGTTTTAGGAAAGAAAAAGTTAACCTTGTTGAATAGTCATATTTCTCTTCCTTGCACAATCTTGTGTAGGAATGCCTTTAATTGGGTTTATATCGTCGGATAGTTTATATTGCTTCAAATCTAAGAAACTCTTTCATATTTGTCAAATGCTCCTATTTTCAACAAAGGATATTTTGAGCTGAAAAGGTAGTTGAATAATGCATTGGTCGTAGTTTTCTCTCCTAAGCAAGATAATATAGTTACTATTTTCAAGTACAACTACTTCTTTTTCTTTAGTTTACGTATAAGAGCAGGTCCTGTATCTACATAGCTGTGATATCTCTATGTGCATTTGTCTTAATATACTATTCACTTGTCTTAATATATTATTCACTTTCAAAAATAAAGACAGATGTGTTTCTATTTCTTAATTAGGCTAAAGTATGCTCATCTCCTCTGTAGATTGATGAGACTTAGCTGCAGGCCAGTTTTTTCAATCTCACGCATAGACTTTTTTATTAAGTCCTATGATTTGAGTAATGTAGGTGGTAATGGTGTGAATTTGATGTCTGCCATGGATGCATGCACCTTGTTTGGTGAGTTCTTTATTGGTCTAATTACTCAAGGCACTTGAGTTATTGTACAACTTGAACGATGACATACCTGTTTGATATTCCACATCATGGATTAGGTCTTTGAAATGCTATTATCCTTTTGGCTCATGATGAAATCTTGAACCATGTTGCTTATTCTACAAACAGTGCTTACAATAATATCCATCACCCAAGCAAGTTAATTATGGGAGCAGACTTTCATTGTTTTAAGCACAAAATTGAGCCAAAGTGGGAAGATCCTGTATGTGCCAATGGAGGGACGTGGAAAATGAGTTTTTCGAAGGGTAAATCTGATACCAGCTGGCTGTATACGGTATTCCGAAGTTATTTCCATCCAGCCCTTAATGATAGGTCATTCTAGTAATGTTATTTTCCCCTTTGATATAATTTCCACTCTTGTTTTCTTATATGGAATTATTGTAGCTGCTGGCAATGATTGGACATCAATTCGATCATGGAGATGAAATTTGTGGAGCAGTTGTTAGTGTCCGGGCTAAGGGAGAAAAAATAGCTTTGTGGACCAAGAATGCTGCAAATGAAACAGCTCAGGTAATTTGCTTTATATTTTTGGTGTCAACGGCCACGTTTGTCATTTTCTTGGATCAAGCGGACAGACATTTTTTGTTGTGTACATACTGTAGTGCTGATGTTTATTCAAAATATACTATGAAATACATTGTACCGTTGAGTATATTGGAAGTTAAGAGGGGAAGTCATCAGATATATAGGAAGTGCTCCTTGTGAGAAATTTCTCTAGTAGGGCTCAAACCCGAGAACCATGGTTAAGGACGGAGGGATCCCTTTGGTGGTATCAAGGGTTAATTATATTATTTCATGTTTCATATGATTGAAACATTTGGATATCCTTGCAAAGTGTGATATTGTTTTGTCTCGTCATTTGTTTTATGCTTCATAAGAATTATCTTTTCTTTCGTCCCCTTCTCTTTGTTTCTTTTTCTCCAGTGTACTTCATTCTTCTAGAATTATATAGTGGTCGGCGTTCCCTTTTGTGCTTCATTGATAATATTGAATCCTTTCAGCTGTTTACCGGTTGATTATTTTTATGTTGGTGCTTATTGCTAGTTTTTTGTTTTTATATCTTTGCAACTATACCTACCATCTTCCTGAAACTTCTCTTTACAGGTTAGCATTGGTAAGCAATGGAAGCAGTTTCTAGATTACAGTGATTCGGTTGGCTTCATATTTCACGTATGAAATCTTGGTTATCATACGCCTTTAATTCAGTTTCTCTTCAATTAGCAAGACTCATAAAGAATCATCTTCTTTTGCAGGACGATGCAAAGAGGCTCGACAGAAATGCCAAGAATCGTTACACCGTATAGTTCTTGATGCAGTGTGGGATTGCAAGAAACACAATTCGTACTGGAAAGGTTGGTAGGTACTAGTTTAGTTTCTCATTTGATAAGCTTCTGGTTTGAGTAACTCGTGTGTTGGTGTTTACACTTTCTAATCGTGGAAAATTGTTTGATTTGAATCCATGCCTCTATGTTTCGTGTGTTCTGTGTTACTTTCCCAGCTTCCCTATTATTTCTCTGCAGTAAAAATCTCTGAAAATATTGTTGATGGAGGTGAAAGTGATACCAAGCACATAACAAAACACAAAT
AGTGCTCCACAGTCCACAGAGCAGCAAAAATGGCAGCAGCTGAAATGGAGAGAACGATGTCGTTTGATGCAGCTGAGAAGTTGAAGGCCGCCGATGGAGGAGGAGGAGAGGTAGACGATGAACTTGAAGAAGGTGAAATTGTTGAAGAATCAAATGATACGGCATCGTATTTAGGGAAAGAAATCACAGTGAAGCATCCATTGGAGCATTCATGGACTTTTTGGTTTGATAACCCTACCACTAAATCTCGACAAACTGCTTGGGGAAGCTCACTTCGAAATGTCTACACTTTCTCCACTGTTGAAGATTTTTGGGGGTAAGTTTTTTTTTTTCCTCTTTCAAATTGGTGATAGTGTAGTGTAAGGGAAAACAGGGAGTGGATTGCAAGGTGGGGAATCGAATCCTCGAGAAAGTTTAGATAGTCAATTAATTGAGCTACTGAGATTCCTCGGATTTTTTAAAAAAAATAAATTGGGGATAGAGGAAGAGGAAATGGGGGAGACTTTTATAAGGTTATACCGTTGTTAACAAGGTGAAATTTTAGGTAGTTAATCAATTGAGCTACTAAGATTCTTTAGATACGATTTTCGTAAGCTCAAATTGGAAAATAAAAAATTAGATTATTACTAAGGAGCTGAAGAAATTCAGAAATGAGTTACCTTTTGAGCCAGCAGAACCAGTTAAGTTGAGATTTCATTGATTTTAGCTTGTTTTTAATGTTGGTTGTGAATTATGGGGTTTTATTATAATGTTCCAACAATTTTGTTGGTGTTGTAGGACTTTTTTGATTTAGCGTTTTGAATGTGTTCTGATTATCTGCCTTCACATAGGTGATATTGAGGTAAAAATGGCATCTTGATTGATTTTGCTCTCATAATTGTTAGATTTTCTTCTTGTACATTTTGCAGTTTTTAGTTAACTTGCCAAGGTGTTTAGTGGATGCACAATATGCGGTATTACTACGGAATGTCTGAATTGGTTTGAGCTTTAGTTTACCCAAGCTGTATTAGTAATTGCACATTGCTTTGTCCTTTTTTAGTTAGTACTTTCCTTAAAACTGGAATTTTGATCTCTTGGTTACTTGCCAATTTAAATTTTAGTTCATGGATCGGATTCAATGAATAGATATATGCTCTTTGGTGGTGGGAGGACAAGGATAGATAAATTAAACTCGGTAAGGAGAGAAAGTGCAGAATGAATGGAAGTTGAGACATTTTGGAGTATGGGGTGAAGAATGACCTGTGAAGTTTTAGGAAAGAAAAAGTTAACCTTGTTGAATAGTCATATTTCTCTTCCTTGCACAATCTTGTGTAGGAATGCCTTTAATTGGGTTTATATCGTCGGATAGTTTATATTGCTTCAAATCTAAGAAACTCTTTCATATTTGTCAAATGCTCCTATTTTCAACAAAGGATATTTTGAGCTGAAAAGGTAGTTGAATAATGCATTGGTCGTAGTTTTCTCTCCTAAGCAAGATAATATAGTTACTATTTTCAAGTACAACTACTTCTTTTTCTTTAGTTTACGTATAAGAGCAGGTCCTGTATCTACATAGCTGTGATATCTCTATGTGCATTTGTCTTAATATACTATTCACTTGTCTTAATATATTATTCACTTTCAAAAATAAAGACAGATGTGTTTCTATTTCTTAATTAGGCTAAAGTATGCTCATCTCCTCTGTAGATTGATGAGACTTAGCTGCAGGCCAGTTTTTTCAATCTCACGCATAGACTTTTTTATTAAGTCCTATGATTTGAGTAATGTAGGTGGTAATGGTGTGAATTTGATGTCTGCCATGGATGCATGCACCTTGTTTGGTGAGTTCTTTATTGGTCTAATTACTCAAGGCACTTGAGTTATTGTACAACTTGAACGATGACATACCTGTTTGATATTCCACATCATGGATTAGGTCTTTGAAATGCTATTATCCTTTTGGCTCATGATGAAATCTTGAACCATGTTGCTTATTCTACAAACAGTGCTTACAATAATATCCATCACCCAAGCAAGTTAATTATGGGAGCAGACTTTCATTGTTTTAAGCACAAAATTGAGCCAAAGTGGGAAGATCCTGTATGTGCCAATGGAGGGACGTGGAAAATGAGTTTTTCGAAGGGTAAATCTGATACCAGCTGGCTGTATACGGTATTCCGAAGTTATTTCCATCCAGCCCTTAATGATAGGTCATTCTAGTAATGTTATTTTCCCCTTTGATATAATTTCCACTCTTGTTTTCTTATATGGAATTATTGTAGCTGCTGGCAATGATTGGACATCAATTCGATCATGGAGATGAAATTTGTGGAGCAGTTGTTAGTGTCCGGGCTAAGGGAGAAAAAATAGCTTTGTGGACCAAGAATGCTGCAAATGAAACAGCTCAGGTAATTTGCTTTATATTTTTGGTGTCAACGGCCACGTTTGTCATTTTCTTGGATCAAGCGGACAGACATTTTTTGTTGTGTACATACTGTAGTGCTGATGTTTATTCAAAATATACTATGAAATACATTGTACCGTTGAGTATATTGGAAGTTAAGAGGGGAAGTCATCAGATATATAGGAAGTGCTCCTTGTGAGAAATTTCTCTAGTAGGGCTCAAACCCGAGAACCATGGTTAAGGACGGAGGGATCCCTTTGGTGGTATCAAGGGTTAATTATATTATTTCATGTTTCATATGATTGAAACATTTGGATATCCTTGCAAAGTGTGATATTGTTTTGTCTCGTCATTTGTTTTATGCTTCATAAGAATTATCTTTTCTTTCGTCCCCTTCTCTTTGTTTCTTTTTCTCCAGTGTACTTCATTCTTCTAGAATTATATAGTGGTCGGCGTTCCCTTTTGTGCTTCATTGATAATATTGAATCCTTTCAGCTGTTTACCGGTTGATTATTTTTATGTTGGTGCTTATTGCTAGTTTTTTGTTTTTATATCTTTGCAACTATACCTACCATCTTCCTGAAACTTCTCTTTACAGGTTAGCATTGGTAAGCAATGGAAGCAGTTTCTAGATTACAGTGATTCGGTTGGCTTCATATTTCACGTATGAAATCTTGGTTATCATACGCCTTTAATTCAGTTTCTCTTCAATTAGCAAGACTCATAAAGAATCATCTTCTTTTGCAGGACGATGCAAAGAGGCTCGACAGAAATGCCAAGAATCGTTACACCGTATAGTTCTTGATGCAGTGTGGGATTGCAAGAAACACAATTCGTACTGGAAAGGTTGGTAGGTACTAGTTTAGTTTCTCATTTGATAAGCTTCTGGTTTGAGTAACTCGTGTGTTGGTGTTTACACTTTCTAATCGTGGAAAATTGTTTGATTTGAATCCATGCCTCTATGTTTCGTGTGTTCTGTGTTACTTTCCCAGCTTCCCTATTATTTCTCTGCAGTAAAAATCTCTGAAAATATTGTTGATGGAGGTGAAAGTGATACCAAGCACATAACAAAACACAAAT
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Get flanking sequences on SL2.50ch03
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![]() ![]() | terms associated with this mRNA |
![]() ![]() | spliced cDNA sequence, including UTRs |
>Solyc03g005870.2.1 Eukaryotic translation initiation factor 4E (AHRD V1 ***- Q199B8_SOLLC); contains Interpro domain(s) IPR001040 Eukaryotic translation initiation factor 4E (eIF-4E)
AGTGCTCCACAGTCCACAGAGCAGCAAAAATGGCAGCAGCTGAAATGGAGAGAACGATGTCGTTTGATGCAGCTGAGAAGTTGAAGGCCGCCGATGGAGGAGGAGGAGAGGTAGACGATGAACTTGAAGAAGGTGAAATTGTTGAAGAATCAAATGATACGGCATCGTATTTAGGGAAAGAAATCACAGTGAAGCATCCATTGGAGCATTCATGGACTTTTTGGTTTGATAACCCTACCACTAAATCTCGACAAACTGCTTGGGGAAGCTCACTTCGAAATGTCTACACTTTCTCCACTGTTGAAGATTTTTGGGGTGCTTACAATAATATCCATCACCCAAGCAAGTTAATTATGGGAGCAGACTTTCATTGTTTTAAGCACAAAATTGAGCCAAAGTGGGAAGATCCTGTATGTGCCAATGGAGGGACGTGGAAAATGAGTTTTTCGAAGGGTAAATCTGATACCAGCTGGCTGTATACGCTGCTGGCAATGATTGGACATCAATTCGATCATGGAGATGAAATTTGTGGAGCAGTTGTTAGTGTCCGGGCTAAGGGAGAAAAAATAGCTTTGTGGACCAAGAATGCTGCAAATGAAACAGCTCAGGTTAGCATTGGTAAGCAATGGAAGCAGTTTCTAGATTACAGTGATTCGGTTGGCTTCATATTTCACGACGATGCAAAGAGGCTCGACAGAAATGCCAAGAATCGTTACACCGTATAGTTCTTGATGCAGTGTGGGATTGCAAGAAACACAATTCGTACTGGAAAGGTTGGTAGGTACTAGTTTAGTTTCTCATTTGATAAGCTTCTGGTTTGAGTAACTCGTGTGTTGGTGTTTACACTTTCTAATCGTGGAAAATTGTTTGATTTGAATCCATGCCTCTATGTTTCGTCACATAACAAAACACAAAT
AGTGCTCCACAGTCCACAGAGCAGCAAAAATGGCAGCAGCTGAAATGGAGAGAACGATGTCGTTTGATGCAGCTGAGAAGTTGAAGGCCGCCGATGGAGGAGGAGGAGAGGTAGACGATGAACTTGAAGAAGGTGAAATTGTTGAAGAATCAAATGATACGGCATCGTATTTAGGGAAAGAAATCACAGTGAAGCATCCATTGGAGCATTCATGGACTTTTTGGTTTGATAACCCTACCACTAAATCTCGACAAACTGCTTGGGGAAGCTCACTTCGAAATGTCTACACTTTCTCCACTGTTGAAGATTTTTGGGGTGCTTACAATAATATCCATCACCCAAGCAAGTTAATTATGGGAGCAGACTTTCATTGTTTTAAGCACAAAATTGAGCCAAAGTGGGAAGATCCTGTATGTGCCAATGGAGGGACGTGGAAAATGAGTTTTTCGAAGGGTAAATCTGATACCAGCTGGCTGTATACGCTGCTGGCAATGATTGGACATCAATTCGATCATGGAGATGAAATTTGTGGAGCAGTTGTTAGTGTCCGGGCTAAGGGAGAAAAAATAGCTTTGTGGACCAAGAATGCTGCAAATGAAACAGCTCAGGTTAGCATTGGTAAGCAATGGAAGCAGTTTCTAGATTACAGTGATTCGGTTGGCTTCATATTTCACGACGATGCAAAGAGGCTCGACAGAAATGCCAAGAATCGTTACACCGTATAGTTCTTGATGCAGTGTGGGATTGCAAGAAACACAATTCGTACTGGAAAGGTTGGTAGGTACTAGTTTAGTTTCTCATTTGATAAGCTTCTGGTTTGAGTAACTCGTGTGTTGGTGTTTACACTTTCTAATCGTGGAAAATTGTTTGATTTGAATCCATGCCTCTATGTTTCGTCACATAACAAAACACAAAT
![]() ![]() | translated polypeptide sequence |
>Solyc03g005870.2.1 Eukaryotic translation initiation factor 4E (AHRD V1 ***- Q199B8_SOLLC); contains Interpro domain(s) IPR001040 Eukaryotic translation initiation factor 4E (eIF-4E)
MAAAEMERTMSFDAAEKLKAADGGGGEVDDELEEGEIVEESNDTASYLGKEITVKHPLEHSWTFWFDNPTTKSRQTAWGSSLRNVYTFSTVEDFWGAYNNIHHPSKLIMGADFHCFKHKIEPKWEDPVCANGGTWKMSFSKGKSDTSWLYTLLAMIGHQFDHGDEICGAVVSVRAKGEKIALWTKNAANETAQVSIGKQWKQFLDYSDSVGFIFHDDAKRLDRNAKNRYTV*
MAAAEMERTMSFDAAEKLKAADGGGGEVDDELEEGEIVEESNDTASYLGKEITVKHPLEHSWTFWFDNPTTKSRQTAWGSSLRNVYTFSTVEDFWGAYNNIHHPSKLIMGADFHCFKHKIEPKWEDPVCANGGTWKMSFSKGKSDTSWLYTLLAMIGHQFDHGDEICGAVVSVRAKGEKIALWTKNAANETAQVSIGKQWKQFLDYSDSVGFIFHDDAKRLDRNAKNRYTV*
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![]() ![]() | [Associate new unigene] |
Unigene ID:
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![]() ![]() | [Associate new genbank sequence] |
DQ537341 Lycopersicon esculentum clone le4I eukaryotic translation initiation factor 4E mRNA, complete cds.
DQ537342 Lycopersicon esculentum clone le4II eukaryotic translation initiation factor 4E mRNA, complete cds.
DQ537343 Lycopersicon esculentum clone le4III eukaryotic translation initiation factor 4E mRNA, complete cds.
CU856538 S.lycopersicum DNA sequence from clone SL_FOS-97P22
GQ451830 Solanum lycopersicum translation initiation factor eIF4E1 (eIF4E1) gene, complete cds.
AY723733 Lycopersicon esculentum cultivar Mospomorist eukaryotic translation initiation factor 4E mRNA, complete cds.
AY723734 Lycopersicon esculentum cultivar Micro-Tom eukaryotic translation initiation factor 4E mRNA, complete cds.
AY723735 Lycopersicon hirsutum cultivar PI 134417 eukaryotic translation initiation factor 4E mRNA, complete cds.
AY723736 Lycopersicon hirsutum cultivar PI 247087 eukaryotic translation initiation factor 4E mRNA, complete cds.
AF259801 Lycopersicon esculentum eIF4E mRNA, complete cds.
DQ537342 Lycopersicon esculentum clone le4II eukaryotic translation initiation factor 4E mRNA, complete cds.
DQ537343 Lycopersicon esculentum clone le4III eukaryotic translation initiation factor 4E mRNA, complete cds.
CU856538 S.lycopersicum DNA sequence from clone SL_FOS-97P22
GQ451830 Solanum lycopersicum translation initiation factor eIF4E1 (eIF4E1) gene, complete cds.
AY723733 Lycopersicon esculentum cultivar Mospomorist eukaryotic translation initiation factor 4E mRNA, complete cds.
AY723734 Lycopersicon esculentum cultivar Micro-Tom eukaryotic translation initiation factor 4E mRNA, complete cds.
AY723735 Lycopersicon hirsutum cultivar PI 134417 eukaryotic translation initiation factor 4E mRNA, complete cds.
AY723736 Lycopersicon hirsutum cultivar PI 247087 eukaryotic translation initiation factor 4E mRNA, complete cds.
AF259801 Lycopersicon esculentum eIF4E mRNA, complete cds.
Other genome matches | None |
![]() ![]() | [Associate publication] [Matching publications] |
Strain-specific interaction of the tobacco etch virus NIa protein with the translation initiation factor eIF4E in the yeast two-hybrid system.
Virology (2000)
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The NIa protein of potyviruses provides VPg and proteolytic functions during virus replication. It has also been shown to confer host genotype-specific movement functions in plants. Specifically, NIa from tobacco etch virus (TEV)-Oxnard, but not from most other strains, confers the ability to move long distances in Nicotiana tabacum cultivar "V-20." This led to the hypothesis that all or part of NIa may interact with one or more cellular factors. To identify cellular proteins that interact with NIa in a host- or strain-specific manner, a yeast two-hybrid search of a tomato cDNA library was done. Ten proteins that interacted with NIa were recovered, with translation initiation factor eIF4E being by far the most common protein identified. Interaction of eIF4E with NIa was shown to be TEV strain-specific. eIF4E from both tomato and tobacco interacted well with NIa from the HAT strain, but not from the Oxnard strain. However, using chimeric NIa proteins, the determinant for systemic infection of V20 plants was found to be genetically distinct from the determinant controlling eIF4E interaction. In TEV-eIF4E coexpression experiments, evidence suggesting that eIF4E provides a positive effect on genome amplification was obtained.
Schaad, MC. Anderberg, RJ. Carrington, JC.
Virology.
2000.
273(2).
300-6.
The recessive potyvirus resistance gene pot-1 is the tomato orthologue of the pepper pvr2-eIF4E gene.
Molecular genetics and genomics : MGG (2005)
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The translation initiation factor 4E (eIF4E) has been implicated in naturally occurring resistance to Potato virus Y (PVY) determined by the pvr2 locus in pepper (Capsicum annuum). Here, the molecular basis of the recessive resistance to PVY and Tobacco etch virus (TEV) controlled by the pot-1 locus in tomato (Lycopersicon esculentum; now Solanum lycopersicum) was investigated. On the basis of genetic mapping data that indicated that pot-1 and pvr2 are located in syntenic regions of the tomato and pepper genomes, the possible involvement of eIF4E in pot-1-mediated resistance was assessed. Genetic mapping of members of the eIF4E multigenic family in tomato introgression lines revealed that an eIF4E locus indeed maps in the same genomic region as pot-1. By comparing eIF4E coding sequences between resistant and susceptible Lycopersicon genotypes, a small number of polymorphisms that co-segregate with the pot-1 locus were identified, suggesting that this gene could be involved in resistance to potyviruses. Functional complementation experiments using Potato virus X-mediated transient expression of eIF4E from a susceptible genotype in a resistant pepper genotype confirmed that a small number of amino acid substitutions in the eIF4E protein indeed account for resistance/susceptibility to both the PVY and TEV, and consequently that pot-1 and pvr2 are orthologues. Taken together, these results support the role of this eIF4E gene as a key component of recessive resistance to potyviruses, and validate the comparative genomic approach for the molecular characterization of recessive resistance genes.
Ruffel, S. Gallois, JL. Lesage, ML. Caranta, C.
Molecular genetics and genomics : MGG.
2005.
274(4).
346-53.
An induced mutation in tomato eIF4E leads to immunity to two potyviruses.
PloS one (2010)
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Mutation analysis of translation initiation factors shows that translation initiation factors of the eIF4E family are determinants of plant susceptibility to RNA viruses and viruses have adopted strategies to use different isoforms. This work also demonstrates the effectiveness of TILLING as a reverse genetics tool to improve crop species. We have also developed a complete tool that can be used for both forward and reverse genetics in tomato, for both basic science and crop improvement. By opening it to the community, we hope to fulfill the expectations of both crop breeders and scientists who are using tomato as their model of study.
Piron, F. Nicolaï, M. Minoïa, S. Piednoir, E. Moretti, A. Salgues, A. Zamir, D. Caranta, C. Bendahmane, A.
PloS one.
2010.
5(6).
e11313.
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