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Tomato locus goblet
| Locus details | Download GMOD XML | Note to Editors | Annotation guidelines | 
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| Registry name: | None | [Associate registry name] | 
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| Image | Description | Type | 
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	 Accessions and images (4)
	 Accessions and images (4)
 | [Associate accession] | 
	 Alleles (3)
	 Alleles (3)
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	 Associated loci (1)
	 Associated loci (1)
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	 Sequence annotations
	 Sequence annotations
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	 Genome features
	 Genome features
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	 Genomic sequence
	 Genomic sequence
 | unprocessed genomic sequence region underlying this gene | 
                
    
  >Solyc07g062840.2 SL2.50ch07:65485289..65487433
    
  
ATGGAGATTTATCATCAGATGCAGTTTGATTGCGGTGATCCGCATTTACCACCGGGGTTTCGGTTTCATCCAACTGACGAAGAACTTATTACTTACTACTTGTTGAAGAAGGTTCTGGACTGCAACTTCACTGCTAGAGCTATTGCTGAAGTTGATCTCAACAAATGTGAACCTTGGGAACTTCCTGGTATGAACTTTTTTTTTTTATTCTCATGTTATATTTGAGTGTGCAAATTTACCATGTTTTACAAGATTTGAACGCTAATTAAATATTTTAACATACTTTTGAGCTTTAACTAAAAAAAAACTAAAATACCCTTATTTTATTAAGGGAAAGCGAAAATGGGAGAAAAAGAATGGTATTTCTTCAGTCTACGTGATCGGAAGTATCCAACAGGGCTGAGGACTAACAGAGCTACTGAAGCGGGTTACTGGAAAGCTACTGGAAAAGATAGAGAAATTTTCAGTTCAAAAACATGTGCACTTGTTGGTATGAAGAAAACCCTAGTTTTTTATCGAGGAAGAGCACCAAAAGGAGAAAAAAGTAACTGGGTTATGCATGAATATCGCCTTGATGGCAAATTTGCCTATCATTATATCTCCAGGAGTTCGAAGGTACTAGAGTATTTTTGTGTTAATAATTAACTGATACACATATATTAATGAATTTTGATGAAGAAAACTGATCTACATGTTTTGTGTTACAACTCATACTTTTTTTTGTATTTGGATTAAAGAGATCAGATTTACTGGAGATATTCTGTGCACAAATATATCATTGATATTACTGCTAGAGCCAGAGATTCTGAAGCAGAAAGTTTTGTGAAACTTCGTTTTCAATGTCTCAATTGCTTATGATTAAGTTGGAAGTATACATAGTCTGAAAAATAACAGAAAAACAAATTAAAAGAGAAAAAAAAGAATTTGCTTTTATTATGATTTATGATCAAAGCAATTAAGACTTTACAGAATAATATACTGTCATATTGATAGCGATTTAATATAATCTCTTTCCAAACTTATTTTATTAGCCTTATCAATGTGTAAGCATGCTTACGTAAATTCATCAGTCTGTTAGATTTTGACTTTTAGCGTTTTGGCATTAATTTAAATGCTTCTTTTTTTAAAATTGCATCATAATGAGCTTCATATTTGTTAGATTACAAACATTTCTTTAATAACAAAATAAGATTCGTAGACGCTAAAAATTAGGTCTTGCCCCAAAAAATGTTGTATATTTGTTTTTCATGGTAAAGTTAAAAGCCTGATGCGGGTTTTATGAAATTTGTAGCTTTCACAAGTTCATAAAATATGTAAACATGCTTGTAGTTATAAATTTTAAATTTTGAATTCGTTTTTTCGTGTTTCCATTGTTCTCATATATTTTTTGGCTACAGGACGAGTGGGTTATCTCGCGGGTCTTTCAAAAAAGCACCGGTTCTAATGGTGCCGCTACTTCAACTGGTGGCGGCAAAAAAAGGCTAAGTTCAAGTATAAACATGTACCAGGAAGTGAGTTCACCGTCTTCCGTCTCTCACCTTCCGCCGCTCCTCGATTCCTCTCCGTATAGCACTACCGCCACTTCCGCCGCAGCTATCGTAATCGGCGACCGCGATCGTGATCATAGCTTCAAGAAGGAGCACGTGCCCTGTTTCTCCACAACTGCTACTGCTACAATAACTGCACAGAGTCTAACTTTCGATCCAACTTCTGTCTTCGACATTTCATCAAACACCTTGCATGCACTACAGCCAACTCCAAGTTTCGCTTCTATTTTGGACTCTTCTCCATCTAATTTCACTAATTACACAAGGAATTCAACTTTTCCAAGCTTAAGATCACTCCATGAGAATCTCCAGCTTCCGTTATTCTCCGGCGGAACCTCCGCCATGCACGGCGGATTTTCTAATCCGATGGTTAATTGGACCGTGCCGGAGACTCAGAAAGTTGAACAGTCTGAACTTGACTGTATGTGGAGCTACTGAATTAGCAAGTGCTTAATTTTAATTAAGACGTTAATTAATTAAGTAATCAGTGTGTTAATCTTTGCTTTTTGTTTAGTATGTACTGCGTGTGGCAGCTTTAGTGGTATTGTCACTTTGTTGTAAACGTTCAGCGTAATTTAATGCATGCTATTATTTCTCG
              
ATGGAGATTTATCATCAGATGCAGTTTGATTGCGGTGATCCGCATTTACCACCGGGGTTTCGGTTTCATCCAACTGACGAAGAACTTATTACTTACTACTTGTTGAAGAAGGTTCTGGACTGCAACTTCACTGCTAGAGCTATTGCTGAAGTTGATCTCAACAAATGTGAACCTTGGGAACTTCCTGGTATGAACTTTTTTTTTTTATTCTCATGTTATATTTGAGTGTGCAAATTTACCATGTTTTACAAGATTTGAACGCTAATTAAATATTTTAACATACTTTTGAGCTTTAACTAAAAAAAAACTAAAATACCCTTATTTTATTAAGGGAAAGCGAAAATGGGAGAAAAAGAATGGTATTTCTTCAGTCTACGTGATCGGAAGTATCCAACAGGGCTGAGGACTAACAGAGCTACTGAAGCGGGTTACTGGAAAGCTACTGGAAAAGATAGAGAAATTTTCAGTTCAAAAACATGTGCACTTGTTGGTATGAAGAAAACCCTAGTTTTTTATCGAGGAAGAGCACCAAAAGGAGAAAAAAGTAACTGGGTTATGCATGAATATCGCCTTGATGGCAAATTTGCCTATCATTATATCTCCAGGAGTTCGAAGGTACTAGAGTATTTTTGTGTTAATAATTAACTGATACACATATATTAATGAATTTTGATGAAGAAAACTGATCTACATGTTTTGTGTTACAACTCATACTTTTTTTTGTATTTGGATTAAAGAGATCAGATTTACTGGAGATATTCTGTGCACAAATATATCATTGATATTACTGCTAGAGCCAGAGATTCTGAAGCAGAAAGTTTTGTGAAACTTCGTTTTCAATGTCTCAATTGCTTATGATTAAGTTGGAAGTATACATAGTCTGAAAAATAACAGAAAAACAAATTAAAAGAGAAAAAAAAGAATTTGCTTTTATTATGATTTATGATCAAAGCAATTAAGACTTTACAGAATAATATACTGTCATATTGATAGCGATTTAATATAATCTCTTTCCAAACTTATTTTATTAGCCTTATCAATGTGTAAGCATGCTTACGTAAATTCATCAGTCTGTTAGATTTTGACTTTTAGCGTTTTGGCATTAATTTAAATGCTTCTTTTTTTAAAATTGCATCATAATGAGCTTCATATTTGTTAGATTACAAACATTTCTTTAATAACAAAATAAGATTCGTAGACGCTAAAAATTAGGTCTTGCCCCAAAAAATGTTGTATATTTGTTTTTCATGGTAAAGTTAAAAGCCTGATGCGGGTTTTATGAAATTTGTAGCTTTCACAAGTTCATAAAATATGTAAACATGCTTGTAGTTATAAATTTTAAATTTTGAATTCGTTTTTTCGTGTTTCCATTGTTCTCATATATTTTTTGGCTACAGGACGAGTGGGTTATCTCGCGGGTCTTTCAAAAAAGCACCGGTTCTAATGGTGCCGCTACTTCAACTGGTGGCGGCAAAAAAAGGCTAAGTTCAAGTATAAACATGTACCAGGAAGTGAGTTCACCGTCTTCCGTCTCTCACCTTCCGCCGCTCCTCGATTCCTCTCCGTATAGCACTACCGCCACTTCCGCCGCAGCTATCGTAATCGGCGACCGCGATCGTGATCATAGCTTCAAGAAGGAGCACGTGCCCTGTTTCTCCACAACTGCTACTGCTACAATAACTGCACAGAGTCTAACTTTCGATCCAACTTCTGTCTTCGACATTTCATCAAACACCTTGCATGCACTACAGCCAACTCCAAGTTTCGCTTCTATTTTGGACTCTTCTCCATCTAATTTCACTAATTACACAAGGAATTCAACTTTTCCAAGCTTAAGATCACTCCATGAGAATCTCCAGCTTCCGTTATTCTCCGGCGGAACCTCCGCCATGCACGGCGGATTTTCTAATCCGATGGTTAATTGGACCGTGCCGGAGACTCAGAAAGTTGAACAGTCTGAACTTGACTGTATGTGGAGCTACTGAATTAGCAAGTGCTTAATTTTAATTAAGACGTTAATTAATTAAGTAATCAGTGTGTTAATCTTTGCTTTTTGTTTAGTATGTACTGCGTGTGGCAGCTTTAGTGGTATTGTCACTTTGTTGTAAACGTTCAGCGTAATTTAATGCATGCTATTATTTCTCG
| Download sequence region | 
    Get flanking sequences on SL2.50ch07
     | 
	 mRNA Solyc07g062840.2.1
	 mRNA Solyc07g062840.2.1
 | 
	 Ontology terms
	 Ontology terms
 | terms associated with this mRNA | 
	 cDNA sequence
	 cDNA sequence
 | spliced cDNA sequence, including UTRs | 
       
    
  >Solyc07g062840.2.1 NAC domain protein IPR003441 (AHRD V1 ***- B9N1D6_POPTR); contains Interpro domain(s)  IPR003441  No apical meristem (NAM) protein 
    
  
ATGGAGATTTATCATCAGATGCAGTTTGATTGCGGTGATCCGCATTTACCACCGGGGTTTCGGTTTCATCCAACTGACGAAGAACTTATTACTTACTACTTGTTGAAGAAGGTTCTGGACTGCAACTTCACTGCTAGAGCTATTGCTGAAGTTGATCTCAACAAATGTGAACCTTGGGAACTTCCTGGGAAAGCGAAAATGGGAGAAAAAGAATGGTATTTCTTCAGTCTACGTGATCGGAAGTATCCAACAGGGCTGAGGACTAACAGAGCTACTGAAGCGGGTTACTGGAAAGCTACTGGAAAAGATAGAGAAATTTTCAGTTCAAAAACATGTGCACTTGTTGGTATGAAGAAAACCCTAGTTTTTTATCGAGGAAGAGCACCAAAAGGAGAAAAAAGTAACTGGGTTATGCATGAATATCGCCTTGATGGCAAATTTGCCTATCATTATATCTCCAGGAGTTCGAAGGACGAGTGGGTTATCTCGCGGGTCTTTCAAAAAAGCACCGGTTCTAATGGTGCCGCTACTTCAACTGGTGGCGGCAAAAAAAGGCTAAGTTCAAGTATAAACATGTACCAGGAAGTGAGTTCACCGTCTTCCGTCTCTCACCTTCCGCCGCTCCTCGATTCCTCTCCGTATAGCACTACCGCCACTTCCGCCGCAGCTATCGTAATCGGCGACCGCGATCGTGATCATAGCTTCAAGAAGGAGCACGTGCCCTGTTTCTCCACAACTGCTACTGCTACAATAACTGCACAGAGTCTAACTTTCGATCCAACTTCTGTCTTCGACATTTCATCAAACACCTTGCATGCACTACAGCCAACTCCAAGTTTCGCTTCTATTTTGGACTCTTCTCCATCTAATTTCACTAATTACACAAGGAATTCAACTTTTCCAAGCTTAAGATCACTCCATGAGAATCTCCAGCTTCCGTTATTCTCCGGCGGAACCTCCGCCATGCACGGCGGATTTTCTAATCCGATGGTTAATTGGACCGTGCCGGAGACTCAGAAAGTTGAACAGTCTGAACTTGACTGTATGTGGAGCTACTGAATTAGCAAGTGCTTAATTTTAATTAAGACGTTAATTAATTAAGTAATCAGTGTGTTAATCTTTGCTTTTTGTTTAGTATGTACTGCGTGTGGCAGCTTTAGTGGTATTGTCACTTTGTTGTAAACGTTCAGCGTAATTTAATGCATGCTATTATTTCTCG
     
    
ATGGAGATTTATCATCAGATGCAGTTTGATTGCGGTGATCCGCATTTACCACCGGGGTTTCGGTTTCATCCAACTGACGAAGAACTTATTACTTACTACTTGTTGAAGAAGGTTCTGGACTGCAACTTCACTGCTAGAGCTATTGCTGAAGTTGATCTCAACAAATGTGAACCTTGGGAACTTCCTGGGAAAGCGAAAATGGGAGAAAAAGAATGGTATTTCTTCAGTCTACGTGATCGGAAGTATCCAACAGGGCTGAGGACTAACAGAGCTACTGAAGCGGGTTACTGGAAAGCTACTGGAAAAGATAGAGAAATTTTCAGTTCAAAAACATGTGCACTTGTTGGTATGAAGAAAACCCTAGTTTTTTATCGAGGAAGAGCACCAAAAGGAGAAAAAAGTAACTGGGTTATGCATGAATATCGCCTTGATGGCAAATTTGCCTATCATTATATCTCCAGGAGTTCGAAGGACGAGTGGGTTATCTCGCGGGTCTTTCAAAAAAGCACCGGTTCTAATGGTGCCGCTACTTCAACTGGTGGCGGCAAAAAAAGGCTAAGTTCAAGTATAAACATGTACCAGGAAGTGAGTTCACCGTCTTCCGTCTCTCACCTTCCGCCGCTCCTCGATTCCTCTCCGTATAGCACTACCGCCACTTCCGCCGCAGCTATCGTAATCGGCGACCGCGATCGTGATCATAGCTTCAAGAAGGAGCACGTGCCCTGTTTCTCCACAACTGCTACTGCTACAATAACTGCACAGAGTCTAACTTTCGATCCAACTTCTGTCTTCGACATTTCATCAAACACCTTGCATGCACTACAGCCAACTCCAAGTTTCGCTTCTATTTTGGACTCTTCTCCATCTAATTTCACTAATTACACAAGGAATTCAACTTTTCCAAGCTTAAGATCACTCCATGAGAATCTCCAGCTTCCGTTATTCTCCGGCGGAACCTCCGCCATGCACGGCGGATTTTCTAATCCGATGGTTAATTGGACCGTGCCGGAGACTCAGAAAGTTGAACAGTCTGAACTTGACTGTATGTGGAGCTACTGAATTAGCAAGTGCTTAATTTTAATTAAGACGTTAATTAATTAAGTAATCAGTGTGTTAATCTTTGCTTTTTGTTTAGTATGTACTGCGTGTGGCAGCTTTAGTGGTATTGTCACTTTGTTGTAAACGTTCAGCGTAATTTAATGCATGCTATTATTTCTCG
	 Protein sequence
	 Protein sequence
 | translated polypeptide sequence | 
       
    
  >Solyc07g062840.2.1 NAC domain protein IPR003441 (AHRD V1 ***- B9N1D6_POPTR); contains Interpro domain(s)  IPR003441  No apical meristem (NAM) protein 
    
  
MEIYHQMQFDCGDPHLPPGFRFHPTDEELITYYLLKKVLDCNFTARAIAEVDLNKCEPWELPGKAKMGEKEWYFFSLRDRKYPTGLRTNRATEAGYWKATGKDREIFSSKTCALVGMKKTLVFYRGRAPKGEKSNWVMHEYRLDGKFAYHYISRSSKDEWVISRVFQKSTGSNGAATSTGGGKKRLSSSINMYQEVSSPSSVSHLPPLLDSSPYSTTATSAAAIVIGDRDRDHSFKKEHVPCFSTTATATITAQSLTFDPTSVFDISSNTLHALQPTPSFASILDSSPSNFTNYTRNSTFPSLRSLHENLQLPLFSGGTSAMHGGFSNPMVNWTVPETQKVEQSELDCMWSY*
    
MEIYHQMQFDCGDPHLPPGFRFHPTDEELITYYLLKKVLDCNFTARAIAEVDLNKCEPWELPGKAKMGEKEWYFFSLRDRKYPTGLRTNRATEAGYWKATGKDREIFSSKTCALVGMKKTLVFYRGRAPKGEKSNWVMHEYRLDGKFAYHYISRSSKDEWVISRVFQKSTGSNGAATSTGGGKKRLSSSINMYQEVSSPSSVSHLPPLLDSSPYSTTATSAAAIVIGDRDRDHSFKKEHVPCFSTTATATITAQSLTFDPTSVFDISSNTLHALQPTPSFASILDSSPSNFTNYTRNSTFPSLRSLHENLQLPLFSGGTSAMHGGFSNPMVNWTVPETQKVEQSELDCMWSY*
	 Gene model matches
	 Gene model matches
 | 
	 SGN Unigenes
	 SGN Unigenes
 | [Associate new unigene] | 
    Unigene ID:
    
    
  
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	 GenBank accessions
	 GenBank accessions
 | [Associate new genbank sequence] | 
         EU670749 Nam-like protein 1 [Solanum lycopersicum] 
      
        
FJ435163 NO APICAL MERISTEM [Solanum lycopersicum]
HM210879 Solanum lycopersicum goblet gene, complete cds.
AY498713 Lycopersicon esculentum NAC domain protein mRNA, complete cds.
AY573802 Lycopersicon esculentum NAC domain protein (NAC-NOR) mRNA, complete cds.
 
   
FJ435163 NO APICAL MERISTEM [Solanum lycopersicum]
HM210879 Solanum lycopersicum goblet gene, complete cds.
AY498713 Lycopersicon esculentum NAC domain protein mRNA, complete cds.
AY573802 Lycopersicon esculentum NAC domain protein (NAC-NOR) mRNA, complete cds.
| Other genome matches | None | 
	 Literature annotations [4]
	 Literature annotations [4]
 | [Associate publication] [Matching publications] | 
    A NAC domain protein interacts with tomato leaf curl virus replication accessory protein and enhances viral replication.   
    The Plant cell (2005) 
  
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  Show / hide abstract
       Geminivirus replication enhancer (REn) proteins dramatically increase the accumulation of viral DNA species by an unknown mechanism. In this study, we present evidence implicating SlNAC1, a new member of the NAC domain protein family from tomato (Solanum lycopersicum), in Tomato leaf curl virus (TLCV) REn function. We isolated SlNAC1 using yeast (Saccharomyces cerevisiae) two-hybrid technology and TLCV REn as bait, and confirmed the interaction between these proteins in vitro. TLCV induces SlNAC1 expression specifically in infected cells, and this upregulation requires REn. In a transient TLCV replication system, overexpression of SlNAC1 resulted in a substantial increase in viral DNA accumulation. SlNAC1 colocalized with REn to the nucleus and activated transcription of a reporter gene in yeast, suggesting that in healthy cells it functions as a transcription factor. Together, these results imply that SlNAC1 plays an important role in the process by which REn enhances TLCV replication.
    
     
       Selth, LA. Dogra, SC. Rasheed, MS. Healy, H. Randles, JW. Rezaian, MA.
       The Plant cell.
       2005.
        17(1).
       311-25.
      
  
    Meristem maintenance and compound-leaf patterning utilize common genetic mechanisms in tomato.   
    Planta (2007) 
  
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  Show / hide abstract
       Balancing shoot apical meristem (SAM) maintenance and organ formation from its flanks is essential for proper plant growth and development and for the flexibility of organ production in response to internal and external cues. Leaves are formed at the SAM flanks and display a wide variability in size and form. Tomato (Solanum lycopersicum) leaves are compound with lobed margins. We exploited 18 recessive tomato mutants, representing four distinct phenotypic classes and six complementation groups, to track the genetic mechanisms involved in meristem function and compound-leaf patterning in tomato. In goblet (gob) mutants, the SAM terminates following cotyledon production, but occasionally partially recovers and produces simple leaves. expelled shoot (exp) meristems terminate after the production of several leaves, and these leaves show a reduced level of compoundness. short pedicel (spd) mutants are bushy, with impaired meristem structure, compact inflorescences, short pedicels and less compound leaves. In multi drop (mud) mutants, the leaves are more compound and the SAM tends to divide into two active meristems after the production of a few leaves. The range of leaf-compoundness phenotypes observed in these mutants suggests that compound-leaf patterning involves an array of genetic factors, which act successively to elaborate leaf shape. Furthermore, the results indicate that similar mechanisms underlie SAM activity and compound-leaf patterning in tomato.
    
     
       Brand, A. Shirding, N. Shleizer, S. Ori, N.
       Planta.
       2007.
        226(4).
       941-51.
      
  
    A conserved molecular framework for compound leaf development.   
    Science (New York, N.Y.) (2008) 
  
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  Show / hide abstract
       Diversity in leaf shape is produced by alterations of the margin: for example, deep dissection leads to leaflet formation and less-pronounced incision results in serrations or lobes. By combining gene silencing and mutant analyses in four distantly related eudicot species, we show that reducing the function of NAM/CUC boundary genes (NO APICAL MERISTEM and CUP-SHAPED COTYLEDON) leads to a suppression of all marginal outgrowths and to fewer and fused leaflets. We propose that NAM/CUC genes promote formation of a boundary domain that delimits leaflets. This domain has a dual role promoting leaflet separation locally and leaflet formation at distance. In this manner, boundaries of compound leaves resemble boundaries functioning during animal development.
    
     
       Blein, T. Pulido, A. Vialette-Guiraud, A. Nikovics, K. Morin, H. Hay, A. Johansen, IE. Tsiantis, M. Laufs, P.
       Science (New York, N.Y.).
       2008.
        322(5909).
       1835-9.
      
  
    The NAC-domain transcription factor GOBLET specifies leaflet boundaries in compound tomato leaves.   
    Development (Cambridge, England) (2009) 
  
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  Show / hide abstract
       Leaves are formed at the flanks of the shoot apical meristem (SAM) and develop into a variety of forms. In tomato, prolonged leaf patterning enables the elaboration of compound leaves by reiterative initiation of leaflets with lobed margins. In goblet (gob) loss-of-function mutants, primary leaflets are often fused, secondary leaflets and marginal serrations are absent, and SAMs often terminate precociously. We show that GOB encodes a NAC-domain transcription factor expressed in narrow stripes at the leaf margins, flanking the distal side of future leaflet primordia, and at the boundaries between the SAM and leaf primordia. Leaf-specific overexpression of the microRNA miR164, a negative regulator of GOB-like genes, also leads to loss of secondary-leaflet initiation and to smooth leaflet margins. Plants carrying a dominant gob allele with an intact ORF but disrupted miR164 binding site produce more cotyledons and floral organs, have split SAMs and, surprisingly, simpler leaves. Overexpression of a form of GOB with an altered miR164 binding site in leaf primordia leads to delayed leaflet maturation, frequent, improperly timed and spaced initiation events, and a simple mature leaflet form owing to secondary-leaflet fusion. miR164 also affects leaflet separation in Cardamine hirsuta, a Brassicaceae species with complex leaves. Genetic and molecular analyses suggest that GOB expression is intact in the simplified leaves of entire tomato mutants, which have a defect in a putative repressor of auxin responses. Our results show that GOB marks leaflet boundaries and that its accurate spatial, temporal and quantitative activity affects leaf elaboration in a context-dependent manner.
    
     
       Berger, Y. Harpaz-Saad, S. Brand, A. Melnik, H. Sirding, N. Alvarez, JP. Zinder, M. Samach, A. Eshed, Y. Ori, N.
       Development (Cambridge, England).
       2009.
        136(5).
       823-32.
      
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