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Tomato locus ovate
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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![]() | fruits from left to right: TA493 Heinz 1706, LA0025, TA503 Yellow pear, and TA496 | locus | |
![]() | Cross sections of the above fruits | locus |
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![]() ![]() | [Associate accession] |
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Tegucigalpa | ![]() | ![]() | ![]() | ![]() | ![]() | ... (Total 36 images) | |
Long John | ![]() | ![]() | ![]() | ![]() | ![]() | ... (Total 6 images) | |
Principe Borghese | ![]() | ![]() | ![]() | ![]() | ![]() |
See 147 more accessions
LA0754 LA2480 LA3377 LA3378 LA3379 LA3482 LA3483 LA3484 LA4038 LA4039 LA4040 Sunripe Grape TM
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![]() ![]() | unprocessed genomic sequence region underlying this gene |
>Solyc02g085500.2 SL2.50ch02:48367481..48369215
AAAAAAAAGCAGAGACAAAAAGAATGGGAAAAAGTTTGAAGCTTCGGTTCTCCAGAGTTATTGCTTCTTTCAATTCGTGCCGTTCGAAAAACCCTTCTTCTCTTCCCCAAAATCCTAATTTCTTCCCACATAAGCTCACTAGTACAAAACACATTTCCCCCGATTTCCCTCTTATTGATCAAAATCAAAATCAAAATCACCGTAATTACGTGCCAGAATCCACGATGATCTCCGTTGGGTGTTGTAGATCAGAATTCAAGTGGGAGAAAGAAGAGAAGTTTCACGTGGTTTCTAGTTCCTTCGTGTCTGAAGAAGAAGAATGTGAAGAGGAGATCAATTTGGCCTTACGACCTCCTCTTACACCTCCGCGATTCAGTAGAATTGTTGTTGAGAAGAAGAAGAAGAAACAACAGCGAGTTAAAAAAACGAAAACAAAAAGTAGAATCATCCGAATGAGTACTTCCTCAGCTGATGAGTACAGCGGGATATTAAGCGGTACTAATACTGATTGGGATAATAATGAAGAGGAAACTGAATCTTTAGTTTCATCTTCCAGAAGCTGTTACGATTTCTCAAGCGATGACTCATCTACTGATTTCAACCCTCACTTAGAAACCATATGTGAGACCACTACAATGAGGCGTCGTCACAAGAGAAATGCCAACACCAAGAGGAGATCAATCAAGCAATCCAGACCAAGTTTTTCCTCTTCAAAAGGTAAAAGTACTATTTGTGCGATCAAATCTTTTATATTTACAGATAATTTTACAGTCACATTAATAAGTATTGCTTTTCGCGTGTGGAATTTGGAGAGGACAGAGTAAACATAGATCTTATAGCTATTTTGTGGAGAGATTAATTTCAAAAGACACCCAATAACAATAACATATTCAATAAAATTCCACTAACTAGAGTAGAAAAAGGATAGAGTTTACACGGAGCTTACCGTTCAAAAATTCTGGCTCAAAGCAAATGCATATCTTATTTAGAGATCAATAATTTTATTTTAAATATTTTTATCGTCTTTTTCTTTGGGAAATAGTGTATATGTAATTGTCGTACAAAAATATATGAAGCTTAATCAAAATTCATTACATTAATTAAAACGGAAAACTATTTAATTTATAATTATGTCTCAACATGCATGCTTCCTTTGTTACTTGTTTATTATTGGGTCGAATATATGAAAATATATTTTGGAAAGACTTTTGTTGCGCTAGTATTTAAAAAACTAGTACTGATTAATTATATTATGTTTGAACAGGTAGAAGATCGTCGGTTTCTACGTCATCAGATAGCGAGCTACCGGCAAGGTTATCGGTGTTTAAGAAGCTGATACCGTGTAGTGTGGATGGGAAAGTGAAGGAGAGTTTCGCGATAGTGAAGAAATCTCAGGACCCGTACTAAGATTTCAAGAGATCGATGATGGAAATGATTTTAGAGAAGGAAATGTTTGAGAAGAATGAGCTGGAACAGCTTTTACAATGTTTTCTGTCGTTGAACGGAAAGCATTATCATGGAGTGATAGTTGAGGCGTTCTCAGACATTTGGGAGACTTTGTTTTTAGGTAATAATGATAGAGTAAGGAGGATGTCAATTCATGATCCCACACCCACCTACTGTAGGTAGTAGTAGAAGAACCTCCTTTGATTAATCATGATTTAGTTGTTAATTAATAAATTTAACTTTTCTTTTATGTGTTAATTGTGATTTAATTGGAGTACGATATTTCACT
AAAAAAAAGCAGAGACAAAAAGAATGGGAAAAAGTTTGAAGCTTCGGTTCTCCAGAGTTATTGCTTCTTTCAATTCGTGCCGTTCGAAAAACCCTTCTTCTCTTCCCCAAAATCCTAATTTCTTCCCACATAAGCTCACTAGTACAAAACACATTTCCCCCGATTTCCCTCTTATTGATCAAAATCAAAATCAAAATCACCGTAATTACGTGCCAGAATCCACGATGATCTCCGTTGGGTGTTGTAGATCAGAATTCAAGTGGGAGAAAGAAGAGAAGTTTCACGTGGTTTCTAGTTCCTTCGTGTCTGAAGAAGAAGAATGTGAAGAGGAGATCAATTTGGCCTTACGACCTCCTCTTACACCTCCGCGATTCAGTAGAATTGTTGTTGAGAAGAAGAAGAAGAAACAACAGCGAGTTAAAAAAACGAAAACAAAAAGTAGAATCATCCGAATGAGTACTTCCTCAGCTGATGAGTACAGCGGGATATTAAGCGGTACTAATACTGATTGGGATAATAATGAAGAGGAAACTGAATCTTTAGTTTCATCTTCCAGAAGCTGTTACGATTTCTCAAGCGATGACTCATCTACTGATTTCAACCCTCACTTAGAAACCATATGTGAGACCACTACAATGAGGCGTCGTCACAAGAGAAATGCCAACACCAAGAGGAGATCAATCAAGCAATCCAGACCAAGTTTTTCCTCTTCAAAAGGTAAAAGTACTATTTGTGCGATCAAATCTTTTATATTTACAGATAATTTTACAGTCACATTAATAAGTATTGCTTTTCGCGTGTGGAATTTGGAGAGGACAGAGTAAACATAGATCTTATAGCTATTTTGTGGAGAGATTAATTTCAAAAGACACCCAATAACAATAACATATTCAATAAAATTCCACTAACTAGAGTAGAAAAAGGATAGAGTTTACACGGAGCTTACCGTTCAAAAATTCTGGCTCAAAGCAAATGCATATCTTATTTAGAGATCAATAATTTTATTTTAAATATTTTTATCGTCTTTTTCTTTGGGAAATAGTGTATATGTAATTGTCGTACAAAAATATATGAAGCTTAATCAAAATTCATTACATTAATTAAAACGGAAAACTATTTAATTTATAATTATGTCTCAACATGCATGCTTCCTTTGTTACTTGTTTATTATTGGGTCGAATATATGAAAATATATTTTGGAAAGACTTTTGTTGCGCTAGTATTTAAAAAACTAGTACTGATTAATTATATTATGTTTGAACAGGTAGAAGATCGTCGGTTTCTACGTCATCAGATAGCGAGCTACCGGCAAGGTTATCGGTGTTTAAGAAGCTGATACCGTGTAGTGTGGATGGGAAAGTGAAGGAGAGTTTCGCGATAGTGAAGAAATCTCAGGACCCGTACTAAGATTTCAAGAGATCGATGATGGAAATGATTTTAGAGAAGGAAATGTTTGAGAAGAATGAGCTGGAACAGCTTTTACAATGTTTTCTGTCGTTGAACGGAAAGCATTATCATGGAGTGATAGTTGAGGCGTTCTCAGACATTTGGGAGACTTTGTTTTTAGGTAATAATGATAGAGTAAGGAGGATGTCAATTCATGATCCCACACCCACCTACTGTAGGTAGTAGTAGAAGAACCTCCTTTGATTAATCATGATTTAGTTGTTAATTAATAAATTTAACTTTTCTTTTATGTGTTAATTGTGATTTAATTGGAGTACGATATTTCACT
Download sequence region |
Get flanking sequences on SL2.50ch02
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Ontology terms | None | terms associated with this mRNA |
![]() ![]() | spliced cDNA sequence, including UTRs |
>Solyc02g085500.2.1 Ovate protein (AHRD V1 ***- Q8GSM4_SOLLC)
AAAAAAAAGCAGAGACAAAAAGAATGGGAAAAAGTTTGAAGCTTCGGTTCTCCAGAGTTATTGCTTCTTTCAATTCGTGCCGTTCGAAAAACCCTTCTTCTCTTCCCCAAAATCCTAATTTCTTCCCACATAAGCTCACTAGTACAAAACACATTTCCCCCGATTTCCCTCTTATTGATCAAAATCAAAATCAAAATCACCGTAATTACGTGCCAGAATCCACGATGATCTCCGTTGGGTGTTGTAGATCAGAATTCAAGTGGGAGAAAGAAGAGAAGTTTCACGTGGTTTCTAGTTCCTTCGTGTCTGAAGAAGAAGAATGTGAAGAGGAGATCAATTTGGCCTTACGACCTCCTCTTACACCTCCGCGATTCAGTAGAATTGTTGTTGAGAAGAAGAAGAAGAAACAACAGCGAGTTAAAAAAACGAAAACAAAAAGTAGAATCATCCGAATGAGTACTTCCTCAGCTGATGAGTACAGCGGGATATTAAGCGGTACTAATACTGATTGGGATAATAATGAAGAGGAAACTGAATCTTTAGTTTCATCTTCCAGAAGCTGTTACGATTTCTCAAGCGATGACTCATCTACTGATTTCAACCCTCACTTAGAAACCATATGTGAGACCACTACAATGAGGCGTCGTCACAAGAGAAATGCCAACACCAAGAGGAGATCAATCAAGCAATCCAGACCAAGTTTTTCCTCTTCAAAAGGTAGAAGATCGTCGGTTTCTACGTCATCAGATAGCGAGCTACCGGCAAGGTTATCGGTGTTTAAGAAGCTGATACCGTGTAGTGTGGATGGGAAAGTGAAGGAGAGTTTCGCGATAGTGAAGAAATCTCAGGACCCGTACTAAGATTTCAAGAGATCGATGATGGAAATGATTTTAGAGAAGGAAATGTTTGAGAAGAATGAGCTGGAACAGCTTTTACAATGTTTTCTGTCGTTGAACGGAAAGCATTATCATGGAGTGATAGTTGAGGCGTTCTCAGACATTTGGGAGACTTTGTTTTTAGGTAATAATGATAGAGTAAGGAGGATGTCAATTCATGATCCCACACCCACCTACTGTAGGTAGTAGTAGAAGAACCTCCTTTGATTAATCATGATTTAGTTGTTAATTAATAAATTTAACTTTTCTTTTATGTGTTAATTGTGATTTAATTGGAGTACGATATTTCACT
AAAAAAAAGCAGAGACAAAAAGAATGGGAAAAAGTTTGAAGCTTCGGTTCTCCAGAGTTATTGCTTCTTTCAATTCGTGCCGTTCGAAAAACCCTTCTTCTCTTCCCCAAAATCCTAATTTCTTCCCACATAAGCTCACTAGTACAAAACACATTTCCCCCGATTTCCCTCTTATTGATCAAAATCAAAATCAAAATCACCGTAATTACGTGCCAGAATCCACGATGATCTCCGTTGGGTGTTGTAGATCAGAATTCAAGTGGGAGAAAGAAGAGAAGTTTCACGTGGTTTCTAGTTCCTTCGTGTCTGAAGAAGAAGAATGTGAAGAGGAGATCAATTTGGCCTTACGACCTCCTCTTACACCTCCGCGATTCAGTAGAATTGTTGTTGAGAAGAAGAAGAAGAAACAACAGCGAGTTAAAAAAACGAAAACAAAAAGTAGAATCATCCGAATGAGTACTTCCTCAGCTGATGAGTACAGCGGGATATTAAGCGGTACTAATACTGATTGGGATAATAATGAAGAGGAAACTGAATCTTTAGTTTCATCTTCCAGAAGCTGTTACGATTTCTCAAGCGATGACTCATCTACTGATTTCAACCCTCACTTAGAAACCATATGTGAGACCACTACAATGAGGCGTCGTCACAAGAGAAATGCCAACACCAAGAGGAGATCAATCAAGCAATCCAGACCAAGTTTTTCCTCTTCAAAAGGTAGAAGATCGTCGGTTTCTACGTCATCAGATAGCGAGCTACCGGCAAGGTTATCGGTGTTTAAGAAGCTGATACCGTGTAGTGTGGATGGGAAAGTGAAGGAGAGTTTCGCGATAGTGAAGAAATCTCAGGACCCGTACTAAGATTTCAAGAGATCGATGATGGAAATGATTTTAGAGAAGGAAATGTTTGAGAAGAATGAGCTGGAACAGCTTTTACAATGTTTTCTGTCGTTGAACGGAAAGCATTATCATGGAGTGATAGTTGAGGCGTTCTCAGACATTTGGGAGACTTTGTTTTTAGGTAATAATGATAGAGTAAGGAGGATGTCAATTCATGATCCCACACCCACCTACTGTAGGTAGTAGTAGAAGAACCTCCTTTGATTAATCATGATTTAGTTGTTAATTAATAAATTTAACTTTTCTTTTATGTGTTAATTGTGATTTAATTGGAGTACGATATTTCACT
![]() ![]() | translated polypeptide sequence |
>Solyc02g085500.2.1 Ovate protein (AHRD V1 ***- Q8GSM4_SOLLC)
MGKSLKLRFSRVIASFNSCRSKNPSSLPQNPNFFPHKLTSTKHISPDFPLIDQNQNQNHRNYVPESTMISVGCCRSEFKWEKEEKFHVVSSSFVSEEEECEEEINLALRPPLTPPRFSRIVVEKKKKKQQRVKKTKTKSRIIRMSTSSADEYSGILSGTNTDWDNNEEETESLVSSSRSCYDFSSDDSSTDFNPHLETICETTTMRRRHKRNANTKRRSIKQSRPSFSSSKGRRSSVSTSSDSELPARLSVFKKLIPCSVDGKVKESFAIVKKSQDPY*
MGKSLKLRFSRVIASFNSCRSKNPSSLPQNPNFFPHKLTSTKHISPDFPLIDQNQNQNHRNYVPESTMISVGCCRSEFKWEKEEKFHVVSSSFVSEEEECEEEINLALRPPLTPPRFSRIVVEKKKKKQQRVKKTKTKSRIIRMSTSSADEYSGILSGTNTDWDNNEEETESLVSSSRSCYDFSSDDSSTDFNPHLETICETTTMRRRHKRNANTKRRSIKQSRPSFSSSKGRRSSVSTSSDSELPARLSVFKKLIPCSVDGKVKESFAIVKKSQDPY*
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![]() ![]() | [Associate new unigene] |
Unigene ID:
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![]() ![]() | [Associate new genbank sequence] |
Other genome matches | None |
![]() ![]() | [Associate publication] [Matching publications] |
A new class of regulatory genes underlying the cause of pear-shaped tomato fruit.
Proceedings of the National Academy of Sciences of the United States of America (2002)
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A common, recurring theme in domesticated plants is the occurrence of pear-shaped fruit. A major quantitative trait locus (termed ovate) controlling the transition from round to pear-shaped fruit has been cloned from tomato. OVATE is expressed early in flower and fruit development and encodes a previously uncharacterized, hydrophilic protein with a putative bipartite nuclear localization signal, Von Willebrand factor type C domains, and an approximately equal 70-aa C-terminal domain conserved in tomato, Arabidopsis, and rice. A single mutation, leading to a premature stop codon, causes the transition of tomato fruit from round- to pear-shaped. Moreover, ectopic, transgenic expression of OVATE unevenly reduces the size of floral organs and leaflets, suggesting that OVATE represents a previously uncharacterized class of negative regulatory proteins important in plant development.
Liu, J. Van Eck, J. Cong, B. Tanksley, SD.
Proceedings of the National Academy of Sciences of the United States of America.
2002.
99(20).
13302-6.
QTLs mapping for fruit size and shape in chromosomes 2 and 4 in pepper and a comparison of the pepper QTL map with that of tomato.
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik (2005)
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Quantitative trait locus (QTL) mapping for fruit weight and shape in pepper (Capsicum spp.) was performed using C. chinense and C. frutescens introgression lines of chromosomes 2 and 4. In chromosome 2, a single major fruit-weight QTL, fw2.1, was detected in both populations that explained 62% of the trait variation. This QTL, as well as a fruit-shape QTL, fs2.1, which had a more minor effect, were localized to the tomato fruit-shape gene ovate. The cloned tomato fruit-weight QTL, fw2.2, did not play a major role in controlling fruit size variations in pepper. In chromosome 4, two fruit-weight QTLs, fw4.1 and fw4.2, were detected in the same genomic regions in both mapping populations. In addition, a single fruit-shape QTL was detected in each of the mapping populations that co-localized with one of the fruit-weight QTLs, suggesting pleiotropy or close linkage of the genes controlling size and shape. fw2.1 and fw4.2 represent major fruit-weight QTLs that are conserved in the three Capsicum species analyzed to date for fruit-size variations. Co-localization of the pepper QTLs with QTLs identified for similar traits in tomato suggests that the pepper and tomato QTLs are orthologous. Compared to fruit-shape QTLs, fruit-weight QTLs were more often conserved between pepper and tomato. This implies that different modes of selection were employed for these traits during domestication of the two Solanaceae species.
Zygier, S. Chaim, A. Efrati, A. Kaluzky, G. Borovsky, Y. Paran, I.
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik.
2005.
111(3).
437-45.
A comparative analysis into the genetic bases of morphology in tomato varieties exhibiting elongated fruit shape.
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik (2008)
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Fruit shape is a quantitatively inherited character. In tomato, two major loci, sun and ovate, control fruit shape index, which is the ratio of fruit height over width. In this study, we measured many additional fruit shape features in three inter-specific F(2) populations using the software application Tomato Analyzer. These populations were derived from varieties carrying elongated fruit but for which the major shape loci differed. We compared the effect of the major fruit shape loci with overall shape, as well as with the distal and proximal end shape features in each population. sun and ovate represented the largest effect on fruit shape in the Howard German and Sausage F(2) populations, respectively. The largest effect QTL in the Rio Grande population carrying neither sun nor ovate, were fs8.1 on chromosome 8 and tri2.1/dblk2.1 on chromosome 2. These latter loci were also segregating in the other two populations, thus indicating common regions that control shape across the three populations. The phenotypic analyses showed that sun and ovate contributed to almost all aspects of shape such as the distal and proximal end features. In Rio Grande however, the largest effect QTL did not control all aspects of shape and the distal and proximal features were distinctly controlled in that population. Combined, our results implied that within the cultivated tomato germplasm pool the largest effect on elongated fruit shape was controlled by a combination of the loci sun, ovate, fs8.1 and tri2.1/dblk2.1.
Gonzalo, Maria. van der Knaap, Esther.
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik.
2008.
116(5).
647-56.
Distribution of SUN, OVATE, LC, and FAS in the Tomato Germplasm and the Relationship to Fruit Shape Diversity.
Plant physiology (2011)
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Phenotypic diversity within cultivated tomato (Solanum lycopersicum) is particularly evident for fruit shape and size. Four genes that control tomato fruit shape have been cloned. SUN and OVATE control elongated shape whereas FASCIATED (FAS) and LOCULE NUMBER (LC) control fruit locule number and flat shape. We investigated the distribution of the fruit shape alleles in the tomato germplasm and evaluated their contribution to morphology in a diverse collection of 368 predominantly tomato and tomato var. cerasiforme accessions. Fruits were visually classified into eight shape categories that were supported by objective measurements obtained from image analysis using the Tomato Analyzer software. The allele distribution of SUN, OVATE, LC, and FAS in all accessions was strongly associated with fruit shape classification. We also genotyped 116 representative accessions with additional 25 markers distributed evenly across the genome. Through a model-based clustering we demonstrated that shape categories, germplasm classes, and the shape genes were nonrandomly distributed among five genetic clusters (P < 0.001), implying that selection for fruit shape genes was critical to subpopulation differentiation within cultivated tomato. Our data suggested that the LC, FAS, and SUN mutations arose in the same ancestral population while the OVATE mutation arose in a separate lineage. Furthermore, LC, OVATE, and FAS mutations may have arisen prior to domestication or early during the selection of cultivated tomato whereas the SUN mutation appeared to be a postdomestication event arising in Europe.
Rodríguez, GR. Muños, S. Anderson, C. Sim, SC. Michel, A. Causse, M. Gardener, BB. Francis, D. van der Knaap, E.
Plant physiology.
2011.
156(1).
275-85.
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