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Tomato locus obscuravenosa
Locus details | Download GMOD XML | Note to Editors | Annotation guidelines |
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Locus | Solyc05g054030 |
Locus name | obscuravenosa |
Symbol | obv |
Gene activity | C2H2L domain class transcription factor (AHRD V1 **-* D9ZIU3_MALDO); contains Interpro domain(s) IPR007087 Zinc finger, C2H2-type |
Description | OBV controls the formation of bundle sheath extensions in leaves. The obv mutant displays reduced vein density, leaf hydraulic conductance and photosynthetic assimilation rate. The gene also controls leaf insertion angle, leaf margin serration, minor vein density, and fruit shape, via changes in auxin signaling. The gene also controls plasticity of leaf development in response to growth irradiance. |
Chromosome | 5 |
Arm | long |
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Registry name: | None | [Associate registry name] |
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Associated loci - graphical view | None |
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![]() ![]() | unprocessed genomic sequence region underlying this gene |
>Solyc05g054030.2 SL2.50ch05:64011108..64014234
ATGCTAACTAGCAACTCTTTCTTGTTTGGTGCTCCTTCTAATTATTCTGATCCATTTTCTTCCCCAGAAAATGGTTTTAT
TATCAAAAGAAAAAGAAGACCTGCTGGTACTCCAGGTATATATATATATTTTTAATTAATTAATTAGTATATTTTTAAAA
AAAAATTAATTTACATAAATATATGAAGAAAATGGTACTTTTTTTGATAATTATGTGAAAAAACACTTGAGTTTTAGCTC
TTGTGTGTCTATTATATTTCTAAATTGATCAACATGTTCAGTCAGTGACGAAAACAGAATTTTCATCAGAGGATTCATGA
GGATGTAACGAAAAGAATTCAGATGAACCTCCTTTTGGCTTTTTCTATCTCCGACCTTGTGTTTTTGAATTCAGAATTTA
AACGTTATAGATGAGAAAGTTGAATTATGATTTAACCTTATCTTTATAGTCAAGGGCGGAGCTATAGGTAACAAAGATTG
TTTGGTTGATACAACCCCTTTCGTCAGAAAATTATATTTTTATATATTTATTTTTTAAAAAAAATTCTTAACCTAATAGA
TTTAATTTTTTAAAATTTTCTTAACCTAATAAATTTAGATGTGAAAATTATATTTGAATTACTGGCTCCGCTACTATTGC
TAACACACATATGTTTAGGGTTATTCGACTGGTAAGAATGCTATTGAATTCTGTTGAACTCGTAATAATTAAATTTACGA
ATTTGCACAGATCCCGATGCACAAGTTGTATATCTTACAGCTGAGATGTTAATGGAATCTGATCGTTACGTTTGTGAAAT
CTGCAACCTTAGCTTTCAAAGAGAGCAAAATCTACAAATGCATCGTCGTCGCCATAAGGTTCCATGGAAGTTGAAGAAGA
AGGTAGTTTAATTTATGTATAATTACGTCATCAATATATCGTCTCATCTAAAATCTTAAACTGTTCGATAGAACACAAGT
TCTTCATTCGTTCAATAGGGAGTGAGTCTTCCCCTTTTTGAAAAATGAGTTAATATCATGTGTAGACGGAGAATTCATAT
ATCTGATAAGAACAGATGTTACACTTGATCTTAGCCACAAGACCGAGAAAGATATTGATGAGAACTATACAATTTTTATT
TACTAAATTATACTTTATATTTCAACACATCTCCTCACGTGCAAGTCATGAAGTTCTTCTTCTTCTTTTTTATTACGAGA
ACGATACATTTTAATATTTAGAATTTCTCTGTTTATTCTTACTGAAATGATTTATAATAATCACACAAATTGCTAAGGCT
TAGTTTTCGACAATAATTTTCAAAAGTCTTTCAATTCTAGACGTCACTCCCCAGTTAAATATAGTCACATAAATTGTAAC
TGACATATTAGATTATATGATTAGATATGTTAATTTTTTTAATTAAATATAAATATAATTTCATTTACTTGATTATATTT
TCAACGTGATCATCAGGAAGAAGAGAAAAATGAGATGGATCAAGTTATTAAGAAGAGAGTATATGTGTGTCCAGAGCCAA
GTTGTGTGCACCATGATCCATGTCATGCATTAGGTGATCTTGTTGGAATCAAAAAACATTTTAGAAGAAAACGTAGCAAT
TACAAACAATGGATTTGTCAAAAATGCAACAAAGGTTATGCTGTTCAATCAGATTATAAAGCTCACATCAAAACTTGTGG
TACTAGAGGCCATTCTTGTGATTGTGGAAGAGTTTTCTCTAGGTAAATTCATCTTCTTAATTATATATCTGTGTTCTGTT
TTACTTGAGTCGAGAATCTATAAGAAAAAATAGAATCTATTTATCCTCATAGGAGTAAGGTTACAACGTCCTATTCAGAT
TCCACTAAATATGTTATTGTTATAGTAATTTTTATCATCAGCGTATCTTTATTATCTAGGTTATATTAAATATACTACTA
AAAAACGTTAAAGAATTAGCTATGAAATTCGTAGCTGGTTAATTTATAACTAAATAGTCTATATCTACTAAGATTGTCTC
ATTATAAAATGTCATTTCTATGTAGTCAAATAGAATTAGGTTTAATTCATTGTTTAGTGATATAAATTAAATTTATAAAA
ATCTTTTAAGTGACTTAATAGCGTAAAAAGTAAATTTACACTATCTTATATATAAAAATTATACACATATATCAAGATGA
GATTACCACATGTTACTTGAATTGGTAACATCCTTTAGGTCTAAAACCTAATGTATATATATGTCTTGTAAATGTACAAA
CATATTTTGTGTGCTCACATTTGAAAATTTCTTCCTTATCTATATGATTATAAAAATCACTATCTTTTTAGTTAAAAACA
TGAATATTATTATCAGAAAATCACTAATTTTCGACGATATTATATGAGTCAAATTCTGATAGATTTGTTGGAAATATTTT
TAATTAAAAATTAGCGATTTTCTGATAGTAAATTTGAGTTATATATAGTATGTTTCTTCTAATTAATCTACTTTTTTTTT
CCTCCCATTTTTATTGTGTTTTTTTTTTCAGAGTTGAAACATTTATTGAGCATCAAGATTCATGCAAACCACAAAGTACA
ACTACTAAAGAATGTCATGATATGCAAATACCAAAACCAATTTTCTTGCCTACTACTACAACTCATATCCCACCACATGA
TCAATATTCAAAAATATTGCCTAATCTTGATCTTGAGCTTTTCACTTCTCCAAATTATTTCAACCAAAACACACACAATT
TTTCATCATTTGTTGATCAAAGTGATCATCATCATCATAATAATAATTACATAGTCCAAAACAATGATATTGAAGTCAAA
GAAATTATTGAAGAGGCAACAACACAAGTAACAAGATTGAAAAGTGAAGCAAATGAAATACTCAAAATAGCAATGGAAGA
AAAGGCAATGGCTATAGAGAAGAGACAAGAAGCAAAGTGTTTGATTGAATTAGCCAACCTTGAAATGGCAAAAGCAATGG
AAATTAGACAAAGTGTTTGTGCTTCATCATCATCATCATCACATGTCATGAAGATAATAAAATGTAGTTCTTGTAATAAT
AAACAATTTCAAAGTGTGTCATCATCAAAAGATGCTACTTTGACTAATAATTATTATTTGTCATCTTCTATTTATAGAAG
ATGATGA
ATGCTAACTAGCAACTCTTTCTTGTTTGGTGCTCCTTCTAATTATTCTGATCCATTTTCTTCCCCAGAAAATGGTTTTAT
TATCAAAAGAAAAAGAAGACCTGCTGGTACTCCAGGTATATATATATATTTTTAATTAATTAATTAGTATATTTTTAAAA
AAAAATTAATTTACATAAATATATGAAGAAAATGGTACTTTTTTTGATAATTATGTGAAAAAACACTTGAGTTTTAGCTC
TTGTGTGTCTATTATATTTCTAAATTGATCAACATGTTCAGTCAGTGACGAAAACAGAATTTTCATCAGAGGATTCATGA
GGATGTAACGAAAAGAATTCAGATGAACCTCCTTTTGGCTTTTTCTATCTCCGACCTTGTGTTTTTGAATTCAGAATTTA
AACGTTATAGATGAGAAAGTTGAATTATGATTTAACCTTATCTTTATAGTCAAGGGCGGAGCTATAGGTAACAAAGATTG
TTTGGTTGATACAACCCCTTTCGTCAGAAAATTATATTTTTATATATTTATTTTTTAAAAAAAATTCTTAACCTAATAGA
TTTAATTTTTTAAAATTTTCTTAACCTAATAAATTTAGATGTGAAAATTATATTTGAATTACTGGCTCCGCTACTATTGC
TAACACACATATGTTTAGGGTTATTCGACTGGTAAGAATGCTATTGAATTCTGTTGAACTCGTAATAATTAAATTTACGA
ATTTGCACAGATCCCGATGCACAAGTTGTATATCTTACAGCTGAGATGTTAATGGAATCTGATCGTTACGTTTGTGAAAT
CTGCAACCTTAGCTTTCAAAGAGAGCAAAATCTACAAATGCATCGTCGTCGCCATAAGGTTCCATGGAAGTTGAAGAAGA
AGGTAGTTTAATTTATGTATAATTACGTCATCAATATATCGTCTCATCTAAAATCTTAAACTGTTCGATAGAACACAAGT
TCTTCATTCGTTCAATAGGGAGTGAGTCTTCCCCTTTTTGAAAAATGAGTTAATATCATGTGTAGACGGAGAATTCATAT
ATCTGATAAGAACAGATGTTACACTTGATCTTAGCCACAAGACCGAGAAAGATATTGATGAGAACTATACAATTTTTATT
TACTAAATTATACTTTATATTTCAACACATCTCCTCACGTGCAAGTCATGAAGTTCTTCTTCTTCTTTTTTATTACGAGA
ACGATACATTTTAATATTTAGAATTTCTCTGTTTATTCTTACTGAAATGATTTATAATAATCACACAAATTGCTAAGGCT
TAGTTTTCGACAATAATTTTCAAAAGTCTTTCAATTCTAGACGTCACTCCCCAGTTAAATATAGTCACATAAATTGTAAC
TGACATATTAGATTATATGATTAGATATGTTAATTTTTTTAATTAAATATAAATATAATTTCATTTACTTGATTATATTT
TCAACGTGATCATCAGGAAGAAGAGAAAAATGAGATGGATCAAGTTATTAAGAAGAGAGTATATGTGTGTCCAGAGCCAA
GTTGTGTGCACCATGATCCATGTCATGCATTAGGTGATCTTGTTGGAATCAAAAAACATTTTAGAAGAAAACGTAGCAAT
TACAAACAATGGATTTGTCAAAAATGCAACAAAGGTTATGCTGTTCAATCAGATTATAAAGCTCACATCAAAACTTGTGG
TACTAGAGGCCATTCTTGTGATTGTGGAAGAGTTTTCTCTAGGTAAATTCATCTTCTTAATTATATATCTGTGTTCTGTT
TTACTTGAGTCGAGAATCTATAAGAAAAAATAGAATCTATTTATCCTCATAGGAGTAAGGTTACAACGTCCTATTCAGAT
TCCACTAAATATGTTATTGTTATAGTAATTTTTATCATCAGCGTATCTTTATTATCTAGGTTATATTAAATATACTACTA
AAAAACGTTAAAGAATTAGCTATGAAATTCGTAGCTGGTTAATTTATAACTAAATAGTCTATATCTACTAAGATTGTCTC
ATTATAAAATGTCATTTCTATGTAGTCAAATAGAATTAGGTTTAATTCATTGTTTAGTGATATAAATTAAATTTATAAAA
ATCTTTTAAGTGACTTAATAGCGTAAAAAGTAAATTTACACTATCTTATATATAAAAATTATACACATATATCAAGATGA
GATTACCACATGTTACTTGAATTGGTAACATCCTTTAGGTCTAAAACCTAATGTATATATATGTCTTGTAAATGTACAAA
CATATTTTGTGTGCTCACATTTGAAAATTTCTTCCTTATCTATATGATTATAAAAATCACTATCTTTTTAGTTAAAAACA
TGAATATTATTATCAGAAAATCACTAATTTTCGACGATATTATATGAGTCAAATTCTGATAGATTTGTTGGAAATATTTT
TAATTAAAAATTAGCGATTTTCTGATAGTAAATTTGAGTTATATATAGTATGTTTCTTCTAATTAATCTACTTTTTTTTT
CCTCCCATTTTTATTGTGTTTTTTTTTTCAGAGTTGAAACATTTATTGAGCATCAAGATTCATGCAAACCACAAAGTACA
ACTACTAAAGAATGTCATGATATGCAAATACCAAAACCAATTTTCTTGCCTACTACTACAACTCATATCCCACCACATGA
TCAATATTCAAAAATATTGCCTAATCTTGATCTTGAGCTTTTCACTTCTCCAAATTATTTCAACCAAAACACACACAATT
TTTCATCATTTGTTGATCAAAGTGATCATCATCATCATAATAATAATTACATAGTCCAAAACAATGATATTGAAGTCAAA
GAAATTATTGAAGAGGCAACAACACAAGTAACAAGATTGAAAAGTGAAGCAAATGAAATACTCAAAATAGCAATGGAAGA
AAAGGCAATGGCTATAGAGAAGAGACAAGAAGCAAAGTGTTTGATTGAATTAGCCAACCTTGAAATGGCAAAAGCAATGG
AAATTAGACAAAGTGTTTGTGCTTCATCATCATCATCATCACATGTCATGAAGATAATAAAATGTAGTTCTTGTAATAAT
AAACAATTTCAAAGTGTGTCATCATCAAAAGATGCTACTTTGACTAATAATTATTATTTGTCATCTTCTATTTATAGAAG
ATGATGA
Download sequence region |
Get flanking sequences on SL2.50ch05
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![]() ![]() | terms associated with this mRNA |
![]() ![]() | spliced cDNA sequence, including UTRs |
>Solyc05g054030.2.1 C2H2L domain class transcription factor (AHRD V1 **-* D9ZIU3_MALDO); contains Interpro domain(s) IPR007087 Zinc finger, C2H2-type
ATGCTAACTAGCAACTCTTTCTTGTTTGGTGCTCCTTCTAATTATTCTGATCCATTTTCTTCCCCAGAAAATGGTTTTAT
TATCAAAAGAAAAAGAAGACCTGCTGGTACTCCAGATCCCGATGCACAAGTTGTATATCTTACAGCTGAGATGTTAATGG
AATCTGATCGTTACGTTTGTGAAATCTGCAACCTTAGCTTTCAAAGAGAGCAAAATCTACAAATGCATCGTCGTCGCCAT
AAGGTTCCATGGAAGTTGAAGAAGAAGGAAGAAGAGAAAAATGAGATGGATCAAGTTATTAAGAAGAGAGTATATGTGTG
TCCAGAGCCAAGTTGTGTGCACCATGATCCATGTCATGCATTAGGTGATCTTGTTGGAATCAAAAAACATTTTAGAAGAA
AACGTAGCAATTACAAACAATGGATTTGTCAAAAATGCAACAAAGGTTATGCTGTTCAATCAGATTATAAAGCTCACATC
AAAACTTGTGGTACTAGAGGCCATTCTTGTGATTGTGGAAGAGTTTTCTCTAGAGTTGAAACATTTATTGAGCATCAAGA
TTCATGCAAACCACAAAGTACAACTACTAAAGAATGTCATGATATGCAAATACCAAAACCAATTTTCTTGCCTACTACTA
CAACTCATATCCCACCACATGATCAATATTCAAAAATATTGCCTAATCTTGATCTTGAGCTTTTCACTTCTCCAAATTAT
TTCAACCAAAACACACACAATTTTTCATCATTTGTTGATCAAAGTGATCATCATCATCATAATAATAATTACATAGTCCA
AAACAATGATATTGAAGTCAAAGAAATTATTGAAGAGGCAACAACACAAGTAACAAGATTGAAAAGTGAAGCAAATGAAA
TACTCAAAATAGCAATGGAAGAAAAGGCAATGGCTATAGAGAAGAGACAAGAAGCAAAGTGTTTGATTGAATTAGCCAAC
CTTGAAATGGCAAAAGCAATGGAAATTAGACAAAGTGTTTGTGCTTCATCATCATCATCATCACATGTCATGAAGATAAT
AAAATGTAGTTCTTGTAATAATAAACAATTTCAAAGTGTGTCATCATCAAAAGATGCTACTTTGACTAATAATTATTATT
TGTCATCTTCTATTTATAGAAGATGATGA
ATGCTAACTAGCAACTCTTTCTTGTTTGGTGCTCCTTCTAATTATTCTGATCCATTTTCTTCCCCAGAAAATGGTTTTAT
TATCAAAAGAAAAAGAAGACCTGCTGGTACTCCAGATCCCGATGCACAAGTTGTATATCTTACAGCTGAGATGTTAATGG
AATCTGATCGTTACGTTTGTGAAATCTGCAACCTTAGCTTTCAAAGAGAGCAAAATCTACAAATGCATCGTCGTCGCCAT
AAGGTTCCATGGAAGTTGAAGAAGAAGGAAGAAGAGAAAAATGAGATGGATCAAGTTATTAAGAAGAGAGTATATGTGTG
TCCAGAGCCAAGTTGTGTGCACCATGATCCATGTCATGCATTAGGTGATCTTGTTGGAATCAAAAAACATTTTAGAAGAA
AACGTAGCAATTACAAACAATGGATTTGTCAAAAATGCAACAAAGGTTATGCTGTTCAATCAGATTATAAAGCTCACATC
AAAACTTGTGGTACTAGAGGCCATTCTTGTGATTGTGGAAGAGTTTTCTCTAGAGTTGAAACATTTATTGAGCATCAAGA
TTCATGCAAACCACAAAGTACAACTACTAAAGAATGTCATGATATGCAAATACCAAAACCAATTTTCTTGCCTACTACTA
CAACTCATATCCCACCACATGATCAATATTCAAAAATATTGCCTAATCTTGATCTTGAGCTTTTCACTTCTCCAAATTAT
TTCAACCAAAACACACACAATTTTTCATCATTTGTTGATCAAAGTGATCATCATCATCATAATAATAATTACATAGTCCA
AAACAATGATATTGAAGTCAAAGAAATTATTGAAGAGGCAACAACACAAGTAACAAGATTGAAAAGTGAAGCAAATGAAA
TACTCAAAATAGCAATGGAAGAAAAGGCAATGGCTATAGAGAAGAGACAAGAAGCAAAGTGTTTGATTGAATTAGCCAAC
CTTGAAATGGCAAAAGCAATGGAAATTAGACAAAGTGTTTGTGCTTCATCATCATCATCATCACATGTCATGAAGATAAT
AAAATGTAGTTCTTGTAATAATAAACAATTTCAAAGTGTGTCATCATCAAAAGATGCTACTTTGACTAATAATTATTATT
TGTCATCTTCTATTTATAGAAGATGATGA
![]() ![]() | translated polypeptide sequence |
>Solyc05g054030.2.1 C2H2L domain class transcription factor (AHRD V1 **-* D9ZIU3_MALDO); contains Interpro domain(s) IPR007087 Zinc finger, C2H2-type
MLTSNSFLFGAPSNYSDPFSSPENGFIIKRKRRPAGTPDPDAQVVYLTAEMLMESDRYVCEICNLSFQREQNLQMHRRRH
KVPWKLKKKEEEKNEMDQVIKKRVYVCPEPSCVHHDPCHALGDLVGIKKHFRRKRSNYKQWICQKCNKGYAVQSDYKAHI
KTCGTRGHSCDCGRVFSRVETFIEHQDSCKPQSTTTKECHDMQIPKPIFLPTTTTHIPPHDQYSKILPNLDLELFTSPNY
FNQNTHNFSSFVDQSDHHHHNNNYIVQNNDIEVKEIIEEATTQVTRLKSEANEILKIAMEEKAMAIEKRQEAKCLIELAN
LEMAKAMEIRQSVCASSSSSSHVMKIIKCSSCNNKQFQSVSSSKDATLTNNYYLSSSIYRR*
MLTSNSFLFGAPSNYSDPFSSPENGFIIKRKRRPAGTPDPDAQVVYLTAEMLMESDRYVCEICNLSFQREQNLQMHRRRH
KVPWKLKKKEEEKNEMDQVIKKRVYVCPEPSCVHHDPCHALGDLVGIKKHFRRKRSNYKQWICQKCNKGYAVQSDYKAHI
KTCGTRGHSCDCGRVFSRVETFIEHQDSCKPQSTTTKECHDMQIPKPIFLPTTTTHIPPHDQYSKILPNLDLELFTSPNY
FNQNTHNFSSFVDQSDHHHHNNNYIVQNNDIEVKEIIEEATTQVTRLKSEANEILKIAMEEKAMAIEKRQEAKCLIELAN
LEMAKAMEIRQSVCASSSSSSHVMKIIKCSSCNNKQFQSVSSSKDATLTNNYYLSSSIYRR*
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![]() ![]() | [Associate new unigene] |
Unigene ID:
none
GenBank accessions | None | [Associate new genbank sequence] |
Other genome matches | None |
![]() ![]() | [Associate publication] [Matching publications] |
Genealogy and fine mapping of obscuravenosa, a gene affecting the distribution of chloroplasts in leaf veins, and evidence of selection during breeding of tomatoes (Lycopersicon esculentum; Solanaceae).
American journal of botany (2012)
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In the processes of plant domestication and variety development, some traits are under direct selection, while others may be introduced by indirect selection or linkage. In the cultivated tomato (Lycopersicon esculentum = Solanum lycopersicum), and all other Solanaceae examined, chloroplasts are normally absent from subepidermal and mesophyll cells surrounding the leaf veins, and thus, veins appear clear upon subillumination. The tomato mutant obscuravenosa (obv), in contrast, contains chloroplasts in cells around the vein, and thus, veins appear as dark as the surrounding leaf tissue. Among tomato cultivars, the obv allele is common in processing varieties bred for mechanical harvest, but is otherwise rare. We traced the source of obv in processing tomatoes to the cultivar Earliana, released in the 1920s. The obv locus was mapped to chromosome 5, bin 5G, using introgression lines containing single chromosome segments from the wild species L. pennellii. This region also contains a quantitative trait locus (QTL) for plant height, pht5.4, which cosegregated with SP5G, a paralog of self-pruning (sp), the gene that controls the switch between determinate and indeterminate growth in tomato. The pht5.4 QTL was partially dominant and associated with a reduced percentage of red fruit at harvest. Our data suggest that the prevalence of obv in nearly all processing varieties may have resulted from its tight linkage to a QTL conferring a more compact, and horticulturally desirable, plant habit.
Jones, CM. Rick, CM. Adams, D. Jernstedt, J. Chetelat, RT.
American journal of botany.
2012.
94(6).
935-47.
A mutation that eliminates bundle sheath extensions reduces leaf hydraulic conductance, stomatal conductance and assimilation rates in tomato (Solanum lycopersicum).
The New phytologist (2015)
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Bundle sheath extensions (BSEs) are key features of leaf structure whose distribution differs among species and ecosystems. The genetic control of BSE development is unknown, so BSE physiological function has not yet been studied through mutant analysis. We screened a population of ethyl methanesulfonate (EMS)-induced mutants in the genetic background of the tomato (Solanum lycopersicum) model Micro-Tom and found a mutant lacking BSEs. The leaf phenotype of the mutant strongly resembled the tomato mutant obscuravenosa (obv). We confirmed that obv lacks BSEs and that it is not allelic to our induced mutant, which we named obv-2. Leaves lacking BSEs had lower leaf hydraulic conductance and operated with lower stomatal conductance and correspondingly lower assimilation rates than wild-type leaves. This lower level of function occurred despite similarities in vein density, midvein vessel diameter and number, stomatal density, and leaf area between wild-type and mutant leaves, the implication being that the lack of BSEs hindered water dispersal within mutant leaves. Our results comparing near-isogenic lines within a single species confirm the hypothesised role of BSEs in leaf hydraulic function. They further pave the way for a genetic model-based analysis of a common leaf structure with deep ecological consequences.
Zsögön, A. Negrini, AC. Peres, LE. Nguyen, HT. Ball, MC.
The New phytologist.
2015.
205(2).
618-26.
Bundle sheath extensions affect leaf structural and physiological plasticity in response to irradiance.
Plant, cell & environment (2020)
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Coordination between structural and physiological traits is key to plants' responses to environmental fluctuations. In heterobaric leaves, bundle sheath extensions (BSEs) increase photosynthetic performance (light-saturated rates of photosynthesis, Amax ) and water transport capacity (leaf hydraulic conductance, Kleaf ). However, it is not clear how BSEs affect these and other leaf developmental and physiological parameters in response to environmental conditions. The obscuravenosa (obv) mutation, found in many commercial tomato varieties, leads to absence of BSEs. We examined structural and physiological traits of tomato heterobaric and homobaric (obv) near-isogenic lines grown at two different irradiance levels. Kleaf , minor vein density, and stomatal pore area index decreased with shading in heterobaric but not in homobaric leaves, which show similarly lower values in both conditions. Homobaric plants, on the other hand, showed increased Amax , leaf intercellular air spaces, and mesophyll surface area exposed to intercellular airspace (Smes ) in comparison with heterobaric plants when both were grown in the shade. BSEs further affected carbon isotope discrimination, a proxy for long-term water-use efficiency. BSEs confer plasticity in traits related to leaf structure and function in response to irradiance levels and might act as a hub integrating leaf structure, photosynthetic function, and water supply and demand.
Barbosa, MAM. Chitwood, DH. Azevedo, AA. Araújo, WL. Ribeiro, DM. Peres, LEP. Martins, SCV. Zsögön, A.
Plant, cell & environment.
2020.
42(5).
1575-1589.
Auxin-driven ecophysiological diversification of leaves in domesticated tomato.
Plant physiology (2022)
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Heterobaric leaves have bundle sheath extensions (BSEs) that compartmentalize the parenchyma, whereas homobaric leaves do not. The presence of BSEs affects leaf hydraulics and photosynthetic rate. The tomato (Solanum lycopersicum) obscuravenosa (obv) mutant lacks BSEs. Here, we identify the obv gene and the causative mutation, a nonsynonymous amino acid change that disrupts a C2H2 zinc finger motif in a putative transcription factor. This mutation exists as a polymorphism in the natural range of wild tomatoes but has increased in frequency in domesticated tomatoes, suggesting that the latter diversified into heterobaric and homobaric leaf types. The obv mutant displays reduced vein density, leaf hydraulic conductance and photosynthetic assimilation rate. We show that these and other pleiotropic effects on plant development, including changes in leaf insertion angle, leaf margin serration, minor vein density, and fruit shape, are controlled by OBV via changes in auxin signaling. Loss of function of the transcriptional regulator AUXIN RESPONSE FACTOR 4 (ARF4) also results in defective BSE development, revealing an additional component of a genetic module controlling aspects of leaf development important for ecological adaptation and subject to breeding selection.
Moreira, JDR. Rosa, BL. Lira, BS. Lima, JE. Correia, LNF. Otoni, WC. Figueira, A. Freschi, L. Sakamoto, T. Peres, LEP. Rossi, M. Zsögön, A.
Plant physiology.
2022.
190(1).
113-126.
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