- -

A cytochrome P450 regulates a domestication trait in cultivated tomato

RiuNet: Repositorio Institucional de la Universidad Politécnica de Valencia

Compartir/Enviar a

Citas

Estadísticas

  • Estadisticas de Uso

A cytochrome P450 regulates a domestication trait in cultivated tomato

Mostrar el registro completo del ítem

Chakrabarti, M.; Zhang, N.; Sauvage, C.; Muños, S.; Blanca Postigo, JM.; Cañizares Sales, J.; Díez Niclós, MJTDJ.... (2013). A cytochrome P450 regulates a domestication trait in cultivated tomato. Proceedings of the National Academy of Sciences. 110(42):17125-17130. doi:10.1073/pnas.1307313110

Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10251/62559

Ficheros en el ítem

Metadatos del ítem

Título: A cytochrome P450 regulates a domestication trait in cultivated tomato
Autor: Chakrabarti, Manohar Zhang, Na Sauvage, Christopher Muños, Stéphane Blanca Postigo, José Miguel Cañizares Sales, Joaquín Díez Niclós, Mª José Teresa de Jesús Schneider, Rhiannon Mazourek, Michael McClead, Jammi Causse, Mathilde Van Der Knaap, Esther Klazina Maria
Entidad UPV: Universitat Politècnica de València. Departamento de Biotecnología - Departament de Biotecnologia
Fecha difusión:
Resumen:
Domestication of crop plants had effects on human lifestyle and agriculture. However, little is known about the underlying molecular mechanisms accompanying the changes in fruit appearance as a consequence of selection by ...[+]
Palabras clave: Fruit size , Maternal control , Shape variation , Gene family , Organ size , Seed size , Loci , Plants , Expression , Variants
Derechos de uso: Cerrado
Fuente:
Proceedings of the National Academy of Sciences. (issn: 0027-8424 ) (eissn: 1091-6490 )
DOI: 10.1073/pnas.1307313110
Editorial:
National Academy of Sciences
Versión del editor: http://dx.doi.org/10.1073/pnas.1307313110
Código del Proyecto:
info:eu-repo/grantAgreement/NSF//0922661/US/Discovery of Genes and Networks Regulating Tomato Fruit Morphology/
Agradecimientos:
We thank Dr. D. Choi (Seoul National University) for providing DNA sequence of chile pepper CaKLUH region; and Molecular and Cellular Imaging Center, The Ohio State University, for assistance with microscopy. This work was ...[+]
Tipo: Artículo

References

Pickersgill, B. (2007). Domestication of Plants in the Americas: Insights from Mendelian and Molecular Genetics. Annals of Botany, 100(5), 925-940. doi:10.1093/aob/mcm193

Blanca, J., Cañizares, J., Cordero, L., Pascual, L., Diez, M. J., & Nuez, F. (2012). Variation Revealed by SNP Genotyping and Morphology Provides Insight into the Origin of the Tomato. PLoS ONE, 7(10), e48198. doi:10.1371/journal.pone.0048198

Klee, H. J., & Giovannoni, J. J. (2011). Genetics and Control of Tomato Fruit Ripening and Quality Attributes. Annual Review of Genetics, 45(1), 41-59. doi:10.1146/annurev-genet-110410-132507 [+]
Pickersgill, B. (2007). Domestication of Plants in the Americas: Insights from Mendelian and Molecular Genetics. Annals of Botany, 100(5), 925-940. doi:10.1093/aob/mcm193

Blanca, J., Cañizares, J., Cordero, L., Pascual, L., Diez, M. J., & Nuez, F. (2012). Variation Revealed by SNP Genotyping and Morphology Provides Insight into the Origin of the Tomato. PLoS ONE, 7(10), e48198. doi:10.1371/journal.pone.0048198

Klee, H. J., & Giovannoni, J. J. (2011). Genetics and Control of Tomato Fruit Ripening and Quality Attributes. Annual Review of Genetics, 45(1), 41-59. doi:10.1146/annurev-genet-110410-132507

Paran, I., & van der Knaap, E. (2007). Genetic and molecular regulation of fruit and plant domestication traits in tomato and pepper. Journal of Experimental Botany, 58(14), 3841-3852. doi:10.1093/jxb/erm257

Tanksley, S. D. (2004). The Genetic, Developmental, and Molecular Bases of Fruit Size and Shape Variation in Tomato. THE PLANT CELL ONLINE, 16(suppl_1), S181-S189. doi:10.1105/tpc.018119

Grandillo, S., Ku, H. M., & Tanksley, S. D. (1999). Identifying the loci responsible for natural variation in fruit size and shape in tomato. Theoretical and Applied Genetics, 99(6), 978-987. doi:10.1007/s001220051405

Frary, A. (2000). fw2.2: A Quantitative Trait Locus Key to the Evolution of Tomato Fruit Size. Science, 289(5476), 85-88. doi:10.1126/science.289.5476.85

Guo, M., Rupe, M. A., Dieter, J. A., Zou, J., Spielbauer, D., Duncan, K. E., … Simmons, C. R. (2010). Cell Number Regulator1 Affects Plant and Organ Size in Maize: Implications for Crop Yield Enhancement and Heterosis. The Plant Cell, 22(4), 1057-1073. doi:10.1105/tpc.109.073676

Libault, M., Zhang, X.-C., Govindarajulu, M., Qiu, J., Ong, Y. T., Brechenmacher, L., … Stacey, G. (2010). A member of the highly conserved FWL (tomato FW2.2-like) gene family is essential for soybean nodule organogenesis. The Plant Journal, 62(5), 852-864. doi:10.1111/j.1365-313x.2010.04201.x

Van der Knaap, E., & Tanksley, S. D. (2003). The making of a bell pepper-shaped tomato fruit: identification of loci controlling fruit morphology in Yellow Stuffer tomato. Theoretical and Applied Genetics, 107(1), 139-147. doi:10.1007/s00122-003-1224-1

Zhang, N., Brewer, M. T., & van der Knaap, E. (2012). Fine mapping of fw3.2 controlling fruit weight in tomato. Theoretical and Applied Genetics, 125(2), 273-284. doi:10.1007/s00122-012-1832-8

Blas, A. L., Yu, Q., Veatch, O. J., Paull, R. E., Moore, P. H., & Ming, R. (2011). Genetic mapping of quantitative trait loci controlling fruit size and shape in papaya. Molecular Breeding, 29(2), 457-466. doi:10.1007/s11032-011-9562-1

Costantini, L., Battilana, J., Lamaj, F., Fanizza, G., & Grando, M. (2008). Berry and phenology-related traits in grapevine (Vitis vinifera L.): From Quantitative Trait Loci to underlying genes. BMC Plant Biology, 8(1), 38. doi:10.1186/1471-2229-8-38

Eduardo, I., Pacheco, I., Chietera, G., Bassi, D., Pozzi, C., Vecchietti, A., & Rossini, L. (2010). QTL analysis of fruit quality traits in two peach intraspecific populations and importance of maturity date pleiotropic effect. Tree Genetics & Genomes, 7(2), 323-335. doi:10.1007/s11295-010-0334-6

Zhang, G., Sebolt, A. M., Sooriyapathirana, S. S., Wang, D., Bink, M. C., Olmstead, J. W., & Iezzoni, A. F. (2009). Fruit size QTL analysis of an F1 population derived from a cross between a domesticated sweet cherry cultivar and a wild forest sweet cherry. Tree Genetics & Genomes, 6(1), 25-36. doi:10.1007/s11295-009-0225-x

Ranc, N., Muños, S., Santoni, S., & Causse, M. (2008). A clarified position for solanum lycopersicum var. cerasiforme in the evolutionary history of tomatoes (solanaceae). BMC Plant Biology, 8(1), 130. doi:10.1186/1471-2229-8-130

Anastasiou, E., Kenz, S., Gerstung, M., MacLean, D., Timmer, J., Fleck, C., & Lenhard, M. (2007). Control of Plant Organ Size by KLUH/CYP78A5-Dependent Intercellular Signaling. Developmental Cell, 13(6), 843-856. doi:10.1016/j.devcel.2007.10.001

Paterson, A. H., Lin, Y.-R., Li, Z., Schertz, K. F., Doebley, J. F., Pinson, S. R. M., … Irvine, J. E. (1995). Convergent Domestication of Cereal Crops by Independent Mutations at Corresponding Genetic Loci. Science, 269(5231), 1714-1718. doi:10.1126/science.269.5231.1714

Adamski, N. M., Anastasiou, E., Eriksson, S., O’Neill, C. M., & Lenhard, M. (2009). Local maternal control of seed size by KLUH/CYP78A5-dependent growth signaling. Proceedings of the National Academy of Sciences, 106(47), 20115-20120. doi:10.1073/pnas.0907024106

Fang, W., Wang, Z., Cui, R., Li, J., & Li, Y. (2012). Maternal control of seed size by EOD3/CYP78A6 in Arabidopsis thaliana. The Plant Journal, 70(6), 929-939. doi:10.1111/j.1365-313x.2012.04907.x

Ito, T., & Meyerowitz, E. M. (2000). Overexpression of a Gene Encoding a Cytochrome P450, CYP78A9, Induces Large and Seedless Fruit in Arabidopsis. The Plant Cell, 12(9), 1541-1550. doi:10.1105/tpc.12.9.1541

Miyoshi, K., Ahn, B.-O., Kawakatsu, T., Ito, Y., Itoh, J.-I., Nagato, Y., & Kurata, N. (2004). PLASTOCHRON1, a timekeeper of leaf initiation in rice, encodes cytochrome P450. Proceedings of the National Academy of Sciences, 101(3), 875-880. doi:10.1073/pnas.2636936100

KATSUMATA, T., FUKAZAWA, J., MAGOME, H., JIKUMARU, Y., KAMIYA, Y., NATSUME, M., … YAMAGUCHI, S. (2011). Involvement of the CYP78A Subfamily of Cytochrome P450 Monooxygenases in Protonema Growth and Gametophore Formation in the MossPhyscomitrella patens. Bioscience, Biotechnology, and Biochemistry, 75(2), 331-336. doi:10.1271/bbb.100759

Meyer, K. B., Maia, A.-T., O’Reilly, M., Ghoussaini, M., Prathalingam, R., Porter-Gill, P., … Ponder, B. A. J. (2011). A Functional Variant at a Prostate Cancer Predisposition Locus at 8q24 Is Associated with PVT1 Expression. PLoS Genetics, 7(7), e1002165. doi:10.1371/journal.pgen.1002165

Näkki, A., Kouhia, S. T., Saarela, J., Harilainen, A., Tallroth, K., Videman, T., … Kujala, U. M. (2010). Allelic variants of IL1R1gene associate with severe hand osteoarthritis. BMC Medical Genetics, 11(1). doi:10.1186/1471-2350-11-50

Nischwitz, S., Cepok, S., Kroner, A., Wolf, C., Knop, M., Müller-Sarnowski, F., … Weber, F. (2010). More CLEC16A gene variants associated with multiple sclerosis. Acta Neurologica Scandinavica, 123(6), 400-406. doi:10.1111/j.1600-0404.2010.01421.x

Uno, S., Zembutsu, H., Hirasawa, A., Takahashi, A., Kubo, M., Akahane, T., … Nakamura, Y. (2010). A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese. Nature Genetics, 42(8), 707-710. doi:10.1038/ng.612

Sandal, N. N., Bojsen, K., & Marcker, K. A. (1987). A small family of nodule specific genes from soybean. Nucleic Acids Research, 15(4), 1507-1519. doi:10.1093/nar/15.4.1507

Stougaard, J., J�rgensen, J.-E., Christensen, T., K�hle, A., & Marcker, K. A. (1990). Interdependence and nodule specificity of cis-acting regulatory elements in the soybean leghemoglobin lbc 3 and N23 gene promoters. MGG Molecular & General Genetics, 220(3), 353-360. doi:10.1007/bf00391738

Vieweg, M. F., Frühling, M., Quandt, H.-J., Heim, U., Bäumlein, H., Pühler, A., … Perlick, A. M. (2004). The Promoter of theVicia fabaL. Leghemoglobin GeneVfLb29Is Specifically Activated in the Infected Cells of Root Nodules and in the Arbuscule-Containing Cells of Mycorrhizal Roots from Different Legume and Nonlegume Plants. Molecular Plant-Microbe Interactions, 17(1), 62-69. doi:10.1094/mpmi.2004.17.1.62

Gillaspy, G., Ben-David, H., & Gruissem, W. (1993). Fruits: A Developmental Perspective. The Plant Cell, 1439-1451. doi:10.1105/tpc.5.10.1439

Iglesias, D. J., Cercós, M., Colmenero-Flores, J. M., Naranjo, M. A., Ríos, G., Carrera, E., … Talon, M. (2007). Physiology of citrus fruiting. Brazilian Journal of Plant Physiology, 19(4), 333-362. doi:10.1590/s1677-04202007000400006

Marcelis, L. F. M., & Baan Hofman-Eijer, L. R. (1993). Cell division and expansion in the cucumber fruit. Journal of Horticultural Science, 68(5), 665-671. doi:10.1080/00221589.1993.11516398

Xiao, H., Radovich, C., Welty, N., Hsu, J., Li, D., Meulia, T., & van der Knaap, E. (2009). Integration of tomato reproductive developmental landmarks and expression profiles, and the effect of SUN on fruit shape. BMC Plant Biology, 9(1), 49. doi:10.1186/1471-2229-9-49

Cong, B., Liu, J., & Tanksley, S. D. (2002). Natural alleles at a tomato fruit size quantitative trait locus differ by heterochronic regulatory mutations. Proceedings of the National Academy of Sciences, 99(21), 13606-13611. doi:10.1073/pnas.172520999

Rao, G. U., Ben Chaim, A., Borovsky, Y., & Paran, I. (2003). Mapping of yield-related QTLs in pepper in an interspecific cross of Capsicum annuum and C. frutescens. Theoretical and Applied Genetics, 106(8), 1457-1466. doi:10.1007/s00122-003-1204-5

Brewer, M. T., Lang, L., Fujimura, K., Dujmovic, N., Gray, S., & van der Knaap, E. (2006). Development of a Controlled Vocabulary and Software Application to Analyze Fruit Shape Variation in Tomato and Other Plant Species. Plant Physiology, 141(1), 15-25. doi:10.1104/pp.106.077867

Xiao, H., Jiang, N., Schaffner, E., Stockinger, E. J., & van der Knaap, E. (2008). A Retrotransposon-Mediated Gene Duplication Underlies Morphological Variation of Tomato Fruit. Science, 319(5869), 1527-1530. doi:10.1126/science.1153040

Huang, Z., Van Houten, J., Gonzalez, G., Xiao, H., & van der Knaap, E. (2013). Genome-wide identification, phylogeny and expression analysis of SUN, OFP and YABBY gene family in tomato. Molecular Genetics and Genomics, 288(3-4), 111-129. doi:10.1007/s00438-013-0733-0

Ben-Chaim, A., Borovsky, Y., Falise, M., Mazourek, M., Kang, B.-C., Paran, I., & Jahn, M. (2006). QTL analysis for capsaicinoid content in Capsicum. Theoretical and Applied Genetics, 113(8), 1481-1490. doi:10.1007/s00122-006-0395-y

Schardl, C. L., Byrd, A. D., Benzion, G., Altschuler, M. A., Hildebrand, D. F., & Hunt, A. G. (1987). Design and construction of a versatile system for the expression of foreign genes in plants. Gene, 61(1), 1-11. doi:10.1016/0378-1119(87)90359-3

Ossowski, S., Schwab, R., & Weigel, D. (2008). Gene silencing in plants using artificial microRNAs and other small RNAs. The Plant Journal, 53(4), 674-690. doi:10.1111/j.1365-313x.2007.03328.x

Bradbury, P. J., Zhang, Z., Kroon, D. E., Casstevens, T. M., Ramdoss, Y., & Buckler, E. S. (2007). TASSEL: software for association mapping of complex traits in diverse samples. Bioinformatics, 23(19), 2633-2635. doi:10.1093/bioinformatics/btm308

FALUSH, D., STEPHENS, M., & PRITCHARD, J. K. (2007). Inference of population structure using multilocus genotype data: dominant markers and null alleles. Molecular Ecology Notes, 7(4), 574-578. doi:10.1111/j.1471-8286.2007.01758.x

Hardy, O. J., & Vekemans, X. (2002). spagedi: a versatile computer program to analyse spatial genetic structure at the individual or population levels. Molecular Ecology Notes, 2(4), 618-620. doi:10.1046/j.1471-8286.2002.00305.x

Librado, P., & Rozas, J. (2009). DnaSP v5: a software for comprehensive analysis of DNA polymorphism data. Bioinformatics, 25(11), 1451-1452. doi:10.1093/bioinformatics/btp187

Tamura, K., Peterson, D., Peterson, N., Stecher, G., Nei, M., & Kumar, S. (2011). MEGA5: Molecular Evolutionary Genetics Analysis Using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods. Molecular Biology and Evolution, 28(10), 2731-2739. doi:10.1093/molbev/msr121

[-]

recommendations

 

Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro completo del ítem