
Plant and inflorescence architecture
Research line: Molecular mechanisms of development and morphogenesis

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Research
RESEARCH
Plants exhibit a remarkable diversity of forms in nature, reflecting variation in the size, shape, and position of their different organs. The number and arrangement of these organs form the basis of plant architecture. Our laboratory is focused on understanding the control of inflorescence architecture, the region of the plant where flowers are formed. We aim to uncover the genetic networks that regulate inflorescence development and how these networks have evolved in different species to generate the vast diversity of architectures observed in nature.
Different Types of Inflorescences
In the classification of inflorescences, one important distinction is between determinate and indeterminate types. Inflorescences in which the apical meristem of the stem has unlimited growth capacity are termed indeterminate. In contrast, inflorescences in which the apical meristem forms a terminal flower are termed determinate. Another key distinction is between simple and compound inflorescences. In simple inflorescences, flowers develop directly from the shoot apical meristem, meaning they form directly on the main inflorescence axis. In contrast, in compound inflorescences, the primary inflorescence axis does not produce the flowers itself but branches to form secondary or higher-order axes where flowers develop.
The position where flowers are formed depends on the identity of the inflorescence meristems—whether the apical meristem remains as an inflorescence meristem or becomes floral, and whether the primary inflorescence meristem gives rise to floral or secondary inflorescence meristems. We study the gene network that confers identity to inflorescence meristems. Our research is mainly divided into two lines of investigation.
FOCUS
Control of Inflorescence Architecture in Arabidopsis
On one hand, we work with the model species *Arabidopsis thaliana*, which has a simple indeterminate inflorescence. The indeterminate growth of the Arabidopsis inflorescence, as well as that of many other species with indeterminate inflorescences, is due to the activity of the *TERMINAL FLOWER1* (*TFL1*) gene, which prevents the inflorescence meristem from becoming floral. To achieve this, *TFL1* is expressed in the inflorescence meristem, thereby repressing the expression of the floral identity genes *LFY* and *AP1* in that region. We study how *TFL1* expression is established in the inflorescence meristem, which genes regulate its expression, and how these genes influence inflorescence architecture.
In situ hybridization showing expression of TFL1 (blue) and LFY (red) in an Arabidopsis inflorescence apex. (Image courtesy of Cristina Ferrándiz) Control of Inflorescence Development in Legume Compound Inflorescences
As a comparative system, we also work with model legume species, such as pea and *Medicago truncatula*, which exhibit indeterminate compound inflorescences where flowers are formed on lateral secondary inflorescences. In the genetic network that specifies meristem identity in legumes, in addition to homologs of *TFL1*, *LFY*, and *AP1*, new genes are also involved, such as *VEG1*, which is responsible for the formation of secondary inflorescences. We are engaged in the identification and characterization of genes that define secondary inflorescence identity and in the analysis of how the meristem identity gene network has evolved in legumes to give rise to compound inflorescences.
Staff
Staff Researchers
Contract Staff and Fellows
Publications
Praena-Tamayo Jesús Tamayo, Ilara Gabriela, Frasson Budzinski, Nicolas Delhomme, Thomas Moritz, Francisco Madueño, Reyes Benlloch (2022) CHARACTERIZATION OF METABOLIC CHANGES ASSOCIATED WITH FLORAL TRANSITION IN ARABIDOPSIS: RAFFINOSE SYNTHASE 5 CONTRIBUTES TO DETERMINE THE TIMING OF FLORAL TRANSITION BioRxiv2022, .04.29.490013; doi: https://doi.org/10.1101/2022.04.29.490013
Pautot, V.; Berbel, A.; Cayla, T.; Eschstruth, A.; Adroher, B.; Ratet, P.; Madueño, F.; Laufs, P (2022). Arabidopsis thaliana SHOOT MERISTEMLESS SUBSTITUTES FOR Medicago truncatula SINGLE LEAFLET1 TO FORM COMPLEX LEAVES AND PETALS. J. Mol. Sci. 2022, 23, 14114. https://doi.org/10.3390/ijms232214114
Serra-Picó M, Hecht V, Weller JL, Benlloch R*, Madueño F*. (2022) IDENTIFICATION AND CHARACTERIZATION OF PUTATIVE TARGETS OF VEGETATIVE1/FULc, A KEY REGULATOR OF DEVELOPMENT OF THE COMPOUND INFLORESCENCE IN PEA AND RELATED LEGUMES. Front Plant Sci. 2022 Sep 21;13:765095. doi: 10.3389/fpls.2022.765095. PMID: 36212341; PMCID: PMC9533771.
Cristina Caballo*†, Ana Berbel†, Raul Ortega, Juan Gil, Teresa Millán, Josefa Rubio, Francisco Madueño* †co-first authors (2020) THE SINGLE FLOWER (SFL) GENE ENCODES A MYB TRANSCRIPTION FACTOR THAT REGULATES THE NUMBER OF FLOWERS PRODUCED BY THE INFLORESCENCE OF CHICKPEA.
New Phytol. May;234(3):827-836. doi: 10.1111/nph.18019.
Azpeitia E, Tichtinsky G, Le Masson M, Serrano-Mislata A, Lucas J, Gregis V, Gimenez C, Prunet N, Farcot E, Kater MM, Bradley D, Madueño F, Godin C, Parcy F. CAULIFLOWER FRACTAL FORMS ARISE FROM PERTURBATIONS OF FLORAL GENE NETWORKS. Science. 2021 Jul 9;373(6551):192-197
Hamza R, Roque E, Gómez-Mena C, Madueño F, Beltrán JP, Cañas LA (2021). PSEND1 IS A KEY PLAYER IN PEA POLLEN DEVELOPMENT THROUGHOMEOSTASIS. Front Plant Sci. 12:765277. doi: 10.3389/fpls.2021.765277.
Joelma O Cruz, Juca Abramo Barrera San Martin, Greice Lubini, Rómulo Sobral, Vitor F Pinoti, Pedro B Ferreira, Vanessa Thomé, Andréa C Quiapim, Marcelo Carnier Dornelas, Maria-Cristina da Silva Pranchevicius, Francisco Madueño, Maria Manuela Ribeiro Costa and Maria Helena S. Goldman. SCI1 IS A DIRECT TARGET OF AGAMOUS AND WUSCHEL AND IS SPECIFICALLY EXPRESSED IN THE FLORAL MERISTEMATIC CELLS. Frontiers in Plant Sciences. Mar 18;12:642879. doi: 10.3389/fpls.2021.642879.
Goretti D1, Silvestre M1, Collani S, Langenecker T, Méndez C, Madueño F*, Schmidt M* (2020) TERMINAL FLOWER 1 FUNCTIONS AS A MOBILE TRANSCRIPTIONAL CO-FACTOR IN THE Arabidopsis thaliana SHOOT APICAL MERISTEM. 1co-first authors, *corresponding authors. Plant Physiol, 182(4):2081-2095. doi: 10.1104/pp.19.00867
Plant Journal, DOI: 10.1111/tpj.13905
Plant Signaling & Behavior, 12(10)
Plant Physiol, 174: 1097-1109
Plant Journal, 88: 437-451
Development, 142: 3315-27
Baumann K, Venail J, Berbel A, Domenech MJ, Money T, Conti L, Hanzawa Y, Madueno F, Bradley D (2015)
Journal of Experimental Botany 66: 4769-4780
Frontiers in Plant Science 6: 543
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Sussmilch Frances C, Berbel A, Hecht V, Vander Schoor JK, Ferrandiz C, Madueno F, Weller JL (2015)Pea VEGETATIVE2 Is an FD Homolog That Is Essential for Flowering and Compound Inflorescence Development
Plant Cell 27: 1046-1060
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Fernández-Nohales P, Domenech MJ, Martínez de Alba AE, Micol JL, Ponce MR and Madueño F (2014)AGO1 CONTROLS INFLORESCENCE ARCHITECTURE POSSIBLY BY REGULATING TFL1 EXPRESSION
Annals of Botany, 114: 1471-81
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Ge L, Peng J, Ana Berbel A, Madueño F and Chen R (2014)REGULATION OF COMPOUND LEAF DEVELOPMENT BY PHANTASTICA IN Medicago truncatula
Plant Physiol, 164(1):216-28
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Coego A, Brizuela E, Castillejo P, Ruíz S, Koncz C, del Pozo C, Pineiro M, Jarillo JA, Paz-Ares J, Leon J and the TRANSPLANTA Consortium (2014)THE TRANSPLANTA COLLECTION OF ARABIDOPSIS LINES: A RESOURCE FOR FUNCTIONAL ANALYSIS OF TRANSCRIPTION FACTORS BASED ON THEIR CONDITIONAL OVEREXPRESSION
Plant Journal, 77:944-53
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Berbel A, Ferrándiz C, Hecht V, Dalmais M, Lund OS, Sussmilch FC, Taylor SA, Bendahmane A, Ellis TH, Beltrán JP, Weller JL, Madueño F (2012)VEGETATIVE1 is essential for development of the compound inflorescence in pea
Nature Communications 3: 797
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Tadege M, Lin H, Bedair M, Berbel A, Wen J, Rojas CM, Tang Y, Sumner L, Ratet P, McHale NA, Madueño F, Mysore KS (2011)STENOFOLIA is a key regulator of blade outgrowth and leaf vascular patterning in Medicago truncatula and Nicotiana sylvestris
Plant Cell 23: 2125-2142
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Chen J, Yu J, Ge L, Wang H, Berbel A, Liu Y, Chen Y, Li G, Tadege M, Wen J, Cosson V, Mysore KS, Ratet P, Madueño F, Bai G, Chen R (2010)Control of dissected leaf morphology by a CYS(2)HIS(2) zinc finger transcription factor in the model legume Medicago truncatula
Proceedings of the National Academy of Sciences USA 107: 10754-10759
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Kaufmann K, Wellmer F, Muiño JM, Ferrier T, Wuest SE, Kumar V, Serrano-Mislata A, Madueño F, Krajewski P, Meyerowitz EM, Angenent GC, Riechmann JL (2010)Orchestration of floral initiation by APETALA1
Science 328: 85-89
- Benlloch R, Roque E, Ferrandiz C, Cosson V, Caballero MT, Penmetsa RV, Cañas LA, Beltrán JP, Ratet P, Madueño F (2009)
Plant Journal 60: 102-111
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Benlloch R, Berbel A, Serrano-Mislata A, Madueño F (2007)Floral initiation and inflorescence architecture: a comparative view
Annals of Botany 100: 659-676
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Roque E, Gómez MD, Ellul P, Wallbraun M, Madueño F, Beltrán JP, Cañas LA (2007)The PsEND1 promoter: a novel tool to produce genetically engineered male-sterile plants by early anther ablation
Plant Cell Reports 26: 313-325
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Sohn EJ, Rojas-Pierce M, Pan S, Carter C, Serrano-Mislata A, Madueño F, Rojo E, Surpin M, Raikhel NV (2007)The shoot meristem identity gene TFL1 demonstrates a role for the protein storage vacuole in plant development
Proceedings of the National Academy of Sciences USA 104: 18801-18806
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Domoney C, Duc G, Ellis THN, Ferrándiz C, Firnhaber C, Gallardo K, Hofer J, Kopka J, Küster H, Madueño F, Munier-Jolain NG, Mayer K, Thompson R, Udvardi M, Salon C (2006)Genetic and genomic analysis of legume flowers and seeds
Current Opinion in Plant Biology 9: 133-141
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Blázquez MA, Ferrándiz C, Madueño F, Parcy F (2006)How floral meristems are built
Plant Molecular Biology 60: 855-870
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Benlloch R, d’Erfurth I, Ferrandiz C, Cosson V, Beltrán JP, Cañas LA, Kondorosi A, Madueño F, Ratet P (2006)Isolation of mtpim proves Tnt1 a useful reverse genetics tool in Medicago truncatula and uncovers new aspects of AP1-like functions in legumes
Plant Physiology 142: 972-983
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Forment J, Gadea J, Huerta L, Abizanda L, Agusti J, Alamar S, Alos E, Andres F, Arribas R, Beltran JP, Berbel A, Blazquez MA, Brumos J, Canas LA, Cercos M, Colmenero-Flores JM, Conesa M, Estables B, Gandia M, Garcia-Martinez JL, Gimeno J, Gisbert A, Gomez G, Gonzalez-Candelas L, Granell A, Guerri J, Lafuente MT, Madueno F, Marcos JF, Marques MC, Martinez F, Martinez-Godoy MA, Miralles S, Moreno P, Navarro L, Pallas V, Perez-Amador MA, Perez-Valle J, Pons C, Rodrigo I, Rodriguez PL, Royo C, Serrano R, Soler G, Tadeo F, Talon M, Terol J, Trenor M, Vaello L, Vicente O, Vidal Ch, Zacarias L, Conejero V (2005)Development of a Citrus genome-wide EST collection and cDNA microarray as resources for genomic studies
Plant Molecular Biology 57: 375-391
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Berbel A, Navarro C, Ferrándiz C, Cañas LA, Beltrán JP, Madueño F (2005)Functional conservation of PISTILLATA activity in a pea homolog lacking the PI motif
Plant Physiology 139: 174-185
Projects
Patent
Thesis
Tipo: Tesis Doctorales