BLADE-ON-PETIOLE–Dependent Signaling Controls Leaf and Floral Patterning in Arabidopsis

Hepworth, Shelley R.; Zhang, Yuelin; McKim, Sarah; Li, Xin; Haughn, George W.

doi:10.1105/tpc.104.030536

Cited by 352Plant Molecular Biology ResearchDevelopmental Biology and Gene RegulationPlant Parasitism and Resistance

BLADE-ON-PETIOLE–Dependent Signaling Controls Leaf and Floral Patterning in Arabidopsis

Open access

Hepworth, Shelley R., Zhang, Yuelin, McKim, Sarah, Li, Xin, Haughn, George W.·2005·The Plant Cell

DOI 10.1105/tpc.104.030536

Open this paper in CoChat — free account

Abstract

NONEXPRESSOR OF PR GENES1 (NPR1) is a key regulator of the plant defense response known as systemic acquired resistance. Accumulation of the signal molecule salicylic acid (SA) leads to a change in intracellular redox potential, enabling NPR1 to enter the nucleus and interact with TGACG sequence-specific binding protein (TGA) transcription factors, which in turn bind to SA-responsive elements in the promoters of defense genes. Here, we show that two NPR1-like genes, BLADE-ON-PETIOLE1 (BOP1) and BOP2, function redundantly to control growth asymmetry, an important aspect of patterning in leaves and flowers. Phenotypes in the double mutant include leafy petioles, loss of floral organ abscission, and asymmetric flowers subtended by a bract. We demonstrate that BOP2 is localized to both the nucleus and the cytoplasm, but unlike NPR1, it is highly expressed in young floral meristems and in yeast interacts preferentially with the TGA transcription factor encoded by PERIANTHIA (PAN). In support of a biological relevance for this interaction, we show that bop1 bop2 and pan mutants share a pentamerous arrangement of first whorl floral organs, a patterning defect that is retained in bop1 bop2 pan triple mutants. Our data provide evidence that BOP proteins control patterning via direct interactions with TGA transcription factors and demonstrate that a signaling mechanism similar to that formally associated with plant defense is likely used for the control of developmental patterning.

Integrity signals

Registry

Crossref · 10.1105/tpc.104.030536

Cites

72 of 72 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Both bop1 and bop2 mutants display defects in inflorescence development, frequently forming fused inflorescences and generating multiple flowers from the same node.
“Both bop1 and bop2 mutants display defects in inflorescence development, as they frequently form fused inflorescences and generate multiple flowers from the same node (Hepworth et al., 2005;Ha et al., 2007).”
From Divide et impera: boundaries shape the plant body and initiate new meristems (2016) · cites this paper as Hepworth et al., 2005

CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
Thompson, J. D., Higgins, D. G., & Gibson, T. J. (1994) · Nucleic Acids Research · doi:10.1093/nar/22.22.4673 · Cited by 64,617 · see citing works
Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
Clough, S. J., & Bent, A. F. (1998) · The Plant Journal · doi:10.1046/j.1365-313x.1998.00343.x · Cited by 22,014 · see citing works
A novel genetic system to detect protein–protein interactions
Fields, S., & Song, O.-K. (1989) · Nature · doi:10.1038/340245a0 · Cited by 6,152 · see citing works
Genome-Wide Insertional Mutagenesis of Arabidopsis thaliana
Alonso, J. M., Stepanova, A. N., Leisse, T. J., Kim, C. J., Chen, H., Shinn, P., Stevenson, D. K., Zimmerman, J., Barajas, P., Cheuk, R., et al. (2003) · Science · doi:10.1126/science.1086391 · Cited by 5,105 · see citing works
MYB transcription factors in Arabidopsis
Dubos, C., Stracke, R., Erich Grotewold, A., Weißhaar, B., Martin, C. R., & Lepiniec, L. (2010) · Trends in Plant Science · doi:10.1016/j.tplants.2010.06.005 · Cited by 4,885 · see citing works
Local, Efflux-Dependent Auxin Gradients as a Common Module for Plant Organ Formation
Benková, E., Michniewicz, M., Sauer, M., Teichmann, T., Seifertová, D., Jürgens, G., & Friml, J. (2003) · Cell · doi:10.1016/s0092-8674(03)00924-3 · Cited by 2,637 · see citing works
Early flower development in Arabidopsis.
Smyth, D. R., Bowman, J. L., & Meyerowitz, E. M. (1990) · The Plant Cell · doi:10.1105/tpc.2.8.755 · Cited by 2,155 · see citing works
The promoter of TL-DNA gene 5 controls the tissue-specific expression of chimaeric genes carried by a novel type of Agrobacterium binary vector
Koncz, C., & Schell, J. (1986) · Molecular and General Genetics MGG · doi:10.1007/bf00331014 · Cited by 2,034 · see citing works
bZIP transcription factors in Arabidopsis
Jakoby, M. J., Weißhaar, B., Dröge‐Laser, W., Vicente‐Carbajosa, J., Tiedemann, J., Kroj, T., & Parcy, F. (2002) · Trends in Plant Science · doi:10.1016/s1360-1385(01)02223-3 · Cited by 1,862 · see citing works
Inducers of Plant Systemic Acquired Resistance Regulate NPR1 Function through Redox Changes
Mou, Z., Fan, W., & Dong, X. (2003) · Cell · doi:10.1016/s0092-8674(03)00429-x · Cited by 1,588 · see citing works
The Arabidopsis NPR1 Gene That Controls Systemic Acquired Resistance Encodes a Novel Protein Containing Ankyrin Repeats
Cao, H., Glazebrook, J., Clarke, J. D., Volko, S. M., & Dong, X. (1997) · Cell · doi:10.1016/s0092-8674(00)81858-9 · Cited by 1,572 · see citing works
pGreen: a versatile and flexible binary Ti vector for Agrobacterium-mediated plant transformation
Hellens, R. P., Edwards, E. A., Leyland, N., Bean, S., & Mullineaux, P. M. (2000) · Plant Molecular Biology · doi:10.1023/a:1006496308160 · Cited by 1,568 · see citing works
SMART: a web-based tool for the study of genetically mobile domains
Schultz, J. (2000) · Nucleic Acids Research · doi:10.1093/nar/28.1.231 · Cited by 1,373 · see citing works
Removal of a cryptic intron and subcellular localization of green fluorescent protein are required to mark transgenic Arabidopsis plants brightly
Haseloff, J. P., Siemering, K. R., Prasher, D. C., & Hodge, S. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.6.2122 · Cited by 1,322 · see citing works
NPR1, all things considered.
Dong, X.-N. (2004) · Current opinion in plant biology · doi:10.1016/j.pbi.2004.07.005 · Cited by 841 · see citing works
Asymmetric leaves1 mediates leaf patterning and stem cell function in Arabidopsis
Byrne, M. E., Barley, R., Curtis, M. D., Arroyo, J. M., Dunham, M. J., Hudson, A., & Martienssen, R. A. (2000) · Nature · doi:10.1038/35050091 · Cited by 816 · see citing works
Origin of floral asymmetry in Antirrhinum
Luo, D., Carpenter, R., Vincent, C. A., Copsey, L., & Coen, E. (1996) · Nature · doi:10.1038/383794a0 · Cited by 783 · see citing works
Cell Cycling and Cell Enlargement in Developing Leaves of Arabidopsis
Donnelly, P. M., Bonetta, D. T., Tsukaya, H., Dengler, R. E., & Dengler, N. G. (1999) · Developmental Biology · doi:10.1006/dbio.1999.9443 · Cited by 758 · see citing works
Auxin transport — shaping the plant
Friml, J. (2003) · Current Opinion in Plant Biology · doi:10.1016/s1369526602000031 · Cited by 739 · see citing works
Nuclear Localization of NPR1 Is Required for Activation of PR Gene Expression
Kinkema, M., Fan, W., & Dong, X. (2000) · The Plant Cell · doi:10.1105/tpc.12.12.2339 · Cited by 718 · see citing works
Interaction of NPR1 with basic leucine zipper protein transcription factors that bind sequences required for salicylic acid induction of the PR-1 gene
Zhang, Y., Fan, W., Kinkema, M., Li, X., & Dong, X. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.11.6523 · Cited by 717 · see citing works
Self-citation
The A. thaliana disease resistance gene RPS2 encodes a protein containing a nucleotide-binding site and leucine-rich repeats
Mindrinos, M. N., Katagiri, F., Yu, G.-L., & Ausubel, F. M. (1994) · Cell · doi:10.1016/0092-8674(94)90282-8 · Cited by 713 · see citing works
The Arabidopsis NPR1/NIM1 Protein Enhances the DNA Binding Activity of a Subgroup of the TGA Family of bZIP Transcription Factors
Després, C., DeLong, C. M. O., Glaze, S., Liu, E., & Fobert, P. R. (2000) · The Plant Cell · doi:10.1105/tpc.12.2.279 · Cited by 599 · see citing works
Leaf polarity and meristem formation in Arabidopsis
McConnell, J. R., & Barton, M. K. (1998) · Development · doi:10.1242/dev.125.15.2935 · Cited by 592 · see citing works
The Arabidopsis NPR1 Disease Resistance Protein Is a Novel Cofactor That Confers Redox Regulation of DNA Binding Activity to the Basic Domain/Leucine Zipper Transcription Factor TGA1
Després, C., Chubak, C., Rochon, A., Clark, R., Bethune, T. D., Desveaux, D., & Fobert, P. R. (2003) · The Plant Cell · doi:10.1105/tpc.012849 · Cited by 592 · see citing works
NPR1 Differentially Interacts with Members of the TGA/OBF Family of Transcription Factors That Bind an Element of the PR-1 Gene Required for Induction by Salicylic Acid
Zhou, J., Trifa, Y., Silva, H., Pontier, D., Lam, E., Shah, J., & Klessig, D. F. (2000) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2000.13.2.191 · Cited by 541 · see citing works
A BSCISSION , D EHISCENCE, AND O THER C ELL S EPARATION P ROCESSES
Roberts, J. A., Elliott, K. A., & González-Carranza, Z. H. (2002) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.53.092701.180236 · Cited by 527 · see citing works
Knockout Analysis of Arabidopsis Transcription Factors TGA2 , TGA5 , and TGA6 Reveals Their Redundant and Essential Roles in Systemic Acquired Resistance
Zhang, Y., Tessaro, M. J., Lassner, M., & Li, X. (2003) · The Plant Cell · doi:10.1105/tpc.014894 · Cited by 518 · see citing works
Self-citation
phantastica: a gene required for dorsoventrality of leaves in Antirrhinum majus
Waites, R., & Hudson, A. (1995) · Development · doi:10.1242/dev.121.7.2143 · Cited by 504 · see citing works
The PHANTASTICA Gene Encodes a MYB Transcription Factor Involved in Growth and Dorsoventrality of Lateral Organs in Antirrhinum
Waites, R., Selvadurai, H. R. N., Oliver, I. R., & Hudson, A. (1998) · Cell · doi:10.1016/s0092-8674(00)81439-7 · Cited by 487 · see citing works
Cell Biology of Abscission
Sexton, R., & Roberts, J. A. (1982) · Annual Review of Plant Physiology · doi:10.1146/annurev.pp.33.060182.001025 · Cited by 473 · see citing works
The ASYMMETRIC LEAVES2 gene of Arabidopsis thaliana regulates formation of a symmetric lamina, establishment of venation and repression of meristem-related homeobox genes in leaves
Semiarti, E., Ueno, Y., Tsukaya, H., Iwakawa, H., Machida, C., & Machida, Y. (2001) · Development · doi:10.1242/dev.128.10.1771 · Cited by 470 · see citing works
ETTIN patterns the Arabidopsis floral meristem and reproductive organs
Sessions, A., Nemhauser, J. L., McCall, A., Roe, J. L., Feldmann, K. A., & Zambryski, P. (1997) · Development · doi:10.1242/dev.124.22.4481 · Cited by 465 · see citing works
THE ROLE OF KNOX GENES IN PLANT DEVELOPMENT
Hake, S., Smith, H. M. S., Holtan, H., Magnani, E., Mele, G., & Ramirez, J. C. (2004) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.20.031803.093824 · Cited by 456 · see citing works
Mechanisms that control knox gene expression in the Arabidopsis shoot
Ori, N., Eshed, Y., Chuck, G. S., Bowman, J. L., & Hake, S. (2000) · Development · doi:10.1242/dev.127.24.5523 · Cited by 455 · see citing works
Last exit: senescence, abscission, and meristem arrest in Arabidopsis.
Bleecker, A. B., & Patterson, S. E. (1997) · The Plant Cell · doi:10.1105/tpc.9.7.1169 · Cited by 436 · see citing works
The ASYMMETRIC LEAVES2 Gene of Arabidopsis thaliana, Required for Formation of a Symmetric Flat Leaf Lamina, Encodes a Member of a Novel Family of Proteins Characterized by Cysteine Repeats and a Leucine Zipper
Iwakawa, H., Ueno, Y., Semiarti, E., Onouchi, H., Kojima, S., Tsukaya, H., Hasebe, M., Soma, T., Ikezaki, M., Machida, C., et al. (2002) · Plant and Cell Physiology · doi:10.1093/pcp/pcf077 · Cited by 428 · see citing works
Control of Organ Asymmetry in Flowers of Antirrhinum
Luo, D., Carpenter, R., Copsey, L., Vincent, C. A., Clark, J., & Coen, E. (1999) · Cell · doi:10.1016/s0092-8674(00)81523-8 · Cited by 427 · see citing works
Cullin‐based ubiquitin ligases: Cul3–BTB complexes join the family
Pintard, L., Willems, A. R., & Peter, M. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600186 · Cited by 413 · see citing works
ASYMMETRIC LEAVES1revealsknoxgene redundancy inArabidopsis
Byrne, M. E., Simorowski, J., & Martienssen, R. A. (2002) · Development · doi:10.1242/dev.129.8.1957 · Cited by 407 · see citing works
Novelas1andas2defects in leaf adaxial-abaxial polarity reveal the requirement forASYMMETRIC LEAVES1and2andERECTAfunctions in specifying leaf adaxial identity
Xu, L., Xu, Y., Dong, A., Sun, Y., Pi, L., Xu, Y., & Huang, H. Y. (2003) · Development · doi:10.1242/dev.00622 · Cited by 356 · see citing works
All in the Family: the BTB/POZ, KRAB, and SCAN Domains
Collins, T., Stone, J. R., & Williams, A. J. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.11.3609-3615.2001 · Cited by 345 · see citing works
The Arabidopsis LATERAL ORGAN BOUNDARIES-Domain Gene ASYMMETRIC LEAVES2 Functions in the Repression of KNOX Gene Expression and in Adaxial-Abaxial Patterning
Lin, W.-C. (2003) · The Plant Cell · doi:10.1105/tpc.014969 · Cited by 316 · see citing works
Significance of the Expression of the CER6 Condensing Enzyme for Cuticular Wax Production in Arabidopsis
Hooker, T. S., Millar, A. A., & Kunst, L. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.003707 · Cited by 312 · see citing works
The role of JAGGED in shaping lateral organs
Dinneny, J. R., Yadegari, R., Fischer, R. L., Yanofsky, M. F., & Weigel, D. (2004) · Development · doi:10.1242/dev.00949 · Cited by 311 · see citing works
Establishment of polarity in angiosperm lateral organs
Bowman, J. L., Eshed, Y., & Baum, S. F. (2002) · Trends in Genetics · doi:10.1016/s0168-9525(01)02601-4 · Cited by 299 · see citing works
Plant Respiratory Burst Oxidase Homologs Impinge on Wound Responsiveness and Development inLycopersicon esculentum [W]
Sagi, M., Davydov, O., Orazova, S., Yesbergenova, Z., Ophir, R., Stratmann, J. W., & Fluhr, R. (2004) · The Plant Cell · doi:10.1105/tpc.019398 · Cited by 278 · see citing works
The Arabidopsis JAGGED gene encodes a zinc finger protein that promotes leaf tissue development
Ohno, C. K., Reddy, G. V., Heisler, M. G., & Meyerowitz, E. M. (2004) · Development · doi:10.1242/dev.00991 · Cited by 271 · see citing works
AP2 Gene Determines the Identity of Perianth Organs in Flowers of Arabidopsis thaliana.
Kunst, L., Klenz, J. E., Martínez-Zapater, J. M., & Haughn, G. W. (1989) · The Plant Cell · doi:10.1105/tpc.1.12.1195 · Cited by 247 · see citing works
Self-citation
The Arabidopsis BELL1 and KNOX TALE Homeodomain Proteins Interact through a Domain Conserved between Plants and Animals
Bellaoui, M., Pidkowich, M. S., Samach, A., Kushalappa, K., Kohalmi, S. E., Modrusan, Z., Crosby, W. L., & Haughn, G. W. (2001) · The Plant Cell · doi:10.1105/tpc.010161 · Cited by 232 · see citing works
Self-citation
The PERIANTHIA gene encodes a bZIP protein involved in the determination of floral organ number in Arabidopsis thalianaPreprint
Chuang, C., Running, M., Williams, R. W., & Meyerowitz, E. M. (1999) · Genes & Development · doi:10.1101/gad.13.3.334 · Cited by 231 · see citing works
The cellular parameters of leaf development in tobacco: a clonal analysis
Poethig, R. S., & Sussex, I. M. (1985) · Planta · doi:10.1007/bf00395039 · Cited by 218 · see citing works
Evolution of floral symmetry
Endress, P. K. (2001) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(00)00140-0 · Cited by 212 · see citing works
TheBLADE-ON-PETIOLE 1gene controls leaf pattern formation through the modulation of meristematic activity inArabidopsis
Ha, C. M., Kim, G., Kim, B. C., Jun, J. H., Soh, M., Ueno, Y., Machida, Y., Tsukaya, H., & Nam, H. G. (2002) · Development · doi:10.1242/dev.00196 · Cited by 202 · see citing works
Homeotic Transformation of Ovules into Carpel-like Structures in Arabidopsis.
Modrusan, Z. D., Reiser, L., Feldmann, K. A., Fischer, R. L., & Haughn, G. W. (1994) · The Plant Cell · doi:10.1105/tpc.6.3.333 · Cited by 201 · see citing works
Self-citation
MUCILAGE-MODIFIED4 Encodes a Putative Pectin Biosynthetic Enzyme Developmentally Regulated by APETALA2, TRANSPARENT TESTA GLABRA1 , and GLABRA2 in the Arabidopsis Seed Coat
Western, T. L., Young, D. S., Dean, G. H., Tan, W. L., Samuels, L., & Haughn, G. W. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.035519 · Cited by 197 · see citing works
Self-citation
Nuclear export of proteins in plants: AtXPO1 is the export receptor for leucine‐rich nuclear export signals in Arabidopsis thaliana
Haasen, D., Köhler, C., Neuhaus, G., & Merkle, T. (1999) · The Plant Journal · doi:10.1046/j.1365-313x.1999.00644.x · Cited by 197 · see citing works
BLADE-ON-PETIOLE1 Encodes a BTB/POZ Domain Protein Required for Leaf Morphogenesis in Arabidopsis thaliana
Ha, C. M., Jun, J. H., Nam, H. G., & Fletcher, J. C. (2004) · Plant and Cell Physiology · doi:10.1093/pcp/pch201 · Cited by 190 · see citing works
A role for salicylic acid and NPR1 in regulating cell growth in Arabidopsis
Vanacker, H., Lu, H., Rate, D. N., & Greenberg, J. T. (2001) · The Plant Journal · doi:10.1046/j.1365-313x.2001.01158.x · Cited by 186 · see citing works
Mutations in the PERIANTHIA gene of Arabidopsis specifically alter floral organ number and initiation pattern
Running, M., & Meyerowitz, E. M. (1996) · Development · doi:10.1242/dev.122.4.1261 · Cited by 164 · see citing works
Activation tagging of theLEAFY PETIOLEgene affects leaf petiole development inArabidopsis thaliana
van der Graaff, E., den Dulk‐Ras, A., Hooykaas, P. J. J., & Keller, B. (2000) · Development · doi:10.1242/dev.127.22.4971 · Cited by 155 · see citing works
Ancient asymmetries in the evolution of flowers
Cubas, P., Coen, E., & Martínez-Zapater, J. M. (2001) · Current Biology · doi:10.1016/s0960-9822(01)00295-0 · Cited by 149 · see citing works
ASYMMETRIC LEAVES1 , an Arabidopsis gene that is involved in the control of cell differentiation in leaves
Sun, Y., Zhou, Q., Zhang, W., Fu, Y.-L., & Huang, H. Y. (2002) · Planta · doi:10.1007/s004250100673 · Cited by 125 · see citing works
Coordinated activation of as-1-type elements and a tobacco glutathione S-transferase gene by auxins, salicylic acid, methyl-jasmonate and hydrogen peroxide
Xiang, C., Miao, Z., & Lam, E. (1996) · Plant Molecular Biology · doi:10.1007/bf00019093 · Cited by 124 · see citing works
The ULTRAPETALA gene controls shoot and floral meristem size in Arabidopsis
Fletcher, J. C. (2001) · Development · doi:10.1242/dev.128.8.1323 · Cited by 119 · see citing works
Development of leaf shape
Byrne, M. E., Timmermans, M. C. P., Kidner, C. A., & Martienssen, R. A. (2001) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(00)00133-3 · Cited by 88 · see citing works
D EVELOPMENT OF S YMMETRY IN P LANTS
Hudson, A. (2000) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.51.1.349 · Cited by 67 · see citing works
Auxin Signaling
Rogg, L. E., & Bartel, B. (2001) · Developmental Cell · doi:10.1016/s1534-5807(01)00077-6 · Cited by 66 · see citing works
Morphogenesis of Flowers—Our Evolving View
Smyth, D. R. (2005) · The Plant Cell · doi:10.1105/tpc.104.030353 · Cited by 61 · see citing works
Protein Degradation: CUL-3 and BTB – Partners in Proteolysis
van den Heuvel, S. (2004) · Current Biology · doi:10.1016/j.cub.2003.12.044 · Cited by 52 · see citing works
Identification and characterization of protein interactions using the yeast 2-hybrid system
Kohalmi, S. E., Reader, L. J. V., Samach, A., Nowak, J., Haughn, G. W., & Crosby, W. L. (1998) · Springer eBooks · doi:10.1007/978-94-011-5242-6_6 · Cited by 34 · see citing works
Self-citation
A New Twist on Systemic Acquired Resistance: Redox Control of the NPR1–TGA1 Interaction by Salicylic Acid
Eckardt, N. A. (2003) · The Plant Cell · doi:10.1105/tpc.150910 · Cited by 18 · see citing works

Flagged first, then by citations

Sorted by citations

Redox Regulation in Photosynthetic Organisms: Signaling, Acclimation, and Practical Implications
Foyer, C. H., & Noctor, G. (2008) · Antioxidants and Redox Signaling · doi:10.1089/ars.2008.2177 · Cited by 1,436 · see citing works
The Cullin-RING Ubiquitin-Protein Ligases
Hua, Z., & Vierstra, R. D. (2011) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-042809-112256 · Cited by 509 · see citing works
Identification of the Wax Ester Synthase/Acyl-Coenzyme A:Diacylglycerol Acyltransferase WSD1 Required for Stem Wax Ester Biosynthesis in Arabidopsis
Li, F., Wu, X., Lam, P. M. W., Bird, D. A., Zheng, H., Samuels, L., Jetter, R., & Kunst, L. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.123471 · Cited by 454 · see citing works
MECHANISM OF LEAF-SHAPE DETERMINATION
Tsukaya, H. (2006) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.57.032905.105320 · Cited by 383 · see citing works
The EPIP Peptide of INFLORESCENCE DEFICIENT IN ABSCISSION Is Sufficient to Induce Abscission in Arabidopsis through the Receptor-Like Kinases HAESA and HAESA-LIKE2
Stenvik, G., Tandstad, N. M., Guo, Y., Shi, C., Kristiansen, W., Holmgren, A., Clark, S. E., Aalen, R. B., & Butenko, M. A. (2008) · The Plant Cell · doi:10.1105/tpc.108.059139 · Cited by 341 · see citing works
Resistance to pathogens and host developmental stage: a multifaceted relationship within the plant kingdom.
Develey-Rivière, M.-P., & Galiana, E. (2007) · New Phytologist · doi:10.1111/j.1469-8137.2007.02130.x · Cited by 304 · see citing works
Twenty years on: The inner workings of the shoot apical meristem, a developmental dynamo
Barton, M. K. (2010) · Developmental Biology · doi:10.1016/j.ydbio.2009.11.029 · Cited by 372 · see citing works
The NONEXPRESSOR OF PATHOGENESIS-RELATED GENES 1 (NPR1) and Related Family: Mechanistic Insights in Plant Disease Resistance
Backer, R., Naidoo, S., & van den Berg, N. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.00102 · Cited by 325 · see citing works
Elucidating mechanisms underlying organ abscission
Estornell, L. H., Agustí, J., Merelo, P., Talón, M., & Tadeo, F. R. (2012) · Plant Science · doi:10.1016/j.plantsci.2012.10.008 · Cited by 317 · see citing works
Molecular Mechanisms of Leaf Morphogenesis
Du, F., Guan, C., & Jiao, Y. (2018) · Molecular Plant · doi:10.1016/j.molp.2018.06.006 · Cited by 283 · see citing works
Salicylic acid signal transduction: the initiation of biosynthesis, perception and transcriptional reprogramming
Seyfferth, C., & Tsuda, K. (2014) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00697 · Cited by 278 · see citing works
Negative regulation of defense responses in Arabidopsis by two NPR1 paralogs
Zhang, Y., Cheng, Y., Qu, N., Zhao, Q., Bi, D.-L., & Li, X. (2006) · The Plant Journal · doi:10.1111/j.1365-313x.2006.02903.x · Cited by 271 · see citing works
Self-citation
CRISPR/Cas9-Mediated SlNPR1 mutagenesis reduces tomato plant drought tolerance
Li, R., Liu, C., Zhao, R., Wang, L., Chen, L., Yu, W., Zhang, S., Sheng, J., & Shen, L. (2019) · BMC Plant Biology · doi:10.1186/s12870-018-1627-4 · Cited by 269 · see citing works
Arabidopsis Basic Leucine-Zipper Transcription Factors TGA9 and TGA10 Interact with Floral Glutaredoxins ROXY1 and ROXY2 and Are Redundantly Required for Anther Development
Murmu, J., Bush, M. J., DeLong, C. M. O., Li, S., Xu, M., Khan, M., Malcolmson, C., Fobert, P. R., Zachgo, S., & Hepworth, S. R. (2010) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.159111 · Cited by 254 · see citing works
Self-citation
The maize SBP-box transcription factor encoded by tasselsheath4 regulates bract development and the establishment of meristem boundaries
Chuck, G. S., Whipple, C., Jackson, D. P., & Hake, S. (2010) · Development · doi:10.1242/dev.048348 · Cited by 246 · see citing works
From Pioneers to Team Players: TGA Transcription Factors Provide a Molecular Link Between Different Stress Pathways
Gatz, C. (2012) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-04-12-0078-ia · Cited by 227 · see citing works
Stamen Abscission Zone Transcriptome Profiling Reveals New Candidates for Abscission Control: Enhanced Retention of Floral Organs in Transgenic Plants Overexpressing ArabidopsisZINC FINGER PROTEIN2
Cai, S., & Lashbrook, C. C. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.107.110908 · Cited by 220 · see citing works
Tell me more: roles of NPRs in plant immunity
Pajerowska-Mukhtar, K. M., Emerine, D. K., & Mukhtar, M. S. (2013) · Trends in Plant Science · doi:10.1016/j.tplants.2013.04.004 · Cited by 218 · see citing works
TheBLADE-ON-PETIOLEgenes are essential for abscission zone formation inArabidopsis
McKim, S. M., Stenvik, G., Butenko, M. A., Kristiansen, W., Cho, S. K., Hepworth, S. R., Aalen, R. B., & Haughn, G. W. (2008) · Development · doi:10.1242/dev.012807 · Cited by 212 · see citing works
Self-citation
The LEAFY target LMI1 is a meristem identity regulator and acts together with LEAFY to regulate expression of CAULIFLOWER
Saddic, L., Huvermann, B., Bezhani, S., Su, Y., Winter, C. M., Kwon, C. S., Collum, R. P., & Wagner, D. (2006) · Development · doi:10.1242/dev.02331 · Cited by 200 · see citing works
TheArabidopsisBEL1-LIKE HOMEODOMAIN Proteins SAW1 and SAW2 Act Redundantly to RegulateKNOXExpression Spatially in Leaf Margins
Kumar, R. S., Kushalappa, K. M., Godt, D. E., Pidkowich, M. S., Pastorelli, S., Hepworth, S. R., & Haughn, G. W. (2007) · The Plant Cell · doi:10.1105/tpc.106.048769 · Cited by 199 · see citing works
Self-citation
Plant separation: 50 ways to leave your mother
Lewis, M. W., Leslie, M. E., & Liljegren, S. J. (2005) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2005.11.009 · Cited by 188 · see citing works
Repression of the Arabidopsis thaliana Jasmonic Acid/Ethylene-Induced Defense Pathway by TGA-Interacting Glutaredoxins Depends on Their C-Terminal ALWL Motif
Zander, M., Chen, S., Imkampe, J., Thurow, C., & Gatz, C. (2011) · Molecular Plant · doi:10.1093/mp/ssr113 · Cited by 186 · see citing works
BLADE-ON-PETIOLE1and2ControlArabidopsisLateral Organ Fate through Regulation of LOB Domain and Adaxial-Abaxial Polarity Genes
Ha, C. M., Jun, J. H., Nam, H. G., & Fletcher, J. C. (2007) · The Plant Cell · doi:10.1105/tpc.107.051938 · Cited by 187 · see citing works
Overexpression of INFLORESCENCE DEFICIENT IN ABSCISSION Activates Cell Separation in Vestigial Abscission Zones in Arabidopsis
Stenvik, G., Butenko, M. A., Urbanowicz, B. R., Rose, J. K. C., & Aalen, R. B. (2006) · The Plant Cell · doi:10.1105/tpc.106.042036 · Cited by 173 · see citing works
Ubiquitin ligases mediate growth and development by promoting protein death
Stone, S. L., & Callis, J. (2007) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2007.07.010 · Cited by 170 · see citing works
Control of inflorescence architecture in tomato by BTB/POZ transcriptional regulatorsPreprint
Cao, X., Park, S. J., Eck, J. M. V., & Lippman, Z. B. (2016) · Genes & Development · doi:10.1101/gad.288415.116 · Cited by 169 · see citing works
Post-translational regulation of plant bZIP factors
Schütze, K., Harter, K., & Chaban, C. (2008) · Trends in Plant Science · doi:10.1016/j.tplants.2008.03.002 · Cited by 166 · see citing works
LATERAL ORGAN FUSION1 and LATERAL ORGAN FUSION2 function in lateral organ separation and axillary meristem formation in Arabidopsis
Lee, D.-K., Geisler, M., & Springer, P. S. (2009) · Development · doi:10.1242/dev.031971 · Cited by 164 · see citing works
Active suppression of a leaf meristem orchestrates determinate leaf growth
Alvarez, J. P., Furumizu, C., Efroni, I., Eshed, Y., & Bowman, J. L. (2016) · eLife · doi:10.7554/elife.15023 · Cited by 155 · see citing works
Arabidopsis Class I KNOTTED-Like Homeobox Proteins Act Downstream in the IDA-HAE/HSL2 Floral Abscission Signaling Pathway
Shi, C., Stenvik, G., Vie, A. K., Bones, A. M., Pautot, V., Proveniers, M. C. G., Aalen, R. B., & Butenko, M. A. (2011) · The Plant Cell · doi:10.1105/tpc.111.084608 · Cited by 160 · see citing works
NUBBINandJAGGEDdefine stamen and carpel shape inArabidopsis
Dinneny, J. R., Weigel, D., & Yanofsky, M. F. (2006) · Development · doi:10.1242/dev.02335 · Cited by 156 · see citing works
Genetic control of shoot organ boundaries
Aida, M., & Tasaka, M. (2005) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2005.11.011 · Cited by 155 · see citing works
Insertional mutant analysis reveals that long-chain acyl-CoA synthetase 1 (LACS1), but not LACS8, functionally overlaps with LACS9 in Arabidopsis seed oil biosynthesis
Zhao, L., Katavić, V., Li, F., Haughn, G. W., & Kunst, L. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04396.x · Cited by 151 · see citing works
Self-citation
Transcription Repressor HANABA TARANU Controls Flower Development by Integrating the Actions of Multiple Hormones, Floral Organ Specification Genes, and GATA3 Family Genes inArabidopsis
Zhang, X., Zhou, Y., Ding, L., Wu, Z., Liu, R., & Meyerowitz, E. M. (2013) · The Plant Cell · doi:10.1105/tpc.112.107854 · Cited by 148 · see citing works
BLADE-ON-PETIOLE1 Coordinates Organ Determinacy and Axial Polarity in Arabidopsis by Directly Activating ASYMMETRIC LEAVES2
Jun, J. H., Ha, C. M., & Fletcher, J. C. (2010) · The Plant Cell · doi:10.1105/tpc.109.070763 · Cited by 145 · see citing works
BLADE-ON-PETIOLE proteins act in an E3 ubiquitin ligase complex to regulate PHYTOCHROME INTERACTING FACTOR 4 abundance
Zhang, B., Holmlund, M., Lorrain, S., Norberg, M., Bakó, L., Fankhauser, C., & Nilsson, O. R. (2017) · eLife · doi:10.7554/elife.26759 · Cited by 143 · see citing works
FASCIATED EAR4 Encodes a bZIP Transcription Factor That Regulates Shoot Meristem Size in Maize
Pautler, M., Eveland, A. L., LaRue, T., Yang, F., Weeks, R., Lunde, C. F., Je, B. I., Meeley, R. B., Komatsu, M., Vollbrecht, E., et al. (2015) · The Plant Cell · doi:10.1105/tpc.114.132506 · Cited by 141 · see citing works
The Nitrate-Responsive Protein MdBT2 Regulates Anthocyanin Biosynthesis by Interacting with the MdMYB1 Transcription Factor
Wang, X., An, J., Liu, X., Su, L., You, C., & Hao, Y. (2018) · PLANT PHYSIOLOGY · doi:10.1104/pp.18.00244 · Cited by 141 · see citing works
LnIs a Key Regulator of Leaflet Shape and Number of Seeds per Pod in Soybean
Jeong, N., Suh, S. J., Kim, M.-H., Lee, S.-K., Moon, J., Kim, H. S., & Jeong, S. (2012) · The Plant Cell · doi:10.1105/tpc.112.104968 · Cited by 140 · see citing works
Control of lateral organ development and flowering time by the Arabidopsis thaliana MADS-box Gene AGAMOUS-LIKE6
Koo, S. C., Bracko, O., Park, M. S., Schwab, R., Chun, H. J., Park, K. M., Seo, J. S., Grbić, V., Balasubramanian, S., Schmid, M., et al. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04192.x · Cited by 133 · see citing works
NODULE ROOT and COCHLEATA Maintain Nodule Development and Are Legume Orthologs of Arabidopsis BLADE-ON-PETIOLE Genes
Couzigou, J.-M., Zhukov, V., Mondy, S., Abu el Heba, G., Cosson, V., Ellis, T. H. N., Ambrose, M., Wen, J., Tadege, M., Tikhonovich, I., et al. (2012) · The Plant Cell · doi:10.1105/tpc.112.103747 · Cited by 145 · see citing works
Regulation of membrane trafficking and organ separation by the NEVERSHED ARF-GAP protein
Liljegren, S. J., Leslie, M. E., Darnielle, L., Lewis, M. W., Taylor, S. M., Luo, R., Geldner, N., Chory, J., Randazzo, P. A., Yanofsky, M. F., et al. (2009) · Development · doi:10.1242/dev.033605 · Cited by 122 · see citing works
Shoot Apical Meristem Form and Function
Ha, C. M., Jun, J. H., & Fletcher, J. C. (2010) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(10)91004-1 · Cited by 119 · see citing works
Nitric oxide molecular targets: reprogramming plant development upon stress
Sánchez-Vicente, I., Fernández-Espinosa, M. G., & Lorenzo, Ó. (2019) · Journal of Experimental Botany · doi:10.1093/jxb/erz339 · Cited by 121 · see citing works
The MADS box gene, FOREVER YOUNG FLOWER, acts as a repressor controlling floral organ senescence and abscission in Arabidopsis
Chen, M., Hsu, W., Lee, P., Thiruvengadam, M., Chen, H., & Yang, C. (2011) · The Plant Journal · doi:10.1111/j.1365-313x.2011.04677.x · Cited by 121 · see citing works
BTB and TAZ domain scaffold proteins perform a crucial function in Arabidopsis development
Robert, H. S., Quint, A., Brand, D., Vivian‐Smith, A., & Offringa, R. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2008.03764.x · Cited by 119 · see citing works
Class I KNOX transcription factors promote differentiation of cambial derivatives into xylem fibers in the Arabidopsis hypocotyl
Liebsch, D., Sunaryo, W., Holmlund, M., Norberg, M., Zhang, J., Hall, H., Helizon, H., Jin, X., Helariutta, Y., Nilsson, O. R., et al. (2014) · Development · doi:10.1242/dev.111369 · Cited by 116 · see citing works
NONEXPRESSOR OF PATHOGENESIS‐RELATED PROTEINS1 (NPR1) and some NPR1‐related proteins are sensitive to salicylic acid
Maier, F., ZWICKER, S., Hückelhoven, A. G., MEISSNER, M., FUNK, J., Pfitzner, A. J. P., & Pfitzner, U. M. (2010) · Molecular Plant Pathology · doi:10.1111/j.1364-3703.2010.00653.x · Cited by 116 · see citing works
Ideal crop plant architecture is mediated by tassels replace upper ears1, a BTB/POZ ankyrin repeat gene directly targeted by TEOSINTE BRANCHED1
Dong, Z., Li, W., Unger‐Wallace, E., Yang, J., Vollbrecht, E., & Chuck, G. S. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1714960114 · Cited by 113 · see citing works
ROS-mediated redox signaling during cell differentiation in plants
Schmidt, R., & Schippers, J. H. M. (2014) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2014.12.020 · Cited by 111 · see citing works
Characterization of Vitis vinifera NPR1 homologs involved in the regulation of Pathogenesis-Related gene expression
Hénanff, G. L., Heitz, T., Mestre, P., Mutterer, J., Walter, B., & Chong, J. (2009) · BMC Plant Biology · doi:10.1186/1471-2229-9-54 · Cited by 111 · see citing works
Clade I TGACG-Motif Binding Basic Leucine Zipper Transcription Factors Mediate BLADE-ON-PETIOLE-Dependent Regulation of Development
Wang, Y., Salasini, B. C., Khan, M., Devi, B., Bush, M. J., Subramaniam, R., & Hepworth, S. R. (2019) · PLANT PHYSIOLOGY · doi:10.1104/pp.18.00805 · Cited by 107 · see citing works
Self-citation
Divide et impera: boundaries shape the plant body and initiate new meristems
Wang, Q., Hasson, A., Rossmann, S., & Theres, K. (2016) · New Phytologist · doi:10.1111/nph.13641 · Cited by 106 · see citing works
A Conserved Mechanism of Bract Suppression in the Grass Family
Whipple, C., Hall, D. H., DeBlasio, S. L., Taguchi‐Shiobara, F., Schmidt, R. J., & Jackson, D. P. (2010) · The Plant Cell · doi:10.1105/tpc.109.073536 · Cited by 106 · see citing works
ArabidopsisClade I TGA Transcription Factors Regulate Plant Defenses in an NPR1-Independent Fashion
Shearer, H. L., Cheng, Y., Wang, L., Liu, J., Boyle, P., Després, C., Zhang, Y., Li, X., & Fobert, P. R. (2012) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-09-11-0256 · Cited by 105 · see citing works
Self-citation
Cloning and characterization of a Verticillium wilt resistance gene from Gossypium barbadense and functional analysis in Arabidopsis thaliana
Zhang, Y., Wang, X., Yang, S., Chi, J., Zhang, G., & Ma, Z. (2011) · Plant Cell Reports · doi:10.1007/s00299-011-1115-x · Cited by 103 · see citing works
Self-citation
Overexpression of NPR1 in Brassica juncea Confers Broad Spectrum Resistance to Fungal Pathogens
Ali, S., Mir, Z. A., Tyagi, A., Gebremedhn, H. M., Meena, R. P., Bhat, J. A., Yadav, P., Papalou, P., Rawat, S., & Grover, A. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.01693 · Cited by 102 · see citing works
Beyond the Divide: Boundaries for Patterning and Stem Cell Regulation in Plants
Hepworth, S. R., & Pautot, V. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.01052 · Cited by 102 · see citing works
Self-citation
Patterning the female side of Arabidopsis: the importance of hormones
Balanzà, V., Navarrete, M., Trigueros, M., & Ferrándiz, C. (2006) · Journal of Experimental Botany · doi:10.1093/jxb/erl188 · Cited by 97 · see citing works
Functional Overlap of Long-Chain Acyl-CoA Synthetases in Arabidopsis
Zhao, L., Haslam, T. M., Sonntag, A., Molina, I., & Kunst, L. (2019) · Plant and Cell Physiology · doi:10.1093/pcp/pcz019 · Cited by 98 · see citing works
Arabidopsis BLADE-ON-PETIOLE1 and 2 promote floral meristem fate and determinacy in a previously undefined pathway targeting APETALA1 and AGAMOUS-LIKE24
Xu, M., Hu, T., McKim, S. M., Murmu, J., Haughn, G. W., & Hepworth, S. R. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04299.x · Cited by 97 · see citing works
Self-citation
Structure‐function analysis of npr1 alleles in Arabidopsis reveals a role for its paralogs in the perception of salicylic acid
Canet, J. V., Dobón, A., ROIG, A., & Tornero, P. (2010) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2010.02194.x · Cited by 96 · see citing works
Core Mechanisms Regulating Developmentally Timed and Environmentally Triggered Abscission
Patharkar, O. R., & Walker, J. C. (2016) · PLANT PHYSIOLOGY · doi:10.1104/pp.16.01004 · Cited by 96 · see citing works
From genes to networks: The genetic control of leaf development
Wang, H., Kong, F., & Zhou, C. (2021) · Journal of Integrative Plant Biology · doi:10.1111/jipb.13084 · Cited by 98 · see citing works
The Barley Uniculme4 Gene Encodes a BLADE-ON-PETIOLE-Like Protein That Controls Tillering and Leaf Patterning
Tavakol, E., Okagaki, R., Verderio, G., Shariati J., V., Hussien, A., Bilgic, H., Scanlon, M. J., Todt, N. R., Close, T. J., Druka, A., et al. (2015) · Plant Physiology · doi:10.1104/pp.114.252882 · Cited by 97 · see citing works
HAWAIIAN SKIRT: An F-Box Gene That Regulates Organ Fusion and Growth in Arabidopsis
González-Carranza, Z. H., Rompa, U., Peters, J. L., Bhatt, A. M., Wagstaff, C., Stead, A. D., & Roberts, J. A. (2007) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.092288 · Cited by 90 · see citing works
Antagonistic Interaction of BLADE-ON-PETIOLE1 and 2 with BREVIPEDICELLUS and PENNYWISE Regulates Arabidopsis Inflorescence Architecture
Khan, M., Xu, M., Murmu, J., Tabb, P., Liu, Y., Storey, K. M., McKim, S. M., Douglas, C. J., & Hepworth, S. R. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.188573 · Cited by 93 · see citing works
Self-citation
A Role forArabidopsis PUCHIin Floral Meristem Identity and Bract Suppression
Karim, M. R., Hirota, A., Kwiatkowska, D., Tasaka, M., & Aida, M. (2009) · The Plant Cell · doi:10.1105/tpc.109.067025 · Cited by 93 · see citing works
Four shades of detachment: Regulation of floral organ abscission
Kim, J. (2014) · Plant Signaling & Behavior · doi:10.4161/15592324.2014.976154 · Cited by 92 · see citing works
The poetry of reproduction: the role of LEAFY in Arabidopsis thaliana flower formation
Siriwardana, N. S., & Lamb, R. S. (2012) · The International Journal of Developmental Biology · doi:10.1387/ijdb.113450ns · Cited by 91 · see citing works
CUL3 E3 ligases in plant development and environmental response
Ban, Z., & Estelle, M. A. (2021) · Nature Plants · doi:10.1038/s41477-020-00833-6 · Cited by 88 · see citing works
Pyridine Nucleotide Cycling and Control of Intracellular Redox State in Relation to Poly (ADP-Ribose) Polymerase Activity and Nuclear Localization of Glutathione during Exponential Growth of Arabidopsis Cells in Culture
Pellny, T. K., Locato, V., Díaz‐Vivancos, P., Marković, J., Gara, L. D., Pallardó, F. V., & Foyer, C. H. (2009) · Molecular Plant · doi:10.1093/mp/ssp008 · Cited by 89 · see citing works
Transcriptional landscapes of de novo root regeneration from detached Arabidopsis leaves revealed by time-lapse and single-cell RNA sequencing analyses
Liu, W., Zhang, Y., Fang, X., Tran, S., Zhai, N., Yang, Z., Guo, F., Chen, L., Yu, J., Ison, M., et al. (2022) · Plant Communications · doi:10.1016/j.xplc.2022.100306 · Cited by 88 · see citing works
Self-citation
The meristem-to-organ boundary: more than an extremity of anything
Rast-Somssich, M. I., & Simon, R. G. (2008) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2008.05.005 · Cited by 86 · see citing works
FOREVER YOUNG FLOWER Negatively Regulates Ethylene Response DNA-Binding Factors by Activating an Ethylene-Responsive Factor to Control Arabidopsis Floral Organ Senescence and Abscission
Chen, W., Li, P., Chen, M.-K., Lee, Y., & Yang, C. (2015) · PLANT PHYSIOLOGY · doi:10.1104/pp.15.00433 · Cited by 85 · see citing works
BLADE-ON-PETIOLE genes: Setting boundaries in development and defense
Khan, M., Xu, H., & Hepworth, S. R. (2014) · Plant Science · doi:10.1016/j.plantsci.2013.10.019 · Cited by 81 · see citing works
Self-citation
PETAL LOSS is a boundary gene that inhibits growth between developing sepals in Arabidopsis thaliana
Lampugnani, E. R., Kilinc, A., & Smyth, D. R. (2012) · The Plant Journal · doi:10.1111/j.1365-313x.2012.05023.x · Cited by 81 · see citing works
Overview of molecular mechanisms of plant leaf development: a systematic review
Lv, Z., Zhao, W., Kong, S., Li, L., & Lin, S. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2023.1293424 · Cited by 81 · see citing works
The ubiquitin–proteasome system as a transcriptional regulator of plant immunity
Adams, E. H. G., & Spoel, S. H. (2018) · Journal of Experimental Botany · doi:10.1093/jxb/ery216 · Cited by 79 · see citing works
Vitis vinifera VvNPR1.1 is the functional ortholog of AtNPR1 and its overexpression in grapevine triggers constitutive activation of PR genes and enhanced resistance to powdery mildew
Hénanff, G. L., Farine, S., Kieffer, F., Miclot, A.-S., Heitz, T., Mestre, P., Bertsch, C., & Chong, J. (2011) · Planta · doi:10.1007/s00425-011-1412-1 · Cited by 79 · see citing works
Repression of lateral organ boundary genes by PENNYWISE and POUND-FOOLISH is essential for meristem maintenance and flowering in Arabidopsis thaliana1
Khan, M., Ragni, L., Tabb, P., Salasini, B. C., Chatfield, S. P., Datla, R., Lock, J., Kuai, X., Després, C., Proveniers, M. C. G., et al. (2015) · PLANT PHYSIOLOGY · doi:10.1104/pp.15.00915 · Cited by 79 · see citing works
Self-citation
ORGAN BOUNDARY1 defines a gene expressed at the junction between the shoot apical meristem and lateral organs
Cho, E., & Zambryski, P. C. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1018542108 · Cited by 91 · see citing works
Multifunctional evolution of B and AGL6 MADS box genes in orchids
Hsu, H., Chen, W., Shen, Y., Hsu, W., Mao, W., & Yang, C. (2021) · Nature Communications · doi:10.1038/s41467-021-21229-w · Cited by 77 · see citing works
Carpel Development
Ferrándiz, C., Fourquin, C., Prunet, N., Scutt, C. P., Sundberg, E., Tréhin, C., & Vialette‐Guiraud, A. (2010) · Advances in botanical research · doi:10.1016/b978-0-12-380868-4.00001-6 · Cited by 75 · see citing works
A Genomic-Scale Artificial MicroRNA Library as a Tool to Investigate the Functionally Redundant Gene Space inArabidopsis
Hauser, F., Chen, W., Deinlein, U., Chang, K., Ossowski, S., Fitz, J., Hannon, G. J., & Schroeder, J. I. (2013) · The Plant Cell · doi:10.1105/tpc.113.112805 · Cited by 76 · see citing works
BLADE-ON-PETIOLE genes temporally and developmentally regulate the sheath to blade ratio of rice leaves
Toriba, T., Tokunaga, H., Shiga, T., Nie, F., Naramoto, S., Honda, E., Tanaka, K., Taji, T., Itoh, J., & Kyozuka, J. (2019) · Nature Communications · doi:10.1038/s41467-019-08479-5 · Cited by 76 · see citing works
Keeping it together: co-ordinating plant growth
Ingram, G. C., & Waites, R. (2005) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2005.11.007 · Cited by 76 · see citing works
HANABA TARANU (HAN) Bridges Meristem and Organ Primordia Boundaries through PINHEAD, JAGGED, BLADE-ON-PETIOLE2 and CYTOKININ OXIDASE 3 during Flower Development in Arabidopsis
Ding, L., Yan, S., Jiang, L., Zhao, W., Ning, K., Zhao, J., Liu, X., Zhang, J., Wang, Q., & Zhang, X. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005479 · Cited by 74 · see citing works
The Light-Response BTB1 and BTB2 Proteins Assemble Nuclear Ubiquitin Ligases That Modify Phytochrome B and D Signaling in Arabidopsis
Christians, M. J., Gingerich, D. J., Hua, Z., Lauer, T., & Vierstra, R. D. (2012) · PLANT PHYSIOLOGY · doi:10.1104/pp.112.199109 · Cited by 69 · see citing works
The Salicylic Acid Receptor NPR3 Is a Negative Regulator of the Transcriptional Defense Response during Early Flower Development in Arabidopsis
Shi, Z., Maximova, S. N., Liu, Y., Verica, J. A., & Guiltinan, M. J. (2012) · Molecular Plant · doi:10.1093/mp/sss091 · Cited by 73 · see citing works
Arabidopsis clade IV TGA transcription factors, TGA10 and TGA9, are involved in ROS-mediated responses to bacterial PAMP flg22
Noshi, M., Mori, D., Tanabe, N., Maruta, T., & Shigeoka, S. (2016) · Plant Science · doi:10.1016/j.plantsci.2016.06.019 · Cited by 73 · see citing works
Redox Regulation and Flower Development: A Novel Function for Glutaredoxins
Xing, S., Lauri, A., & Zachgo, S. (2006) · Plant Biology · doi:10.1055/s-2006-924278 · Cited by 71 · see citing works
A comprehensive review of TGA transcription factors in plant growth, stress responses, and beyond
Lu, C., Liu, X., Tang, Y., Fu, Y., Zhang, J., Yang, L., Li, P., Zhu, Z., & Dong, P. (2023) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2023.128880 · Cited by 71 · see citing works
Behavior of Leaf Meristems and Their Modification
Ichihashi, Y., & Tsukaya, H. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.01060 · Cited by 70 · see citing works
NPR1 paralogs of Arabidopsis and their role in salicylic acid perception
Castelló, M. J., Medina‐Puche, L., Lamilla, J., & Tornero, P. (2018) · PLoS ONE · doi:10.1371/journal.pone.0209835 · Cited by 69 · see citing works
The influence of abscisic acid on the ethylene biosynthesis pathway in the functioning of the flower abscission zone in Lupinus luteus
Wilmowicz, E., Frankowski, K., Kućko, A., Świdziński, M., Ramírez, J. D. D. A., Nowakowska, A., & Kopcewicz, J. (2016) · Journal of Plant Physiology · doi:10.1016/j.jplph.2016.08.018 · Cited by 69 · see citing works
CRISPR/Cas9-Mediated Multiplex Genome Editing of JAGGED Gene in Brassica napus L.
Zaman, Q. U., Chu, W., Hao, M., Shi, Y., Sun, M., Sang, S., Mei, D., Cheng, H., Liu, J., Li, C., et al. (2019) · Biomolecules · doi:10.3390/biom9110725 · Cited by 68 · see citing works
SPINDLY, ERECTA, and Its Ligand STOMAGEN Have a Role in Redox-Mediated Cortex Proliferation in the Arabidopsis Root
Cui, H., Kong, D., Wei, P., Hao, Y., Torii, K. U., Lee, J. S., & Li, J. (2014) · Molecular Plant · doi:10.1093/mp/ssu106 · Cited by 67 · see citing works
Letting Go is Never Easy: Abscission and Receptor‐ L ike Protein Kinases
Niederhuth, C. E., Cho, S. K., Seitz, K. A., & Walker, J. C. (2013) · Journal of Integrative Plant Biology · doi:10.1111/jipb.12116 · Cited by 66 · see citing works

BLADE-ON-PETIOLE genes: Setting boundaries in development and defense
Khan, M., Xu, H., & Hepworth, S. R. (2014) · Plant Science · doi:10.1016/j.plantsci.2013.10.019 · Cited by 81 · see citing works
Self-citation
Investigating a Role for BLADE-ON-PETIOLE Genes in Plant Defense
Bergin, C. J. (2018) · doi:10.22215/etd/2018-13450 · Cited by 2 · see citing works
Antagonistic Interaction of BLADE-ON-PETIOLE1 and 2 with BREVIPEDICELLUS and PENNYWISE Regulates Arabidopsis Inflorescence Architecture
Khan, M., Xu, M., Murmu, J., Tabb, P., Liu, Y., Storey, K. M., McKim, S. M., Douglas, C. J., & Hepworth, S. R. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.188573 · Cited by 93 · see citing works
Self-citation
The Salicylic Acid Receptor NPR3 Is a Negative Regulator of the Transcriptional Defense Response during Early Flower Development in Arabidopsis
Shi, Z., Maximova, S. N., Liu, Y., Verica, J. A., & Guiltinan, M. J. (2012) · Molecular Plant · doi:10.1093/mp/sss091 · Cited by 73 · see citing works
Roles of the BLADE-ON-PETIOLE genes in Arabidopsis thaliana lateral organ development
McKim, S. M. (2009) · cIRcle (University of British Columbia) · doi:10.14288/1.0070846 · Cited by 1 · see citing works
Self-citation

Authors: Hepworth, S. R., Zhang, Y., McKim, S., Li, X., & Haughn, G. W.
Affiliations: University of British Columbia (CA)
ORCID: Hepworth, Shelley R.
Zhang, Yuelin
McKim, Sarah
Li, Xin
Haughn, George W.
Venue: The Plant Cell
Publisher: Oxford University Press (OUP)
Published: 2005-04-01
Volume: 17
Issue: 5
Pages: 1434-1448
ISSN: 1040-4651 (ISSN-L)
1532-298X
DOI: 10.1105/tpc.104.030536
OpenAlex: W2153891726
Cited by: 351
References: 72
Citations by year: 2026: 14 · 2025: 18 · 2024: 14 · 2023: 23 · 2022: 18 · 2021: 32 · 2020: 13 · 2019: 17 · 2018: 18 · 2017: 14 · 2016: 12 · 2015: 21 · 2014: 14 · 2013: 14 · 2012: 21
FWCI: 15.24
Type: journal article
Language: en
Open access: green
dx.doi.org
Licence: aspb.org/publications/aspb-journals/open-articles (vor, 395 d)
Locations: The Plant Cell (publishedVersion)
PubMed (publishedVersion)
PubMed Central (publishedVersion)
Funders: University of British Columbia
Directorate for Biological Sciences
Microscopy Imaging Center, University of Bern
Natural Sciences and Engineering Research Council of Canada
Topics: Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Parasitism and Resistance
Keywords: TGA transcription factors, floral organ patterning, floral meristem, floral organ abscission, bracts, plant defense signaling, salicylic acid, redox signaling, Arabidopsis thaliana
MeSH terms: Cell Nucleus, Cytoplasm, Molecular Sequence Data, Mutation, Phylogeny, Sequence Homology, Nucleic Acid, Transcription Factors, Signal Transduction, Arabidopsis, Gene Expression Regulation, Plant, Plant Leaves, Arabidopsis Proteins, Flowers, Regulatory Elements, Transcriptional

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

BLADE-ON-PETIOLE–Dependent Signaling Controls Leaf and Floral Patterning in Arabidopsis

Abstract

Integrity signals

Claims the paper makes

Claims other papers make about this one

Cites

Cited by

Related

Record

About these checks