Cited by 1,537Plant Molecular Biology ResearchDevelopmental Biology and Gene RegulationPlant Parasitism and Resistance

The DOI matches its Crossref record; 20 of the 20 references it cites were found in a registry or an index.

A member of the KNOTTED class of homeodomain proteins encoded by the STM gene of Arabidopsis

Long, Jeff A., Moan, Erich I., Medford, June I., Barton, M. Kathryn·1996·Nature

Open this paper in CoChat — free account

Abstract

The KNOTTED class of plant genes encodes homeodomain proteins. These genes have been found in all plant species where they have been sought and, where examined, show expression patterns that suggest they play an important role in shoot meristem function. Until now, all mutant phenotypes associated with these genes have been due to gain-of-function mutations, making it difficult to deduce their wild-type function. Here we present evidence that the Arabidopsis SHOOT-MERISTEMLESS (STM) gene, required for shoot apical meristem formation during embryogenesis, encodes a class I KNOTTED-like protein. We also describe the expression pattern of this gene in the wild-type plant. To our knowledge, STM is the first gene shown to mark a specific pattern element in the developing plant embryo both phenotypically and molecularly.

Integrity signals

Registry

Crossref · 10.1038/379066a0

Cites

20 of 20 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?

The developmental gene Knotted-1 is a member of a maize homeobox gene family
Vollbrecht, E., Veit, B. E., Sinha, N. R., & Hake, S. (1991) · Nature · doi:10.1038/350241a0 · Cited by 760
Expression of maize KNOTTED1 related homeobox genes in the shoot apical meristem predicts patterns of morphogenesis in the vegetative shoot
Jackson, D., Veit, B. E., & Hake, S. (1994) · Development · doi:10.1242/dev.120.2.405 · Cited by 754
A knotted1-Like Homeobox Gene in Arabidopsis Is Expressed in the Vegetative Meristem and Dramatically Alters Leaf Morphology When Overexpressed in Transgenic Plants
Lincoln, C., Long, J. C., Yamaguchi, J., Serikawa, K. A., & Hake, S. (1994) · The Plant Cell · doi:10.1105/tpc.6.12.1859 · Cited by 684
Self-citation
Formation of the shoot apical meristem in Arabidopsis thaliana: an analysis of development in the wild type and in the shoot meristemless mutant
Barton, M. K., & Poethig, R. S. (1993) · Development · doi:10.1242/dev.119.3.823 · Cited by 626
Self-citation
Overexpression of the maize homeo box gene, KNOTTED-1, causes a switch from determinate to indeterminate cell fates.Preprint
Sinha, N. R., Williams, R., & Hake, S. (1993) · Genes & Development · doi:10.1101/gad.7.5.787 · Cited by 457
A dominant mutation in the maize homeobox gene, Knotted-1, causes its ectopic expression in leaf cells with altered fates
Smith, L. G., Greene, B. A., Veit, B. E., & Hake, S. (1992) · Development · doi:10.1242/dev.116.1.21 · Cited by 441
Sequence analysis and expression patterns divide the maize knotted1-like homeobox genes into two classes.
Kerstetter, R. A., Vollbrecht, E., Lowe, B., Veit, B. E., Yamaguchi, J., & Hake, S. (1994) · The Plant Cell · doi:10.1105/tpc.6.12.1877 · Cited by 332
The barley Hooded mutation caused by a duplication in a homeobox gene intron
Müller, K. J., Romano, N., Gerstner, O., García‐Maroto, F., Pozzi, C. M., Salamini, F., & Rohde, W. (1995) · Nature · doi:10.1038/374727a0 · Cited by 217
Early embryogenesis in Arabidopsis thaliana. I. The mature embryo sac
Mansfield, S. G., BRIARTY, L. G., & Erni, S. (1991) · Canadian Journal of Botany · doi:10.1139/b91-062 · Cited by 171
Effect of mutations in the PINHEAD gene of Arabidopsis on the formation of shoot apical meristems
McConnell, J. R., & Barton, M. K. (1995) · Developmental Genetics · doi:10.1002/dvg.1020160409 · Cited by 129
Self-citation

Flagged first, then by citations

Show all 20 references

Research works printed but not linked: 1

Arabidopsis: An Atlas or Morphology and Development (ed. Bowman, J.) 133–172 (Springer, New York, 1994).

Sorted by citations

Items 701–800 of 1,000

Molecular Insights into Inflorescence Meristem Specification for Yield Potential in Cereal Crops
Wang, C., Yang, X., & Li, G. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22073508 · Cited by 39
Translational fusions with the engrailed repressor domain efficiently convert plant transcription factors into dominant-negative functions
Markel, H. (2002) · Nucleic Acids Research · doi:10.1093/nar/gkf591 · Cited by 39
Acquisition and Diversification of Cladodes: Leaf-Like Organs in the Genus Asparagus
Nakayama, H., Yamaguchi, T., & Tsukaya, H. (2012) · The Plant Cell · doi:10.1105/tpc.111.092924 · Cited by 39
Altered seed oil and glucosinolate levels in transgenic plants overexpressing the Brassica napus SHOOTMERISTEMLESS gene
Elhiti, M., Yang, C., Chan, A. C., Durnin, D. C., Belmonte, M. F., Ayele, B. T., Tahir, M., & Stasolla, C. (2012) · Journal of Experimental Botany · doi:10.1093/jxb/ers125 · Cited by 39
Signalling in Plant Lateral Organ Development
Golz, J. F., & Hudson, A. (2002) · The Plant Cell · doi:10.1105/tpc.000828 · Cited by 39
Induction of a homeodomain–leucine zipper gene by auxin is inhibited by cytokinin in Arabidopsis roots
Son, O., Cho, H., Kim, M., Lee, H., Lee, M., Song, E., Park, J. H., Nam, K. H., Chun, J.-Y., Kim, H.-J., et al. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.11.014 · Cited by 39
Wood Formation in Populus
Groover, A. T., Nieminen, K. M., Helariutta, Y., & Mansfield, S. D. (2009) · Springer eBooks · doi:10.1007/978-1-4419-1541-2_10 · Cited by 39
Cellular basis of shoot apical meristem development
Traas, J. A., & Doonan, J. H. (2001) · International review of cytology · doi:10.1016/s0074-7696(01)08004-4 · Cited by 39
Patterning the Flower
Irish, V. F. (1999) · Developmental Biology · doi:10.1006/dbio.1999.9226 · Cited by 39
Arabidopsis floral phytomer development: auxin response relative to biphasic modes of organ initiation
Chandler, J., & Werr, W. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru153 · Cited by 41
Expression patterns of STM-like KNOX and Histone H4 genes in shoot development of the dissected-leaved basal eudicot plants Chelidonium majus and Eschscholzia californica (Papaveraceae)
Groot, E. P., Sinha, N. R., & Gleissberg, S. (2005) · Plant Molecular Biology · doi:10.1007/s11103-005-4548-1 · Cited by 38
Synergistic action of GCN5 and CLAVATA1 in the regulation of gynoecium development in Arabidopsis thaliana
Poulios, S., & Vlachonasios, K. E. (2018) · New Phytologist · doi:10.1111/nph.15303 · Cited by 38
Phloem Companion Cell-Specific Transcriptomic and Epigenomic Analyses Identify MRF1, a Regulator of Flowering
You, Y., Sawikowska, A., Lee, J. E., Benstein, R. M., Neumann, M., Krajewski, P., & Schmid, M. (2019) · The Plant Cell · doi:10.1105/tpc.17.00714 · Cited by 38
Emergent Protective Organogenesis in Date Palms: A Morpho-Devo-Dynamic Adaptive Strategy during Early Development
Xiao, T. T., Aragón-Raygoza, A., Caballero-Pérez, J., Kirschner, G. K., Deng, Y., Atkinson, B. S., Sturrock, C. J., Lube, V., Wang, J. Y., Gilles Lubineau, A., et al. (2019) · The Plant Cell · doi:10.1105/tpc.19.00008 · Cited by 38
A Molecular Switch for Initiating Cell Differentiation in Arabidopsis
Sanmartín, M., Sauer, M., Muñoz, A., Zouhar, J., Ordóñez, A., van de Ven, W. T. G., Caro, E., Sánchez, M. D. L. P., Raikhel, N. V., Gutiérrez, C., et al. (2011) · Current Biology · doi:10.1016/j.cub.2011.04.041 · Cited by 40
Overexpression of HBK3, a class I KNOX homeobox gene, improves the development of Norway spruce (Picea abies) somatic embryos
Belmonte, M. F., Tahir, M., Schroeder, D., & Stasolla, C. (2007) · Journal of Experimental Botany · doi:10.1093/jxb/erm099 · Cited by 38
De novo Transcriptome Sequencing and Development of Abscission Zone-Specific Microarray as a New Molecular Tool for Analysis of Tomato Organ Abscission
Sundaresan, S., Philosoph‐Hadas, S., Riov, J., Mugasimangalam, R. C., Kuravadi, N. A., Kochanek, B., Salim, S., Tucker, M. L., & Meir, S. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2015.01258 · Cited by 38
Characterization of the KNOX class homeobox genes Oskn2 and Oskn3 identified in a collection of cDNA libraries covering the early stages of rice embryogenesis
Postma-Haarsma, A. D., Verwoert, I. I. G. S., Stronk, O. P., Koster, J., Lamers, G. E. M., Hoge, J. H. C., & Meijer, A. H. (1999) · Plant Molecular Biology · doi:10.1023/a:1006153506868 · Cited by 38
KNOX homeobox genes are sufficient in maintaining cultured cells in an undifferentiated state in rice
Ito, Y., Eiguchi, M., & Kurata, N. (2001) · genesis · doi:10.1002/gene.1069 · Cited by 38
KNOTTED1-like homeobox genes of a gymnosperm, Norway spruce, expressed during somatic embryogenesis
Hjortswang, H. I., Larsson, A. S., Geeta, R., Bozhkov, P. V., von Arnold, S., & Vahala, T. (2002) · Plant Physiology and Biochemistry · doi:10.1016/s0981-9428(02)01445-6 · Cited by 38
Models of shoot apical meristem function
Tooke, F., & Battey, N. H. (2003) · New Phytologist · doi:10.1046/j.1469-8137.2003.00803.x · Cited by 38
Transposon Tagging of the Defective embryo and meristems Gene of Tomato
Keddie, J. S., Carroll, B. S., Thomas, C. M., Reyes, M., Klimyuk, V. I., Holtan, H., Gruissem, W., & Jones, J. D. G. (1998) · The Plant Cell · doi:10.1105/tpc.10.6.877 · Cited by 38
Diving into the Water: Amphibious Plants as a Model for Investigating Plant Adaptations to Aquatic Environments
Koga, H., Ikematsu, S., & Kimura, S. (2024) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-062923-024919 · Cited by 37
Asymmetric morphogenetic cues along the transverse plane: Shift from disymmetry to zygomorphy in the flower of Fumarioideae
Damerval, C., Citerne, H. L., Guilloux, M. L., Domenichini, S., Dutheil, J., Craene, L. P. R. D., & Nadot, S. (2013) · American Journal of Botany · doi:10.3732/ajb.1200376 · Cited by 37
Genetic integration of DORNRÖSCHEN and DORNRÖSCHEN-LIKE reveals hierarchical interactions in auxin signalling and patterning of the Arabidopsis apical embryo
Chandler, J., Cole, M., Jacobs, B., Comelli, P., & Werr, W. (2010) · Plant Molecular Biology · doi:10.1007/s11103-010-9721-5 · Cited by 39
Identification of the Key Regulatory Genes Involved in Elaborate Petal Development and Specialized Character Formation in Nigelladamascena (Ranunculaceae)
Zhang, R., Fu, X., Zhao, C., Cheng, J., Liao, H., Wang, P., Yao, X., Duan, X., Yuan, Y., Xu, G., et al. (2020) · The Plant Cell · doi:10.1105/tpc.20.00330 · Cited by 39
Condensation of STM is critical for shoot meristem maintenance and salt tolerance in Arabidopsis
Cao, X., Du, Q., Guo, Y., Wang, Y., & Jiao, Y. (2023) · Molecular Plant · doi:10.1016/j.molp.2023.09.005 · Cited by 37
Transcription factors and hormones: new insights into plant cell differentiation
Long, T. A., & Benfey, P. N. (2006) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2006.09.004 · Cited by 37
Metabolic aspects of organogenesis in the shoot apical meristem
Fleming, A. J. (2006) · Journal of Experimental Botany · doi:10.1093/jxb/erj178 · Cited by 37
Did auxin play a crucial role in the evolution of novel body plans during the Late Silurian-Early Devonian radiation of land plants?
Cooke, T. J., Poli, D., & Cohen, J. D. (2004) · Elsevier eBooks · doi:10.1016/b978-012339552-8/50006-8 · Cited by 37
Arabidopsis histone H3 lysine 9 methyltransferases KYP/SUVH5/6 are involved in leaf development by interacting with AS1-AS2 to repress KNAT1 and KNAT2
Hung, F., Feng, Y., Hsin, K., Shih, Y., Chang, C., Zhong, W., Lai, Y., Xu, Y., Yang, S., Sugimoto, K., et al. (2023) · Communications Biology · doi:10.1038/s42003-023-04607-6 · Cited by 36
Drawing a Line: Grasses and Boundaries
Richardson, A. E., & Hake, S. (2018) · Plants · doi:10.3390/plants8010004 · Cited by 38
Transcriptional, Posttranscriptional, and Posttranslational Regulation of SHOOT MERISTEMLESS Gene Expression in Arabidopsis Determines Gene Function in the Shoot Apex
Aguilar-Martínez, J. A., Uchida, N., Townsley, B. T., West, D. A., Yanez, A., Lynn, N., Kimura, S., & Sinha, N. R. (2014) · PLANT PHYSIOLOGY · doi:10.1104/pp.114.248625 · Cited by 36
stem fasciated, a Recessive Mutation in Sunflower (Helianthus annuus), Alters Plant Morphology and Auxin Level
Fambrini, M., BONSIGNORI, E., Rapparini, F., Cionini, G., Michelotti, V., BERTINI, D., Baraldi, R., & Pugliesi, C. (2006) · Annals of Botany · doi:10.1093/aob/mcl153 · Cited by 37
Partitioning the Apical Domain of the Arabidopsis Embryo Requires the BOBBER1 NudC Domain Protein
Jurkuta, R. E. J., Kaplinsky, N. J., Spindel, J. E., & Barton, M. K. (2009) · The Plant Cell · doi:10.1105/tpc.108.065284 · Cited by 37
Self-citation
Simple and compound leaves: reduction or multiplication?
Sinha, N. R. (1997) · Trends in Plant Science · doi:10.1016/s1360-1385(97)90055-8 · Cited by 36
Xyloglucan endotransglucosylase/hydrolase genes in cucumber (Cucumis sativus) – differential expression during somatic embryogenesis†
Malinowski, R., Filipecki, M., Tagashira, N., Wiśniewska, A., Gaj, P., Pląder, W., & Malepszy, S. (2004) · Physiologia Plantarum · doi:10.1111/j.0031-9317.2004.0289.x · Cited by 36
Developmental control of cell division patterns in the shoot apex
Vernoux, T., Autran, D., & Traas, J. A. (2000) · Plant Molecular Biology · doi:10.1023/a:1006464430936 · Cited by 36
YABBY and diverged KNOX1 genes shape nodes and internodes in the stem
Tsuda, K., Maeno, A., Otake, A., Kato, K., Tanaka, W., Hibara, K., & Nonomura, K. (2024) · Science · doi:10.1126/science.adn6748 · Cited by 35
CIN-like TCP13 is essential for plant growth regulation under dehydration stress
Urano, K., Maruyama, K., Koyama, T., González, N., Inzé, D., Yamaguchi‐Shinozaki, K., & Shinozaki, K. (2022) · Plant Molecular Biology · doi:10.1007/s11103-021-01238-5 · Cited by 35
Genetic Control of Seed Development and Seed Mass
Ohto, M., Stone, S. L., & Harada, J. J. (2007) · Blackwell Publishing Ltd eBooks · doi:10.1002/9780470988848.ch1 · Cited by 35
Characterization of CsSEF1 gene encoding putative CCCH-type zinc finger protein expressed during cucumber somatic embryogenesis
Grabowska, A., Wiśniewska, A., Tagashira, N., Malepszy, S., & Filipecki, M. (2008) · Journal of Plant Physiology · doi:10.1016/j.jplph.2008.06.005 · Cited by 35
Truncated Hemoglobins in Actinorhizal Nodules of Datisca glomerata
Pawlowski, K., Jacobsen, K. R., Alloisio, N., Denison, R. F., Klein, M., Tjepkema, J. D., Winzer, T., Sirrenberg, A., Guan, C., & Berry, A. M. (2007) · Plant Biology · doi:10.1055/s-2007-965258 · Cited by 35
TANMEI/EMB2757 Encodes a WD Repeat Protein Required for Embryo Development in Arabidopsis
Yamagishi, K., Nagata, N., Yee, K. M., Braybrook, S. A., Pelletier, J., Fujioka, S., Yoshida, S., Fischer, R. L., Goldberg, R. B., & Harada, J. J. (2005) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.060467 · Cited by 35
Negative regulation of KNOX expression in tomato leaves
Jasinski, S., Kaur, H., Tattersall, A. D., & Tsiantis, M. (2007) · Planta · doi:10.1007/s00425-007-0572-5 · Cited by 35
Intragenic diversity and functional conservation of the three homoeologous loci of the KN1-type homeobox gene Wknox1 in common wheat
Morimoto, R., Kosugi, T., Nakamura, C., & Takumi, S. (2005) · Plant Molecular Biology · doi:10.1007/s11103-005-3247-2 · Cited by 35
Genome-wide analyses for dissecting gene regulatory networks in the shoot apical meristem
Bustamante, M., Matus, J. T., & Riechmann, J. L. (2016) · Journal of Experimental Botany · doi:10.1093/jxb/erw058 · Cited by 34
Control of stem cell activity in the carpel margin meristem (CMM) in Arabidopsis
Reyes‐Olalde, J. I., & de Folter, S. (2019) · Plant Reproduction · doi:10.1007/s00497-018-00359-0 · Cited by 35
Same Actor in Different Stages: Genes in Shoot Apical Meristem Maintenance and Floral Meristem Determinacy in Arabidopsis
Chang, W., Guo, Y., Zhang, H., Liu, X., & Guo, L. (2020) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2020.00089 · Cited by 34
Genetic analysis of plant morphogenesis in vitro
Sugiyama, M. (2000) · International review of cytology · doi:10.1016/s0074-7696(00)96002-9 · Cited by 34
Regulation and a conserved intron sequence of liguleless3/4 knox class-I homeobox genes in grasses
Bauer, P., Lubkowitz, M. A., Tyers, R. G., Nemoto, K., Meeley, R. B., Goff, S. A., & Freeling, M. (2004) · Planta · doi:10.1007/s00425-004-1233-6 · Cited by 34
Cell division pattern influences gene expression in the shoot apical meristem
Wyrzykowska, J., & Fleming, A. J. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0930352100 · Cited by 34
Phyllotaxis: from patterns of organogenesis at the meristem to shoot architecture
Galván-Ampudia, C. S., Chaumeret, A., Godin, C., & Vernoux, T. (2016) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.231 · Cited by 35
Identification of Polycomb Repressive Complex1, Trithorax group genes and their simultaneous expression with WUSCHEL, WUSCHEL-related Homeobox5 and SHOOT MERISTEMLESS during the induction phase of somatic embryogenesis in Medicago truncatula Gaertn.
Orłowska, A., & Kępczyńska, E. (2018) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-018-1425-6 · Cited by 34
Hormonal Studies of fass, an Arabidopsis Mutant That Is Altered in Organ Elongation
Fisher, R. H., Barton, M. K., Cohen, J. D., & Cooke, T. J. (1996) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.4.1109 · Cited by 34
Self-citation
The cytokinin receptor OHK4/OsHK4 regulates inflorescence architecture in rice via an IDEAL PLANT ARCHITECTURE1/WEALTHY FARMER’S PANICLE-mediated positive feedback circuit
Chun, Y., Fang, J., Savelieva, E. M., Lomin, S. N., Shang, J., Sun, Y., Zhao, J., Kumar, A., Yuan, S., Yao, X., et al. (2023) · The Plant Cell · doi:10.1093/plcell/koad257 · Cited by 33
Sugar signaling modulates SHOOT MERISTEMLESS expression and meristem function in Arabidopsis
Lopes, F. L., Formosa-Jordan, P., Malivert, A., Margalha, L., Confraria, A., Feil, R., Lunn, J. E., Jönsson, H., Landrein, B., & Gonzalez, E. B. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2408699121 · Cited by 33
Calpain-Mediated Positional Information Directs Cell Wall Orientation to Sustain Plant Stem Cell Activity, Growth and Development
Liang, Z., Brown, R. C., Fletcher, J. C., & Opsahl-Sorteberg, H.-G. (2015) · Plant and Cell Physiology · doi:10.1093/pcp/pcv110 · Cited by 33
Interplay between miRNA regulation and mechanical stress forCUCgene expression at the shoot apical meristem
Fal, K., Landrein, B., & Hamant, O. (2015) · Plant Signaling & Behavior · doi:10.1080/15592324.2015.1127497 · Cited by 34
Genetic control of compound leaf development in the mungbean (Vigna radiata L.)
Jiao, K., Li, X., Su, S., Guo, W., Guo, Y., Guan, Y., Hu, Z., Shen, Z., & Luo, D. (2019) · Horticulture Research · doi:10.1038/s41438-018-0088-0 · Cited by 33
Quantum Molecular Dynamics, Topological, Group Theoretical and Graph Theoretical Studies of Protein-Protein Interactions
Balasubramanian, K., & Gupta, S. P. (2019) · Current Topics in Medicinal Chemistry · doi:10.2174/1568026619666190304152704 · Cited by 33
Control of cell fate during axillary meristem initiation
Cao, X., & Jiao, Y. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03407-8 · Cited by 35
A coiled-coil protein associates Polycomb Repressive Complex 2 with KNOX/BELL transcription factors to maintain silencing of cell differentiation-promoting genes in the shoot apex
Tan, F., Wang, W., Li, J., Lu, Y., Zhu, B., Hu, F., Li, Q., Zhao, Y. J., & Zhou, D. (2022) · The Plant Cell · doi:10.1093/plcell/koac133 · Cited by 33
How was apical growth regulated in the ancestral land plant? Insights from the development of non-seed plants
Fouracre, J. P., & Harrison, C. J. O. (2022) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiac313 · Cited by 33
The cellular basis for synergy between RCO and KNOX1 homeobox genes in leaf shape diversity
Wang, Y., Strauss, S., Liu, S., Pieper, B., Lymbouridou, R., Runions, A., & Tsiantis, M. (2022) · Current Biology · doi:10.1016/j.cub.2022.08.020 · Cited by 33
Molecular Analysis of In Vitro Shoot Organogenesis
Zhang, S., & Lemaux, P. G. (2004) · Critical Reviews in Plant Sciences · doi:10.1080/07352680490484569 · Cited by 33
A new class of plant homeobox genes is expressed in specific regions of determinate symbiotic root nodules
Jørgensen, J.-E., Grønlund, M., Pallisgaard, N., Larsen, K., Marcker, K. A., & Jensen, E. Ø. (1999) · Plant Molecular Biology · doi:10.1023/a:1026463506376 · Cited by 33
A novel role of BELL1-like homeobox genes, PENNYWISE and POUND-FOOLISH, in floral patterning
Yu, L., Patibanda, V., & Smith, H. M. S. (2008) · Planta · doi:10.1007/s00425-008-0867-1 · Cited by 33
Cell type specification and self renewal in the vegetative shoot apical meristem
Barton, M. K. (1998) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(98)80125-8 · Cited by 33
Self-citation
Use of Petunia to unravel plant meristem functioning
Angenent, G. C., Stuurman, J., Snowden, K. C., & Koes, R. E. (2005) · Trends in Plant Science · doi:10.1016/j.tplants.2005.03.004 · Cited by 33
Cell signaling in the shoot apical meristem
Wang, Y., & Jiao, Y. (2023) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiad309 · Cited by 32
The Arabidopsis MERISTEM DISORGANIZATION 1 gene is required for the maintenance of stem cells through the reduction of DNA damage
侑磨, 橋., & Ueguchi, C. (2011) · The Plant Journal · doi:10.1111/j.1365-313x.2011.04718.x · Cited by 33
Ectopic KNOX Expression Affects Plant Development by Altering Tissue Cell Polarity and Identity
Richardson, A. E., Rebocho, A. B., & Coen, E. (2016) · The Plant Cell · doi:10.1105/tpc.16.00284 · Cited by 32
Regulation of Meristem Size by Cytokinin SignalingF
Skylar, A., & Wu, X. (2011) · Journal of Integrative Plant Biology · doi:10.1111/j.1744-7909.2011.01045.x · Cited by 32
ZLL/AGO10 maintains shoot meristem stem cells during Arabidopsis embryogenesis by down-regulating ARF2-mediated auxin response
Roodbarkelari, F., Du, F., Truernit, E., & Laux, T. (2015) · BMC Biology · doi:10.1186/s12915-015-0180-y · Cited by 35
Molecular characterization of PgAGO, a novel conifer gene of the ARGONAUTE family expressed in apical cells and required for somatic embryo development in spruce
Tahir, M., Law, D. A., & Stasolla, C. (2006) · Tree Physiology · doi:10.1093/treephys/26.10.1257 · Cited by 32
A Strawberry KNOX Gene Regulates Leaf, Flower and Meristem Architecture
Chatterjee, M., Bermudez-Lozano, C. L., Clancy, M. A., Davis, T. M., & Folta, K. M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0024752 · Cited by 32
Auxin and cytokinin act during gynoecial patterning and the development of ovules from the meristematic medial domain
Sehra, B., & Franks, R. G. (2015) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.193 · Cited by 32
Arabidopsis PRC1 core component AtRING1 regulates stem cell-determining carpel development mainly through repression of class I KNOX genes
Chen, D., Molitor, A. M., Xu, L., & Shen, W. (2016) · BMC Biology · doi:10.1186/s12915-016-0336-4 · Cited by 32
Phytochrome A, phytochrome B and other phytochrome(s) regulate ATHB‐2 gene expression in etiolated and green Arabidopsis plants
Steindler, C., Carabelli, M., Borello, U., Morelli, G., & Ruberti, I. (1997) · Plant Cell & Environment · doi:10.1046/j.1365-3040.1997.d01-123.x · Cited by 32
Embryonic shoot apical meristem formation in higher plants
Takada, S., & Tasaka, M. (2002) · Journal of Plant Research · doi:10.1007/s10265-002-0061-7 · Cited by 32
Seed development in Arabidopsis: what we have learnt in the past 30 years
Huang, X., Zhao, P., Peng, X., & Sun, M. (2023) · Seed Biology · doi:10.48130/seedbio-2023-0006 · Cited by 31
A rapid and sensitive, multiplex, whole mount RNA fluorescence in situ hybridization and immunohistochemistry protocol
Huang, T., Guillotin, B., Rahni, R., Birnbaum, K. D., & Wagner, D. (2023) · Plant Methods · doi:10.1186/s13007-023-01108-9 · Cited by 31
Phylogenomic Analyses of the BARREN STALK1/LAX PANICLE1 (BA1/LAX1) Genes and Evidence for Their Roles During Axillary Meristem Development
Woods, D. P., Hope, C. L., & Malcomber, S. T. (2011) · Molecular Biology and Evolution · doi:10.1093/molbev/msr036 · Cited by 32
PtWOX11 acts as master regulator conducting the expression of key transcription factors to induce de novo shoot organogenesis in poplar
Liu, B., Zhang, J., Yang, Z., Matsui, A., Seki, M., Li, S., Yan, X., Kohnen, M. V., Gu, L., Prasad, K., et al. (2018) · Plant Molecular Biology · doi:10.1007/s11103-018-0786-x · Cited by 31
Cell- and noncell-autonomous AUXIN RESPONSE FACTOR3 controls meristem proliferation and phyllotactic patterns
Zhang, K., Zhang, H., Pan, Y., Niu, Y., Guo, L., Ma, Y., Tian, S., Wei, J., Wang, C., Yang, X., et al. (2022) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiac370 · Cited by 33
Identification of differentially expressed cDNA sequences and histological characteristics of Hevea brasiliensis calli in relation to their embryogenic and regenerative capacities
Charbit, E., Legavre, T., Lardet, L., Bourgeois, E., Ferri�re, N., & Carron, M. P. (2004) · Plant Cell Reports · doi:10.1007/s00299-003-0737-z · Cited by 31
Cyclin-dependent kinase activity retains the shoot apical meristem cells in an undifferentiated state
Gaamouche, T., Manes, C.-L. D. O., Kwiatkowska, D., Berckmans, B., Koumproglou, R., Maes, S., Beeckman, T., Vernoux, T., Doonan, J. H., Traas, J. A., et al. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04317.x · Cited by 33
EMBRYO YELLOW gene, encoding a subunit of the conserved oligomeric Golgi complex, is required for appropriate cell expansion and meristem organization in Arabidopsis thaliana
Ishikawa, T., Machida, C., Yoshioka, Y., Ueda, T., Nakano, A., & Machida, Y. (2008) · Genes to Cells · doi:10.1111/j.1365-2443.2008.01186.x · Cited by 31
Signaling pathways maintaining stem cells at the plant shoot apex
Rieu, I., & Laux, T. (2009) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2009.09.013 · Cited by 31
The SHOOT ORGANIZATION2 Gene Coordinates Leaf Domain Development Along the Central-Marginal Axis in Rice
Itoh, J.-I., Sato, Y., & Nagato, Y. (2008) · Plant and Cell Physiology · doi:10.1093/pcp/pcn099 · Cited by 31
Plastid osmotic stress influences cell differentiation at the plant shoot apex
Wilson, M. E., Mixdorf, M., Berg, R. H., & Haswell, E. S. (2016) · Development · doi:10.1242/dev.136234 · Cited by 31
Different subcellular localization and trafficking properties of KNOX class 1 homeodomain proteins from rice
Kuijt, S. J. H., Lamers, G. E. M., Rueb, S., Scarpella, E., Ouwerkerk, P. B. F., Spaink, H. P., & Meijer, A. H. (2004) · Plant Molecular Biology · doi:10.1007/s11103-004-1967-3 · Cited by 31
Regulation of developmental transitions
Chuck, G. S., & Hake, S. (2004) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2004.11.002 · Cited by 31
Transcriptome profiling reveals phase-specific gene expression in the developing barley inflorescence
Liu, H., Li, G., Yang, X., Kuijer, H. N. J., Liang, W., & Zhang, D. (2019) · The Crop Journal · doi:10.1016/j.cj.2019.04.005 · Cited by 30
The role of auxin and sugar signaling in dominance inhibition of inflorescence growth by fruit load
Goetz, M., Rabinovich, M. I., & Smith, H. M. S. (2021) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiab237 · Cited by 31
Two citrus KNAT-like genes, CsKN1 and CsKN2, are involved in the regulation of spring shoot development in sweet orange
Zeng, R., Zhou, H., Fu, L., Yan, Z., Ye, L., Hu, S., Gan, Z., Ai, X., Hu, C., & Zhang, J. (2021) · Journal of Experimental Botany · doi:10.1093/jxb/erab311 · Cited by 30
The evolution of plant regulatory networks: what Arabidopsis cannot say for itself
Nardmann, J., & Werr, W. (2007) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2007.07.009 · Cited by 30
Control of division and differentiation of plant stem cells and their derivatives
Nieuwland, J., Scofield, S., & Murray, J. A. H. (2009) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2009.09.011 · Cited by 31
Genetics of Barley Hooded Suppression
Roig, C., Pozzi, C. M., Santi, L., Müller, J., Wang, Y., Stile, M. R., Rossini, L., Stanca, M., & Salamini, F. (2004) · Genetics · doi:10.1534/genetics.167.1.439 · Cited by 30

Authors: Long, J. A., Moan, E. I., Medford, J. I., & Barton, M. K.
Affiliations: University of Wisconsin–Madison (US)
Pennsylvania State University (US)
ORCID: Long, Jeff A.
Medford, June I.
Barton, M. Kathryn
Venue: Nature
Publisher: Springer Science and Business Media LLC
Published: 1996-01
Volume: 379
Issue: 6560
Pages: 66-69
ISSN: 0028-0836 (ISSN-L)
1476-4687
DOI: 10.1038/379066a0
OpenAlex: W1980630177
Cited by: 1,537
References: 20
Citations by year: 2026: 19 · 2025: 36 · 2024: 46 · 2023: 41 · 2022: 71 · 2021: 37 · 2020: 45 · 2019: 36 · 2018: 35 · 2017: 48 · 2016: 45 · 2015: 43 · 2014: 49 · 2013: 54 · 2012: 63
FWCI: 78.23
Type: journal article
Language: en
Open access: closed
Licence: www.springer.com/tdm (tdm)
Locations: Nature (publishedVersion)
PubMed (publishedVersion)
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: STM, Arabidopsis thaliana, shoot apical meristem, embryonic development, gene expression patterns, gain-of-function mutations, plant development
MeSH terms: Amino Acid Sequence, Molecular Sequence Data, Plant Proteins, Gene Expression, Genes, Plant, Arabidopsis, Sequence Homology, Amino Acid, Homeodomain Proteins, Plant Shoots, RNA, Plant, Arabidopsis Proteins

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

A member of the KNOTTED class of homeodomain proteins encoded by the STM gene of Arabidopsis

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks