The DOI matches its Crossref record; 47 of the 47 references it cites were found in a registry or an index.
The homeotic gene long sterile lemma ( G1 ) specifies sterile lemma identity in the rice spikelet
Open accessAbstract
The mechanism of floral organ specification is principally conserved in angiosperms, as demonstrated by the ABC model. By contrast, mechanisms that regulate the development of organs or structures specific to a group of species remain unclear. Grasses have unique inflorescence units, comprising spikelets and florets. In the genus Oryza (rice), the single spikelet consists of a fertile floret subtended by a lemma and a palea, two sterile lemmas, and rudimentary glumes. Each sterile lemma is a tiny glume-like organ with a smooth surface. Here, we have examined a long sterile lemma1 ( g1 ) mutant, in which the sterile lemma is enlarged like the lemma. Detailed phenotypic analysis reveals that the large sterile lemma in the g1 mutant appears to be caused by homeotic transformation of the sterile lemma into a lemma, suggesting that G1 is involved in the repression of lemma identity to specify the sterile lemma. Gene isolation reveals that G1 is a member of a plant-specific gene family that encodes proteins with a previously uncharacterized domain, named here ALOG ( Arabidopsis LSH1 and Oryza G1 ). G1 mRNA is expressed in sterile lemma primordia throughout their development, and G1 protein is localized in the nucleus. A trans-activation assay using the yeast GAL4 system suggests that G1 is involved in transcriptional regulation. Repression of lemma identity by G1 is consistent with a hypothesis proposed to explain the morphological evolution of rice spikelets. We also show that a wild rice species, Oryza grandiglumis , that forms large sterile lemmas has serious mutations in the G1 gene.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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 cited source says what the claim attributes to it.
In the citing paper
“| LSH3/4 | G1 (rice) | ALOG | Only gain-of-function | SAM and lateral organs | Takeda et al. (2011); Cho & Zam- |”
From Divide et impera: boundaries shape the plant body and initiate new meristems (2016) · cites this paper as Yoshida et al. (2009)
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
The neighbor-joining method: a new method for reconstructing phylogenetic trees.
Saitou, N., & Nei, M. (1987) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a040454 · Cited by 59,959
Hiei, Y., Ohta, S., Komari, T., & Kumashiro, T. (1994) · The Plant Journal · doi:10.1046/j.1365-313x.1994.6020271.x · Cited by 3,558
The war of the whorls: genetic interactions controlling flower development
Coen, E., & Meyerowitz, E. M. (1991) · Nature · doi:10.1038/353031a0 · Cited by 3,045
The Physcomitrella Genome Reveals Evolutionary Insights into the Conquest of Land by Plants
Rensing, S. A., Lang, D., Zimmer, A. D., Terry, A. Y., Salamov, A. A., Shapiro, H., Nishiyama, T., Perroud, P., Lindquist, E., Kamisugi, Y., et al. (2007) · Science · doi:10.1126/science.1150646 · Cited by 1,856
Nakagawa, T., Kurose, T., Hino, T., Tanaka, K., Kawamukai, M., Niwa, Y., Toyooka, K., Matsuoka, K., Jinbo, T., & Kimura, T. (2007) · Journal of Bioscience and Bioengineering · doi:10.1263/jbb.104.34 · Cited by 1,644
Evolutionary History of the Grasses
Kellogg, E. A. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.125.3.1198 · Cited by 811
A short history of MADS-box genes in plants
Theißen, G., Becker, A., Rosa, A. D., Kanno, A., Kim, J. T., Münster, T., Winter, K., & Saedler, H. (2000) · Springer eBooks · doi:10.1007/978-94-011-4221-2_6 · Cited by 676
Grass Systematics and Evolution.
Thomas, W. W., Soderstrom, T. R., Hilu, K. W., Campbell, C. S., & Barkworth, M. E. (1988) · Brittonia · doi:10.2307/2807477 · Cited by 640
A short history of MADS-box genes in plants
Theißen, G., Becker, A., Rosa, A. D., Kanno, A., Kim, J. T., Münster, T., Winter, K., & Saedler, H. (2000) · Plant Molecular Biology · doi:10.1023/a:1006332105728 · Cited by 632
Ambrose, B. A., Lerner, D. R., Ciceri, P., Padilla, C. M., Yanofsky, M. F., & Schmidt, R. J. (2000) · Molecular Cell · doi:10.1016/s1097-2765(00)80450-5 · Cited by 462
Flagged first, then by citations
Research works printed but not linked: 1
- I Takamure, T Kinoshita, Modification of glume characters due to genic interactions and environmental conditions. Rice Genet Newslett 9, 85–88 (1992).
Cited by
Sorted by citations
Items 101–194 of 194
Form follows function in Triticeae inflorescences
Sakuma, S., & Koppolu, R. (2023) · Ikushugaku zasshi · doi:10.1270/jsbbs.22085 · Cited by 9
“Several studies suggest that the putative Oryza ancestor had three florets, with the two lateral florets degenerated during evolution (Ren et al. 2013, Yoshida et al. 2009).”
BackgroundNon-cell-autonomous signaling associated with barley ALOG1 specifies spikelet meristem determinacy
Jiang, G., Koppolu, R., Rutten, T. L. M., Hensel, G., Lundqvist, U., Moya, Y. A. T., Huang, Y., Rajaraman, J., Poursarebani, N., Nicolaus Von Wirén, A., et al. (2024) · Current Biology · doi:10.1016/j.cub.2024.04.083 · Cited by 9
“22,23,25,27,29,32,34 In a parallel study on the ALOG family in wheat, 70 the authors revealed that the wheat (i.e., ALOG-1 ) ortholog of HvALOG1 is involved in the regulation of inflorescence development; consistent with this, absence of ALOG-1 in wheat facilitates formation of a secondary spikelet…”
BackgroundFormation of two florets within a single spikelet in the rice tongari-boushi1 mutant
Tanaka, W., Toriba, T., Ohmori, Y., et al. (2012) · Plant Signaling & Behavior · doi:10.4161/psb.20522 · Cited by 9
“In rice, each spikelet forms a single fertile floret that is flanked by the sterile lemmas, putative degenerated lemmas derived from lateral sterile florets.(1,3,4) The TOB1 loss-of-function mutant exhibits a unique spikelet phenotype, the formation of two florets within a spikelet, in addition to the formation of a c…”
BackgroundSelf-citationLi, Y., Wang, W., Hu, C., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24129794 · Cited by 8
Yu, H., Ruan, B., Wang, Z., et al. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.00486 · Cited by 8
“The bract-like glume organs of maize and wheat are severely reduced and equivalent to the rudimentary glume in rice, and are similar to the lemma in size and structure (Kellogg, 2001; Yoshida et al., 2009; Hong et al., 2010).”
BackgroundMethodResultInfluentialApical stem cells sustaining prosperous evolution of land plants
Nishihama, R., & Naramoto, S. (2020) · Journal of Plant Research · doi:10.1007/s10265-020-01198-9 · Cited by 8
Kyozuka, J. (2014) · Advances in botanical research · doi:10.1016/b978-0-12-417162-6.00007-9 · Cited by 8
Li, Z. A., Wang, Z., Wang, C., Zeng, X., Tang, J., Zhu, H., Lin, H., Zhu, S., Li, Y. Y., Yao, P., et al. (2025) · New Phytologist · doi:10.1111/nph.20455 · Cited by 7
Genetic Analysis of Anthocyanin Pigmentation in Sterile Lemma and Apiculus in Rice
Kim, W., Adeva, C. C., Lee, H., et al. (2020) · Plant Breeding and Biotechnology · doi:10.9787/pbb.2020.8.4.378 · Cited by 7
Synergistic roles of LAX1 and FZP in the development of rice sterile lemma
Wang, Y., Wei, S., He, Y., Yan, L., Wang, R., & Zhao, Y. (2019) · The Crop Journal · doi:10.1016/j.cj.2019.06.006 · Cited by 7
G1 Interacts with OsMADS1 to Regulate the Development of the Sterile Lemma in Rice
Fang, H., Chen, H., Wang, J., et al. (2024) · Plants · doi:10.3390/plants13040505 · Cited by 6
“In addition to two E-class genes, OsMADS1 and OsMADS34 , the LONG STERILE LEMMA1 ( G1 ) /Elongated empty glume ( ELE ) gene is also involved in the development of sterile lemmas [22,25].”
BackgroundInfluentialGenome-wide identification and evolutionary view of ALOG gene family in Solanaceae
Turchetto, C., Silvério, A. D. C., Waschburger, E. L., Lacerda, M. E. G., Quintana, I. V., & Turchetto‐Zolet, A. C. (2023) · Genetics and Molecular Biology · doi:10.1590/1415-4757-gmb-2023-0142 · Cited by 6
“1; Yoshida et al ., 2009) as a query.”
Kim, D. S., Li, Y., Ahn, H., et al. (2024) · New Phytologist · doi:10.1111/nph.19790 · Cited by 6
K-Domain Splicing Factor OsMADS1 Regulates Open Hull Male Sterility in Rice
Lian-ping, S., Zhang, Y., Zhang, P., et al. (2015) · Rice Science · doi:10.1016/j.rsci.2015.09.001 · Cited by 6
Luo, X., Wei, Y., Zheng, Y., et al. (2023) · BMC Plant Biology · doi:10.1186/s12870-022-04012-x · Cited by 5
Yang, D., He, N., Zheng, X., et al. (2020) · BMC Plant Biology · doi:10.1186/s12870-020-02776-8 · Cited by 5
ALOG/LSHs: a novel class of transcription factors that regulate plant growth and development
Upadhyaya, G., Sethi, V., Modak, A., et al. (2024) · Journal of Experimental Botany · doi:10.1093/jxb/erae409 · Cited by 5
Ren, D., Li, Y., Zeng, W. A. N. G., et al. (2012) · Journal of Integrative Agriculture · doi:10.1016/s2095-3119(12)60160-9 · Cited by 5
Genetic analysis and gene cloning of a triangular hull 1 (tri1) mutant in rice (Oryza sativa L.)
Feng, G., Zhang, C., Tang, M., et al. (2013) · Chinese Science Bulletin · doi:10.1007/s11434-012-5642-9 · Cited by 5
Characterization and Gene Mapping of non-open hull 1 (noh1) Mutant in Rice (Oryza sativa L.)
Zhang, J., Zheng, H., Zeng, X., et al. (2019) · Agronomy · doi:10.3390/agronomy9020056 · Cited by 5
Zhang, Y., Shen, C., Shi, J., Shi, J., & Zhang, D. (2023) · Journal of Experimental Botany · doi:10.1093/jxb/erad386 · Cited by 5
Rice AGL1 determines grain size and sterile lemma identity
Yu, H., Wang, A., Zhang, G., et al. (2024) · The Crop Journal · doi:10.1016/j.cj.2024.02.003 · Cited by 4
Comprehensive identification and analysis of DUF640 genes associated with rice growth
Wang, Z., Wang, R., Yuan, H., et al. (2024) · Gene · doi:10.1016/j.gene.2024.148404 · Cited by 4
Liu, Z., Fan, Z., Wang, L., et al. (2024) · Frontiers in Genetics · doi:10.3389/fgene.2024.1381690 · Cited by 4
Jiang, Q., Zeng, Y., Yu, B., Cen, W., Lu, S., Jia, P., Wang, X., Qin, B., Cai, Z., & Luo, J. (2019) · BMC Plant Biology · doi:10.1186/s12870-019-1805-z · Cited by 4
Zhuang, H. S., Lan, J., Yang, Q., et al. (2023) · Journal of Integrative Agriculture · doi:10.1016/j.jia.2023.07.010 · Cited by 4
Zirkel, J. W., Hulse‐Kemp, A. M., & Storm, A. R. (2022) · PubMed · doi:10.17912/micropub.biology.000670 · Cited by 4
“…of GhLSH4L-A0A1U8MC48 ( Figure 1B ) that have been studied experimentally and computationally (Takeda et al., 2011; Iyer and Aravind, 2012; Yoshida et al., 2009; Zhao et al., 2004), including the closest homologs in Arabidopsis (LSH1-4) and rice (G1) as well as the structural analog viral…”
BackgroundQTL Mapping for Hull Thickness and Related Traits in Hybrid Rice Xieyou 9308
Li-li, L. U. O., Zhang, Y., Chen, D., et al. (2014) · Rice Science · doi:10.1016/s1672-6308(13)60156-0 · Cited by 4
Genetic analysis and gene mapping of a dwarf and liguleless mutation in barley
Guo, B., Jiang, Q., Li, D., et al. (2022) · The Crop Journal · doi:10.1016/j.cj.2022.01.006 · Cited by 4
Ahmad, M. Z., Ahmad, B., Nasir, J. A., et al. (2024) · Genetic Resources and Crop Evolution · doi:10.1007/s10722-024-02239-1 · Cited by 3
“Specifically, there are 11 ALOG members in P. axillaris (Chen et al. 2019), 13 in P. inflate (Chen et al. 2019), 14 in rice (Yoshida et al. 2009; Li et al. 2019), 4 in P. patens (Li et al. 2019) , 9 in B. distachyon (Li et al. 2019), 19 in Z. mays (Li et al. 2019), 11 in S. bicolor (Li et al.…”
Zamzam, M. M., Basak, R., Singh, S. K., Prakash, S., Peesapati, R., Khanday, I., Simonini, S., Grossniklaus, U., & Vijayraghavan, U. (2025) · The Plant Journal · doi:10.1111/tpj.70490 · Cited by 3
Suzuki, C., Tanaka, W., & Hirano, H. (2015) · Genes & Genetic Systems · doi:10.1266/ggs.90.181 · Cited by 3
Self-citationMapping and candidate gene analysis for a new top spikelet abortion mutant in rice
Shu, J., Wang, J., Liu, D., et al. (2016) · Plant Breeding · doi:10.1111/pbr.12342 · Cited by 3
Tang, W., & Tang, A. Y. (2017) · Journal of Forestry Research · doi:10.1007/s11676-017-0414-7 · Cited by 3
“…reveals that the large sterile lemma in the g1 mutant appears to be caused by homeotic transformation of the sterile lemma into a lemma, suggesting that the homeotic gene long sterile lemma G1 is involved in the repression of lemma identity to specify sterile lemma identity (Yoshida et al. 2009).”
BackgroundTsuruta, M., & Mukai, Y. (2019) · Ikushugaku zasshi · doi:10.1270/jsbbs.19078 · Cited by 3
G1-mediated OsMADS1 repression regulates sterile lemma development in rice
Qin, X., Sun, J., Li, R., Cen, W., Li, R., & Luo, J. (2025) · Plant Cell Reports · doi:10.1007/s00299-025-03619-2 · Cited by 2
“Previous studies have reported that knockout of G1 results in the elongation of the sterile lemmas (Yoshida et al. 2009; Hong et al. 2010; Liu et al. 2016).”
InfluentialPolar patterning of the spikelet is disrupted in the two opposite lemma mutant in rice
Sugiyama, S.-H., Tanaka, W., & Hirano, H. (2016) · Genes & Genetic Systems · doi:10.1266/ggs.16-00014 · Cited by 2
“, 2011), whereas the G1 gene encoding a plant-specific nuclear factor specifies sterile lemma identity by repressing lemma identity (Yoshida et al., 2009).”
BackgroundSelf-citationCharacterization and Expression Analysis of the ALOG Gene Family in Rice (Oryza sativa L.)
Luo, X., Wang, H., Wei, Y., et al. (2025) · Plants · doi:10.3390/plants14081208 · Cited by 2
“In 2009, Yoshida et al. classified the Domains of Unknown Function 640 (DUF640) proteins in the Pfam protein family database as the ALOG ( Arabidopsis LSH1 and Oryza G1) domain [1].”
Li, J., Li, B., Zhou, X., et al. (2025) · New Phytologist · doi:10.1111/nph.70291 · Cited by 2
“In rice, the ALOG gene G1 is highly expressed in the sterile lemma primordia, acting as a transcription inhibitor conferring the identity of the sterile lemma (Yoshida et al ., 2009).”
Homeotic genes and their role in development of morphological traits in wheat
Prokopyk, D. O., & Ternovska, T. (2011) · Cytology and Genetics · doi:10.3103/s0095452711010099 · Cited by 2
Yang, D., YE, X. F., Zheng, X., et al. (2016) · The Journal of Agricultural Science · doi:10.1017/s0021859615000866 · Cited by 2
“For example, G1 is involved in the repression of lemma identity to specify the sterile lemma (Yoshida et al. 2009).”
BackgroundCharacterization and fine mapping of nonstop glumes 2 (nsg2) mutant in rice (Oryza sativa L.)
Li, Y., Zeng, X., Zhuang, H., et al. (2019) · Plant Biotechnology · doi:10.5511/plantbiotechnology.19.0506a · Cited by 2
“In the g1 mutant, the sterile lemma is larger than that of the wild-type, and has structural features resembling those of the lemma in the top fertile floret (Yoshida et al. 2009).”
BackgroundResultInfluentialConstruction and application of functional gene modules to regulatory pathways in rice
Hong, W., Chandran, A. K. N., Jeon, J., & Jung, K. (2017) · Journal of Plant Biology · doi:10.1007/s12374-017-0034-y · Cited by 2
“Among the genes controlling flower morphological characteristics, Floral organ regulator 1(OsFOR1), FLORAL ORGAN NUMBER1 (fon1), and Long sterile lemma 1(g1) regulate floral organ identity (Jang et al. 2003; Suzaki et al. 2004; Yoshida et al. 2009), whereas Triangular hull1 (th1) has a role in lemma and palea developm…”
BackgroundPeng, Q., Liu, C., Zou, Z., et al. (2023) · BMC Plant Biology · doi:10.1186/s12870-023-04085-2 · Cited by 1
Genome-wide identification and characterization of ALOG domain genes in Rosa
Chen, F., Lv, B., Guo, J., et al. (2025) · Frontiers in Plant Science · doi:10.3389/fpls.2025.1690365 · Cited by 1
A pendant awn phenotype linked to the EMBRYONIC FLOWER 1 LIKE (EMF1L) gene in barley
Jhingan, S., Boyny, Z. Z. F., Rutten, T. L. M., et al. (2025) · Theoretical and Applied Genetics · doi:10.1007/s00122-025-05105-5 · Cited by 1
“Similarly, in rice, LONG STERILE LEMMA1 ( G1 ) represses lemma identity to maintain the sterile lemma (Liu et al. 2016; Yoshida et al. 2009).”
Jin, D., Yang, C.-Y., Liu, X., et al. (2026) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2026.04.019 · Cited by 1
MULTI-FLORET SPIKELET 4 (MFS4) Regulates Spikelet Development and Grain Size in Rice
Wang, Y., Xiaoqin, Z., Lu, L., et al. (2021) · Rice Science · doi:10.1016/j.rsci.2021.05.005 · Cited by 1
Screening and identification of photoresponse factors in kiwifruit (Actinidia arguta) development
Huang, H., Lin, M., Sun, L., et al. (2024) · Molecular Biology Reports · doi:10.1007/s11033-023-09073-1 · Cited by 1
Cereal genetics: Novel modulators of spikelet number and flowering time
Li, M., & Jiao, Y. (2024) · Current Biology · doi:10.1016/j.cub.2024.04.071 · Cited by 1
Designer Rice in Quest of High Grain Filling
Mohapatra, P. K., & Sahu, B. B. (2021) · Springer eBooks · doi:10.1007/978-3-030-67897-5_13 · Cited by 1
Lateral organ diversification in plants mediated by the ALOG protein family of transcription factorsPreprint
Naramoto, S., Jones, V. A. S., Trozzi, N., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/689109 · Cited by 1
Huang, X., Xiao, N., Xie, Y., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.03.18.435998 · Cited by 1
“…and other nightshades (Solanaceae) have reported important roles of ALOG genes in floral organ specification, light signaling (Chen et al., 2019; Cho and Zambryski, 2011; Lei et al., 2019; Naramoto et al., 2019; Sato et al., 2014; Takeda et al., 2011; Yoshida et al., 2009, 2013; Zhao et al., 2004).”
BackgroundKim, D. S., Woods‐Tör, A., Çevik, V., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.04.25.538220 · Cited by 1
Zhang, X., Liu, D., Shu, J., et al. (2014) · Plant Omics
Mapping and allelic sequencing of a long sterile lemma trait in rice
Jiang, L., Zhu, Z., Huang, R., et al. (2017) · Bragantia · doi:10.1590/1678-4499.098
“G1 was cloned by the map-based cloning method (Yoshida et al. 2009).”
BackgroundMethodInfluentialKraehmer, H. (2019) · Grasses · doi:10.1002/9781119417095.ch4
Phan, M. S. V., Keren, I., Tran, P. T., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.07.30.502139
“The presence of DNA binding motifs, transcriptional regulation activity, nuclear localization, and homodimerization ability (21, 35-37) suggest that the ALOG proteins may function as specific transcription factors.”
BackgroundPhan, M. S. V., Tran, P. T., & Citovsky, V. (2022) · Journal of Visualized Experiments · doi:10.3791/64656
Dabing Zhang (July 5, 1967–June 22, 2023)
Yuan, Z., Shi, J., Yang, L., et al. (2023) · Seed Biology · doi:10.48130/seedbio-2023-0011
Cytokinins specify pluripotent stem cell identity in the moss Physcomitrium patensPreprint
Hata, Y., Ohtsuka, J., Hiwatashi, Y., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.19.572286
Kuroha, T., Lombardo, F., Iwasaki, W. M., Chechetka, S. A., Kawahara, Y., Yoshida, A., Kyozuka, J., Makino, T. T., & Yoshida, H. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.17.612847
Self-citationThe genetic control of long sterile lemma during African rice domestication
Luo, L., Luo, W., Gao, B., Wang, K., Ma, S., Ndjiondjop, M.-N., Sun, C., Zhu, Z., & Chang, L. (2024) · Journal of Integrative Agriculture · doi:10.1016/j.jia.2024.11.031
Luo, X., Wang, H., Wei, Y., et al. (2025) · Chinese Science Bulletin (Chinese Version) · doi:10.1360/tb-2024-1267
Genetic regulation of rice panicle architecture: a molecular approach
Kyozuka, J. (2025) · Breeding Research · doi:10.1270/jsbbr.25j13
Modular 3D-printed biophotonic platform for cost-effective hyperspectral and polarimetric imaging
Boateng, R., Månefjord, H., Opoku-Ansah, J., et al. (2025) · Optics Continuum · doi:10.1364/optcon.575071
Luo, X., Wei, Y., Zheng, Y., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26559437
Luo, X., Wei, Y., Zheng, Y., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26559446
Luo, X., Wei, Y., Zheng, Y., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26559422
Yang, D., He, N., Zheng, X., et al. (2020) · Figshare · doi:10.6084/m9.figshare.13467327
Luo, X., Wei, Y., Zheng, Y., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26559431
Luo, X., Wei, Y., Zheng, Y., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26559425
Luo, X., Wei, Y., Zheng, Y., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26559455
Luo, X., Wei, Y., Zheng, Y., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26559434
Luo, X., Wei, Y., Zheng, Y., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26559452
Luo, X., Wei, Y., Zheng, Y., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26559461
Luo, X., Wei, Y., Zheng, Y., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26559440
Luo, X., Wei, Y., Zheng, Y., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26559458
Peng, Q., Liu, C., Zou, Z., et al. (2023) · Figshare · doi:10.6084/m9.figshare.22609621
Huang, X., Xiao, N., Zou, Y., et al. (2022) · Figshare · doi:10.6084/m9.figshare.19359573
Luo, X., Wei, Y., Zheng, Y., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26559464
Yang, D., He, N., Zheng, X., et al. (2020) · Figshare · doi:10.6084/m9.figshare.13467323
Luo, X., Wei, Y., Zheng, Y., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26559443
Huang, X., Xiao, N., Zou, Y., et al. (2022) · Figshare · doi:10.6084/m9.figshare.19359570
Luo, X., Wei, Y., Zheng, Y., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26559428
Luo, X., Wei, Y., Zheng, Y., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26559449
Luo, X., Wei, Y., Zheng, Y., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26559419
Li, X., Gu, S., Huang, D., et al. (2025) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2025.110983
Genomic and Functional Analysis of the ALOG Gene Family in Dioscorea alata
Zhang, Y., Wu, J., Lin, H., et al. (2026) · Plants · doi:10.3390/plants15050718
Yuan, Z., & Zhang, D. (2026) · Springer eBooks · doi:10.1007/978-981-95-7033-1_7
Ohyama, A., Toriba, T., Sato, M., Tsuji, H., & Tanaka, W. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.19.726093
Self-citationZhang, G., Hu, Y., Huang, N., McIntyre, C. A., & Ma, H. (2026) · Plant Communications · doi:10.1016/j.xplc.2026.101937
Metadata
- Authors
- Yoshida, A., Suzaki, T., Tanaka, W., & Hirano, H.-Y.
- Affiliations
- The University of Tokyo (JP)
- University of California San Diego (US)
- Department of Biological Sciences, Graduate School of Science, University of Tokyo, Tokyo 113-8654, Japan
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2009-11-24
- Volume
- 106
- Issue
- 47
- Pages
- 20103-20108
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC2775035
- OpenAlex
- W2032677611
- Semantic Scholar
- 82ab49c65d5a71c52986815cb49faa36656b9119
- Cited by
- 194
- References
- 47
- Citations by year
- 2026: 5 · 2025: 13 · 2024: 33 · 2023: 18 · 2022: 13 · 2021: 7 · 2020: 15 · 2019: 20 · 2018: 10 · 2017: 9 · 2016: 9 · 2015: 6 · 2014: 10 · 2013: 9 · 2012: 7
- FWCI
- 6.88
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Ministry of Education, Culture, Sports, Science and Technology
- Japan Science Society
- Japan Society for the Promotion of Science (20061006, 20380005)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Genetic and Mutation Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Mapping and Diversity in Plants and Animals
- Keywords
- homeotic transformation, transcriptional regulation, Oryza grandiglumis, floral organ specification, rice
- MeSH terms
- Genes, Homeobox, Mutation, Phenotype, Phylogeny, Plant Proteins, Oryza, Genes, Plant, Gene Expression Regulation, Plant, Flowers
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