The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.
Insights into the Origin and Evolution of the Plant Hormone Signaling Machinery
Open accessAbstract
Plant hormones modulate plant growth, development, and defense. However, many aspects of the origin and evolution of plant hormone signaling pathways remain obscure. Here, we use a comparative genomic and phylogenetic approach to investigate the origin and evolution of nine major plant hormone (abscisic acid, auxin, brassinosteroid, cytokinin, ethylene, gibberellin, jasmonate, salicylic acid, and strigolactone) signaling pathways. Our multispecies genome-wide analysis reveals that: (1) auxin, cytokinin, and strigolactone signaling pathways originated in charophyte lineages; (2) abscisic acid, jasmonate, and salicylic acid signaling pathways arose in the last common ancestor of land plants; (3) gibberellin signaling evolved after the divergence of bryophytes from land plants; (4) the canonical brassinosteroid signaling originated before the emergence of angiosperms but likely after the split of gymnosperms and angiosperms; and (5) the origin of the canonical ethylene signaling pathway postdates shortly the emergence of angiosperms. Our findings might have important implications in understanding the molecular mechanisms underlying the emergence of land plants.
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FastTree 2 – Approximately Maximum-Likelihood Trees for Large Alignments
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The F-box protein TIR1 is an auxin receptor
Dharmasiri, N., Dharmasiri, S., & Estelle, M. (2005) · Nature · doi:10.1038/nature03543 · Cited by 2,083
Jasmonate perception by inositol-phosphate-potentiated COI1–JAZ co-receptor
Sheard, L. B., Tan, X., Mao, H., Withers, J., Ben-Nissan, G., Hinds, T. R., Kobayashi, Y., Hsu, F.-F., Sharon, M., Browse, J., et al. (2010) · Nature · doi:10.1038/nature09430 · Cited by 1,497
How significant is a protein structure similarity with TM-score = 0.5?
Xu, J., & Zhang, Y. (2010) · Bioinformatics · doi:10.1093/bioinformatics/btq066 · Cited by 1,142
D14–SCFD3-dependent degradation of D53 regulates strigolactone signalling
Zhou, F., Lin, Q., Zhu, L., Ren, Y., Zhou, K., Shabek, N., Wu, F., Mao, H., Dong, W., Gan, L., et al. (2013) · Nature · doi:10.1038/nature12878 · Cited by 891
DWARF 53 acts as a repressor of strigolactone signalling in rice
Jiang, L., Liu, X., Xiong, G., Liu, H., Chen, F., Wang, L., Meng, X., Liu, G., Yu, H., Yuan, Y., et al. (2013) · Nature · doi:10.1038/nature12870 · Cited by 868
The Origin and Establishment of the Plastid in Algae and Plants
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Insights into Land Plant Evolution Garnered from the Marchantia polymorpha Genome
Bowman, J. L., Kohchi, T., Yamato, K. T., Jenkins, J., Shu, S., Ishizaki, K., Yamaoka, S., Nishihama, R., Nakamura, Y., Berger, F., et al. (2017) · Cell · doi:10.1016/j.cell.2017.09.030 · Cited by 1,205
Modularity in Jasmonate Signaling for Multistress Resilience
Howe, G. A., Major, I. T., & Koo, A. J. (2018) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-042817-040047 · Cited by 697
Evolution of Hormone Signaling Networks in Plant Defense
Berens, M. L., Berry, H. M., Mine, A., Argueso, C. T., & Tsuda, K. (2017) · Annual Review of Phytopathology · doi:10.1146/annurev-phyto-080516-035544 · Cited by 563
Cui, H., Gobbato, E., Kracher, B., Qiu, J., Bautor, J., & Parker, J. E. (2017) · New Phytologist · doi:10.1111/nph.14302 · Cited by 299
Hormones as go‐betweens in plant microbiome assembly
Eichmann, R., Richards, L., & Schäfer, P. (2021) · The Plant Journal · doi:10.1111/tpj.15135 · Cited by 299
Metadata
- Authors
- Wang, C., Liu, Y., Li, S.-S., & Han, G.-Z.
- Venue
- Plant Physiology
- Publisher
- Oxford University Press (OUP)
- Published
- 2015-01-05
- Volume
- 167
- Issue
- 3
- Pages
- 872-886
- ISSN
- 0032-0889 (ISSN-L)
- 1532-2548
- OpenAlex
- W1968823787
- Cited by
- 244
- References
- 7
- FWCI
- 26.67
- Type
- journal article
- Language
- en
- Open access
- green
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