Difference between revisions of "Os05g0482400"
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Transgenic RNA interference of the Eui gene effectively increased plant height and improved heading performance. Furthermore, the eui mutant was defective in starch granule development in root caps and Eui overexpression enhanced starch granule generation and gravity responses, revealing a role for Eui in root starch granule development and gravity responses<ref name="ref15" />. | Transgenic RNA interference of the Eui gene effectively increased plant height and improved heading performance. Furthermore, the eui mutant was defective in starch granule development in root caps and Eui overexpression enhanced starch granule generation and gravity responses, revealing a role for Eui in root starch granule development and gravity responses<ref name="ref15" />. | ||
| − | [[File:6-2.jpg|right|thumb|150px|'' Eui mutants are more susceptible to bacterial blight (from reference <ref name="ref18" />).'']] | + | [[File:6-2.jpg|right|thumb|150px|''Eui mutants are more susceptible to bacterial blight (from reference <ref name="ref18" />).'']] |
The mutants displayed significantly longer lesion to PXO99A than their controls. Similar results were obtained with infection by DY89031. Similarly, the representative transgenic lines S73 and S74,in which Eui expression was knocked down with RNAi<ref name="ref15" />, phenocopied the susceptibility of the eui mutants to both the strains. Slightly enhanced resistance to Xoo in semi-dwarf rice containing the mutant "Green Revolution" gene sd1, in comparison with the near-isogenic tall rice carrying the wild-type Sd1 gene that encodes a GA20 oxidase<ref name="ref17" />. Therefore, the loss of function of Eui decreased disease resistance, suggesting that EUI might be a positive modulator of basal disease resistance in rice<ref name="ref18" />. | The mutants displayed significantly longer lesion to PXO99A than their controls. Similar results were obtained with infection by DY89031. Similarly, the representative transgenic lines S73 and S74,in which Eui expression was knocked down with RNAi<ref name="ref15" />, phenocopied the susceptibility of the eui mutants to both the strains. Slightly enhanced resistance to Xoo in semi-dwarf rice containing the mutant "Green Revolution" gene sd1, in comparison with the near-isogenic tall rice carrying the wild-type Sd1 gene that encodes a GA20 oxidase<ref name="ref17" />. Therefore, the loss of function of Eui decreased disease resistance, suggesting that EUI might be a positive modulator of basal disease resistance in rice<ref name="ref18" />. | ||
Revision as of 15:15, 11 June 2014
The rice EUI1 (ELONGATED UPPERMOST INTERNODE) gene controls the growth of the first internode at the top of rice, and the recessive mutations of this site cause the abnormal elongation of internodes at the top of rice.
Annotated Information
Function
EUI gene is a recessive gene which was first reported by Rutger and Carnahan [1], which is characterized by the near doubling length of the uppermost internode, excess panicle exsertion and an increased panicle length in comparison with the wild type.The EUI mutant shows notably rapid elongation of the uppermost internode at the heading stage. Because of its prospective application to amend panicle enclosure in the male-sterile lines, this recessive trait, along with male sterility,maintainer and restorer, was referred to as the fourth genetic element of hybrid rice production [1].
The EUI1 gene was mapped on the central part of the long arm of chromosome 5, and located within two overlapping bacterial artificial chromosome (BAC) clones, OSJNBa0018K15 and OSJNBa0095J22, in an interval of 98 kb between markers M0387 and M01 [2].The EUI1 gene encodes a putative cytochrome P450 protein, CYP714D1. It can control the elongation of internodes and determines the plant height and underlies the grain yield .EUI1 plays a negative role in gibberellinmediated regulation of cell elongation in the uppermost internode of rice [3][4].
Rice internodes are important organs that affect plant height, yield, lodging resistance, and panicle exsertion, and also constitute a unique system for the study of gibberellic acid (GA) signaling. A spontaneous recessive tall mutant in rice called eui, which shows notably rapid elongation of the uppermost internode at the heading stage, was picked up in a japonica variety of rice some years ago [1]. The mutant (zeui stock) is characterized by a near-doubling in the length of the uppermost internode, extreme panicle exsertion, and an increase in panicle length, with little or no effect on other internodes or plant characters. This recessive genotype with the elongated uppermost internode is a very useful trait in hybrid rice seed production, and was referred to as the fourth genetic element of hybrid rice, in addition to the traits male sterility, maintainer and restorer [1]. Panicle enclosure, a phenotype which is typical of almost all male-sterile (MS) lines [5] [6] [7], greatly reduces seed production by hybrid rice, necessitating the use of large amounts of exogenous GA to cause panicle exsertion. However, GA application not only increases the cost of seed production, but also greatly increases the rate of seed germination on the panicle, resulting in decreased quality and shortened storage life of hybrid seeds. In contrast, eui MS plants need little or no exogenous GA application for hybrid seed production[6] [8]. Therefore, the eui mutant represents a breakthrough in hybrid rice production[9].Previous genetic and physiological studies have shown that the eui phenotype is due to a recessive mutation in a single gene, which functions similarly in both japonica and indica subspecies and confers highest sensitivity to exogenously applied GA3 at the seedling and heading stages among the genotypes studied, although the level of GAs in eui plants is already higher than that in wild-type plants [9][10][11]. These results strongly suggested that the Eui gene is likely to be involved in GA metabolism or signaling.
The eui1 mutants have increased cell elongation, higher levels of endogenous active gibberellin, and also a higher sensitivity to exogenously applied GA3During the seedling and tillering stages, eui plants were morphologically similar to wild-type plants[8].However, at the heading stage, the eui mutant exhibited an extremely elongated uppermost internode, with slightly elongated second and third internodes and panicle. Because of the enhanced internode elongation, the stem exposed between the ear and the flag leaf sheath (panicle exsertion) is much longer in the eui mutant than in wild-type plants . The enhanced internode elongation of the eui mutant was due to longitudinally increased cell lengths but not to an increase in the number of cells (Figure . These observations suggested that the uppermost internode of the eui mutant might accumulate an excessive amount of biologically active GAs or exhibit an enhanced GA sensitivity[13].
EUI catalyzed 16a,17-epoxidation of non-13-hydroxylated GAs. Consistent with the tall and dwarfed phenotypes of the eui mutant and Eui-overexpressing transgenic plants, respectively, 16a,17-epoxidation reduced the biological activity of GA4 in rice, demonstrating that EUI functions as a GA deactivating enzyme[13].
Overexpression of EUI1 gave rise to the gibberellin-deficient-like phenotypes, which could be partially reversed by supplementation with gibberellin .Furthermore, apart from the alteration of expression levels of the gibberellin biosynthesis genes, accumulation of SLR1 protein was found in the overexpressing transgenic plants,indicating that the expression level of EUI1 is implicated in both gibberellin-mediated SLR1 destruction and a feedback regulation in gibberellin biosynthesis.The rice EUI gene encodes a cytochrome P450 monooxygenase that deactivates bioactive gibberellins (GAs)[3].
An early study showed that GA plus kinetin treatment could remove starch granules in amyloplasts and therefore change gravisensitivity of cress roots[15]. Starch granules were almost completely absent in eui root-tip cells, while their generation was enhanced in the roots of Eui-OX plants compared with WT plants. As a consequence of the altered starch granule development, Eui-OX roots were more hypersensitive than the WT to gravity. After 2h of rotation away from vertical, most Eui-OX root tips bended near vertical. All WT and Eui-OX root tips bended vertically when roots were rotated over 12h. These results indicate that Eui is also involved in GA homeostasis in rice roots and reveal a novel role for GA in gravity responses[14].
The eui phenotype that has increased panicle exertion (heading performance) has been used in breeding for male sterile varieties of hybrid riceCite error: Closing </ref> missing for <ref> tag
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Structured Information
| Gene Name |
Os05g0482400 |
|---|---|
| Description |
Cytochrome P450 family protein |
| Version |
NM_001062401.1 GI:115464532 GeneID:4339131 |
| Length |
9805 bp |
| Definition |
Oryza sativa Japonica Group Os05g0482400, complete gene. |
| Source |
Oryza sativa Japonica Group ORGANISM Oryza sativa Japonica Group
Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;
Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP
clade; Ehrhartoideae; Oryzeae; Oryza.
|
| Chromosome | |
| Location |
Chromosome 5:23775727..23785531 |
| Sequence Coding Region |
23775837..23776191,23784066..23785444 |
| Expression | |
| Genome Context |
<gbrowseImage1> name=NC_008398:23775727..23785531 source=RiceChromosome05 preset=GeneLocation </gbrowseImage1> |
| Gene Structure |
<gbrowseImage2> name=NC_008398:23775727..23785531 source=RiceChromosome05 preset=GeneLocation </gbrowseImage2> |
| Coding Sequence |
<cdnaseq>atggagagcttcttcgtcttcttcacggcggcggcgttgccggtggtggtggcggcggcggtgatcgccgggctgtgcattacggcggcgtggctggcgaggccgcggcgcgtggcggaggtgttccggaggcaggggatcgacggcccgccgccgtcgtcgttcctggcggggaacctcccggagatgaaggcgagggtggccgccgcggcgtcggcggcggcgccaacggcggacggggaggagaccgcctccgccggcggcggcggcggtggccgggacttcgagaaggacgggttcgacgactactgcaccaggatcttcccttacttccacaagtggaggaaagcctacggcgagacgtacctgtactggctgcggcggcggccggcgctgtacgtgacggacccggagctcatcggcgagatcgggcggtgcgtgtcgctcgacatgggcaagcccaagtacctccagaaaggccaggagccactcttcggcggcggcgtcctcaaggccaacggcgcgtgctgggcgcgccagcgcaaggtcatcgcgccggagttctacatggcccgtgtcagggccatggtccagctcatggtcgacgccgcgcagccgctgatcgcctcctgggaatccaggatcgacgccgctggaggcgcggcggcggcggaggtcgtcgtcgacggcgacctccggagcttctccttcgatgtgatatcgcgggcttgctttgggagtgattactcgagggggagggagatcttcctccgcctccgtgagctgtccgggctcatgtcggagaccagcgtcatcttcagcatcccttcgctgaggcacctgccgacggggaagaaccggaggatctggaggctcacgggggagatccggtcgctgatcatggagctcgtcagggagcggaggtgcgcggcgagggcggcgagggagcacggcgggaaggcggcgccgccgtcgccgccggagcgcgacttcctcggctccatcatcgagaacagcggcgggcagccgcggccggacgacttcgtggtggacaactgcaagaacatctacttcgccgggcacgagacgagcgcggtcaccgcgacgtggtgcctcatgctgctcgccgcgcacccggagtggcaggaccgcgcccgcgccgaggtgctcgaggtctgcggcggcgacggcgccgccgcccccgccgcgccggacttcgacatggtgtcccggatgcggacggtggggatggtggtgcaggaaacgctgcggctgttcccgccgtcgtcgttcgtggtgcgggagacgttccgggacatgcagttgggtaggctgctggcgcccaagggcacctacctgttcgtcccggtgtccaccatgcaccacgacgtcgccgcctggggcccgacggcgaggctgttcgacccgtcccgcttccgcgacggcgtggcggcggcgtgcaagcacccgcaggcgtcgttcatgccgttcggcctcggcgcccgcacctgcctcggccagaacctcgcgctcgtcgaggtcaagacgctcgtcgccgtcgtcctcgcccggttcgagttcacgctctcgccggagtacaggcactcgccggcgttccggctcatcatcgagccggagttcggcctccgcctccgcatccgccgcgccggcggtcaggacgccacgtcacaagttgacacatctactgcacccgtgcatagttctcataattaa</cdnaseq> |
| Protein Sequence |
<aaseq>MESFFVFFTAAALPVVVAAAVIAGLCITAAWLARPRRVAEVFRR QGIDGPPPSSFLAGNLPEMKARVAAAASAAAPTADGEETASAGGGGGGRDFEKDGFDD YCTRIFPYFHKWRKAYGETYLYWLRRRPALYVTDPELIGEIGRCVSLDMGKPKYLQKG QEPLFGGGVLKANGACWARQRKVIAPEFYMARVRAMVQLMVDAAQPLIASWESRIDAA GGAAAAEVVVDGDLRSFSFDVISRACFGSDYSRGREIFLRLRELSGLMSETSVIFSIP SLRHLPTGKNRRIWRLTGEIRSLIMELVRERRCAARAAREHGGKAAPPSPPERDFLGS IIENSGGQPRPDDFVVDNCKNIYFAGHETSAVTATWCLMLLAAHPEWQDRARAEVLEV CGGDGAAAPAAPDFDMVSRMRTVGMVVQETLRLFPPSSFVVRETFRDMQLGRLLAPKG TYLFVPVSTMHHDVAAWGPTARLFDPSRFRDGVAAACKHPQASFMPFGLGARTCLGQN LALVEVKTLVAVVLARFEFTLSPEYRHSPAFRLIIEPEFGLRLRIRRAGGQDATSQVD TSTAPVHSSHN</aaseq> |
| Gene Sequence |
<dnaseqindica>111..465#8340..9718#aagggcgaggtgagcgaggcgagactcgagagagaggagaagatccagaaatcgcaagctgcacgctatagctaggtagctatctccggggaaagagagagtaggctgccatggagagcttcttcgtcttcttcacggcggcggcgttgccggtggtggtggcggcggcggtgatcgccgggctgtgcattacggcggcgtggctggcgaggccgcggcgcgtggcggaggtgttccggaggcaggggatcgacggcccgccgccgtcgtcgttcctggcggggaacctcccggagatgaaggcgagggtggccgccgcggcgtcggcggcggcgccaacggcggacggggaggagaccgcctccgccggcggcggcggcggtggccgggacttcgagaaggacgggttcgacgactactgcaccaggatcttcccttacttccacaagtggaggaaagcctacggtacgtgtacacaagcctctctcctctctactgctcgatttcacatcactagctacatgcatgatgcttgcttgctttgcctgttaattactccgctcatgtgtgcttaattagcttaattaattcacactccggttaatcaagtcatgcaaaacccacaattaatcagctatcaattgagatgagtatataccagaatatatatacttacagtaaatttaataaaaaaataaaaaaaagaaaagaaaagctctctcgatctctctgtgacgatgatacaagaaatttgtggttgccctagtaacaagttgactagagtataaaagctgctaaaatgtcaagagctctccatataaaaaagaacagtgggggagaataattaatactgtcccaaacagcgagaggaagagagggggcaaacgagaaaagagagaataaacaaaattaatgcaggatggaaaccgtggttgggacgaactactcggtttgcttccagtcaaccgtcctgcatcattaagctatggattaataattaattaactgcagtatataaatatatatactcccccacatatattaatcggtcgttggtccaattagacaacagcaaagccatgcctaggtacctgtctaggtaggctatgactgtagtacactcgtactactcacttaatagcacattagtgctcttattttgcgaattaatgaaactttaatcaataataactatatataactataatatatttagtataatttaacaatatatctattcagcgtgctatcgtttcttcagcctatcaatcaacttaaaaaacttagtgttaaattgattttggtgttttcttatcgtaatttttcttcagttttggattgttttttaagttgctaacaattttagttaacaaagctatttggaaggagaggaataatgcatccatgacaaaagtatatgcttcataataattttcatataccagatcttgcccctggtggtgacgtgttaccaaataccgactggaattaatttcttctctctttctttttctctctgccggtgcaatgaggcgacatttttgagttataactgtgcgtatgaatgcatgtattaattgctgtttgctgaggttaataggctagcaataccgttgttttgggggaccccgcagtttgacctagtagagtttatcatggacgcagactgcccctacctgttcttcttcacggacagcatgattaattagctatactagtggtagtactcgatgtcattaataattggtctctccgtacgtgaataattatcgatttttgactttgacaagtactccctccgtacttgttaaggaagtcgttttagacagcaacacggtctccaaaacacaactttaacttcttatttctataaaaatatttattgaaaagtgatatatgtatacttttatgaaatattttttaagacaaatatattcatataatttttacattttaaaacttaatggaaagttacttttccaagatttgactcaaacattgttctaaacgatttcctttatgagtacggaaaaagtatgttttttcactgttcttatgaagtgtacatggaaagtgatcgaatagctctgagcagtactctaggtagggaattacttttagttgcgtacaaatctaacaattaattaatatgccatttttagtgaacataattgtatattttctccgtttcacaatgtaagacattctagcattttccacatgcatattaatgttaatatgtctagattcattaacatcaatataaatataagaaatgctagaatgacttacattataaaacggaggaagtaatttatgctagaatgacttacattataaaacggaggaagtaatttagtacatcaccttcgtcgattattacgaaaacatccatcatatcgatcgatatctgtgtatttgctactccagaaaaatattttctgagaccgacccacagatgcatatatatgcacattattgtggcggttttcctttctttttagatcaatcggtggcctgacggccggcccagcttcgattgaaattaagctgaataattattgtggccgtcatgtgctaatcacccatataattaggcgtggttagaacctgactaagctatttaagccggtcagttaggctttcccaaaacggccatcaggccatgcatgttgccattagctgtccgagcacgccggccaaagctcaaccctcgtgatcacatcaactcgatctccccgatgcttatccctttttgcaagcaaccggtatgtggtgcttagataattaatgcaagaattaacagtgtacctcctatcaatttgccgttagctatgcatgtaatggattagaaattctatatgcatgttttcgtctaacagagtttgatcagcagcagtacttagctaactaattattctgtaatttatataactactataagctagagtttaagcagagtatgtaagtatgatattttaactaatttagttcttgtcatatggcactgtagttgaaaccataaaccgatcaattaataggacaaatattcaacctggttgcctcactgcatgcgttgttttagtttgacaaatgcatgcatgtgtatgatattttatttgcttggcccttaataagtatattatgttgaagtcatgcatcttgacacagaaacttggagcaaaaactatataatatatttcaagaaccaaagggcctgaatactagtacttgcctacatcgatcacatgatgctagtgtcaatcttatttaaggtttttatttcttctttaatgtcaaaatggctattgtttaactatctaaaaacaccaataattagaagactcccactagaccatctcatgatgcattgcacgtaggatcgatatatatggcaacattaattattttacttgaacatctaatcgcgttcgctattattcaacttatgttacatgttctcccctaatttaagcaaaggccggtttgaccaacgggaaacaaataattaaattgatcttccaggcccagtacttatattaattacctagtcattaactacattttctccatatttaatttgaatgcttcgttctgaaatatttaaaggccattaacactaacacggcacacaagaaattaatttaaatatttaatttggctagcatgtatacatatatatgttgatatgcatggatatatatatatatatatatatatatatatatatatatatgtatatatatatatatgtatatatatgtatatatgtatgtatatgtatatgtatatgtatatgtgtgtgtgtgtgtgtgtgtgtgacaatagctaactttagatatgtttttttttcgatgatacatggtcccggcctctgcatcacaaatgcacacatccaacgaatatcgtacaaataataataaaaaaagtgatgggacaaaactcccgactcctacataagacttaggactagtgagctaagggtgtgtttagttcaccaaaattggaaatttgattgaaattagaatgatgtgacggaaaagttgaaagtttgtgtgtgtaggaaagttttgatgtgatggaaaatttggaagtttgaagaaaaagtttagaactaaactcggcctaactgaaaacaaatcaattgatatttgttttcagttatgccgagtttagtttgacaaaattaaacgaaaccatacaatatataattacaaatcaataattaattcctaatgctgcttgatgctactagcttctctcctacacagtgccattgactaggtaattgctcctaaccctagctagctaagcatgcagctcgatcgaatcgatcgagcatgaaagcaacaggtcgatcgatagatggtaagccatgacgatcaatatgatcatatcatgcatgcatgacactgtagagtgtgtactacgtactaccaccactccaccaaccatgcatgcattcctcccccctctctcttgcaccttttaaagctagctaggacgtgtggggacttcaatatatttcttgtgcattgtctctcctacaaggattccacatggagatgtgcatatgcatggggttacaccaattaaaagtgcagcccacactctatggattgaaggtgctagctagatctctgtactctatccgtcccaaaatataagcatttttagttataaatccagatagatagttatccagattcgtagctaaaagttattatattttaggatggaggtaatatagtttagatggtggaaattaagtctagtagctatggggaaaaatggcaaaaataaaattacagtatggggttgtactggaaaattttcatttgaatatatctcttcacaaatatgtaagcctaaatttaatctaaatatatatgggcacaaatgaattaaaaaacatattttctatgaacatatatagcaggaataatatgcattcctcgattttatt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| External Link(s) |
- ↑ 1.0 1.1 1.2 1.3 Cite error: Invalid
<ref>tag; no text was provided for refs namedref1 - ↑ 2.0 2.1 Xu, Y.H., Zhu, Y.Y., Zhou, H.C., Li, Q., Sun, Z.X., Liu, Y.G., Lin, H.X. and He,Z.H. (2004) Identification of a 98-kb DNA segment containing the rice EUI gene controlling uppermost internode elongation, and construction of a TAC transgene sublibrary. Mol. Gen. Genet. 272: 149–155.
- ↑ 3.0 3.1 3.2 3.3 3.4 3.5 3.6 3.7 3.8 3.9 Anding Luo;Qian Qian;Hengfu Yin;Xiaoqiang Liu;Changxi Yin;Ying Lan;Jiuyou Tang;Zuoshun Tang;Shouyun Cao;Xiujie Wang;Kai Xia;Xiangdong Fu;Da Luo;and Chengcai Chu.(2006) EUI1, Encoding a Putative Cytochrome P450 Monooxygenase, Regulates the Internodes Elongation by Modulating GA Responses in Rice.Plant and Cell Physiology 47(2): 181-191.
- ↑ 4.0 4.1 Ma Hongli;Zhang Shubiao;Ji Lan;Zhu Hongbo;Yang Shulan;Fang Xuanjun;Yang Rencui.(2006) Fine Mapping and in silico Isolation of the EUI1 Gene Controlling Upper Internode Elongation in Rice.Plant Molecular Biology 60(1): 87-94.
- ↑ 5.0 5.1 Shen ZT, Yang CD, He ZH (1987) Studies on eliminating panicle enclosure in WA type MS line of rice Oryza sativa subsp. indica).Chin J Rice Sci 1:95–99.
- ↑ 6.00 6.01 6.02 6.03 6.04 6.05 6.06 6.07 6.08 6.09 6.10 6.11 6.12 6.13 6.14 6.15 6.16 6.17 6.18 6.19 Shen ZT, He ZH (1989) Interaction between eui gene and WAMS cytoplasm of rice and improvement of panicle exsertion of MS line. SABRAO J 6:753–756. Cite error: Invalid
<ref>tag; name "ref6" defined multiple times with different content Cite error: Invalid<ref>tag; name "ref6" defined multiple times with different content Cite error: Invalid<ref>tag; name "ref6" defined multiple times with different content Cite error: Invalid<ref>tag; name "ref6" defined multiple times with different content Cite error: Invalid<ref>tag; name "ref6" defined multiple times with different content Cite error: Invalid<ref>tag; name "ref6" defined multiple times with different content Cite error: Invalid<ref>tag; name "ref6" defined multiple times with different content Cite error: Invalid<ref>tag; name "ref6" defined multiple times with different content Cite error: Invalid<ref>tag; name "ref6" defined multiple times with different content Cite error: Invalid<ref>tag; name "ref6" defined multiple times with different content Cite error: Invalid<ref>tag; name "ref6" defined multiple times with different content Cite error: Invalid<ref>tag; name "ref6" defined multiple times with different content Cite error: Invalid<ref>tag; name "ref6" defined multiple times with different content Cite error: Invalid<ref>tag; name "ref6" defined multiple times with different content Cite error: Invalid<ref>tag; name "ref6" defined multiple times with different content Cite error: Invalid<ref>tag; name "ref6" defined multiple times with different content Cite error: Invalid<ref>tag; name "ref6" defined multiple times with different content - ↑ 7.0 7.1 Yang RC, Zhang SB, Huang RH, Yang SL, Zhang QQ (2002) Breeding technology of eui hybrids of rice. Scientia Agricultura Sinica 35:233–237.
- ↑ 8.0 8.1 8.2 He ZH, Shen ZT (1994) Sensitivity of elongated internode gene to GA3 and improvement of MS line in rice. Acta Agronomica Sinica 20:161–167.
- ↑ 9.0 9.1 9.2 Zhang QQ, Yang RC (2003) The effect of different eui genes on biological characters of e-hybrid rice. Scientia Agricultura Sinica 36:735–739.
- ↑ 10.0 10.1 He ZH, ETOH K, Shi CH, Shen ZT (1993) Sensitivity of plant height genes to GA3 and their relationship with enzymes in rice. Chin J Rice Sci 7:143–147.
- ↑ 11.0 11.1 He ZH, Shen ZT, Li DB (1994) Relations of plant height genes to the sensitivity of GA3 and to the regulation of endogenous hormones in different rice growth stages. Plant Physiol Commun 30:170–174.
- ↑ 12.0 12.1 Itoh, H., Ueguchi-Tanaka, M., Sato, Y., Ashikari, M. and Matsuoka, M. (2002)The gibberellin signaling pathway is regulated by the appearance and disappearance of SLENDER RICE1 in nuclei. Plant Cell 14: 57–70.
- ↑ 13.0 13.1 13.2 13.3 13.4 Yongyou Zhu;Takahito Nomura;Yonghan Xu;Yingying Zhang;Yu Peng;Bizeng Mao;Atsushi Hanada;Haicheng Zhou;Renxiao Wang;Peijin Li;Xudong Zhu;Lewis N. Mander;Yuji Kamiya;Shinjiro Yamaguchi;Zuhua He.(2006)ELONGATED UPPERMOST INTERNODEEncodes a Cytochrome P450 Monooxygenase That Epoxidizes Gibberellins in a Novel Deactivation Reaction in Rice.The Plant Cell 18(2): 442-456.
- ↑ 14.0 14.1 14.2 14.3 Yingying Zhang;Yongyou Zhu;Yu Peng;Dawei Yan;Qun Li;Jianjun Wang;Linyou Wang;Zuhua He.(2008)Gibberellin homeostasis and plant height control by EUI and a role for gibberellin in root gravity responses in rice.Cell Research 18(3): 412-421.
- ↑ 15.0 15.1 Busch MB, Sievers A.(1990).Hormone treatment of roots causes not only a reversible loss of starch but also of structural polarity in statocytes. Planta 181:358-364.
- ↑ Mei C, Zhou X, Yang Y.(2006)Use of RNA interference to dissect defense-signaling pathways in rice. Methods Mol Biol.354:161-172.
- ↑ Sasaki,A.,et al.(2002). Green revolution: a mutant gibberellinsynthesis gene in rice. Nature 416, 701–702.
- ↑ Dong-Lei Yang;Qun Li;Yi-Wen Deng;Yong-Gen Lou;Mu-Yang Wang;Guo-Xing Zhou;Ying-Ying Zhang;Zu-Hua He.(2008) Altered Disease Development in the eui Mutants and Eui Overexpressors Indicates that Gibberellins Negatively Regulate Rice Basal Disease Resistance.Molecular Plant 1(3): 528-537 .