Rice leaf inclination2, a VIN3-like protein, regulates leaf angle through modulating cell division of the collar

Cell Research

Volumn 20, Issue 8, 2010, Pages 935-947

  Zhao, Shu Qing ^a   Hu, Jiang ^b   Guo, Long Biao ^b   Qian, Qian ^b   Xue, Hong Wei ^a  

^a INSTITUTE OF PLANT PHYSIOLOGY AND ECOLOGY   (China)

^b CHINA NATIONAL RICE RESEARCH INSTITUTE   (China)

Author keywords

[No Author keywords available]

Indexed keywords

VEGETABLE PROTEIN;

AMINO ACID SEQUENCE; ARTICLE; CELL DIVISION; CLASSIFICATION; GENETICS; GROWTH, DEVELOPMENT AND AGING; HISTOLOGY; METABOLISM; MOLECULAR GENETICS; MUTATION; PLANT LEAF; PROTEIN TERTIARY STRUCTURE; RICE; ANATOMY AND HISTOLOGY;

AMINO ACID SEQUENCE; CELL DIVISION; MOLECULAR SEQUENCE DATA; MUTATION; ORYZA SATIVA; PLANT LEAVES; PLANT PROTEINS; PROTEIN STRUCTURE, TERTIARY;

EID: 77955268516     PISSN: 10010602     EISSN: 17487838     Source Type: Journal    
DOI: 10.1038/cr.2010.109     Document Type: Article

References (48)

1. Hoshikawa K. The growing rice plant: An anatomical monograph. 1st Edition, Okyo: Nosan Gyoson Bunka Kyokai (Nobunkyo), 1989.
2. Sinclair TR, Sheehy JE. Erect leaves and photosynthesis in rice. Science 1999; 283:1455.
3. Sakamoto T, Morinaka Y, Ohnishi T, et al. Erect leaves caused by brassinosteroid deficiency increase biomass production and grain yield in rice. Nat Biotechnol 2006; 24:105-109. (Pubitemid 43083174)
4. Hong Z, Ueguchi-Tanaka M, Matsuoka M. Brassinosteroids and rice architecture. J Pestic Sci 2004; 29:184-188.
5. Cao HP, Chen SK. Brassinosteroid-induced rice lamina joint inclination and its relation to indole-3-acetic acid and ethylene. J Plant Growth Regul 1995; 16:189-196.
6. Duan K, Li L, Hu P, Xu ZH, Xue HW. A brassinolidesuppressed rice MADS-box transcription factor, OsMDP1, has a negative regulatory role in BR signaling. Plant J 2006; 47:519-531.
7. Li ZK, Paterson AH, Pinson SRM, Khush GS. A major gene, Ta1 and QTLs affecting tiller and leaf angles in rice. Rice Genetics Newslett 1998; 15:154-156.
8. Li ZK, Paterson AH, Pinson SRM, Stansel JW. RFLP facilitated analysis of tiller and leaf angles in rice (Oryza sativa L). Euphytica 1999; 9:79-84.
9. Hong Z, Ueguchi-Tanaka M, Shimizu-Sato S, et al. Loss-offunction of a rice brassinosteroid biosynthetic enzyme, C-6 oxidase, prevents the organized arrangement and polar elongation of cells in the leaves and stem. Plant J 2002; 32:495-508.
10. Hong Z, Ueguchi-Tanaka M, Umemura K, et al. A rice brassinosteroid- deficient mutant, ebisu dwarf (d2), is caused by a loss of function of a new member of cytochrome P450. Plant Cell 2003; 15:2900-2910.
11. Wada K, Marumo S, Ikekawa N, Morisaki M, Mori K. Brassinolide and homobrassinolide promotion of lamina inclination of rice seedlings. Plant Cell Physiol 1981; 22:323-325.
12. Wada K, Marumo S, Abe H, et al. A rice lamina inclination test - a micro-quantitative bioassay for brassinosteroids. Agric Biol Chem 1984; 48:719-726.
13. Yamamuro C, Ihara Y, Wu X. Loss of function of a rice brassinosteroid insensitive1 homolog prevents internode elongation and bending of the lamina joint. Plant Cell 2000; 12:1591-1605.
14. Morinaka Y, Sakamoto T, Inukai Y, et al. Morphological alteration caused by brassinosteroid insensitivity increases the biomass and grain production of rice. Plant Physiol 2006; 141:924-931. (Pubitemid 44061599)
15. Bai MY, Zhang LY, Gampala SS, et al. Functions of OsBZR1 and 14-3-3 proteins in brassinosteroid signaling in rice. Proc Natl Acad Sci USA 2007; 104:13839-13844.
16. Wu CY, Trieu A, Radhakrishnan P, et al. Brassinosteroids regulate grain filling in rice. Plant Cell 2008; 20:2130-2145.
17. Nakamura A, Fujioka S, Takatsuto S, et al. Involvement of C-22-hydroxylated brassinosteroids in auxin-induced lamina joint bending in rice. Plant Cell Physiol 2009; 50:1627-1635.
18. Shimada A, Ueguchi-Tanaka M, Sakamoto T, et al. The rice SPINDLY gene functions as a negative regulator of gibberellin signaling by controlling the suppressive function of the DELLA protein, SLR1, and modulating brassinosteroid synthesis. Plant J 2006; 48:390-402.
19. Komatsu K, Maekawa M, Ujiie S, et al. LAX and SPA: major regulators of shoot branching in rice. Proc Natl Acad Sci USA 2003; 100:11765-11770.
20. Tanaka A, Nakagawa H, Tomita C, et al. BRASSINOSTEROID UPREGULATED 1, encoding a helix-loop-helix protein, is a novel gene involved in brassinosteroid signaling and controls bending of the lamina joint in rice. Plant Physiol 2009; 151:669-680.
21. Lee J, Park JJ, Kim SL, Yim J, An G. Mutations in the rice liguleless gene result in a complete loss of the auricle, ligule, and laminar joint. Plant Mol Biol 2007; 65:487-499.
22. Wang DK, Zhang HX, Hu GC, Fu YP, Si HM, Sun ZX. Genetic analysis and identification of a large leaf angles (lla) mutant in rice. Chinese Sci Bull 2005; 50:492-494.
23. Lee S, Choi SC, An G. Rice SVP-group MADS-box proteins, OsMADS22 and OsMADS55, are negative regulators of brassinosteroid responses. Plant J 2008; 54:93-105. (Pubitemid 351406021)
24. Wang L, Xu YY, Zhang C, et al. OsLIC, a novel CCCH-type zinc finger protein with transcription activation, mediates rice architecture via brassinosteroids signaling. PLoS ONE 2008; 3:e3521. DOI: 10.1371/journal.pone. 0003521.
25. Zhang LY, Bai MY, Wu J, et al. Antagonistic HLH/bHLH transcription factors mediate brassinosteroid regulation of cell elongation and plant development in rice and Arabidopsis. Plant Cell 2009; 21:3767-3780.
26. Shi Z, Wang J, Wan X, Shen G, Wang X, Zhang J. Overexpression of rice OsAGO7 gene induces upward curling of the leaf blade that enhanced erect-leaf habit. Planta 2007; 226:99-108.
27. Sung S, Amasino RM. Vernalization in Arabidopsis thaliana is mediated by the PHD finger protein VIN3. Nature 2004; 427:159-164.
28. Sung S, Schmitz RJ, Amasino RM. A PHD finger protein involved in both the vernalization and photoperiod pathways in Arabidopsis. Genes Dev 2006; 20:3244-3248.
29. Fu D, Dunbar M, Dubcovsky J. Wheat VIN3-like PHD finger genes are up-regulated by vernalization. Mol Genet Genomics 2007; 277:301-313.
30. Aasland R, Gibson TJ, Stewart AF. The PHD-finger: implications for chromatin-mediated transcriptional regulation. Trends Biochem Sci 1995; 20:56-59.
31. Mariann B. The PHD finger, a nuclear protein-interaction domain. Trends Biochem Sci 2006; 31:35-40.
32. Aspberg A, Miura R, Bourdoulous S, et al. The C-type lectin domains of lecticans, a family of aggregating chondroitin sulfate proteoglycans, bind tenascin-R by protein-protein interactions independent of carbohydrate moiety. Proc Natl Acad Sci USA 1997; 94:10116-10121.
33. Pankov R, Yamada KM. Fibronectin at a glance. J Cell Sci 2002; 115:3861-3863.
34. Fabian-Marwedel T, Umeda M, Sauter M. The rice cyclindependent kinase-activating kinase R2 regulates S-phase progression. Plant Cell 2002; 14:197-210.
35. Renaudin JP, Doonan JH, Freeman D, et al. Plant cyclins: a unified nomenclature for plant A-, B- and D-type cyclins based on sequence organisation. Plant Mol Biol 1996; 32:1003-1018.
36. Sauter M. Differential expression of a CAK (cdc2-activating kinase)-like protein kinase, cyclins and cdc2 genes from rice during the cell cycle and in response to gibberellin. Plant J 1997; 11:181-190.
37. Lee Y, Kende H. Expression of β-expansins is correlated with internodal elongation in deepwater rice. Plant Physiol 2001; 127:645-654.
38. Uozu S, Tanaka-Ueguchi M, Kitano H, Hattori K, Matsuoka M. Characterization of XET-related genes of rice. Plant Physiol 2000; 122:853-859.
39. Sakamoto T, Miura K, Itoh H, et al. An overview of gibberellin metabolism enzyme genes and their related mutants in rice. Plant Physiol 2004; 134:1642-1653.
40. Jain M, Kaur N, Garg R, Thakur JK, Tyagi AK, Khurana JP. Structure and expression analysis of early auxin-responsive Aux/IAA gene family in rice (Oryza sativa). Funct Integr Genomics 2006; 6:47-59. (Pubitemid 43013208)
41. Bienz M. The PHD finger, a nuclear protein-interaction domain. Trends Biochem Sci 2006; 31:35-40.
42. Wood CC, Robertson M, Tanner G, Peacock WJ, Dennis ES, Helliwell CA. The Arabidopsis thaliana vernalization response requires a polycomb-like protein complex that also includes VERNALIZATION INSENSITIVE 3. Proc Natl Acad Sci USA 2006; 103:14631-14636.
43. Sheldon CC, Finnegan EJ, Dennis ES, Peacock WJ. Quantitative effects of vernalization on FLC and SOC1 expression. Plant J 2006; 45:871-883.
44. Mori M, Nomura T, Ooka H, et al. Isolation and characterization of a rice dwarf mutant with a defect in brassinosteroid biosynthesis. Plant Physiol 2002; 130:1152-1161.
45. Hiei Y, Ohta S, Komari T, Kumashiro T. Efficient transformation of rice (Oryza sativa L.) mediated by Agrobacterium and sequence analysis of the boundaries of the T-DNA. Plant J 1994; 6:271-282.
46. Liu W, Xu ZH, Luo D, Xue HW. Roles of OsCKI1, a rice casein kinase I, in root development and plant hormone sensitivity. Plant J 2003; 36:189-202.
47. Jefferson RA, Kavanagh TA, Bevan MW. GUS fusions: betaglucuronidase as a sensitive and versatile gene fusion marker in higher plants. EMBO J 1987; 6:3901-3907.
48. Lou Y, Gou JY, Xue HW. PIP5K9, an Arabidopsis phosphatidylinositol monophosphate kinase, interacts with a cytosolic invertase to negatively regulate sugar-mediated root growth. Plant Cell 2007; 19:163-181.