Please wait a minute...
Journal of Integrative Agriculture  2016, Vol. 15 Issue (7): 1441-1448    DOI: 10.1016/S2095-3119(15)61208-4
Crop Genetics · Breeding · Germplasm Resources Advanced Online Publication | Current Issue | Archive | Adv Search |
Identification of a novel gain-of-function mutant allele, slr1-d5, of rice DELLA protein
ZHANG Yun-hui1*, BIAN Xiao-feng1*, ZHANG Suo-bing1, LING Jing1, WANG Ying-jie1, WEI Xiao-ying2, FANG Xian-wen1
1 The Jiangsu Provincial Platform for Conservation and Utilization of Agricultural Germplasm/Jiangsu Provincial Key Laboratory of Agrobiology/Institute of Food Crops, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, P.R.China
2 Shandong Business Institute, Yantai 264670, P.R.China
Download:  PDF in ScienceDirect  
Export:  BibTeX | EndNote (RIS)      
Abstract    Controlling the height of crops plays a crucial role for their yields. The large scale utilization of semi-dwarf varieties has greatly improved crop yield, providing an effective support for world food security. In rice, a main food for over half of the world’s population, a number of dwarf loci have been identified. However, most of them are recessive, such as the ‘green revolution’ gene sd1. To gain more beneficial loci for rice breeding programs, exploring new mutations is needed, especially the dominant loci which can be used broadly for hybrid breeding. Here, we isolated a novel dominant dwarf rice mutant, slr1-d5. All of the internodes of slr1-d5 are reduced. We find that the responsiveness of slr1-d5 to gibberellin (GA), GA3, was significantly reduced. Map-based cloning revealed that the dominant dwarfism of slr1-d5 was caused by an amino acid substitution in the N-terminal TVHYNP domain of rice DELLA protein, SLR1, where the conserved amino acid Pro (P) was substituted to His (H). Our findings not only further prove the pivotal role of TVHYNP motif in regulating SLR1 stability, but also provide a new dwarf source for improvement of rice germplasms.
Keywords:  rice        dominant dwarf        DELLA protein        gibberellin  
Received: 09 June 2015   Accepted:
Fund: 

This work was supported by the National Natural Science Foundation of China (31401036), the Jiangsu Independent Innovation Project (CX(14)5005), the Natural Science Foundation of Jiangsu Province, China (BK20130706), and the Basal Research Fund of Jiangsu Acadamy of Agricultural Sciences, China (ZX(15)4015).

Corresponding Authors:  FANG Xian-wen, Tel: +86-25-84390321, E-mail: xianwen_fang@hotmail.com    
About author:  HANG Yun-hui, E-mail: zyhrice@163.com; BIAN Xiao-feng, E-mail: bianxiaofeng2@163.com

Cite this article: 

ZHANG Yun-hui, BIAN Xiao-feng, ZHANG Suo-bing, LING Jing, WANG Ying-jie, WEI Xiao-ying, FANG Xian-wen. 2016. Identification of a novel gain-of-function mutant allele, slr1-d5, of rice DELLA protein. Journal of Integrative Agriculture, 15(7): 1441-1448.

Asano K, Hirano K, Ueguchi-Tanaka M, Angeles-Shim R B, Komura T, Satoh H, Kitano H, Matsuoka M, Ashikari M. 2009. Isolation and characterization of dominant dwarf mutants, Slr1-d, in rice. Molecular Genetics and Genomics, 281, 223–231.

Aasno K, Takashi T, Miura K, Qian Q, Kitano H, Matsuoka M, Ashikari M. 2007. Genetic and molecular analysis of utility of sd1 alleles in rice breeding. Breeding Science, 57, 53–58.

Chen X, Temnykh S, Xu Y, Cho Y G, McCouch S R. 1997. Development of a microsatellite framework map providing genome-wide coverage in rice (Oryza sativa L.). Theoretical and Applied Genetics, 95, 553–567.

Dellaporta S L, Wood J, Hicks J B. 1983. A plant DNA mini preparation: Version II. Plant Molecular Biology Reporter, 1, 19–21.

Dill A, Jung H S, Sun T P. 2001. The DELLA motif is essential for gibberellin-induced degradation of RGA. Proceedings of the National Academy of Sciences of the United States of America, 98, 14162–14167.

Fleet C M, Sun T P. 2005. A DELLAcate balance: The role of gibberellin in plant morphogenesis. Current Opinion in Plant Biology, 8, 77–85.

Gomi K, Sasaki A, Itoh H, Ueguchi-Tanaka M, Ashikari M, Kitano H, Matsuoka M. 2004. GID2, an F-box subunit of the SCF E3 complex, specifically interacts with phosphorylated SLR1 protein and regulates the gibberellin-dependent degradation of SLR1 in rice. The Plant Journal, 37, 626–634.

Griffiths J, Murase K, Rieu I, Zentella R, Zhang Z L, Powers S J, Gong F, Phillips A L, Hedden P, Sun T P, Thomas S G. 2006. Genetic characterization and functional analysis of the GID1 gibberellin receptors in Arabidopsis. The Plant Cell, 18, 3399–3414.

Hargrove T R, Cabanilla V L. 1979. The impact of semi-dwarf varieties on Asian rice-breeding programs. Bioscience, 29, 731–735.

Hedden P. 2003. The genes of the green revolution. Trends in Genetics, 19, 5–9.

Hedden P, Phillips A L. 2000. Gibberellin metabolism: New insights revealed by the genes. Trends in Plant Science, 5, 523–530.

Hirano K, Asano K, Tsuji H, Kawamura M, Mori H, Kitano H, Ueguchi-Tanaka M, Matsuoka M. 2010. Characterization of the molecular mechanism underlying gibberellin perception complex formation in rice. The Plant Cell, 22, 2680–2696.

Ikeda A, Ueguchi-Tanaka M, Sonoda Y, Kitano H, Koshioka M, Futsuhara Y, Matsuoka M, Yamaguchi J. 2001. slender rice, a constitutive gibberellin response mutant, is caused by a null mutation of the SLR1 gene, an ortholog of the height-regulating gene GAI/RGA/RHT/D8. The Plant Cell, 13, 999–1010.

Khush G S. 2001. Green revolution: The way forward. Nature Reviews Genetics, 2, 815–822.

Kikuchi F, Futsuhara Y. 1997. Inheritance of morphological characters. 2. Inheritance of semi-dwarf. In: Matsuo T, Kumazawa K, Ishii R, Ishihara K, Hirata H, eds., Science of the Rice Plant. vol 3. Food and Agricultural Policy Research Center, Tokyo, Japan. pp. 309–317.

Monna L, Kitazawa N, Yoshino R, Suzuki J, Masuda H, Maehara Y, Tanji M, Sato M, Nasu S, Minobe Y. 2002. Positional cloning of rice semidwarfing gene, sd-1: Rice “green revolution gene” encodes a mutant enzyme involved in gibberellins synthesis. DNA Research, 9, 11–17.

Murase K, Hirano Y, Sun T P, Hakoshima T. 2008. Gibberellin-induced DELLA recognition by the gibberellin receptor GID1. Nature, 456, 459–464.

Nishimura A, Aichi I, Matsuoka M. 2006. A protocol for Agrobacterium-mediated transformation in rice. Nature Protocol, 1, 2796–2802.

Peng J, Carol P, Richards D E, King K E, Cowling R J, Murphy G P, Harberd N P. 1997. The Arabidopsis GAI gene defines a signaling pathway that negatively regulates gibberellin responses. Genes & Development, 11, 3194–3205.

Peng J, Richards D E, Hartley N M, Murphy G P, Devos K M, Flintham J E, Beales J, Fish L J, Worland A J, Pelica F, Sudhakar D, Christou P, Snape J W, Gale M D, Harberd N P. 1999. ‘Green revolution’ genes encode mutant gibberellin response modulators. Nature, 400, 256–261.

Richards D E, King K E, Ait-ali T, Harberd N P. 2001. How gibberellins regulates plant growth and development: A molecular genetic analysis of gibberellins signaling. Annual Review Plant Physiology and Plant Molecular Biology, 52, 67–88.

Sakamoto T, Miura K, Itoh H, Tatsumi T, Ueguchitanaka M, Ishiyama K. 2004. An overview of gibberellin metabolism enzyme genes and their related mutants in rice. Plant Physiology, 134, 1642–1653.

Sanguinetti C J, Dias N E, Simpson A J G. 1994. Rapid silver staining and recover of PCR products separated on polyacrylamide gels. Biotechniques, 17, 915–919.

Sasaki A, Ashikari M, Ueguchi-Tanaka M, Itoh H, Nishimura A, Swapan D, Ishiyama K, Saito T, Kobayashi M, Khush G S, Kitano H, Matsuoka M. 2002. Green revolution: A mutant gibberellin-synthesis gene in rice. Nature, 416, 701–702.

Sasaki A, Itoh H, Gomi K, Ueguchi-Tanaka M, Ishiyama K, Kobayashi M, Jeong D H, An G, Kitano H, Ashikari M, Matsuoka M. 2003. Accumulation of phosphorylated repressor for gibberellins signaling in an F-box mutant. Science, 299, 1896–1898.

Spielmeyer W, Ellis M, Chandler P. 2002. Semidwarf (sd-1), “green revolution” rice, contains a defective gibberellin 20-oxidase gene. Proceedings of the National Academy of Sciences of the United States of America, 99, 9043–9048.

Sun T P, Gubler F. 2004. Molecular mechanism of gibberellin signalingin plants. Annual Review of Plant Biology, 55, 197–223.

Takeda K. 1977. Internode elongation and dwarfism in some graminaeous plants. Gamma Field Symposia, 16, 1–18.

Ueguchi-Tanaka M, Ashikari M, Nakajima M, Itoh H, Katoh E, Kobayashi M, Chow T Y, Hsing Y I, Kitano H, Yamaguchi I, Matsuoka M. 2005. GIBBERELLIN INSENSITIVE DWARF1 encodes a soluble receptor for gibberellin. Nature, 437, 693–698.

Ueguchi-Tanaka M, Nakajima M, Katoh E, Ohmiya H, Asano K, Saji S, Hongyu X, Ashikari M, Kitano H, Yamaguchi I, Matsuoka M. 2007. Molecular interactions of a soluble gibberellin receptor, GID1, with a rice DELLA protein, SLR1, and gibberellin. The Plant Cell, 19, 2140–2155.

Willige B C, Ghosh S, Nill C, Zourelidou M, Dohmann E M, Maier A, Schwechheimer C. 2007. The DELLA domain of GA INSENSITIVE mediates the interaction with the GA INSENSITIVE DWARF1A gibberellin receptor of Arabidopsis. The Plant Cell, 19, 1209–1220.

Yamaguchi S. 2008. Gibberellin metabolism and its regulation. Annual Review of Plant Biology, 59, 225–251.

Zhang Y H, Zhang S B, Lin J, Wang Y J, Fang X W. 2014. Research progress on cloning and functional analysis of plant height in rice (Oryza sativa L.). Chinese Agricultural Science Bulletin, 30, 1–7. (in Chinese)
[1] ZHAO Jun-yang, LU Hua-ming, QIN Shu-tao, PAN Peng, TANG Shi-de, CHEN Li-hong, WANG Xue-li, TANG Fang-yu, TAN Zheng-long, WEN Rong-hui, HE Bing. Soil conditioners improve Cd-contaminated farmland soil microbial communities to inhibit Cd accumulation in rice[J]. >Journal of Integrative Agriculture, 2023, 22(8): 2521-2535.
[2] GAO Peng, ZHANG Tuo, LEI Xing-yu, CUI Xin-wei, LU Yao-xiong, FAN Peng-fei, LONG Shi-ping, HUANG Jing, GAO Ju-sheng, ZHANG Zhen-hua, ZHANG Hui-min. Improvement of soil fertility and rice yield after long-term application of cow manure combined with inorganic fertilizers[J]. >Journal of Integrative Agriculture, 2023, 22(7): 2221-2232.
[3] SHI Shi-jie, ZHANG Gao-yu, CAO Cou-gui, JIANG Yang . Untargeted UHPLC–Q-Exactive-MS-based metabolomics reveals associations between pre- and post-cooked metabolites and the taste quality of geographical indication rice and regular rice[J]. >Journal of Integrative Agriculture, 2023, 22(7): 2271-2281.
[4] CHEN Guang-yi, PENG Li-gong, LI Cong-mei, TU Yun-biao, LAN Yan, WU Chao-yue, DUAN Qiang, ZHANG Qiu-qiu, YANG Hong, LI Tian. Effects of the potassium application rate on lipid synthesis and eating quality of two rice cultivars[J]. >Journal of Integrative Agriculture, 2023, 22(7): 2025-2040.
[5] WEI Huan-he, GE Jia-lin, ZHANG Xu-bin, ZHU Wang, DENG Fei, REN Wan-jun, CHEN Ying-long, MENG Tian-yao, DAI Qi-gen. Decreased panicle N application alleviates the negative effects of shading on rice grain yield and grain quality[J]. >Journal of Integrative Agriculture, 2023, 22(7): 2041-2053.
[6] DU Xiang-bei, XI Min, WEI Zhi, CHEN Xiao-fei, WU Wen-ge, KONG Ling-cong. Raised bed planting promotes grain number per spike in wheat grown after rice by improving spike differentiation and enhancing photosynthetic capacity[J]. >Journal of Integrative Agriculture, 2023, 22(6): 1631-1644.
[7] LIU Yu, LIU Wen-wen, LI Li, Frederic FRANCIS, WANG Xi-feng. Transcriptome analysis reveals different response of resistant and susceptible rice varieties to rice stripe virus infection[J]. >Journal of Integrative Agriculture, 2023, 22(6): 1750-1762.
[8] ZHANG Zi-han, NIE Jun, LIANG Hai, WEI Cui-lan, WANG Yun, LIAO Yu-lin, LU Yan-hong, ZHOU Guo-peng, GAO Song-juan, CAO Wei-dong. The effects of co-utilizing green manure and rice straw on soil aggregates and soil carbon stability in a paddy soil in southern China[J]. >Journal of Integrative Agriculture, 2023, 22(5): 1529-1545.
[9] LI Min, ZHU Da-wei, JIANG Ming-jin, LUO De-qiang, JIANG Xue-hai, JI Guang-mei, LI Li-jiang, ZHOU Wei-jia. Dry matter production and panicle characteristics of high yield and good taste indica hybrid rice varieties[J]. >Journal of Integrative Agriculture, 2023, 22(5): 1338-1350.
[10] CHEN Chang-zhao, WANG Ya-Liang, HE Meng-xing, LI Zhi-wen, SHEN Lan, LI Qing, RE De-yong, HU Jiang, ZHU Li, ZHANG Guang-heng, GAO Zhen-yu, ZENG Da-li, GUO Long-biao, QIAN Qian, ZHANG Qiang. OsPPR9 encodes a DYW-type PPR protein that affects editing efficiency of multiple RNA editing sites and is essential for chloroplast development[J]. >Journal of Integrative Agriculture, 2023, 22(4): 972-980.
[11] WANG Xin-yu, YANG Guo-dong, XU Le, XIANG Hong-shun, YANG Chen, WANG Fei, PENG Shao-bing. Grain yield and nitrogen use efficiency of an ultrashort-duration variety grown under different nitrogen and seeding rates in direct-seeded and double-season rice in Central China[J]. >Journal of Integrative Agriculture, 2023, 22(4): 1009-1020.
[12] Kanokwan KAEWMUNGKUN, Keasinee TONGMARK, Sriprapai CHAKHONKAEN, Numphet SANGARWUT, Thiwawan WASINANON, Natjaree PANYAWUT, Khanittha DITTHAB, Kannika SIKAEWTUNG, QI Yong-bin, Sukanya DAPHA, Atikorn PANYA, Natthaporn PHONSATTA, Amorntip MUANGPROM. Development of new aromatic rice lines with high eating and cooking qualities[J]. >Journal of Integrative Agriculture, 2023, 22(3): 679-690.
[13] CAO Peng-hui, WANG Di, GAO Su, LIU Xi, QIAO Zhong-ying, XIE Yu-lin, DONG Ming-hui, DU Tan-xiao, ZHANG Xian, ZHANG Rui, JI Jian-hui. OsDXR interacts with OsMORF1 to regulate chloroplast development and the RNA editing of chloroplast genes in rice[J]. >Journal of Integrative Agriculture, 2023, 22(3): 669-678.
[14] WANG Yuan-zheng, Olusegun IDOWU, WANG Yun, HOMMA Koki, NAKAZAKI Tetsuya, ZHENG Wen-jing, XU Zheng-jin, SHIRAIWA Tatsuhiko.
Effects of erect panicle genotype and environment interactions on rice yield and yield components
[J]. >Journal of Integrative Agriculture, 2023, 22(3): 716-726.
[15] REN Chuan-ying, ZHANG Shan, HONG Bin, GUAN Li-jun, HUANG Wen-gong, FENG Jun-ran, SHA Di-xin, YUAN Di, LI Bo, JI Ni-na, LIU Wei, LU Shu-wen. Germinated brown rice relieves hyperlipidemia by alleviating gut microbiota dysbiosis[J]. >Journal of Integrative Agriculture, 2023, 22(3): 945-957.
No Suggested Reading articles found!