Reviews and Special Topics

Advances in the Molecular Mechanism of Rice Plant Type

Expand
  • Rice Research Institute College of Agronomy and Biotechnology, Southwest University/ Key Laboratory of Application and Safety Control of Genetically Modified Crops, Chongqing 400715, China

Received date: 2022-11-04

  Revised date: 2022-11-30

  Online published: 2023-09-13

Abstract

The plant type of rice is one of the major factors determining rice yield. The ideotype of high-yielding rice cultivar is an important way to increase rice yield potential in rice breeding. Dwarf breeding in the 1950s and hybrid rice breeding in the 1970s are two revolutions in rice yield. However, the growth rate of rice yield has slowed down significantly in recent years. The third yield breakthrough depends on the super-high-yield breeding that combines ideotype with heterosis. We briefly reviewed the advances in the regulation mechanism of rice plant architecture, focusing on the progress achieved in leaf, panicle, grain and other aspects, and looked forward to the future research trends rice ideotype. It will lay a solid foundation for improving rice plant type and further increasing rice yield through molecular breeding.

Cite this article

LAN Jinsong, ZHUANG Hui . Advances in the Molecular Mechanism of Rice Plant Type[J]. Chinese Journal OF Rice Science, 2023 , 37(5) : 449 -458 . DOI: 10.16819/j.1001-7216.2023.221102

References

[1] 张启发. 绿色超级稻培育的设想[J]. 分子植物育种, 2005, 3(5): 601-602.
[1] Zhang Q F. Strategies for developing green super rice[J]. Molecular Plant Breeding, 2005, 3(5): 601-602. (in Chinese)
[2] Boysen-Jensen P. Die Stoffproduktion der Pflanzen[J]. Protoplasma, 1933, 18(1): 311.
[3] Heath O V S, Gregory F G. The constancy of the mean net assimilation rate and its ecological importance[J]. Annals of Botany, 1938, 2(4): 811-818.
[4] Donald C M. The breeding of crop ideotypes[J]. Euphytica, 1968, 17(3): 385-403.
[5] 马梦影, 巩文靓, 康雪蒙, 段海燕. 水稻理想株型改良的研究进展[J]. 中国农学通报, 2020, 36(29): 1-6.
[5] Ma M Y, Gong W L, Kang X M, Duan H Y. The improvement of ideal plant type of rice: A review[J]. China Agricultural Science Bulletin, 2020, 36(29): 1-6. (in Chinese with English abstract)
[6] 黄耀祥. 水稻超高产育种研究[J]. 作物杂志, 1990(4): 1-2.
[6] Huang Y X. Study on super high yield rice breeding[J]. Crops, 1990(4): 1-2. (in Chinese)
[7] 杨守仁, 张龙步, 徐正进, 陈温福, 王进民, 董克. 水稻理想株形育种的基础研究及其与国内外同类研究的比较[J]. 沈阳农业大学学报, 1991(S1): 1-5.
[7] Yang S R, Zhang L B, Xu Z J, Chen W F, Wang J M, Dong K. The research results of ideal morphological breeding in rice and their comparisons with the same studies at home and abroad[J]. Journal of Shenyang Agricultural University, 1991(S1): 1-5. (in English with Chinese abstract)
[8] 杨守仁, 张龙步, 陈温福, 徐正进, 王进民. 水稻超高产育种的理论和方法[J]. 中国水稻科学, 1996, 10(2): 115-120.
[8] Yang S R, Zhang L B, Chen W F, Xu Z J, Wang J M. Theories and methods of rice breeding for maximum yield[J]. Chinese Journal of Rice Science, 1996, 10(2): 115-120. (in Chinese with English abstract)
[9] 周开达, 汪旭东, 李仕贵, 李平, 黎汉云, 黄国寿, 刘太清, 沈茂松. 亚种间重穗型杂交稻研究[J]. 中国农业科学, 1997(5): 92-94.
[9] Zhou K D, Wang X D, Li S G, Li P, Li H Y, Huang G S, Liu T Q, Shen M S. The study on heavy panicle type of inter-subspecific hybrid rice (Oryza sativa L.)[J]. Scientia Agricultura Sinica, 1997(5): 92-94. (in Chinese with English abstract)
[10] 汪开治. 国际水稻所将推出理想株型水稻新品种[J]. 中国农技推广, 1996(4): 26.
[10] Wang K Z. International Rice Research Institute will introduce a new ideal strain type of rice varieties[J]. China Agro-Technology Extension, 1996(4): 26. (in Chinese)
[11] 袁隆平. 杂交水稻超高产育种[J]. 杂交水稻, 1997, 12(6): 1-6.
[11] Yuan L P. Hybrid rice breeding for super high yield[J]. Hybrid Rice, 1997, 12(6): 1-6. (in Chinese)
[12] Li S, Tian Y H, Wu K, Ye Y F, Yu J P, Zhang J Q, Liu Q, Hu M Y, Li H, Tong Y P, Nicholas Harberd P, Fu X D. Modulating plant growth-metabolism coordination for sustainable agriculture[J]. Nature, 2018, 560(7720): 595-600.
[13] 胡茂龙. 水稻光合功能相关性状QTL分析及转绿型白叶突变体基因的图位克隆[D]. 南京: 南京农业大学, 2006.
[13] Hu M L. QTL analysis for traits associated with photosynthetic functions and map-based cloning of virescent white leaf gene in rice (Oryza sativa L.)[D]. Nanjing: Nanjing Agricultural University, 2006. (in Chinese with English abstract)
[14] 陈达刚, 周新桥, 李丽君, 刘传光, 陈友订. 水稻叶厚性状的研究进展[J]. 农学学报, 2015, 5(11): 22-25.
[14] Chen D G, Zhou X Q, Li L J, Liu C G, Chen Y D. Research progress on rice (Oryza sativa L.) leaf thickness[J]. Journal of Agriculture, 2015, 5(11): 22-25. (in Chinese with English abstract)
[15] 高艳红, 吕川根, 王茂青, 王澎, 闫晓燕, 谢坤, 万建民. 水稻卷叶性状QTL的初步定位[J]. 江苏农业学报, 2007, 23(1): 5-10.
[15] Gao Y H, Lü C G, Wang M Q, Wang P, Yan X Y, Xie K, Wan J M. QTL mapping for rolled leaf gene in rice[J]. Jiangsu Journal of Agricultural Science, 2007, 23(1): 5-10. (in Chinese with English abstract)
[16] Yoshida S. Fundamentals of Rice Crop Science[J]. Los Banos, the Philippines: International Rice Research Institute, 1981: 1-61.
[17] 范玉斌, 梁婉琪. 水稻叶极性发育分子机制研究进展[J]. 上海交通大学学报: 农业科学版, 2014, 32(1): 16-22.
[17] Fan Y B, Liang W Q. Research progress on the mechanism of leaf polarity establishment in rice[J]. Journal of Shanghai Jiaotong University: Agricultural Science, 2014, 32(1): 16-22. (in Chinese with English abstract)
[18] Xiang J J, Zhang G H, Qian Q, Xue H W. SEMI-ROLLED LEAF1 encodes a putative GPI-anchored protein and modulates rice leaf rolling by regulating the formation of bulliform cells[J]. Plant Physiology, 2012, 159(4): 1488-1500.
[19] Hibara K I, Obara M, Hayashida E, Abe M, Ishimaru T, Satoh H, Itoh J I, Nagato Y. The ADAXIALIZED LEAF1 gene functions in leaf and embryonic pattern formation in rice[J]. Developmental Biology, 2009, 334(2): 345-354.
[20] Zhang T, You J, Zhang Y, Yao W Y, Chen W B, Duan Q N, Xiao W W, Ye L, Zhou Y, Sang X C, Ling Y H, He G H, Li Y F. LF1 regulates the lateral organs polarity development in rice[J]. The New Phytologist, 2021, 231(3): 1265-1277.
[21] You J, Xiao W W, Zhou Y, Shen W Q, Ye L, Yu P, Yu G L, Duan Q N, Zhang X F, He Z F, Xiang Y, Sang X C, Li Y F, Zhao F M, Ling Y H, He G H, Zhang T. The APC/CTAD1-WIDE LEAF 1-NARROW LEAF 1 pathway controls leaf width in rice[J]. The Plant Cell, 2022, 34(11): 4313-4328.
[22] 姚栋萍. 水稻培矮64S直立叶基因的初步定位[D]. 长沙: 湖南农业大学, 2016.
[22] Yao D P. Preliminary mapping of the rice erect leaf gene from Peiai 64s[D]. Changsha: Hunan Agricultural University, 2016. (in Chinese with English abstract)
[23] Zhao S Q, Hu J, Guo L B, Qian Q, Xue H W. Rice leaf inclination2, a VIN3-like protein, regulates leaf angle through modulating cell division of the collar[J]. Cell Research, 2010, 20(8): 935-947.
[24] Tanaka A, Nakagawa H, Tomita C, Shimatani Z, Ohtake M, Nomura T, Jiang C J, Dubouzet J G, Kikuchi S, Sekimoto H, Yokota T, Asami T, Kamakura T, Mori M. BRASSINOSTEROID UPREGULATED1, encoding a Helix-Loop-Helix protein, is a novel gene involved in brassinosteroid signaling and controls bending of the lamina joint in rice[J]. Plant Physiology, 2009, 151(2): 669-680.
[25] Ning J, Zhang B C, Wang N L, Zhou Y H, Xiong L Z. Increased Leaf Angle1, a Raf-Like MAPKKK that interacts with a nuclear protein family, regulates mechanical tissue formation in the lamina joint of rice[J]. The Plant Cell, 2011, 23(12): 4334-4347.
[26] Wu X R, Tang D, Li M, Wang K J, Cheng Z K. Loose Plant Architecture1, an INDETERMINATE DOMAIN protein involved in shoot gravitropism, regulates plant architecture in rice[J]. Plant Physiology, 2013, 161(1): 317-329.
[27] Yasuno N, Takamure I, Kidou S, Tokuji Y, Ureshi A, Funabiki A, Ashikaga K, Yamanouchi U, Yano M, Kato K. Rice shoot branching requires an ATP-binding cassette subfamily G protein[J]. New Phytologist, 2009, 182(1): 91-101.
[28] Nakagawa M, Shimamoto K, Kyozuka J. Overexpression of RCN1 and RCN2, rice TERMINAL FLOWER 1/CENTRORADIALIS homologs, confers delay of phase transition and altered panicle morphology in rice[J]. The Plant Journal, 2002, 29(6): 743-750.
[29] Terao T, Nagata K, Morino K, Hirose T. A gene controlling the number of primary rachis branches also controls the vascular bundle formation and hence is responsible to increase the harvest index and grain yield in rice[J]. Theoretical and Applied Genetics, 2010, 120(5): 875-893.
[30] Ikeda-Kawakatsu K, Maekawa M, Izawa T, Itoh JI, Nagato Y. ABERRANT PANICLE ORGANIZATION 2/RFL, the rice ortholog of Arabidopsis LEAFY, suppresses the transition from inflorescence meristem to floral meristem through interaction with APO1[J]. The Plant Journal, 2012, 69(1): 168-180.
[31] Zeng X Q, Zhuang H, Cheng Q L, Tang J, Yang F Y, Huang M J, Wang Z Y, Li Z C, Zhu H H, Chen R, He G H, Li Y F. SB1 encoding Ring-Like Zinc-Finger protein regulates branch development as a transcription repressor[J]. Rice Science, 2021, 28(3): 243-256.
[32] Zhang D B, Yuan Z. Molecular control of grass inflorescence development[J]. Annual Review of Plant Biology, 2014, 65(1): 553-578.
[33] Pautler M, Tanaka W, Hirano H Y, Jackson D. Grass meristems: I. Shoot apical meristem maintenance, axillary meristem determinacy and the floral transition[J]. Plant and Cell Physiology, 2013, 54(3): 302-312.
[34] Bradley D, Ratcliffe O, Vincent C, Carpenter R, Coen E. Inflorescence commitment and architecture in Arabidopsis[J]. Science, 1997, 275(5296): 80-83.
[35] Ratcliffe O J, Bradley D J, Coen E S. Separation of shoot and floral identity in Arabidopsis[J]. Development, 1999, 126(6): 1109-1120.
[36] Mimida N, Goto K, Kobayashi Y, Araki T, Ahn J H, Weigel D, Murata M, Motoyoshi F, Sakamoto W. Functional divergence of the TFL1-like gene family in Arabidopsis revealed by characterization of a novel homologue[J]. Genes to Cells, 2001, 6(4): 327-336.
[37] Rao N N, Prasad K, Kumar P R, Vijayraghavan U. Distinct regulatory role for RFL, the rice LFY homolog, in determining flowering time and plant architecture[J]. Proceedings of the National Academy of Sciences of the United States of America, 2008, 105(9): 3646-3651.
[38] Yoshida A, Sasao M, Yasuno N, Takagi K, Daimon Y, Chen R H, Yamazaki R, Tokunaga H, Kitaguchi Y, Sato Y, Nagamura Y, Ushijima T, Kumamaru T, Iida S, Maekawa M, Kyozuka J. TAWAWA1, a regulator of rice inflorescence architecture, functions through the suppression of meristem phase transition[J]. Proceedings of the National Academy of Sciences of the United States of America, 2013, 110(2): 767-772.
[39] Huang Y, Bai X F, Luo M F, Xing Y Z. Short Panicle 3 controls panicle architecture by upregulating APO2/RFL and increasing cytokinin content in rice[J]. Journal of Integrative Plant Biology, 2019, 61(9): 987-999.
[40] Xue W Y, Xing Y Z, Weng X Y, Zhao Y, Tang W J, Wang L, Zhou H J, Yu S B, Xu C G, Li X H, Zhang Q F. Natural variation in Ghd7 is an important regulator of heading date and yield potential in rice[J]. Nature Genetics, 2008, 40(6): 761-767.
[41] Wei X J, Xu J F, Guo H N, Jiang L, Chen S H, Yu C Y, Zhou Z L, Hu P S, Zhai H Q, Wan J M. DTH8 suppresses flowering in rice, influencing plant height and yield potential simultaneously[J]. Plant Physiology, 2010, 153(4): 1747-1758.
[42] Yan W H, Wang P, Chen H X, Zhou H J, Li Q P, Wang C R, Ding Z H, Zhang Y S, Yu S B, Xing Y Z, Zhang Q F. A major QTL, Ghd8, plays pleiotropic roles in regulating grain productivity, plant height, and heading date in rice[J]. Molecular Plant, 2011, 4(2): 319-330.
[43] Dai X D, Ding Y N, Tan L B, Fu Y C, Liu F X, Zhu Z F, Sun X Y, Sun X W, Gu P, Cai H W, Sun C Q. LHD1, an allele of DTH8/Ghd8, controls late heading date in common wild rice (Oryza rufipogon)[J]. Journal of Integrative Plant Biology, 2012, 54(10): 790-799.
[44] Sheng P K, Wu F Q, Tan J J, Zhang H, Ma W W, Chen L P, Wang J C, Wang J, Zhu S S, Guo X P, Wang J L, Zhang X, Cheng Z J, Bao Y Q, Wu C Y, Liu X M, Wan J M. A CONSTANS-like transcriptional activator, OsCOL13, functions as a negative regulator of flowering downstream of OsphyB and upstream of Ehd1 in rice[J]. Plant Molecular Biology, 2016, 92(1-2): 209-222.
[45] Li S B, Qian Q, Fu Z M, Zeng D L, Meng X B, Kyozuka J, Maekawa M, Zhu X D, Zhang J, Li J Y, Wang Y H. Short panicle1 encodes a putative PTR family transporter and determines rice panicle size[J]. The Plant Journal, 2009, 58(4): 592-605.
[46] Jiang G H, Xiang Y H, Zhao J Y, Yin D D, Zhao X F, Zhu L H, Zhai W X. Regulation of inflorescence branch development in rice through a novel pathway involving the pentatricopeptide repeat protein sped1-D[J]. Genetics, 2014, 197(4): 1395-1407.
[47] Qiao Y L, Piao R H, Shi J X, Lee S I, Jiang W Z, Kim B K, Lee J, Han L Z, Ma W B, Koh H J. Fine mapping and candidate gene analysis of dense and erect panicle 3, DEP3, which confers high grain yield in rice (Oryza sativa L.)[J]. Theoretical and Applied Genetics, 2011, 122(7): 1439-1449.
[48] Piao R H, Jiang W Z, Ham T H, Choi M S, Qiao Y, Chu S H, Park J H, Woo M O, Jin Z, An G, Lee J, Koh H J. Map-based cloning of the ERECT PANICLE 3 gene in rice[J]. Theoretical and Applied Genetics, 2009, 119(8): 1497-1506.
[49] Li M, Tang D, Wang K J, Wu X R, Lu L L, Yu H X, Gu M D, Yan C J, Cheng Z K. Mutations in the F-box gene LARGER PANICLE improve the panicle architecture and enhance the grain yield in rice[J]. Plant Biotechnology Journal, 2011, 9(9): 1002-1013.
[50] Gao X C, Liang W Q, Yin C S, Ji S M, Wang H M, Su X, Guo C, Kong H Z, Xue H W, Zhang D B. The SEPALLATA-like gene OsMADS34 is required for rice inflorescence and spikelet development[J]. Plant Physiology, 2010, 153(2): 728-740.
[51] Kobayashi K, Maekawa M, Miyao A, Hirochika H, Kyozuka J. PANICLE PHYTOMER2 (PAP2), encoding a SEPALLATA subfamily MADS-box protein, positively controls spikelet meristem identity in rice[J]. Plant and Cell Physiology, 2010, 51(1): 47-57.
[52] Zhuang H, Wang H L, Zhang T, Zeng X Q, Chen H, Wang Z W, Zhang J, Zheng H, Tang J, Ling Y H, Yang Z L, He G H, Li Y F. NONSTOP GLUMES1 encodes a C2H2 zinc finger protein that regulates spikelet development in rice[J]. The Plant Cell, 2020, 32(2): 392-413.
[53] Zhang T, Li Y F, Ma L, Sang X C, Ling Y H, Wang Y T, Yu P, Zhuang H, Huang J Y, Wang N, Zhao F M, Zhang C W, Yang Z L, Fang L K, He G H. LATERAL FLORET 1 induced the three-florets spikelet in rice[J]. Proceedings of the National Academy of Sciences of the United States of America, 2017, 114(37): 9984-9989.
[54] Ren D Y, Li Y F, Zhao F M, Sang X C, Shi J Q, Wang N, Guo S, Ling Y H, Zhang C W, Yang Z L, He G H. MULTI-FLORET SPIKELET1, which encodes an AP2/ERF protein, determines spikelet meristem fate and sterile lemma identity in rice[J]. Plant Physiology, 2013, 162(2): 872-884.
[55] Li Y F, Zeng X Q, Li Y, Wang L, Zhuang H, Wang Y, Tang J, Wang H L, Xiong M, Yang F Y, Yuan X Z, He G H. MULTI-FLORET SPIKELET 2, a MYB transcription factor, determines spikelet meristem fate and floral organ identity in rice[J]. Plant Physiology, 2020, 184(2): 988-1003.
[56] Wang Y, Zeng X Q, Lu L, Cheng Q L, Yang F Y, Huang M J, Xiong M, Li Y F. MULTI-FLORET SPIKELET 4 (MFS4) regulates spikelet development and grain size in rice[J]. Rice Science, 2021, 28(4): 344-357.
[57] Zheng H, Zhang J, Zhuang H, Zeng X Q, Tang J, Wang H L, Chen H, Li Y, Ling Y H, He G H, Li Y F. mfs3) in rice (Oryza sativa L.)[J]. Journal of Integrative Agriculture, 2019, 18(12): 2673-2681.
[58] Ren D Y, Li Y F, He G H, Qian Q. Multifloret spikelet improves rice yield[J]. New Phytologist, 2020, 225(6): 2301-2306.
[59] 徐建龙, 薛庆中, 罗利军, 黎志康. 水稻粒重及其相关性状的遗传解析[J]. 中国水稻科学, 2002, 16(1): 6-10.
[59] Xu J L, Xue Q Z, Luo L J, Li Z K. Genetic dissection of grain weight and its related traits in rice (Oryza sativa L.)[J]. Chinese Journal of Rice Science, 2002, 16(1): 6-10. (in Chinese with English abstract)
[60] Li N, Xu R, Duan P G, Li Y H. Control of grain size in rice[J]. Plant Reproduction, 2018, 31(3): 237-251.
[61] Li N, Xu R, Li Y H. Molecular networks of seed size control in plants[J]. Annual Review of Plant Biology, 2019, 70(1): 435-463.
[62] Fan Y W, Li Y B. Molecular, cellular and Yin-Yang regulation of grain size and number in rice[J]. Molecular Breeding, 2019, 39(12): 1-25.
[63] Huang X Z, Qian Q, Liu Z B, Sun H Y, He S Y, Luo D, Xia G M, Chu C C, Li J Y, Fu X D. Natural variation at the DEP1 locus enhances grain yield in rice[J]. Nature Genetics, 2009, 41(4): 494-497.
[64] Mao H L, Sun S Y, Yao J L, Wang C R, Yu S B, Xu C G, Li X H, Zhang Q F. Linking differential domain functions of the GS3 protein to natural variation of grain size in rice[J]. Proceedings of the National Academy of Sciences of the United States of America, 2010, 107(45): 19579-19584.
[65] Takano-Kai N, Doi K, Yoshimura A. GS3 participates in stigma exsertion as well as seed length in rice[J]. Breeding Science, 2011, 61(3): 244-250.
[66] Sun S Y, Wang L, Mao H L, Shao L, Li X H, Xiao J H, Ouyang Y D, Zhang Q F. A G-protein pathway determines grain size in rice[J]. Nature Communications, 2018, 9(1): 851.
[67] Huang H X, Ye Y F, Song W Z, Li Q, Han R X, Wu C C, Wang S X, Yu J P, Liu X Y, Fu X D, Liu Q, Wu K. Modulating the C-terminus of DEP1 synergistically enhances grain quality and yield in rice[J]. Journal of Genetics and Genomics, 2022, 49(5): 506-509.
[68] Yamamuro C, Ihara Y, Wu X, Noguchi T, Fujioka S, Takatsuto S, Ashikari M, Kitano H, Matsuok M. Loss of function of a rice brassinosteroid insensitive1 homolog prevents internode elongation and bending of the lamina joint[J]. The Plant Cell, 2000, 12(9): 1591-1606.
[69] Morinaka Y, Sakamoto T, Inukai Y, Agetsuma M, Kitano H, Ashikari M, Matsuoka M. Morphological alteration caused by brassinosteroid insensitivity increases the biomass and grain production of rice[J]. Plant Physiology, 2006, 141(3): 924-931.
[70] Ito Y, Takaya K, Kurata N. Expression of SERK family receptor-like protein kinase genes in rice[J]. Biochimica et Biophysica Acta, 2005, 1730(3): 253-258.
[71] Li D, Wang L, Wang M, Xu Y Y, Luo W, Liu Y J, Xu Z H, Li J. Engineering OsBAK1 gene as a molecular tool to improve rice architecture for high yield[J]. Plant Biotechnology Journal, 2009, 7(8): 791-806.
[72] Tong H N, Liu L C, Jin Y, Du L, Yin Y H, Qian Q, Zhu L H, Chu C C. DWARF AND LOW-TILLERING acts as a direct downstream target of a GSK3/SHAGGY-like kinase to mediate brassinosteroid responses in rice[J]. The Plant Cell, 2012, 24(6): 2562-2577.
[73] Tong H N, Jin Y, Liu W B, Li F, Fang J, Yin Y H, Qian Q, Zhu L H, Chu C C. DWARF AND LOW- TILLERING, a new member of the GRAS family, plays positive roles in brassinosteroid signaling in rice[J]. The Plant Journal, 2009, 58(5): 803-816.
[74] Sun L J, Li X J, Fu Y C, Zhu Z F, Tan L B, Liu F X, Sun X Y, Sun X W, Sun C Q. GS6, a member of the GRAS gene family, negatively regulates grain size in rice[J]. Journal of Integrative Plant Biology, 2013, 55(10): 938-949.
[75] Song X J, Huang W, Shi M, Zhu M Z, Lin H X. A QTL for rice grain width and weight encodes a previously unknown RING-type E3 ubiquitin ligase[J]. Nature Genetics, 2007, 39(5): 623-630.
[76] Hao J Q, Wang D K, Wu Y B, Huang K, Duan P G, Li N, Xu R, Zeng D L, Dong G J, Zhang B L, Zhang L M, Inzé D, Qian Q, Li Y H. The GW2-WG1-OsbZIP47 pathway controls grain size and weight in rice[J]. Molecular Plant, 2021, 14(8): 1266-1280.
[77] Hu X M, Qian Q, Xu T, Zhang Y E, Dong G J, Gao T, Xie Q, Xue Y B. The U-box E3 ubiquitin ligase TUD1 functions with a heterotrimeric G α subunit to regulate Brassinosteroid-mediated growth in rice[J]. PLOS Genetics, 2013, 9(3): e1003391.
[78] Jiao Y Q, Wang Y H, Xue D W, Wang J, Yan M X, Liu G F, Dong G J, Zeng D L, Lu Z F, Zhu X D, Qian Q, Li J Y. Regulation of OsSPL14 by OsmiR156 defines ideal plant architecture in rice[J]. Nature Genetics, 2010, 42(6): 541-544.
Outlines

/

Tel: 0571-63370278 E-mail: cjrs@263.net
Supported by Beijing Magtech Co., Ltd.