Ectopic expression of LjmiR156 delays flowering, enhances shoot branching, and improves forage quality in alfalfa

被引:29
作者
Aung, Banyar [1 ,2 ]
Gruber, Margaret Y. [3 ]
Amyot, Lisa [2 ]
Omari, Khaled [1 ]
Bertrand, Annick [4 ]
Hannoufa, Abdelali [1 ,2 ]
机构
[1] Agr & Agri Food Canada, London, ON N5V 4T3, Canada
[2] Univ Western Ontario, Dept Biol, London, ON N6A 5B7, Canada
[3] Agr & Agri Food Canada, Saskatoon, SK S7N 0X2, Canada
[4] Agr & Agri Food Canada, Quebec City, PQ G1V 2J3, Canada
关键词
LjmiR156a; SPL genes; Flowering time; Shoot branching; Alfalfa biomass; TRANSCRIPTION FACTORS; GENE; ARABIDOPSIS; MIR156; CLEAVAGE; LIGNIN; TARGET; PCR; MICRORNA156; TRANSITION;
D O I
10.1007/s11816-015-0375-2
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
MicroRNA156 (miR156) is a regulator of flowering time and biomass production through regulation of members of SQUAMOSA PROMOTER BINDING PROTEIN-LIKE (SPL) gene family. To expand our investigations on the utility of miR156 in alfalfa, we generated transgenic alfalfa expressing a heterologous miR156 from Lotus japonicus (LjmiR156a). 5' RACE and qRT-PCR analysis confirmed that the same three SPL genes (MsSPL6, MsSPL12, and MsSPL13) targeted by MsmiR156d are also targets of LjmiR156a in alfalfa. Ectopic expression of LjmiR156a down-regulated these SPL genes in transgenic alfalfa, coupled with reduced internode length, a more extreme delay in flowering time than occurred with MsmiR156d, enhanced shoot branching, and elevated biomass production. While root length was maintained, nodulation was reduced in some transgenic genotypes. Furthermore, heterologous expression of LjmiR156a enhanced the contents of starch, soluble sugars, and phenolics in all transgenic genotypes in contrast to the impact from MsmiR156d enhancement, even though the effects on lignin, cellulose, pectin, structural sugars, flavonoids, and carotenoids were variable among the new alfalfa genotypes. The variations among the traits/genotypes reflect the change in expression of alfalfa SPL genes targeted by LjmiR156a and show that LjmiR156a could be employed as a tool to improve quality and yield of alfalfa biomass.
引用
收藏
页码:379 / 393
页数:15
相关论文
共 62 条
[21]   DEGRADATION CHARACTERISTICS OF ISOLATED AND IN-SITU CELL-WALL LUCERNE PECTIC POLYSACCHARIDES BY MIXED RUMINAL MICROBES [J].
HATFIELD, RD ;
WEIMER, PJ .
JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, 1995, 69 (02) :185-196
[22]  
Jefferson RA., 1987, PLANT MOL BIOL REP, V5, P387, DOI DOI 10.1007/BF02667740
[23]  
Jiang Li., 2011, SENSOR FAULT DETECTI
[24]   Regulation of OsSPL14 by OsmiR156 defines ideal plant architecture in rice [J].
Jiao, Yongqing ;
Wang, Yonghong ;
Xue, Dawei ;
Wang, Jing ;
Yan, Meixian ;
Liu, Guifu ;
Dong, Guojun ;
Zeng, Dali ;
Lu, Zefu ;
Zhu, Xudong ;
Qian, Qian ;
Li, Jiayang .
NATURE GENETICS, 2010, 42 (06) :541-U36
[25]  
Kim MY, 2013, PLANT GENOME, DOI [10.3835/plantgenome2013030008, DOI 10.3835/PLANTGENOME2013030008]
[26]   Five decades of alfalfa cultivar improvement: Impact on forage yield, persistence, and nutritive value [J].
Lamb, JFS ;
Sheaffer, CC ;
Rhodes, LH ;
Sulc, RM ;
Undersander, DJ ;
Brummer, EC .
CROP SCIENCE, 2006, 46 (02) :902-909
[27]   THE C-ELEGANS HETEROCHRONIC GENE LIN-4 ENCODES SMALL RNAS WITH ANTISENSE COMPLEMENTARITY TO LIN-14 [J].
LEE, RC ;
FEINBAUM, RL ;
AMBROS, V .
CELL, 1993, 75 (05) :843-854
[28]   Misexpression of miR482, miR1512, and miR1515 Increases Soybean Nodulation [J].
Li, Hui ;
Deng, Ying ;
Wu, Tianlong ;
Subramanian, Senthil ;
Yu, Oliver .
PLANT PHYSIOLOGY, 2010, 153 (04) :1759-1770
[29]   Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method [J].
Livak, KJ ;
Schmittgen, TD .
METHODS, 2001, 25 (04) :402-408
[30]   Cleavage of Scarecrow-like mRNA targets directed by a class of Arabidopsis miRNA [J].
Llave, C ;
Xie, ZX ;
Kasschau, KD ;
Carrington, JC .
SCIENCE, 2002, 297 (5589) :2053-2056