Virus-induced gene silencing (VIGS) as a reverse genetic tool to study development of symbiotic root nodules

被引:21
作者
Constantin, G. D. [1 ]
Gronlund, M. [1 ]
Johansen, I. E. [1 ]
Stougaard, J. [2 ]
Lund, O. S. [1 ,3 ]
机构
[1] Univ Aarhus, Fac Agr Sci, Dept Genet & Biotechnol, DK-1871 Frederiksberg C, Denmark
[2] Univ Aarhus, Dept Mol Biol, Gene Express Lab, DK-8000 Aarhus, Denmark
[3] Univ Copenhagen, Fac Life Sci, Dept Plant Biol, DK-1871 Frederiksberg, Denmark
关键词
sym35; symbiosis; Tobravirus;
D O I
10.1094/MPMI-21-6-0720
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Virus-induced gene silencing (VIGS) can provide a shortcut to plants with altered expression of specific genes. Here, we report that VIGS of the Nodule inception gene (Nin) can alter the nodulation phenotype and Nin gene expression in Pisum sativum. PsNin was chosen as target because of the distinct non-nodulating phenotype of nin mutants in P sativum, Lotus japonicus, and Medicago truncatula. The vector based on Pea early browning virus (PEBV) was engineered to carry one of three nonoverlapping fragments (PsNinA, PsNinB, and PsNinC) derived from the PsNin cDNA. Vector inoculation was mediated by agroinfiltration and, 2 weeks later, a Rhizobium leguminosarum bv. viceae culture was added in order to induce root nodulation. At this time point, it was estimated that systemic silencing was established because leaves of reference plants inoculated with PEBV carrying a fragment of Phytoene desaturase displayed photo bleaching. Three weeks after Rhizobium spp. application, plants inoculated with a control vector nodulated normally, whereas nodulation was almost eliminated in plants inoculated with a vector carrying PsNinA and PsNinC. For plants inoculated with a vector carrying PsNinB, nodulation was reduced by at least 45%. Downregulation of PsNin transcripts in plants inoculated with vectors carrying PsNin cDNA fragments was confirmed and these plants displayed a relative increase in the root/shoot ratio, as expected if nitrogen fixation had been impaired.
引用
收藏
页码:720 / 727
页数:8
相关论文
共 35 条
[1]  
[Anonymous], 2004, PLANT DNA C VALUES D
[2]   Differential effects of combined N sources on early steps of the nod factor-dependent transduction pathway in Lotus japonicus [J].
Barbulova, Ani ;
Rogato, Alessandra ;
D'Apuzzo, Enrica ;
Omrane, Selim ;
Chiurazzi, Maurizio .
MOLECULAR PLANT-MICROBE INTERACTIONS, 2007, 20 (08) :994-1003
[3]   The Mi-1-mediated pest resistance requires Hsp90 and Sgt1 [J].
Bhattarai, Kishor K. ;
Li, Qi ;
Liu, Yule ;
Dinesh-Kumar, Savithramma P. ;
Kaloshian, Isgouhi .
PLANT PHYSIOLOGY, 2007, 144 (01) :312-323
[4]   The sym35 gene required for root nodule development in pea is an ortholog of nin from Lotus japonicus [J].
Borisov, AY ;
Madsen, LH ;
Tsyganov, VE ;
Umehara, Y ;
Voroshilova, VA ;
Batagov, AO ;
Sandal, N ;
Mortensen, A ;
Schauser, L ;
Ellis, N ;
Tikhonovich, IA ;
Stougaard, J .
PLANT PHYSIOLOGY, 2003, 131 (03) :1009-1017
[5]   Stability of Barley stripe mosaic virus -: Induced gene silencing in barley [J].
Bruun-Rasmussen, Marianne ;
Madsen, Christian Toft ;
Jessing, Stine ;
Albrechtsen, Merete .
MOLECULAR PLANT-MICROBE INTERACTIONS, 2007, 20 (11) :1323-1331
[6]   Applications and advantages of virus-induced gene silencing for gene function studies in plants [J].
Burch-Smith, TM ;
Anderson, JC ;
Martin, GB ;
Dinesh-Kumar, SP .
PLANT JOURNAL, 2004, 39 (05) :734-746
[7]   Virus-induced gene silencing as a tool for functional genomics in a legume species [J].
Constantin, GD ;
Krath, BN ;
MacFarlane, SA ;
Nicolaisen, M ;
Johansen, IE ;
Lund, OS .
PLANT JOURNAL, 2004, 40 (04) :622-631
[8]   EFFECTS OF SOIL NUTRIENTS AND MOSITURE ON ROOT/SHOOT RATIOS IN LOLIUM PERENNE L AND TRIFOLIUM REPENS L [J].
DAVIDSON, RL .
ANNALS OF BOTANY, 1969, 33 (131) :571-+
[9]   Antiviral immunity directed by small RNAs [J].
Ding, Shou-Wei ;
Voinnet, Olivier .
CELL, 2007, 130 (03) :413-426
[10]   MUTAGENESIS OF PEA (PISUM-SATIVUM-L) AND THE ISOLATION OF MUTANTS FOR NODULATION AND NITROGEN-FIXATION [J].
DUC, G ;
MESSAGER, A .
PLANT SCIENCE, 1989, 60 (02) :207-213