The effects of spacer sequences on silencing efficiency of plant RNAi vectors

被引:53
作者
Hirai, Sayaka
Oka, Shin-ichiro
Adachi, Eri
Kodama, Hiroaki
机构
[1] Chiba Univ, Fac Hort, Dept Bioprod Sci, Chiba 2718510, Japan
[2] Chiba Univ, Grad Sch Sci & Technol, Inage Ku, Chiba 2638522, Japan
关键词
binary vector; hairpin construct; RNA interference; spacer; transgenic plant;
D O I
10.1007/s00299-006-0277-4
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
RNA interference (RNAi) has been used to suppress gene expression in various eukaryotic organisms. In plants, RNAi can be induced by introduction of an RNAi vector that transcribes a self-complementary hairpin RNA. Most basic RNAi constructs have an inverted repeat interrupted with a spacer sequence. To test silencing capability of RNAi constructs, we developed an in vivo assay that is based on the RNAi-mediated changes of the alpha-linolenic acid content in hairy roots. A tobacco endoplasmic reticulum omega-3 fatty acid desaturase (NtFAD3) is the main enzyme for production of alpha-linolenic acid of root membrane lipids. Tobacco hairy roots transformed with the RNAi vectors against the NtFAD3 gene showed a decrease in alpha-linolenic acid content. The frequency of RNA silencing was more affected by spacer sequence than by spacer length, at least between 100 and 1800 bp. Since significant amounts of hairpin RNA against the NtFAD3 gene remained in the transgenic plants displaying a weak silencing phenotype, low degree of silencing was attributed to low efficiency of hairpin RNA processing mediated by Dicer-like proteins. Our results show the possibility of producing a broad range of the RNAi-induced silencing phenotypes by replacing the spacer sequence of RNAi construct.
引用
收藏
页码:651 / 659
页数:9
相关论文
共 35 条
[1]   RNA interference: Biology, mechanism, and applications [J].
Agrawal, N ;
Dasaradhi, PVN ;
Mohmmed, A ;
Malhotra, P ;
Bhatnagar, RK ;
Mukherjee, SK .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2003, 67 (04) :657-+
[2]  
Akashi Hideo, 2004, Methods Mol Biol, V252, P533
[3]   MAP-BASED CLONING OF A GENE CONTROLLING OMEGA-3-FATTY-ACID DESATURATION IN ARABIDOPSIS [J].
ARONDEL, V ;
LEMIEUX, B ;
HWANG, I ;
GIBSON, S ;
GOODMAN, HM ;
SOMERVILLE, CR .
SCIENCE, 1992, 258 (5086) :1353-1355
[4]   Role for a bidentate ribonuclease in the initiation step of RNA interference [J].
Bernstein, E ;
Caudy, AA ;
Hammond, SM ;
Hannon, GJ .
NATURE, 2001, 409 (6818) :363-366
[5]   Specific and heritable genetic interference by double-stranded RNA in Arabidopsis thaliana [J].
Chuang, CF ;
Meyerowitz, EM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (09) :4985-4990
[6]   Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans [J].
Fire, A ;
Xu, SQ ;
Montgomery, MK ;
Kostas, SA ;
Driver, SE ;
Mello, CC .
NATURE, 1998, 391 (6669) :806-811
[7]   CLONING OF A CDNA-ENCODING TOBACCO OMEGA-3-FATTY-ACID DESATURASE [J].
HAMADA, T ;
KODAMA, K ;
NISHIMURA, M ;
IBA, K .
GENE, 1994, 147 (02) :293-294
[8]   Modification of fatty acid composition by over- and antisense-expression of a microsomal omega-3 fatty acid desaturase gene in transgenic tobacco [J].
Hamada, T ;
Kodama, H ;
Nishimura, M ;
Iba, K .
TRANSGENIC RESEARCH, 1996, 5 (02) :115-121
[9]   An RNA-directed nuclease mediates post-transcriptional gene silencing in Drosophila cells [J].
Hammond, SM ;
Bernstein, E ;
Beach, D ;
Hannon, GJ .
NATURE, 2000, 404 (6775) :293-296
[10]   RNA silencing in plants: a shortcut to functional analysis [J].
Horiguchi, G .
DIFFERENTIATION, 2004, 72 (2-3) :65-73