A Highly Efficient Method for Construction of Rice Artificial MicroRNA Vectors

被引:11
作者
Wang, Xuming
Yang, Yong
Yu, Chulang
Zhou, Jie
Cheng, Ye
Yan, Chengqi
Chen, Jianping [1 ]
机构
[1] Zhejiang Acad Agr Sci, Inst Virol & Biotechnol, MOA, Hangzhou 310021, Zhejiang, Peoples R China
关键词
Oryza sativa; Gene silencing; Artificial miRNA; Vector construction; SMALL RNAS; GENES; ARABIDOPSIS; EXPRESSION; PCR; DNA; MIRNAS; PLANTS;
D O I
10.1007/s12033-010-9291-4
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
Artificial microRNA (amiRNA) has become a powerful tool for gene silencing in plants. A new method for easy and rapid construction of rice artificial miRNA vector is described. The procedure involved modification of the pCAMBIA1300-UR vector by insertion of a 'vector modification fragment'. This was prepared from the precursor of Os-amiR528 by eliminating the central miRNA-containing region while simultaneously creating an AfeI restriction site. The fragment was then introduced to the destination vector to produce a multipurpose 'Highly Efficient gene Silencing Compatible vector' (HESC vector). AfeI was used to produce linearized HESC vectors, and a blunt end PCR product that included amiRNA sequence was cloned into this site by a single ligation reaction to create the completed amiRNA vector. Tests showed that the method was highly efficient, and greatly reduced the time needed for vector construction and resulted in a DNA sequence identical to that of the current method, making it particularly suitable for use in a systems biology approach to functional genomic research.
引用
收藏
页码:211 / 218
页数:8
相关论文
共 28 条
[1]   TURBO CLONING - A FAST, EFFICIENT METHOD FOR CLONING PCR PRODUCTS AND OTHER BLUNT-ENDED DNA FRAGMENTS INTO PLASMIDS [J].
BOYD, AC .
NUCLEIC ACIDS RESEARCH, 1993, 21 (04) :817-821
[2]   Widespread translational inhibition by plant miRNAs and siRNAs [J].
Brodersen, Peter ;
Sakvarelidze-Achard, Lali ;
Bruun-Rasmussen, Marianne ;
Dunoyer, Patrice ;
Yamamoto, Yoshiharu Y. ;
Sieburth, Leslie ;
Voinnet, Olivier .
SCIENCE, 2008, 320 (5880) :1185-1190
[3]   Ubiquitin promoter-based vectors for high-level expression of selectable and/or screenable marker genes in monocotyledonous plants [J].
Christensen, AH ;
Quail, PH .
TRANSGENIC RESEARCH, 1996, 5 (03) :213-218
[4]   TISSUE-SPECIFIC AND LIGHT-REGULATED EXPRESSION OF A PEA NUCLEAR GENE ENCODING THE SMALL SUBUNIT OF RIBULOSE-1,5-BISPHOSPHATE CARBOXYLASE [J].
CORUZZI, G ;
BROGLIE, R ;
EDWARDS, C ;
CHUA, NH .
EMBO JOURNAL, 1984, 3 (08) :1671-1679
[5]   Genetic contributions to agricultural sustainability [J].
Dennis, Elizabeth S. ;
Ellis, Jeffrey ;
Green, Allan ;
Llewellyn, Danny ;
Morell, Matthew ;
Tabe, Linda ;
Peacock, W. J. .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2008, 363 (1491) :591-609
[6]   The widespread impact of mammalian microRNAs on mRNA repression and evolution [J].
Farh, KKH ;
Grimson, A ;
Jan, C ;
Lewis, BP ;
Johnston, WK ;
Lim, LP ;
Burge, CB ;
Bartel, DP .
SCIENCE, 2005, 310 (5755) :1817-1821
[7]   EFFICIENT TRANSFORMATION OF RICE (ORYZA-SATIVA L) MEDIATED BY AGROBACTERIUM AND SEQUENCE-ANALYSIS OF THE BOUNDARIES OF THE T-DNA [J].
HIEI, Y ;
OHTA, S ;
KOMARI, T ;
KUMASHIRO, T .
PLANT JOURNAL, 1994, 6 (02) :271-282
[8]   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
[9]   Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets [J].
Lewis, BP ;
Burge, CB ;
Bartel, DP .
CELL, 2005, 120 (01) :15-20
[10]   Microarray analysis shows that some microRNAs downregulate large numbers of target mRNAs [J].
Lim, LP ;
Lau, NC ;
Garrett-Engele, P ;
Grimson, A ;
Schelter, JM ;
Castle, J ;
Bartel, DP ;
Linsley, PS ;
Johnson, JM .
NATURE, 2005, 433 (7027) :769-773