Particle bombardment and the genetic enhancement of crops: myths and realities

被引:198
作者
Altpeter, F
Baisakh, N
Beachy, R
Bock, R
Capell, T
Christou, P
Daniell, H
Datta, K
Datta, S
Dix, PJ
Fauquet, C
Huang, N
Kohli, A
Mooibroek, H
Nicholson, L
Nguyen, TT
Nugent, G
Raemakers, K
Romano, A
Somers, DA
Stoger, E
Taylor, N
Visser, R
机构
[1] Univ Lleida, Dept Prod Vegetal & Ciencia Forestal, E-25198 Lleida, Spain
[2] Univ Florida, IFAS, Dept Agron, Lab Mol Plant Physiol, Gainesville, FL 32611 USA
[3] Int Rice Res Inst, Div Plant Breeding Genet & Biochem, Manila 1099, Philippines
[4] Danforth Plant Sci Ctr, St Louis, MO USA
[5] Univ Munster, Inst Biochem & Biotechnol Pflanzen, D-48143 Munster, Germany
[6] Max Planck Inst Mol Pflanzenphysiol, D-14476 Golm, Germany
[7] Univ Cent Florida, Dept Mol Biol & Microbiol, Orlando, FL 32816 USA
[8] Natl Univ Ireland Maynooth, Dept Biol, Inst Bioengn & Agroecol, Maynooth, Kildare, Ireland
[9] Danforth Plant Sci Ctr, Int Lab Trop Agr Biotechnol, St Louis, MO USA
[10] Ventria Biosci, Sacramento, CA 95834 USA
[11] Newcastle Univ, Sch Biol, Inst Res Environm & Sustainabil, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[12] Univ Wageningen & Res Ctr, Agrotechnol & Food Innovat BV, Dept Bioconvers, NL-6708 PD Wageningen, Netherlands
[13] John Innes Ctr Plant Sci Res, Norwich NR4 7UH, Norfolk, England
[14] La Trobe Univ, Ctr Plant Biotechnol, Dept Primary Ind, Primary Ind Res Victoria, Bundoora, Vic 3086, Australia
[15] Univ Wageningen & Res Ctr, Lab Plant Breeding, NL-6700 AJ Wageningen, Netherlands
[16] Univ Hosp Maastricht, Dept Obstet & Gynaecol, Res Inst GROW, NL-6202 AZ Maastricht, Netherlands
[17] Univ Minnesota, Dept Agron & Plant Genet, St Paul, MN 55108 USA
[18] Rhein Westfal TH Aachen, Inst Mol Biotechnol, D-52074 Aachen, Germany
关键词
crops; genetic engineering; particle bombardment; transformation; transgene expression; transgene structure; transgenic plants;
D O I
10.1007/s11032-004-8001-y
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
DNA transfer by particle bombardment makes use of physical processes to achieve the transformation of crop plants. There is no dependence on bacteria, so the limitations inherent in organisms such as Agrobacterium tumefaciens do not apply. The absence of biological constraints, at least until DNA has entered the plant cell, means that particle bombardment is a versatile and effective transformation method, not limited by cell type, species or genotype. There are no intrinsic vector requirements so transgenes of any size and arrangement can be introduced, and multiple gene cotransformation is straightforward. The perceived disadvantages of particle bombardment compared to Agrobacterium-mediated transformation, i.e. the tendency to generate large transgene arrays containing rearranged and broken transgene copies, are not borne out by the recent detailed structural analysis of transgene loci produced by each of the methods. There is also little evidence for major differences in the levels of transgene instability and silencing when these transformation methods are compared in agriculturally important cereals and legumes, and other non-model systems. Indeed, a major advantage of particle bombardment is that the delivered DNA can be manipulated to influence the quality and structure of the resultant transgene loci. This has been demonstrated in recently reported strategies that favor the recovery of transgenic plants containing intact, single-copy integration events, and demonstrating high-level transgene expression. At the current time, particle bombardment is the most efficient way to achieve plastid transformation in plants and is the only method so far used to achieve mitochondrial transformation. In this review, we discuss recent data highlighting the positive impact of particle bombardment on the genetic transformation of plants, focusing on the fate of exogenous DNA, its organization and its expression in the plant cell. We also discuss some of the most important applications of this technology including the deployment of transgenic plants under field conditions.
引用
收藏
页码:305 / 327
页数:23
相关论文
共 193 条
[1]   Widely separated multiple transgene integration sites in wheat chromosomes are brought together at interphase [J].
Abranches, R ;
Santos, AP ;
Wegel, E ;
Williams, S ;
Castilho, A ;
Christou, P ;
Shaw, P ;
Stoger, E .
PLANT JOURNAL, 2000, 24 (06) :713-723
[2]   Retrofitting YACs for direct DNA transfer into plant cells [J].
Adam, G ;
Mullen, JA ;
Kindle, KL .
PLANT JOURNAL, 1997, 11 (06) :1349-1358
[3]  
AGRAWAL PK, IN PRESS MOL BREEDIN
[4]   Transgenic insect-resistant maintainer line (IR68899B) for improvement of hybrid rice [J].
Alam, MF ;
Datta, K ;
Abrigo, E ;
Oliva, N ;
Tu, J ;
Virmani, SS ;
Datta, SK .
PLANT CELL REPORTS, 1999, 18 (7-8) :572-575
[5]   Generation of large numbers of independently transformed fertile perennial ryegrass (Lolium perenne L.) plants of forage- and turf-type cultivars [J].
Altpeter, F ;
Xu, JP ;
Ahmed, S .
MOLECULAR BREEDING, 2000, 6 (05) :519-528
[6]   Rapid production of transgenic turfgrass (Festuca rubra L.) plants [J].
Altpeter, F ;
Xu, JP .
JOURNAL OF PLANT PHYSIOLOGY, 2000, 157 (04) :441-448
[7]  
Altpeter F, 2004, DEV PLANT BREED, V11, P255
[8]   Stable expression of 1Dx5 and 1Dy10 high-molecular-weight glutenin subunit genes in transgenic rye drastically increases the polymeric glutelin fraction in rye flour [J].
Altpeter, F ;
Popelka, JC ;
Wieser, H .
PLANT MOLECULAR BIOLOGY, 2004, 54 (06) :783-792
[9]   Integration and expression of the high-molecular-weight glutenin subunit 1Ax1 gene into wheat [J].
Altpeter, F ;
Vasil, V ;
Srivastava, V ;
Vasil, IK .
NATURE BIOTECHNOLOGY, 1996, 14 (09) :1155-1159
[10]  
Altpeter F, 1996, PLANT CELL REP, V16, P12, DOI 10.1007/BF01275440