Transgene organization in rice engineered through direct DNA transfer supports a two-phase integration mechanism mediated by the establishment of integration hot spots

被引:189
作者
Kohli, A [1 ]
Leech, M [1 ]
Vain, P [1 ]
Laurie, DA [1 ]
Christou, P [1 ]
机构
[1] John Innes Ctr Plant Sci Res, Norwich NR4 7UH, Norfolk, England
关键词
D O I
10.1073/pnas.95.12.7203
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Organization of transgenes in rice transformed through direct DNA transfer strongly suggests a two-phase integration mechanism. In the "preintegration" phase, transforming plasmid molecules (either intact or partial) are spliced together, This gives rise to rearranged transgenic sequences, which upon integration do not contain any interspersed plant genomic sequences, Subsequently, integration of transgenic DNA. into the host genome is initiated. Our experiments suggest that the original site of integration acts as a hot spot, facilitating subsequent integration of successive transgenic molecules at the same lotus. The resulting transgenic locus may have plant DNA separating the transgenic sequences. Our data indicate that transformation through direct DNA transfer, specifically particle bombardment, generally results in a single transgenic locus as a result of this two-phase integration mechanism. Transgenic plants generated through such processes may, therefore, be more amenable to breeding programs as the single transgenic locus will be easier to characterize genetically, Results from direct DNA transfer experiments suggest that in the absence of protein factors involved in exogenous DNA transfer through Agrobacterium, the qualitative and/or quantitative efficiency of transformation events is not compromised. Our results cast doubt on the role of Agrobacterium vir genes in the integration process.
引用
收藏
页码:7203 / 7208
页数:6
相关论文
共 62 条
[1]   A risk assessment study of plant genetic transformation using Agrobacterium and implications for analysis of transgenic plants [J].
Barrett, C ;
Cobb, E ;
McNicol, R ;
Lyon, G .
PLANT CELL TISSUE AND ORGAN CULTURE, 1997, 47 (02) :135-144
[2]   REGENERATION OF INTACT TOBACCO PLANTS CONTAINING FULL LENGTH COPIES OF GENETICALLY ENGINEERED T-DNA, AND TRANSMISSION OF T-DNA TO R1-PROGENY [J].
BARTON, KA ;
BINNS, AN ;
MATZKE, AJM ;
CHILTON, MD .
CELL, 1983, 32 (04) :1033-1043
[3]   A CHIMAERIC ANTIBIOTIC-RESISTANCE GENE AS A SELECTABLE MARKER FOR PLANT-CELL TRANSFORMATION [J].
BEVAN, MW ;
FLAVELL, RB ;
CHILTON, MD .
NATURE, 1983, 304 (5922) :184-187
[5]   STRATEGIES FOR VARIETY-INDEPENDENT GENETIC-TRANSFORMATION OF IMPORTANT CEREALS, LEGUMES AND WOODY SPECIES UTILIZING PARTICLE BOMBARDMENT [J].
CHRISTOU, P .
EUPHYTICA, 1995, 85 (1-3) :13-27
[6]   PRODUCTION OF TRANSGENIC RICE (ORYZA-SATIVA L) PLANTS FROM AGRONOMICALLY IMPORTANT INDICA AND JAPONICA VARIETIES VIA ELECTRIC-DISCHARGE PARTICLE-ACCELERATION OF EXOGENOUS DNA INTO IMMATURE ZYGOTIC EMBRYOS [J].
CHRISTOU, P ;
FORD, TL ;
KOFRON, M .
BIO-TECHNOLOGY, 1991, 9 (10) :957-962
[7]   Details of T-DNA structural organization from a transgenic Petunia population exhibiting co-suppression [J].
Cluster, PD ;
ODell, M ;
Metzlaff, M ;
Flavell, RB .
PLANT MOLECULAR BIOLOGY, 1996, 32 (06) :1197-1203
[8]   CHROMATIN STRUCTURE OF INTEGRATED T-DNA IN CROWN GALL TUMORS [J].
COATES, D ;
TALIERCIO, EW ;
GELVIN, SB .
PLANT MOLECULAR BIOLOGY, 1987, 8 (02) :159-168
[9]   MOLECULAR AND GENETIC-CHARACTERIZATION OF ELITE TRANSGENIC RICE PLANTS PRODUCED BY ELECTRIC-DISCHARGE PARTICLE-ACCELERATION [J].
COOLEY, J ;
FORD, T ;
CHRISTOU, P .
THEORETICAL AND APPLIED GENETICS, 1995, 90 (01) :97-104
[10]  
DeNeve M, 1997, PLANT J, V11, P15, DOI 10.1046/j.1365-313X.1997.11010015.x