Evidence for genomic changes in transgenic rice (Oryza sativa L) recovered from protoplasts

被引:29
作者
Bao, PH
Granata, S
Castiglione, S
Wang, GJ
Giordani, C
Cuzzoni, E
Damiani, G
Bandi, C
Datta, SK
Datta, K
Potrykus, I
Callegarin, A
Sala, F
机构
[1] UNIV PAVIA,DEPT GENET & MICROBIOL,CONSORZIO INTERUNIV NAZL BIOL MOL PIANTE,I-27100 PAVIA,ITALY
[2] CNR,IDVGA,I-20133 MILAN,ITALY
[3] IST PATOL GEN VET,MILAN,ITALY
[4] ETH ZENTRUM,SWISS FED INST TECHNOL,CH-8092 ZURICH,SWITZERLAND
[5] CTR RIC RISO,CASTELLO DAGOGNA,PAVIA,ITALY
关键词
transgenic rice; PCR-RAPD; arbitrary DNA primers; genomic changes; somaclonal variation;
D O I
10.1007/BF01969427
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The occurrence of genomic modifications intransgenic rice plants recovered from protoplasts and their transmission to the self-pollination progeny has been verified with the random amplified polymorphic DNA (RAPD) approach. The plant was the Indica-type rice (Oryza sativa L.) cultivar Chinsurah Bore II. The analysed material was: (1) microspore-derived embryogenic rice cells grown in suspension culture, (2) transgenic plants recovered from protoplasts produced from the cultured cells and (3) the self-pollination progeny (two successive generations) of the transgenic plants. DNA purified from samples of these materials was PCR-amplified with different random oligonucleotide primers and the amplification products were analysed by agarose gel electrophoresis. Band polymorphism was scored and used in band-sharing analyses to produce a similarity matrix. Relationships among the analysed genomes were expressed in a dendrogram. The extensive DNA changes evidenced in cultured cells demonstrate the occurrence of somaclonal variation in the material used to produce protoplasts for gene transfer. Quantitatively reduced DNA changes were also found in the resulting transgenic plants and in their self-pollination progenies. While confirming the stability of the foreign gene in transgenic plants, this work gives molecular evidence for the occurrence of stable genomic changes in transgenic plants and points to in vitro cell culture as the causative agent. RAPDs are shown to be a convenient tool to detect and estimate the phenomenon at the molecular level. The methodology is also proposed as a fast tool to select those transgenic individuals that retain the most balanced genomic structure and to control the result of back-crosses planned to restore the original genome.
引用
收藏
页码:97 / 103
页数:7
相关论文
共 27 条
[1]   ANALYSIS OF SINGLE PROTOPLASTS AND REGENERATED PLANTS BY PCR AND RAPD TECHNOLOGY [J].
BROWN, PTH ;
LANGE, FD ;
KRANZ, E ;
LORZ, H .
MOLECULAR AND GENERAL GENETICS, 1993, 237 (03) :311-317
[2]   RAPD FINGERPRINTS FOR IDENTIFICATION AND FOR TAXONOMIC STUDIES OF ELITE POPLAR (POPULUS SPP) CLONES [J].
CASTIGLIONE, S ;
WANG, G ;
DAMIANI, G ;
BANDI, C ;
BISOFFI, S ;
SALA, F .
THEORETICAL AND APPLIED GENETICS, 1993, 87 (1-2) :54-59
[3]   AGROBACTERIUM-MEDIATED PRODUCTION OF TRANSGENIC RICE PLANTS EXPRESSING A CHIMERIC ALPHA-AMYLASE PROMOTER BETA-GLUCURONIDASE GENE [J].
CHAN, MT ;
CHANG, HH ;
HO, SL ;
TONG, WF ;
YU, SM .
PLANT MOLECULAR BIOLOGY, 1993, 22 (03) :491-506
[4]   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
[5]   THE DEVELOPMENT OF A VARIETY-INDEPENDENT GENE-TRANSFER METHOD FOR RICE [J].
CHRISTOU, P ;
FORD, TL ;
KOFRON, M .
TRENDS IN BIOTECHNOLOGY, 1992, 10 (07) :239-246
[6]   PRE-GERMINATION GENOTYPIC SCREENING USING PCR AMPLIFICATION OF HALF-SEEDS [J].
CHUNWONGSE, J ;
MARTIN, GB ;
TANKSLEY, SD .
THEORETICAL AND APPLIED GENETICS, 1993, 86 (06) :694-698
[7]  
CLARK AG, 1993, MOL BIOL EVOL, V10, P1096
[8]   GENE-MAPPING JAPAN NUMBER ONE CROP [J].
CRAWFORD, R .
SCIENCE, 1991, 252 (5013) :1611-1611
[9]   A REPEATED CHROMOSOMAL DNA-SEQUENCE IS AMPLIFIED AS A CIRCULAR EXTRACHROMOSOMAL MOLECULE IN RICE (ORYZA-SATIVA L) [J].
CUZZONI, E ;
FERRETTI, L ;
GIORDANI, C ;
CASTIGLIONE, S ;
SALA, F .
MOLECULAR & GENERAL GENETICS, 1990, 222 (01) :58-64
[10]  
DATTA SK, 1990, PLANT CELL REP, V9, P253, DOI 10.1007/BF00232295