Development of marker-free transformants by site-specific recombinases

被引:1
|
作者
Sekan, A. S. [1 ]
Isayenkov, S. V. [1 ]
Blume, Ya. B. [1 ]
机构
[1] Natl Acad Sci Ukraine, Inst Food Biotechnol & Genom, Kiev, Ukraine
关键词
selectable marker genes; excision of the marker sequences; site-specific recombination system; FREE TRANSGENIC PLANTS; ISOPENTENYL TRANSFERASE GENE; DOUBLE-STRAND BREAKS; SEPARATE T-DNAS; CRE RECOMBINASE; MAMMALIAN-CELLS; HOMOLOGOUS RECOMBINATION; TRANSIENT EXPRESSION; INTEGRATION PATTERNS; TOBACCO PLANTS;
D O I
10.3103/S0095452715060080
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
To produce transgenic plants in current biotechnology, selectable marker genes are used that lead to the selectivity of transformants from non-transformed organisms. However, after the transgenic event has been occured, the presence of these genes in transformants genome is generally of no use. Moreover, the continued presence of this kind of genes in transgenic plants with their further commercialization may raise public concern. Therefore, various techniques have been developed in recent years to obtain marker free transgenic plants. In the present review are described the main strategies for removal of selective marker DNA sequences that are used in genetic engineering so far. The most popular among them is a site-specific recombination technology. The particular attention is paid to site-specific recombinase system Cre/loxP. The using of a new approach with site-specific recombinase system Cre/loxP under the control of 35S promoter to generate marker-free genetically modified plants is described.
引用
收藏
页码:397 / 407
页数:11
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