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Homologous recombination-mediated transgene deletion in plant cells

a plant cell and homologous recombination technology, applied in the field of transgenic cell production methods, to achieve the effect of decreasing the occurrence of co-suppression and increasing the stability of the transgen

Inactive Publication Date: 2005-03-17
GILBERTSON LARRY A
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0017] The invention provides a novel method of removing undesirable DNA sequences as well as a method for resolving complex transgene insertions to simpler insertions, thereby increasing transgene stability and decreasing the occurrence of co-suppression.

Problems solved by technology

Since ancillary sequences do not contribute to the desired crop improvement, efforts have been made to delete them from the GM progeny.
Although each of these methods has been designed specifically to excise unwanted sequences, each also relies upon introduction of ancillary genetic sequences (e.g., recombinase or transposase specific recognition sequences) that ultimately do not contribute to the desired crop improvement.

Method used

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  • Homologous recombination-mediated transgene deletion in plant cells
  • Homologous recombination-mediated transgene deletion in plant cells
  • Homologous recombination-mediated transgene deletion in plant cells

Examples

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Effect test

example 1

[0344] Deletion of the Bar Gene from the Transgenic Event DBT418

[0345] Homologous recombination-mediated transgene deletion is a process whereby the structure of a transgene insert can be altered (see FIG. 1). The process is dependent on the presence of direct repeats of DNA sequences in the transgene insertion. Direct repeats may be present in the transgene used for transformation, or they may arise through multi-element integration at the site of transgene insertion. The direct repeats might be, for example, incomplete parts of a transgene that, upon recombination, produce a complete transgene conferring an identifiable phenotype.

[0346] Line DBT418 was produced by microprojectile bombardment of embryogenic cells with plasmid vectors pDPG354 (FIG. 6), pDPGI65 (FIG. 7) and pDPG320 (FIG. 8). The structure of the transgene insert in the line DBT418 is diagramed in FIG. 9 and described in detail in U.S.D.A. Petition 9629101p for deregulation. The insert has one functional copy of a b...

example 2

[0351] Deletion of nptII or cryIA(b) Gene from the Transgenic Events “MON849” and “MON850”

[0352] Transformation events (MON849) and (MON 850) were produced by microprojectile bombardment of cells with plasmid vector using pMON19344 (FIG. 4). The structure of the MON849 transgene insert is diagramed in FIG. 11. The insert has one copy of an nptII gene conferring resistance to kanamycin and one copy of a cryIA(b) Bt gene conferring resistance to certain insect pests. Both the nptII and cryIA(b) coding regions are flanked on the 5′ ends by identical 35S promoters and hsp70 introns. Both the nptII and cryIA(b) coding regions are flanked on the 3′ ends by identical nos terminators. Recombination events between the 35S promoter and hsp70 intron regions of the cryIA(b) gene and the 35S promoter and hsp70 intron regions of the nptII gene result in the loss of the cryIA(b) gene (FIG. 11). Recombination events between the nos terminator region of the cryIA(b) gene and the nos terminator regio...

example 3

[0358] Alteration of a Transgene Insertion Event in Transformed Cells

[0359] The plasmid vector pMON36133 (FIG. 12) was constructed wherein a neomycin phosphotransferase II (nptII) gene is flanked on both the 5′ and 3′ ends by direct repeats of sequences derived from the 3′ end of the maize hsp70 intron. The vector further comprises a gene encoding green fluorescent protein (GFP) that lacks a promoter and is not expressed in a plant cell. Deletion of the sequences between the repeated hsp70 sequences produces a transgene wherein the 35S promoter and hsp70 intron are operable linked to the GFP gene and therefore, the GFP protein is expressed.

[0360] The plasmid vector pMON36133 was introduced into Black Mexican Sweet maize cells using microprojectile bombardment. Transformed callus was selected based on resistance to kanamycin conferred by the nptII gene. Sectors of GFP expressing tissues were observed in the transformants, indicating that the nptII gene was deleted, thereby activati...

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Abstract

A process to prepare a recombined transgenic Zea mays plant or plant cell from a first transgenic Zea mays plant cell, wherein the transgene in the recombinant plant or plant cell has an altered genetic structure relative to the genetic structure of the transgene in the first transgenic plant cell, due to homologous recombination-mediated transgene deletion.

Description

RELATED APPLICATIONS [0001] This application is a division of application Ser. No. 09 / 801,261 filed Mar. 7, 2001 which is a continuation-in-part of application Ser. No. 09 / 521,557 filed Mar. 9, 2000 which are incorporated herein by reference.FIELD OF THE INVENTION [0002] The present invention relates to methods for producing transgenic cells, preferably plant cells, and transgenic plants in which the transgene insertion has been altered by homologous recombination. Alterations include deletions, modifications, or duplications of transgene sequences. The invention further relates to a method for deleting ancillary sequences, such as selectable marker or reporter genes, from transgenic cells, preferably plant cells, and transgenic plants. DESCRIPTION OF THE RELATED ART [0003] Genetically modified (GM) crops offer many advantages to the farmer in terms of inputs to crop production, e.g. weed and insect control, and improved usage of water and nutrient inputs. GM plants also provide a m...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C12N15/31C12N15/82
CPCC12N15/8213
Inventor GILBERTSON, LARRY A.
Owner GILBERTSON LARRY A
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