Direct comparison of pollen-mediated movement of native and engineered genes
Despite the commercial approval of twenty-five transgenic crops in the U.S. as of mid-1996, concern is still being expressed regarding the potential risks associated with genetically engineered crops. One recurring issue is the possibility of pollen-mediated escape of engineered genes into populatio...
Gespeichert in:
Veröffentlicht in: | Euphytica 1997-01, Vol.96 (3), p.397-403 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Despite the commercial approval of twenty-five transgenic crops in the U.S. as of mid-1996, concern is still being expressed regarding the potential risks associated with genetically engineered crops. One recurring issue is the possibility of pollen-mediated escape of engineered genes into populations of crop wild relatives. To address this concern, the scientific community has depended on literature on pollen dispersal generated from non-transgenic organisms. Utilization of this information requires the assumption that the pollen mediated movement of native and transgenes is the same. To test the validity of this assumption, we directly compared the pollen-mediated gene movement of native and engineered marker genes using melon plants (Cucumis melo L.) expressing dominant morphological and transgenic traits. Movement into both contiguous border plots and non-contiguous satellite plots were monitored. Dispersal of the native gene and transgene into the satellite plots was identical. Dispersal of the two traits into the plot borders was nearly identical. Of the nearly 4600 seedlings screened for both morphological (presence of green vs. virescent cotyledons) and transgene movement (presence of NPT II protein by ELISA), in no case was the NPT II gene observed in the absence of green cotyledons. However, 39 seedlings were green but did not express NPT II as measured by ELISA. PCR analysis revealed transgene inactivation as a cause of the NPT II ELISA-seedlings.[PUBLICATION ABSTRACT] |
---|---|
ISSN: | 0014-2336 1573-5060 |
DOI: | 10.1023/A:1003061501477 |