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Chapter category: Biotechnology

3xP3-EGFP Marker for Screening of Transgenic Silkworm

This chapter appears in the following book:

Transgenic Silkworms

Edited by: Katsutoshi Yoshizato
ISBN: 1-58706-176-7
» Get more information about this book at landesbioscience.com «

Chapter authors:
Jean-Luc Thomas

With the aim of Drosophila transgenesis the use of the transposable P element was the breakthrough for a new age of molecular genetic research in insects biology.1 The concern of experimentators was to identify the transgenic individuals quite easily as much as possible using vital screening markers. This was early possible for laboratory host strains such as Drosophila melanogaster using eye color mutants and their counterpart cloned genes able to rescue the color deficiency by transcomplementation. It was more difficult for other related dipteran species (nondrosophilid flies or mosquitoes) to benefit from such a prior genetic context. The situation was more critical in other insect orders comprising Lepidoptera, Hymenoptera or Orthoptera. It was particularly a slowing down in our attempts to transform Bombyx mori silkworm. I will present here a brief review based on some excellent already published reviews2-7 describing the importance of the availability of vital screening markers as a reliable detection for insect transgenesis technology. Constant progress on the quality and reliability of marker-coding sequences and more precisely the combination of those sequences with a convenient regulatory sequence has to be continued and encouraged. For Bombyx mori, we benefited by such progress as I will explain it in that chapter. Moreover I also consider that new progress could be envisaged using germ cells screening markers allowing very early in situ detection of transformed germ cells. We have also to keep in mind that the discovered fluorescent screening markers are really powerful essentially due to the progress made in the discovery and development of the new insect transposon as gene vectors.

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