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Merck

Gene targeting in the silkworm by use of a baculovirus.

Genes & development (1999-03-11)
M Yamao, N Katayama, H Nakazawa, M Yamakawa, Y Hayashi, S Hara, K Kamei, H Mori
ABSTRACT

The Bombyx mori fibroin light (L)-chain gene was cloned and the green fluorescent protein (GFP) gene inserted into exon 7. The chimeric L-chain-GFP gene was used to replace the polyhedrin gene of Autographa californica nucleopolyhedrovirus (AcNPV). This recombinant virus was used to target the L-chain-GFP gene to the L-chain region of the silkworm genome. Female moths were infected with the recombinant virus and then mated with normal male moths. Genomic DNA from their progenies was screened for the desired targeting event. This analysis showed that the chimeric gene had integrated into the L-chain gene on the genome by homologous recombination and was stably transmitted through generations. The chimeric gene was expressed in the posterior silk gland, and the gene product was spun into the cocoon layer.

MATERIALS
Product Number
Brand
Product Description

ECL Direct Nucleic Acid, Cytiva RPN3000, pack of 1 ea
ECL Direct Nucleic Acid, Cytiva RPN3001, pack of 1 ea
ECL Detection Reagents, Cytiva RPN3004, pack of 1 ea
ECL Direct Nucleic Acid, Cytiva RPN3005, pack of 1 ea