Identification of early genes in the Drosophila immune response by PCR-based differential display: the Attacin A gene and the evolution of attacin-like proteins
We are using the PCR-based differential display technique to isolate genes which are induced during the immune response in Drosophila. In this way, a cDNA clone for a member of the attacin family of antibacterial proteins was isolated. The corresponding Attacin A (AttA) gene is localized at 51A-B on...
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Veröffentlicht in: | Insect biochemistry and molecular biology 1995-04, Vol.25 (4), p.511-518 |
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Sprache: | eng |
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Zusammenfassung: | We are using the PCR-based differential display technique to isolate genes which are induced during the immune response in
Drosophila. In this way, a cDNA clone for a member of the attacin family of antibacterial proteins was isolated. The corresponding
Attacin A (AttA) gene is localized at 51A-B on the second chromosome, and it is closely linked to at least one more cross-hybridizing gene. Injection of bacteria induces a 0.8 kb transcript, with expression kinetics similar to that of cecropin.
Drosophila attacin is most closely related to sarcotoxin II of
Sarcophaga peregrina, but it lacks the extra domains that are unique to this protein, and the overall domain structure of the
AttA gene product is identical to that of the attacins from
Hyalophora cecropia. |
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ISSN: | 0965-1748 1879-0240 |
DOI: | 10.1016/0965-1748(94)00091-C |