| Literature DB >> 8890742 |
D Kang1, A Lundström, H Steiner.
Abstract
The mRNA differential display method was used to isolate antibacterial defense genes from Trichoplusia ni. The mRNA population in last-instar T. ni larvae injected with bacteria was compared to that of untreated larvae. Using a PCR amplified probe corresponding to an induced mRNA, we were able to clone an attacin homolog from a lambda cDNA library from vaccinated larvae. The corresponding protein showed 63% identity to Hyalophora cecropia acidic attacin. The induction kinetics of T. ni attacin A gave optimal mRNA levels at 20 h post-infection. Genomic analysis showed this to be a single-copy gene with two introns.Entities:
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Year: 1996 PMID: 8890742 DOI: 10.1016/0378-1119(96)00089-3
Source DB: PubMed Journal: Gene ISSN: 0378-1119 Impact factor: 3.688