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PMID: 8890742 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Trichoplusia ni attacin A, a differentially displayed insect gene coding for an antibacterial protein.

Gene ·Vol. 174 ·No. 2 ·1996-10-03 ·Pages 245-9

Kang D, Lundström A, Steiner H

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.

MeSH Terms
Amino Acid Sequence Animals Bacterial Infections/immunology Base Sequence Blotting, Southern Cloning, Molecular Gene Expression Regulation Gene Library Insect Hormones/genetics Insect Proteins Introns Larva/genetics,immunology,microbiology Molecular Sequence Data Moths/genetics,immunology RNA, Messenger/genetics Sequence Alignment Sequence Homology, Amino Acid
Chemicals
Insect Hormones Insect Proteins RNA, Messenger attacin antibacterial protein, insect
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Kang D
Department of Microbiology, Stockholm University, Sweden.
Lundström A
Steiner H
Article Info
Journal
Gene
Abbr.
Gene
ISSN
0378-1119
Published
1996-10-03
Pages
245-9
Language
English
Region
Netherlands
NLM ID
7706761
Subset
IM
Databases
GENBANK
U46130
SWISSPROT
UNKNOWN
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