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dc.contributor.authorKaur, Kiranpreeteng
dc.contributor.authorBakke, Marit Jørgenseneng
dc.contributor.authorNilsen, Frankeng
dc.contributor.authorHorsberg, Tor Einareng
dc.description.abstractAcetylcholinesterase (AChE) is an important enzyme in cholinergic synapses. Most arthropods have two genes (ace1 and ace2), but only one encodes the predominant synaptic AChE, the main target for organophosphates. Resistance towards organophosphates is widespread in the marine arthropod Lepeophtheirus salmonis. To understand this trait, it is essential to characterize the gene(s) coding for AChE(s). The full length cDNA sequences encoding two AChEs in L. salmonis were molecularly characterized in this study. The two ace genes were highly similar (83.5% similarity at protein level). Alignment to the L. salmonis genome revealed that both genes were located close to each other (separated by just 26.4 kbp on the L. salmonis genome), resulting from a recent gene duplication. Both proteins had all the typical features of functional AChE and clustered together with AChE-type 1 proteins in other species, an observation that has not been described in other arthropods. We therefore concluded the presence of two versions of ace1 gene in L. salmonis, named ace1a and ace1b. Ace1a was predominantly expressed in different developmental stages compared to ace1b and was possibly active in the cephalothorax, indicating that ace1a is more likely to play the major role in cholinergic synaptic transmission. The study is essential to understand the role of AChEs in resistance against organophosphates in L. salmonis.en_US
dc.rightsAttribution CC BYeng
dc.titleIdentification and molecular characterization of two acetylcholinesterases from the salmon louse, Lepeophtheirus salmonisen_US
dc.typePeer reviewed
dc.typeJournal article
dc.rights.holderCopyright 2015 Kaur et al.en_US
dc.source.journalPLoS ONE

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