Abstract

Typical multicopper oxidases (MCOs) have ten conserved histidines and one conserved cysteine that coordinate four copper atoms. These copper ions are required for oxidase activity. During our studies of insect MCOs, we discovered a gene that we named multicopper oxidase-related protein (MCORP). MCORPs share sequence similarity with MCOs, but lack many of the copper-coordinating residues. We identified MCORP orthologs in many insect species, but not in other invertebrates or vertebrates. We predicted that MCORPs would lack oxidase activity due to the absence of copper-coordinating residues. To test this prediction, we purified recombinant Tribolium castaneum (red flour beetle) MCORP and analyzed its enzymatic activity using a variety of substrates. As expected, no oxidase activity was detected. To study MCORP function in vivo, we analyzed expression profiles of TcMCORP and Anopheles gambiae (African malaria mosquito) MCORP, and assessed RNAi-mediated knockdown phenotypes. We found that both MCORPs are constitutively expressed at a low level in all of the tissues we analyzed. Injection of TcMCORP dsRNA into larvae resulted in 100% mortality prior to adult eclosion, with death occurring mainly during the pharate pupal stage or late pharate adult stage. Injection of TcMCORP dsRNA into pharate pupae resulted in the death of approximately 20% of the treated insects during the pupal to adult transition and a greatly shortened life span for the remaining insects. In addition, knockdown of TcMCORP in females prevented oocyte maturation and, thus, greatly decreased the number of eggs laid. These results indicate that TcMCORP is an essential gene and that its function is required for reproduction. An understanding of the role MCORP plays in insect physiology may help to develop new strategies for controlling insect pests.

Highlights

  • The multicopper oxidase (MCO) family of enzymes is a large group of oxidases that share a similar structure but differ in substrate specificity [1]

  • The multicopper oxidase-related protein (MCORP) sequences are similar to MCO sequences, but they lack the conserved cysteine and many of the conserved histidines that coordinate copper ions

  • During our studies of T. castaneum and A. gambiae MCOs, we discovered that these two insect species have a gene encoding a multicopper oxidase-related protein

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Summary

Introduction

The multicopper oxidase (MCO) family of enzymes is a large group of oxidases that share a similar structure but differ in substrate specificity [1]. The other oxidases tend to oxidize specific substrates such as ascorbate, bilirubin, iron, copper, or manganese [1]. Most enzymes in the MCO family contain four copper atoms, which are essential for oxidase activity. A typical MCO contains three contiguous cupredoxin-like domains [1,5]. The four copper atoms are coordinated by ten conserved histidines (His) and one conserved cysteine (Cys) [1]. One electron is transferred from the substrate to the T1 center, and the electron is passed via intramolecular residues (a conserved His-Cys-His triad) to the pair of T3 copper ions [4]. Molecular oxygen bound between the T3 copper ions is reduced to water after the transfer of four electrons [4]

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