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      A Multicopper Oxidase-Related Protein Is Essential for Insect Viability, Longevity and Ovary Development

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          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.

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          PSORT: a program for detecting sorting signals in proteins and predicting their subcellular localization.

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            Laccases: a never-ending story.

            Laccases (benzenediol:oxygen oxidoreductases, EC 1.10.3.2) are blue multicopper oxidases that catalyze the oxidation of an array of aromatic substrates concomitantly with the reduction of molecular oxygen to water. In fungi, laccases carry out a variety of physiological roles during their life cycle. These enzymes are being increasingly evaluated for a variety of biotechnological applications due to their broad substrate range. In this review, the most recent studies on laccase structural features and catalytic mechanisms along with analyses of their expression are reported and examined with the aim of contributing to the discussion on their structure-function relationships. Attention has also been paid to the properties of enzymes endowed with unique characteristics and to fungal laccase multigene families and their organization.
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              Laccase 2 is the phenoloxidase gene required for beetle cuticle tanning.

              Cuticle tanning (or sclerotization and pigmentation) in invertebrates involves the oxidative conjugation of proteins, which renders them insoluble and hardens and darkens the color of the exoskeleton. Two kinds of phenoloxidases, laccase and tyrosinase, have been proposed to participate in tanning, but proof of the true identity of the enzyme(s) responsible for this process has been elusive. We report the cloning of cDNAs for laccases and tyrosinases from the red flour beetle, Tribolium castaneum, as well as their developmental patterns of expression. To test for the involvement of these types of enzymes in cuticle tanning, we performed RNA interference experiments to decrease the levels of individual phenoloxidases. Normal phenotypes were obtained after dsRNA-mediated transcript depletion for all phenoloxidases tested, with the exception of laccase 2. Insects injected with dsRNA for the laccase 2 gene failed to tan, were soft-bodied and deformed, and subsequently died in a dsRNA dose-dependent fashion. The results presented here support the hypothesis that two isoforms of laccase 2 generated by alternative splicing catalyze larval, pupal, and adult cuticle tanning in Tribolium.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2014
                20 October 2014
                : 9
                : 10
                : e111344
                Affiliations
                [1 ]Department of Biochemistry and Molecular Biophysics, Kansas State University, Manhattan, Kansas, United States of America
                [2 ]Department of Civil and Environmental Engineering, University of California Davis, Davis, California, United States of America
                University of Cincinnati, United States of America
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: ZP PG YA MK MG. Performed the experiments: ZP PG YA. Analyzed the data: ZP PG YA MK MG. Contributed to the writing of the manuscript: ZP PG MK MG.

                [¤]

                Current address: Department of Applied Biology, Chonnam National University, Gwangju, Korea

                Article
                PONE-D-14-38572
                10.1371/journal.pone.0111344
                4203857
                25330116
                f6aba41c-0182-4c95-9b27-453f6471144f
                Copyright @ 2014

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 27 August 2014
                : 30 September 2014
                Page count
                Pages: 12
                Funding
                This work was supported by National Institute of Allergy and Infectious Diseases grant R01 AI070864, National Institute of General Medical Sciences grant R37 GM41247, and National Science Foundation grant IOS-0726425 to M.R.K. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and life sciences
                Anatomy
                Reproductive System
                Ovaries
                Biochemistry
                Biochemical Activity
                Enzymology
                Tissue Distribution
                Genetics
                Epigenetics
                RNA interference
                Genetic Interference
                Phenotypes
                Organisms
                Animals
                Invertebrates
                Arthropoda
                Insects
                Beetles
                Tribolium
                Mosquitoes
                Physiology
                Reproductive Physiology
                Zoology
                Animal Physiology
                Invertebrate Physiology
                Insect Physiology
                Entomology
                Custom metadata
                The authors confirm that all data underlying the findings are fully available without restriction. All relevant data are within the paper and its Supporting Information files.

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                Uncategorized

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