Literature DB >> 26515963

Identification and characterisation of hemocyanin of the fish louse Argulus (Crustacea: Branchiura).

Pauline Pinnow1, Andrej Fabrizius1, Christian Pick1, Thorsten Burmester2.   

Abstract

Hemocyanin transports oxygen in the hemolymph of many arthropod species. Within the crustaceans, this copper-containing protein was thought to be restricted to Malacostraca, while other crustacean classes were assumed to employ hemoglobin or lack any respiratory protein. Only recently it has become evident that hemocyanins also occur in Remipedia and Ostracoda. Here we report for the first time the identification and characterisation of hemocyanin in the fish louse Argulus, which belongs to the class of Branchiura. This finding indicates that hemocyanin was the principal oxygen carrier in the stem lineage of the pancrustaceans, but has been lost independently multiple times in crustacean taxa. We obtained the full-length cDNA sequences of two hemocyanin subunits of Argulus foliaceus by a combination of RT-PCR, RACE and Illumina sequencing of the transcriptome. In addition, one full-length and one partial cDNA sequence were derived from the transcriptome data of Argulus siamensis. Western blot analysis confirmed the presence of at least two hemocyanin subunits in A. foliaceus, which are expressed at the mRNA level at a 1:3.5 ratio. The addition to the branchiuran hemocyanin subunits to a multiple sequence alignment of arthropod, hemocyanins improved the phylogenetic resolution within the pancrustacean hemocyanins. Malacostracan, ostracod and branchiuran hemocyanins are distinct from the hexapod and remipede hemocyanins, reinforcing the hypothesis of a close relationship of Remipedia and Hexapoda. Notably, the ostracod hemocyanins are paraphyletic with respect to the branchiuran hemocyanins, indicating ancient divergence and differential loss of distinct subunit types.

Entities:  

Keywords:  Branchiura; Copper; Crustacea; Hemocyanin; Phylogeny; Respiratory protein

Mesh:

Substances:

Year:  2015        PMID: 26515963     DOI: 10.1007/s00360-015-0943-3

Source DB:  PubMed          Journal:  J Comp Physiol B        ISSN: 0174-1578            Impact factor:   2.200


  47 in total

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4.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

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5.  Evolution of arthropod hemocyanins and insect storage proteins (hexamerins).

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Journal:  Mol Biol Evol       Date:  1994-05       Impact factor: 16.240

6.  The structure of arthropod hemocyanins.

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7.  Functional conversion of hemocyanin to phenoloxidase by horseshoe crab antimicrobial peptides.

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8.  Molecular characterization and evolution of haemocyanin from the two freshwater shrimps Caridina multidentata (Stimpson, 1860) and Atyopsis moluccensis (De Haan, 1849).

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Journal:  J Comp Physiol B       Date:  2013-01-22       Impact factor: 2.200

9.  Quaternary and subunit structure of Calliphora arylphorin as deduced from electron microscopy, electrophoresis, and sequence similarities with arthropod hemocyanin.

Authors:  J Markl; T Burmester; H Decker; A Savel-Niemann; J R Harris; M Süling; U Naumann; K Scheller
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Review 10.  Ontogeny of decapod crustacean hemocyanin: effects of temperature and nutrition.

Authors:  N Terwilliger; K Dumler
Journal:  J Exp Biol       Date:  2001-03       Impact factor: 3.312

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4.  Molecular Cloning, Structure and Phylogenetic Analysis of a Hemocyanin Subunit from the Black Sea Crustacean Eriphia verrucosa (Crustacea, Malacostraca).

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