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Cytochrome Oxidase Subunit (cytochrome + oxidase_subunit)

Distribution by Scientific Domains
Life Sciences100%

Terms modified by Cytochrome Oxidase Subunit

  • cytochrome oxidase subunit i
    		•

    Selected Abstracts

    The mitochondrial genome of the wine yeast Hanseniaspora uvarum: a unique genome organization among yeast/fungal counterparts

    FEMS YEAST RESEARCH, Issue 1 2006
    Paraskevi V. Pramateftaki
    Abstract The complete sequence of the apiculate wine yeast Hanseniaspora uvarum mtDNA has been determined and analysed. It is an extremely compact linear molecule containing the shortest functional region ever found in fungi (11 094 bp long), flanked by Type 2 telomeric inverted repeats. The latter contained a 2704-bp-long subterminal region and tandem repeats of 839-bp units. In consequence, a population of mtDNA molecules that differed at the number of their telomeric reiterations was detected. The functional region of the mitochondrial genome coded for 32 genes, which included seven subunits of respiratory complexes and ATP synthase (the genes encoding for NADH oxidoreductase subunits were absent), two rRNAs and 23 tRNA genes which recognized codons for all amino acids. A single intron interrupted the cytochrome oxidase subunit 1 gene. A number of reasons contributed towards its strikingly small size, namely: (1) the remarkable size reduction (by >40%) of the rns and rnl genes; (2) that most tRNA genes and five of the seven protein-coding genes were the shortest among known yeast homologs; and (3) that the noncoding regions were restricted to 5.1% of the genome. In addition, the genome showed multiple changes in the orientation of transcription and the gene order differed drastically from other yeasts. When all protein coding gene sequences were considered as one unit and were compared with the corresponding molecules from all other complete mtDNAs of yeasts, the phylogenetic trees constructed robustly supported its placement basal to the yeast species of the ,Saccharomyces complex', demonstrating the advantage of this approach over single-gene or multigene approaches of unlinked genes. [source]

    Molecular phylogeny of Diabrotica beetles (Coleoptera: Chrysomelidae) inferred from analysis of combined mitochondrial and nuclear DNA sequences

    INSECT MOLECULAR BIOLOGY, Issue 4 2001
    T. L. Clark
    Abstract The phylogenetic relationships of thirteen Diabrotica (representing virgifera and fucata species groups) and two outgroup Acalymma beetle species (Coleoptera: Chrysomelidae) were inferred from the phylogenetic analysis of a combined data set of 1323 bp of mitochondrial DNA (mtDNA) cytochrome oxidase subunit 1 (COI) and the entire second internal transcribed spacer region (ITS-2) of nuclear ribosomal DNA of 362 characters. Species investigated were D. adelpha, D. balteata, D. barberi, D. cristata, D. lemniscata, D. longicornis, D. porracea, D. speciosa, D. undecimpunctata howardi, D. u. undecimpunctata, D. virgifera virgifera, D. v. zeae, D. viridula, and outgroup A. blandulum and A. vittatum. Maximum parsimony (MP), minimum evolution (ME), and maximum likelihood (ML) analyses of combined COI and ITS-2 sequences clearly place species into their traditional morphological species groups with MP and ME analyses resulting in identical topologies. Results generally confer with a prior work based on allozyme data, but within the virgifera species group, D. barberi and D. longicornis strongly resolve as sister taxa as well as monophyletic with the neotropical species, D. viridula, D. cristata and D. lemniscata also resolve as sister taxa. Both relationships are not in congruence with the prior allozyme-based hypothesis. Within the fucata species group, D. speciosa and D. balteata resolve as sister taxa. Results also strongly supported the D. virgifera and D. undecimpunctata subspecies complexes. Our proposed phylogeny provides some insight into current hypotheses regarding distribution status and evolution of various life history traits for Diabrotica. [source]

    New molecular data for tardigrade phylogeny, with the erection of Paramacrobiotus gen. nov.

    JOURNAL OF ZOOLOGICAL SYSTEMATICS AND EVOLUTIONARY RESEARCH, Issue 4 2009
    R. Guidetti
    Abstract Up to few years ago, the phylogenies of tardigrade taxa have been investigated using morphological data, but relationships within and between many taxa are still unresolved. Our aim has been to verify those relationships adding molecular analysis to morphological analysis, using nearly complete 18S ribosomal DNA gene sequences (five new) of 19 species, as well as cytochrome oxidase subunit 1 (COI) mitochondrial DNA gene sequences (15 new) from 20 species, from a total of seven families. The 18S rDNA tree was calculated by minimum evolution, maximum parsimony (MP) and maximum likelihood (ML) analyses. DNA sequences coding for COI were translated to amino acid sequences and a tree was also calculated by neighbour-joining, MP and ML analyses. For both trees (18S rDNA and COI) posterior probabilities were calculated by MrBayes. Prominent findings are as follows: the molecular data on Echiniscidae (Heterotardigrada) are in line with the phylogenetic relationships identifiable by morphological analysis. Among Eutardigrada, orders Apochela and Parachela are confirmed as sister groups. Ramazzottius (Hypsibiidae) results more related to Macrobiotidae than to the genera here considered of Hypsibiidae. Macrobiotidae and Macrobiotus result not monophyletic and confirm morphological data on the presence of at least two large groups within Macrobiotus. Using 18S rDNA and COI mtDNA genes, a new phylogenetic line has been identified within Macrobiotus, corresponding to the ,richtersi-areolatus group'. Moreover, cryptic species have been identified within the Macrobiotus,richtersi group' and within Richtersius. Some evolutionary lines of tardigrades are confirmed, but others suggest taxonomic revision. In particular, the new genus Paramacrobiotus gen. n. has been identified, corresponding to the phylogenetic line represented by the ,richtersi-areolatus group'. Zusammenfassung Die Anzahl der Arten im Phylum Tardigrada ist in den letzten 25 Jahren von 500 Arten auf inzwischen fast 1000 Arten angestiegen. Zurzeit besteht die Gruppe aus zwei Klassen (Heterotardigrada und Eutardigrada), vier Ordnungen, 21 Familien, und 104 Gattungen. Trotz der Häufigkeit der Tardigraden wurde ihnen seit ihrer Entdeckung im Jahr 1773 nur wenig Aufmerksamkeit geschenkt. Bis vor wenigen Jahren wurden ausschließlich morphologische Merkmale verwendet, um die Phylogenie der Tardigrada zu untersuchen. Dennoch sind die Verhältnisse zwischen und innerhalb vieler Arten noch nicht eindeutig geklärt. Das Ziel der vorliegenden Arbeit war es, die bereits bekannten, morphologischen Verhältnisse mit molekularen Ergebnissen zu belegen. Hierzu wurden nur vollständige Sequenzen der ribosomalen 18S rDNA von 19 Arten verwendet. Fünf neue Sequenzen wurden dabei hinzugefügt. Weiterhin wurden von 15 Arten neue mitochrondriale COI Sequenzen verwendet, die mit fünf bekannten COI Sequenzen zu insgesamt sieben Familien gehören. Der 18S rDNA-Baum wurde durch ME, maximum parsimony (MP) and ML Analysen berechnet. Die für COI kodierenden Sequenzen wurden in Aminosäuren übersetzt und der Baum mit NJ, MP and ML Analysen berechnet. Für beide Bäume (18 rDNA und COI) wurden die Wahrscheinlichkeiten durch MrBayes ermittelt. Dabei ergab sich, dass molekulare Daten mit den morphologischen Untersuchungen bei den Echiniscidae (Heterotardigrada) übereinstimmen. Bei Eutardigrada wurden die Ordnungen Apochela und Parachela als Schwestergruppen bestätigt. Ramazzottius (Hypsibiidae) gehört zu der Familie Macrobiotidae und weniger zu Hypsibiidae, zu der die Gattung gegenwärtig gestellt wird. Die molekularen und morphologischen Daten deuten darauf hin, dass es mindestens zwei großer Gruppen innerhalb von Macrobiotus gibt. Durch die 18 rDNA und COI mtDNA Sequenzen konnte eine neue phylogenetische Linie innerhalb von Macrobiotus, der ,richtersi-areolatus Gruppe' zugehörig, identifiziert werden. Weiterhin sind kryptische Arten innerhalb der Macrobiotus richtersi Gruppe' und innerhalb von Richtersius gefunden worden. Die vorliegende Arbeit verifiziert die in vorangegangene Untersuchungen erarbeitete Phylogenie von Tardigraden. Es konnten einige Entwicklungslinien innerhalb den Tardigraden bestätigt werden, andere deuten zukünftige, taxonomische Revisionen an. So wurde die neue Gattung Paramacrobiotus eingeführt, entsprechend der phylogenetischen Linie, die bisher durch die ,richtersi-areolatus Gruppe' vertreten war. [source]

    Identification of mosquito bloodmeals using mitochondrial cytochrome oxidase subunit I and cytochrome b gene sequences

    MEDICAL AND VETERINARY ENTOMOLOGY, Issue 4 2008
    J. S. TOWNZEN
    Abstract Primer pairs were designed and protocols developed to selectively amplify segments of vertebrate mitochondrial cytochrome oxidase subunit 1 (COI) and cytochrome b (Cyt b) mtDNA from the bloodmeals of mosquitoes (Diptera: Culicidae). The protocols use two pairs of nested COI primers and one pair of Cyt b primers to amplify short segments of DNA. Resultant sequences are then compared with sequences in GenBank, using the BLAST function, for putative host identification. Vertebrate DNA was amplified from 88% of our sample of 162 wild-caught, blood-fed mosquitoes from Oregon, U.S.A. and GenBank BLAST searches putatively identified 98% of the amplified sequences, including one amphibian, seven mammalian and 14 avian species. Criteria and caveats for putative identification of bloodmeals are discussed. [source]

    Molecular data reveals California as the potential source of an invasive leafhopper species, Macrosteles sp. nr. severini, transmitting the aster yellows phytoplasma in Hawaii

    ANNALS OF APPLIED BIOLOGY, Issue 3 2009
    J.J. Le Roux
    Abstract A species of aster leafhopper (Macrosteles sp.) became established in 2001 on Oahu, Hawaii, and through the transmission of the aster yellows phytoplasma, caused devastating losses to the island's watercress industry. DNA sequence data were analysed from two mitochondrial genes [cytochrome oxidase subunit 1(CO1) and nicotinamide adenine dinucleotide 1 (NADH1)] and one nuclear gene (wingless, Wg) (combined total of 1874 bp) to reconstruct phylogenetic relationships between putative US mainland source populations of aster leafhoppers and those introduced to Hawaii. These data were applied to elucidate the origin(s) and identity of Hawaiian infestations and the amount of genetic diversity within introduced invasive populations. Both phylogenetic search criteria (Bayesian and maximum likelihood models) converged onto similar tree topologies for all three gene regions and suggested that Hawaii infestations represent a single undescribed leafhopper species unrelated to the common aster leafhopper, Macrosteles quadrilineatus. An exact haplotype match was found from a specimen intercepted from watercress shipped to Hawaii from Los Angeles, California, suggesting this region as the potential source for Hawaiian infestations. Two mitochondrial haplotypes were identified in Hawaii suggesting two or perhaps just a single introduction of more than one female. [source]