Home  About us  Contact
 

Mitochondrial Cytochrome Oxidase Subunit I (mitochondrial + cytochrome_oxidase_subunit_i)

Distribution by Scientific Domains
Life Sciences100%

Selected Abstracts

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]

DNA barcoding Central Asian butterflies: increasing geographical dimension does not significantly reduce the success of species identification

MOLECULAR ECOLOGY RESOURCES, Issue 5 2009
VLADIMIR A LUKHTANOV
Abstract DNA barcoding employs short, standardized gene regions (5' segment of mitochondrial cytochrome oxidase subunit I for animals) as an internal tag to enable species identification. Prior studies have indicated that it performs this task well, because interspecific variation at cytochrome oxidase subunit I is typically much greater than intraspecific variation. However, most previous studies have focused on local faunas only, and critics have suggested two reasons why barcoding should be less effective in species identification when the geographical coverage is expanded. They suggested that many recently diverged taxa will be excluded from local analyses because they are allopatric. Second, intraspecific variation may be seriously underestimated by local studies, because geographical variation in the barcode region is not considered. In this paper, we analyse how adding a geographical dimension affects barcode resolution, examining 353 butterfly species from Central Asia. Despite predictions, we found that geographically separated and recently diverged allopatric species did not show, on average, less sequence differentiation than recently diverged sympatric taxa. Although expanded geographical coverage did substantially increase intraspecific variation reducing the barcoding gap between species, this did not decrease species identification using neighbour-joining clustering. The inclusion of additional populations increased the number of paraphyletic entities, but did not impede species-level identification, because paraphyletic species were separated from their monophyletic relatives by substantial sequence divergence. Thus, this study demonstrates that DNA barcoding remains an effective identification tool even when taxa are sampled from a large geographical area. [source]

DNA barcoding of the endemic New Zealand leafroller moth genera, Ctenopseustis and Planotortrix

MOLECULAR ECOLOGY RESOURCES, Issue 3 2009
PIA LANGHOFF
Abstract Molecular techniques such as DNA barcoding have become popular in assisting species identification especially for cryptic species complexes. We have analysed data from a 468-bp region of the mitochondrial cytochrome oxidase subunit I (COI) gene from 200 specimens of 12 species of endemic New Zealand leafroller moths (Tortricidae) from the genera Planotortrix and Ctenopseustis to assess whether the DNA barcoding region can distinguish these species. Among the 200 sequences analysed, 72 haplotypes were recovered, with each genus forming a separate major clade. Maximum likelihood phylogenetic methods were used to test whether species fell into reciprocally monophyletic clades. The optimal phylogeny showed that four species within the genus Ctenopseustis (C. obliquana, C. herana, C. filicis and C. fraterna) and three within Planotortrix (P. octo, P. excessana and P. avicenniae) are polyphyletic. Shimodaira,Hasegawa tests rejected a null hypothesis of monophyly for the species C. obliquana, C. herana, P. octo and P. excessana. Comparisons of within and between species levels of sequence divergence for the same set of seven species showed cases where maximum levels of within-species divergence were greater than some levels of between-species divergence. DNA barcoding using this region of the COI gene is able to distinguish the two genera and some species within each genus; however, many species cannot be identified using this method. Finally, we discuss the possible reasons for this polyphyly, including incomplete lineage sorting, introgression, horizontal gene transfer and incorrect taxonomy. [source]

A set of primers conserved in genus Parnassius (Lepidoptera, Papilionidae) for amplification and sequencing of 1016 bp fragment of cytochrome oxidase subunit I from museum specimens

MOLECULAR ECOLOGY RESOURCES, Issue 3 2008
MACIEJ K. KONOPINSKI
Abstract Four short, overlapping amplicons covering a 1016 bp fragment of mitochondrial cytochrome oxidase subunit I were developed. All four fragments were successfully amplified and sequenced in eight species of butterflies belonging to the genus Parnassius including over 100-year-old DNA from pinned museum specimens. The fragment contains sufficient variation for both inter- and intraspecific analyses. A total of 105 sites were polymorphic within 52 haplotypes found in 186 samples from Parnassius mnemosyne. [source]

Description of Crypsiphona tasmanica sp. nov. (Lepidoptera: Geometridae: Geometrinae), with notes on limitations in using DNA barcodes for delimiting species

AUSTRALIAN JOURNAL OF ENTOMOLOGY, Issue 2 2009
Erki Õunap
Abstract External morphological differences were found between Tasmanian and mainland Australian specimens of what was previously considered a single species, the Redlined Geometrid, Crypsiphona ocultaria (Donovan). Examination of genitalia showed constant differences, suggesting that Tasmanian and mainland Australian populations represent distinct species. This hypothesis was tested using DNA sequences from the mitochondrial cytochrome oxidase subunit I (COI) gene and nuclear elongation factor 1-alpha (EF-1,) gene. Tasmanian Crypsiphona Meyrick populations were found to represent a distinct species, described here as C. tasmanica sp. nov. The results show that a phylogeny-based approach allows the delimitation of C. ocultaria (Donovan) and C. tasmanica sp. nov., but distance-based delimitation is problematic due to substantial overlap in intra- and interspecific genetic distances. Using nucleotide data in character-based species delimitations might be possible for discriminating between C. ocultaria and C. tasmanica, but our current knowledge does not allow the assignment of characters required for this purpose. [source]