Cytochrome C Oxidase Genes Research Articles

Metabolic Adaptations in Phosphine-Resistant Tribolium castaneum Driven by Mitochondrial Enzyme Variability and Gene Expression.

Phosphine fumigation is essential for controlling storage pests like Tribolium castaneum, but its frequent application has resulted in resistance, primarily due to mutations in the Dihydrolipoamide dehydrogenase (DLD) gene associated with the rph2 allele. This study demonstrates that the Patiala population exhibits homozygous resistance variations across populations, contrasting with the susceptibility observed in laboratory cultures. Our assessment of mitochondrial DLD and Cytochrome c oxidase (COX) activities showed significantly elevated levels in the Patiala population, with increases of approximately sevenfold for DLD and 6.92-fold for COX, indicating mitochondrial adaptations for enhanced energy production. Kinetic analyses of DLD in the resistant Patiala population showed a higher Vmax (0.005 mmol/min) and a significantly increased Km (16.66 mM), indicating variations in maximal enzyme activity and substrate affinity. Furthermore, resistant T. castaneum populations displayed substantial upregulation of DLD and COX gene expression, with DLD expression increasing by 10.53-fold and COX expression peaking at 102.57-fold in Patiala. Pearson correlation analysis indicated strong positive correlations (r > 0.8) between enzymatic activity and gene expression for both DLD and COX, suggesting a coordinated role in resistance mechanisms. The PCA biplot illustrated distribution patterns of enzymatic activity and gene expression among field-resistant populations, highlighting the association between increased resistance and elevated enzymatic activity and gene expression levels. Therefore, the upregulation of DLD and COX activities in resistant populations underscores their critical roles in counteracting phosphine, reflecting metabolic reprogramming for improved energy production under stress.

Genome-wide identification and evolutionary analysis of the AP2/EREBP, COX and LTP genes in Zea mays L. under drought stress

AP2 (APETALA2)/EREBP (ethylene-responsive element-binding protein), cytochrome c oxidase (COX) and nonspecific lipid transfer proteins (LTP) play important roles in the response to drought stress. This is the first study to identify the COX gene in Zea mays L. via genome-wide analysis. The qRT‒PCR results indicated that AP2/EREBP, COX and LTP were downregulated, with fold changes of 0.84, 0.53 and 0.31, respectively, after 12 h of drought stress. Genome-wide analysis identified 78 AP2/EREBP, 6 COX and 10 LTP genes in Z. mays L. Domain analysis confirmed the presence of the AP2 domain, Cyt_c_Oxidase_Vb domain and nsLTP1 in the AP2/EREBP, COX and LTP proteins, respectively. The AP2/EREBP protein family (AP2) includes five different domain types: the AP2/ERF domain, the EREBP-like factor (EREBP), the ethylene responsive factor (ERF), the dehydration responsive element binding protein (DREB) and the SHN SHINE. Synteny analysis of the AP2/EREBP, COX and LTP genes revealed collinearity orthologous relationships in O. sativa, H. vulgare and A. thaliana. AP2/EREBP genes were found on the 10 chromosomes of Z. mays L. COX genes were found on chromosomes 1, 3, 4, 5, 7 and 8. LTP genes were found on chromosomes 1, 3, 6, 8, 9 and 10. In the present study, the Ka/Ks ratios of the AP2/EREBP paralogous pairs indicated that the AP2/EREBP genes were influenced primarily by purifying selection, which indicated that the AP2/EREBP genes received strong environmental pressure during evolution. The Ka/Ks ratios of the COX-3/COX-4 paralogous pairs indicate that the COX-3/COX-4 genes were influenced primarily by Darwinian selection (driving change). For the LTP genes, the Ka/Ks ratios of the LTP-1/LTP-10, LTP-5/LTP-3 and LTP-4/LTP-8 paralogous pairs indicate that these genes were influenced primarily by purifying selection, while the Ka/Ks ratios of the LTP-2/LTP-6 paralogous pairs indicate that these genes were influenced primarily by Darwinian selection. The duplication time of the AP2/EREBP paralogous gene pairs in Z. mays L. ranged from approximately 9.364 to 100.935 Mya. The duplication time of the COX-3/COX-4 paralogous gene pair was approximately 5.217 Mya. The duplication time of the LTP paralogous gene pairs ranged from approximately 19.064 to 96.477 Mya. The major focus of research is to identify the genes that are responsible for drought stress tolerance to improve maize for drought stress tolerance. The results of the present study will improve the understanding of the functions of the AP2/EREBP, COX and LTP genes in response to drought stress.

Unveiling the molecular identity of the diminutive cyprinid, Horadandia brittani (Teleostei: Cyprinidae), a species endemic to Southern India.

Horadandia brittani is a small cyprinid fish species initially discovered in the coastal floodplains of southern India. For almost 50 years, the genus Horadandia was monotypic with a single species confined to Sri Lanka. In 1992, a new species H. brittani was described from south-western India. Despite being described as a separate species, H. brittani was later considered a synonym of H. atukorali, but in 2013, researchers recognized it as a distinct species based on morphological differences. Despite this clarification, there was still a need to validate the identity of H. brittani and determine its evolutionary relationship with its closely related species using DNA sequences. To address the uncertainties surrounding the identity of H. brittani, the present study utilized molecular techniques to generate DNA sequences. Sample collection involved obtaining specimens of H. brittani from their natural habitats. Subsequently, DNA was extracted from the collected samples, and the mitochondrial cytochrome C oxidase (COI) gene was amplified using appropriate methods. The analysis of DNA sequences obtained from the COI gene revealed significant genetic distinctions between H. brittani and H. atukorali. The genetic distance values between these two species ranged from 3.21 to 3.63%, clearly indicating that these two species are genetically separate entities. The study successfully established the phylogenetic relationships between H. brittani and H. atukorali based on the COI gene sequences, further confirming the validity of H. brittani as a distinct and separate species. The findings of this study conclusively demonstrate that H. brittani is a valid and separate species, distinct from H. atukorali. The genetic analysis based on mitochondrial COI gene sequences provided strong evidence for the differentiation between these two species. The molecular data generated in this research can be used to identify H. brittani quickly and accurately in the future.

Phylogenomic analysis of 155 helminth species reveals widespread absence of oxygen metabolic capacity.

The terminal electron acceptor of most aerobic respiratory chains, cytochrome c oxidase (COX), has been highly conserved throughout evolution, from aerobic prokaryotes to complex eukaryotes. Oxygen metabolism in parasitic helminths differs significantly from that of most aerobic eukaryotes, as these organisms can switch between aerobic and anaerobic metabolisms throughout their life cycles. Early studies suggested a lack of COX activity in certain parasitic helminths, and the role of COX in helminth mitochondria remains unclear. To determine whether a functional COX is widely present in helminths, we analyzed the phylogenetic distribution of oxygen metabolism systems across 155 helminth genomes, investigating three distinct sets of protein-coding genes involved in different aspects of oxygen metabolism: COX and its assembly factors, peroxisomes, and the most abundant reactive oxygen species (ROS)-metabolizing proteins. While glycolytic and citric acid cycle enzymes are highly conserved in helminthic species, we observed an apparent widespread absence of essential COX genes across 52% of helminth species investigated. While the most common proteins involved in the defense against ROS are highly maintained across virtually all lineages, we also observed an apparent absence of essential peroxisomal protein-coding genes in 42% of species investigated. Our results suggest that a subset of parasitic helminths utilize oxygen differently from related, non-parasitic species such as C. elegans, with significant differences in their mitochondrial electron transport chains and peroxisomes. The identification of substantive differences between parasite and host metabolism offers a new avenue for the development of anthelmintic agents that could target these divergent pathways.

First identification of Tyrophagus curvipenis (Acari: Acaridae) and pathogen detection in Apis mellifera colonies in the Republic of Korea

Mites of the genus Tyrophagus (Acari: Acaridae) are among the most widely distributed mites. The species in this genus cause damage to stored products and crops, and pose a threat to human health. However, the influence of Tyrophagus spp. in apiculture remains unknown. In 2022, a study focusing on the identification of Tyrophagus species within five apiaries was conducted in Chungcheongnam Province, Republic of Korea. Its specific objective was to investigate the presence of Tyrophagus mites in response to the reported high mortality of honey bee colonies in this area. Morphological identification and phylogenetic analysis using the mitochondrial gene cytochrome-c oxidase subunit 1 (CO1) confirmed for the first time the presence of the mite species Tyrophagus curvipenis in a honey bee colony in the Republic of Korea. Two honey bee pathogens were detected in the mite, a viral pathogen (deformed wing virus, DWV) and a protozoal pathogen (Trypanosoma spp.). The presence of the two honey bee pathogens in the mite suggests that this mite could contribute to the spread of related honey bee diseases. However, the direct influence of the mite T. curvipenis on honey bee health remains unknown and should be further investigated.

DNA Barcoding of Argyrops filamentosus (Perciformes: Sparidae) Based on Mitochondrial COI Gene and Histopathological Evaluation of Gills Infected by Monogeneans

Background: Sparidae is a fish family that belongs to the order Perciformes and is commonly known as sea breams and porgies. Many species are included in this family and divided into 71 genera that could be barcoded using mitochondrial DNA genes. These fish are vulnerable to different parasitic taxa that affect fish status. The present study is aimed to confirm the molecular status of Argyrops filamentosus fish via the mitochondrial cytochrome c oxidase (COI) gene and to study the pathological changes of gills infested by monogenean parasites. Methods: Thirty Argyrops filamentosus fish were collected from Jeddah (Saudi Arabia) and identified molecularly via the mtCOI gene. Also, gills were isolated and examined microscopically for presence of monogeneans. Histopathological impacts of monogeneans on fish gills were studied in comparison to the gills of non-infected fish. Result: The DNA of fish species was barcoded and showed highly stringent criteria with the previously Argyrops filamentosus sequence data. The obtained host DNA sequences were deposited in NCBI database under accession number OP975758.1. Examination of the investigated fish gills revealed the presence of three monogenean species Protolamellodiscus senilobatus Kritsky, Jiménez-Ruiz and Sey, 2000, Acleotrema maculatus Morsy, El-Fayoumi and Fahmy (2014) and Haliotrema susanae Soo, 2019. Monogenean parasites penetrated deeply with their haptor to the gill lamella and caused damage and degeneration of epithelial cells leading to the formation of a cup-shaped depression. Therefore, the mtDNA gene has the ability for host identification and heavy monogeneans infections lead to severe damage to fish gills.

A huge undescribed diversity of the subgenus Hystricochaetonotus (Gastrotricha, Chaetonotidae, Chaetonotus) in Central Europe

The subgenus Hystricochaetonotus Schwank, 1990 is one of the most species-rich subgenera of Chaetonotus Ehrenberg, 1830. It has a worldwide distribution and encompasses 37 species predominantly living in the benthos and periphyton of limnetic habitats. We have discovered further nine new species in running and stagnant waters in Slovakia (Central Europe): Ch. (H.) arcanus sp. nov., Ch. (H.) avarus sp. nov., Ch. (H.) gulosus sp. nov., Ch. (H.) iratus sp. nov., Ch. (H.) luxus sp. nov., Ch. (H.) mirabilis sp. nov., Ch. (H.) optabilis sp. nov., Ch. (H.) slavicus sp. nov., and Ch. (H.) superbus sp. nov. Their morphology was studied using differential interference contrast microscopy and subsequent morphometric analyses were carried out. In addition, the primary and secondary structures of their 18S, ITS2, and 28S rRNA molecules as well as their barcoding mitochondrial gene encoding for cytochrome c oxidase (COI) were analyzed. Species boundaries were tested also using the compensatory base change analysis. The new species could be well separated both morphologically and molecularly. The present barcoding analyses revealed that the nuclear ITS2 sequences represent a powerful DNA barcode in addition to the mitochondrial COI gene. According to the multi-gene phylogenetic analyses, the lineage leading to the last common ancestor of the ‘Hystricochaetonotus’ clade is the longest internal branch within the family Chaetonotidae Gosse, 1864. Since members of the subgenus Hystricochaetonotus are morphologically highly heterogeneous, parallel evolution of Chaetonotus-like and/or Hystricochaetonotus-like characters of scales and spines occurred during its radiation.

A phylogeny based on cytochrome-c oxidase gene sequences identifies sympatric Ichthyophonus genotypes in the NE Pacific Ocean.

In recent decades, evidence has accumulated to suggest that the widespread and highly variable parasite Ichthyophonus hoferi is actually a species complex. Highly plastic morphology and a general lack of defining structures has contributed to the likely underestimate of biodiversity within this group. Molecular methods are a logical next step in the description of these parasites, but markers used to date have been too conserved to resolve species boundaries. Here we use mitochondrial encoded cytochrome-c oxidase (MTCO1) gene sequences and phylogenic analysis to compare Ichthyophonus spp. isolates from several marine and anadromous fish hosts. The resulting phylogeny displays lineage separation among isolates and possible host/niche segregation not previously described. The parasite type that infects Pacific herring Clupea pallasii, Atlantic herring C. harengus, Atlantic salmon Salmo salar, and Pacific staghorn sculpin Oligocottus maculosus (Clade A) is different from that which infects Chinook salmon Oncorhynchus tshawytscha, walleye pollock Gadus chalcogrammus, Greenland halibut Reinhardtius hippoglossoides, and Pacific halibut Hippoglossus stenolepsis (Clade B). MTCO1 sequences confirmed the presence of a more divergent Ichthyophonus sp. isolated from American shad Alosa sapidissima in rivers of eastern North America (Clade C), while American shad introduced to the Pacific Ocean are infected with the same parasite that infects Pacific herring (Clade A). Currently there are no consensus criteria for delimiting species within Ichthyophonidae, but MTCO1 sequences hold promise as a potential species identifying marker and useful epizootiological tool.

An Explanation Based on Energy-Related Changes for Blue Mussel Mytilus edulis Coping With Seawater Acidification.

As ocean acidification (OA) is gradually increasing, concerns regarding its ecological impacts on marine organisms are growing. Our previous studies have shown that seawater acidification exerted adverse effects on physiological processes of the blue mussel Mytilus edulis, and the aim of the present study was to obtain energy-related evidence to verify and explain our previous findings. Thus, the same acidification system (pH: 7.7 or 7.1; acidification method: HCl addition or CO2 enrichment; experimental period: 21d) was set up, and the energy-related changes were assessed. The results showed that the energy charge (EC) and the gene expressions of cytochrome C oxidase (COX) reflecting the ATP synthesis rate increased significantly after acidification treatments. What’s more, the mussels exposed to acidification allocated more energy to gills and hemocytes. However, the total adenylate pool (TAP) and the final adenosine triphosphate (ATP) in M. edulis decreased significantly, especially in CO2 treatment group at pH 7.1. It was interesting to note that, TAP, ATP, and COXs gene expressions in CO2 treatment groups were all significantly lower than that in HCl treatment groups at the same pH, verifying that CO2-induced acidification exhibited more deleterious impacts on M. edulis, and ions besides H+ produced by CO2 dissolution were possible causes. In conclusion, energy-related changes in M. edulis responded actively to seawater acidification and varied with different acidification conditions, while the constraints they had at higher acidification levels suggest that M. edulis will have a limited tolerance to increasing OA in the future.

A growing genetic tree in the soil of prostate.

In this issue of Cell Stem Cell, Grossmann etal. (2021) reconstructed the developmental history of the prostate gland in a 59-year-old male by 3D tracking of somatic mutations across 319 micro-dissected specimens. It provides a genetic picture of how the human prostate gland is shaped during embryogenesis, puberty, and adult life.

Leeches as the intermediate host for strigeid trematodes: genetic diversity and taxonomy of the genera Australapatemon Sudarikov, 1959 and Cotylurus Szidat, 1928

BackgroundLeeches (Hirudinida) play a significant role as intermediate hosts in the circulation of trematodes in the aquatic environment. However, species richness and the molecular diversity and phylogeny of larval stages of strigeid trematodes (tetracotyle) occurring in this group of aquatic invertebrates remain poorly understood. Here, we report our use of recently obtained sequences of several molecular markers to analyse some aspects of the ecology, taxonomy and phylogeny of the genera Australapatemon and Cotylurus, which utilise leeches as intermediate hosts.MethodsFrom April 2017 to September 2018, 153 leeches were collected from several sampling stations in small rivers with slow-flowing waters and related drainage canals located in three regions of Poland. The distinctive forms of tetracotyle metacercariae collected from leeches supplemented with adult Strigeidae specimens sampled from a wide range of water birds were analysed using the 28S rDNA partial gene, the second internal transcribed spacer region (ITS2) region and the cytochrome c oxidase (COI) fragment.ResultsAmong investigated leeches, metacercariae of the tetracotyle type were detected in the parenchyma and musculature of 62 specimens (prevalence 40.5%) with a mean intensity reaching 19.9 individuals. The taxonomic generic affiliation of metacercariae derived from the leeches revealed the occurrence of two strigeid genera: Australapatemon Sudarikov, 1959 and Cotylurus Szidat, 1928. Phylogenetic reconstructions based on the partial 28S rRNA gene, ITS2 region and partial COI gene confirmed the separation of the Australapatemon and Cotylurus clades. Taking currently available molecular data and our results into consideration, recently sequenced tetracotyle of Australapatemon represents most probably Au. minor; however, unclear phylogenetic relationships between Au. burti and Au. minor reduce the reliability of this conclusion. On the other hand, on the basis of the obtained sequences, supplemented with previously published data, the metacercariae of Cotylurus detected in leeches were identified as two species: C. strigeoides Dubois, 1958 and C. syrius Dubois, 1934. This is the first record of C. syrius from the intermediate host.ConclusionsThe results of this study suggest the separation of ecological niches and life cycles between C. cornutus (Rudolphi, 1808) and C. strigeoides/C. syrius, with potential serious evolutionary consequences for a wide range of host–parasite relationships. Moreover, phylogenetic analyses corroborated the polyphyletic character of C. syrius, the unclear status of C. cornutus and the separate position of Cotylurus raabei Bezubik, 1958 within Cotylurus. The data demonstrate the inconsistent taxonomic status of the sequenced tetracotyle of Australapatemon, resulting, in our opinion, from the limited availability of fully reliable, comparative sequences of related taxa in GenBank.Graphical

G6036A substitution in mitochondrial COX I gene compromises cytochrome c oxidase activity in thiamine responsive Leigh syndrome patients

Cytochrome c oxidase (COX) deficiency is known to be associated with Leigh syndrome (LS), however there are limited studies on genetic screening of mitochondrial (mt) DNA encoding COX genes as well as the functional validation of identified variants. In our previous studies, we cared for total 165 LS patients and analyzed the nucleotide variations across entire mt genome. We observed a high level of genetic heterogeneity in these patients. We identified various reported and novel variation across entire genome including COX genes. In our present study we have further studied and functionally validated the selected novel nucleotide variant of COX I and COX II gene using different in-silico tools and trans mitochondrial cybrid based assays. As a result of our study, G6036A (G45S) variant of COX I gene, reduced the COX activity in both spectrophotometric as well as In-gel BN-PAGE assays. FACS analysis also revealed this variant to affect the mitochondrial membrane potential in the respective cybrids. Interestingly most of our in-silico studies indicated that this variant might affect the secondary structure and confirmation of COX I protein. Thus we report the first missense mutation in the COX I gene of LS patients and justify its pathogenic role in these patients by different assays. Variant A7746G (N54K) in COX II gene was also predicted to affect the secondary structure as well as stability of COX II protein. Though, the effect of this variant was not significant, however it will be interesting to investigate its significance by other assays in future.

A morphological and combined phylogenetic analysis of pirate spiders (Araneae, Mimetidae): evolutionary relationships, taxonomy and character evolution

Mimetidae is one of the three families within Araneoidea whose members do not spin foraging webs, but are unique in displaying a complex prey-capture behaviour known as aggressive mimicry. Mimetids are distributed worldwide and are most diverse in the tropics of Central and South America. Here we provide a comprehensive phylogeny of pirate spiders (Mimetidae) based on analyses that combine morphological and multigene nucleotide sequence data. We scored 147 morphological characters for 55 mimetids and 16 outgroup taxa and combined it in a total-evidence approach with the sequence data of Benavides et al. (2017) which included two nuclear ribosomal genes, 18S rRNA and 28S rRNA, two mitochondrial ribosomal genes, 12S rRNA and 16S rRNA, the nuclear protein-encoding gene histone H3 and the mitochondrial protein-encoding gene cytochromec oxidase subunitI. We analysed the combined dataset using parsimony, maximum-likelihood and Bayesian inference methods. Our results support the monophyly of Mimetidae and of the genera Gelanor, Ero, Anansi and Australomimetus. Mimetidae is sister to Arkyidae + Tetragnathidae. Mimetus as currently circumscribed is not monophyletic under any analytical approach used, although several lineages within the genus are consistently found in our analyses. We describe, illustrate and discuss the morphological synapomorphies that support the main clades of Mimetidae. The following nomenclatural changes are proposed: Ermetus koreanus (Paik, 1967), the sole species of the genus, is transferred to Ero C.L. Koch, 1836 and thus Ermetus Ponomarev, 2008 is a junior synonym of Ero C.L. Koch, 1836 (new synonymy) and Ero koreana Paik, 1967 becomes a revalidated combination. Phobetinus sagittifer Simon, 1895, the type species of the genus, is transferred to Mimetus Hentz, 1832 and thus Phobetinus Simon, 1895 is a junior synonym of Mimetus Hentz, 1832 (new synonymy), which results in two changes: Mimetus sagittifer (Simon, 1895), new combination and Mimetus investus (Simon, 1909), new combination. Reo latro Brignoli, 1979, the type species of the genus, is transferred to Mimetus and thus Reo Brignoli, 1979 is a junior synonym of Mimetus (new synonymy), which results in the following two changes: Mimetus latro Brignoli, 1979, new combination and Mimetus eutypus Chamberlin & Ivie, 1935, revalidated combination. Arochoides integrans Mello-Leitão, 1935 is transferred to Tetragnathidae (new family placement). The type specimen of Arochoides integrans, the only species in this genus, is a subadult male of Azilia (Tetragnathidae), most likely Azilia histrio Simon, 1895. Arochoides is a junior synonym of Azilia (new synonymy). http://zoobank.org/urn:lsid:zoobank.org:pub:90F6B3DA-232B-428C-BF38-AEA8953D7685

Predator performance of Coccinella transversalis and its molecular identification

Predatory efficacy of Coccinella transversalis (Coleoptera: Coccinellidae) on three detrimental agriculturally important aphids (Aphis craccivora, A. fabae and A. gossypii) was studied under laboratory condition. The 4th instar larvae of C. transversalis consumed highest (21.56 ± 1.72) number of A. craccivora aphids followed by A. fabae (12.33 ± 1.74) and A. gossypii (13.99 ± 0.77). Life cycle studies of C. transversalis on the above three aphid species revealed that it took maximum (27.66 ± 3.06) days to complete life cycle while reared on A. craccivora followed by A. fabae (25.66 ± 0.58 days) and A. gossypii (22.33 ± 1.52 days) respectively. As C. transversalis is a potential predator, an attempt was taken to identify this biological control agent based on mitochondrial cytochrome c oxidase (COI) gene sequence. Sequenced gene was submitted to the NCBI GenBank database (Accession NO. MG 587947.1) followed by proper procedure. Phylogenetic relationship of the beetle was constructed based on mitochondrial COI gene. The nucleotide composition analysis revealed that the value of A+T (69.3%) was greater than G+C (30.7%). Such study of C. transversalis would be helpful in biological control programme of aphid pest.
 Bangladesh J. Zool. 47(2): 229-241, 2019

Cr-induced disturbance on expression of six COX genes in rice seedlings

Cytochrome c oxidase (COX) is one of the principle enzymes involved in cell apoptosis in plants, due to oxidative stresses and mitochondrial dysfunction. In this study, hydroponic experiment was conduced to investigate transcriptional changes of six selected COX genes in rice seedlings (Oryza sativa L. cv. XZX 45) exposed to potassium chromate Cr(VI) or chromium nitrate Cr(III) using quantitative real-time RT-PCR. Uptake and accumulation of both Cr species by rice seedlings and their effect on COX activity were also determined. Results indicated that accumulation of Cr in rice tissues was evident, in which much more Cr was detected in roots rather than shoots from both Cr treatments. Significant increase in COX activity was only observed in shoots at the highest Cr treatment concentration from both Cr variants, whereas changes of COX activity in roots responded biphasically. Six selected target genes of COX1, COX2, COX5B, COX6A, COX6B, and COX7A from the rice COX gene family were expressed differentially in response to both Cr variants. Expression pattern of these selected COX genes was also variable in rice tissues. Information collected here suggests that selected COX genes from the rice COX gene family may play different roles during detoxification of Cr stress.

Complete Mitochondrial Genome of Papilio protenor (Lepidoptera, Papilionidae) and Implications for Papilionidae Taxonomy

The complete mitochondrial genome (mitogenome) of Papilio protenor (Lepidoptera: Papilionidae) was sequenced and annotated in this study. The mitogenome comprised a typical circular, double-stranded DNA molecule of 15,268 bp in length including 13 protein-coding genes (PCGs), two ribosomal RNA genes, 22 transfer RNA (tRNA) genes, and an A+T-rich region. The gene order and mitogenome orientation were similar to those of all known Papilionidae species. The nucleotide composition of the P. protenor mitogenome exhibits considerable A+T bias (80.5%) and the AT (−0.019) and GC (−0.231) skewness is slightly negative. All of the PCGs except for cytochrome c oxidase (COI) start with a canonical ATN start codon, whereas the COI gene is tentatively designated by the CGA codon. Of the 13 PCGs, 11 contain the complete stop codon TAA or TAG, whereas COI and COII were terminated with a single T nucleotide. All tRNAs exhibit the typical cloverleaf structure, except for tRNASer(AGN), which does not contain the dihydrouridine arm. The 458 bp A+T-rich region is comprised of nonrepetitive sequences including the motif ATAGA followed by a poly-T stretch and a microsatellite-like (AT)6 element preceded by the ATTTA motif. Phylogenetic analysis of the 13 PCGs data using Bayesian inference, maximum likelihood methods, and maximum parsimony support the view that the subfamily Parnassiinae is regarded as an independent subfamily within Papilionidae and that Zerynthiini should be treated as one of the two clades of the subfamily Parnassiinae along with Parnasiini. In addition, the analysis strongly supports the monophyly of the subfamily Parnassiinae.

Identification of sequence polymorphisms in the mitochondrial cytochrome c oxidase genes as risk factors for hepatocellular carcinoma.

Single nucleotide polymorphisms (SNPs) accumulated in the mitochondrial DNA (mtDNA) is susceptible to the tumor formation. We discovered previously that SNPs in the mitochondrial displacement loop (D-loop) was associated with the risk of hepatocellular carcinoma (HCC). The cytochrome c oxidase (COX) genes of mtDNA were sequenced between 107 HCC patients and 100 matched healthy controls. The χ2 test was used to analyze single SNPs' statistical difference between HCC patients and healthy controls. In this study, cancer risk-associated SNPs in the COX genes of mtDNA coding region were assessed in HCC patients and health controls. The nucleotide position at site 9545A/G (P=.036) was identified its association for HCC with the 9545G allele susceptible to cancer risk. The SNPs in the COX genes may help us to evaluate the cancer risk of HCC.

Downregulation of cytochrome c oxidase subunit 7A1 expression is important in enhancing cell proliferation in adenocarcinoma cells

Mitochondrial Dysfunction has been implicated in multiple human diseases, including cancer. Among all cancer, lung cancer is the most common type of cancer worldwide with low survival rates. Mammals possess multiple subunits of the mitochondrial enzyme Cytochrome C oxidase (COX). The COX subunits are expressed in a tissue specific manner and have been implicated in cancer cell metabolism although their molecular and regulatory mechanisms are not clearly understood. In this study, we aimed at identifying novel gene signatures in lung cancer. We performed extensive analysis of seven different Gene Expression Omnibus (GEO) datasets pertaining to different stages of lung adenocarcinoma and identified that multiple subunits of COX genes are differentially expressed in these patients. Amongst all COX genes, the expression of COX7A1 gene was observed to be highly down regulated in these patients. In order to validate the GEO datasets, we looked at the expression of multiple COX genes using quantitative real time PCR (qPCR) using human lung adenocarcinoma cell line A549. Our results confirmed that COX 7A1 gene expression was indeed highly reduced in these cells. Overexpression of COX7A1 in human lung cancer cells led to inhibition of cell proliferation and increase in cell death via apoptosis. These results indicated that low level of COX7A1 gene expression is essential to regulate cell viability and inhibit cell death in lung adenocarcinoma. Our study has identified COX7A1 as a novel gene that might play a crucial role in the etiology of lung adenocarcinoma and can serve as a biomarker for lung cancer disease progression.

Divergence of the Populations of Yellow Wagtail Motacilla flaval Linnaeus, 1758, And Citrine Wagtail Motacilla citreola Pallas, 1776, (Motacillidae, Passeriformes) in Middle Volga Region of Russia

<p class="1Body">Blood samples of so-called “yellow” wagtails collected in geographical areas of Middle Volga breeding populations of these species were studied. After mtDNA isolation barcoding of studied species of "yellow" wagtails was performed. Site of gene cytochromec-oxidase I was amplified. This gene was used as a genetic marker for the comparison of obtained samples. After sequencing and sequence alignment of gene cytochrome c-oxidase I, based on the comparison of genetic distances between specimens of the studied species using Jalview software, phylogenetic trees of populations of species <em>Motacilla flava</em> L. and <em>Motacilla citreola</em> Pall. were constructed.</p>

Prediction of genetic risk factors of atherosclerosis using various bioinformatic tools.

The aim of this study was to identify potential markers of atherosclerosis development in familial hypercholesterolemia (FH) patients. GSE13985 microarray data, generated using blood samples from 5 FH patients and 5 matched controls, was downloaded from the Gene Expression Omnibus. Differentially expressed genes (DEGs) between FH and controls were identified and a protein-protein interaction (PPI) network was constructed. Module and hub proteins were screened in this network. The module genes were subjected to a gene ontology (GO) analysis, and a Kyoto Encyclopedia of Genes and Genomes enrichment analysis was also performed. A total of 394 genes, including 125 up- and 269 down-regulated genes, were differentially expressed. Ribosomal proteins L9 (RPL9), L35 (RPL35), and S7 (RPS7) were designated as hub nodes in the PPI network. The DEGs were found to be significantly enriched in ribosomal and oxidative phosphorylation pathways. Ribosomal protein genes were found to be involved in the ribosomal pathway. The cytochrome-c oxidase (COX) genes COX subunit VIIa polypeptide 2 (COX7A2), COX subunit VIIb (COX7B), COX subunit VIIc (COX7C), and COX subunit VIc (COX6C) were enriched in the oxidative phosphorylation pathway. Module analysis and GO enrichment analysis identified ribosomal proteins as important regulators of FH. Ribosomal and oxidative phosphorylation pathways may be closely associated with atherosclerosis development. Ribosomal protein genes and cytochrome-coxidase genes may be potential therapeutic targets for atherosclerosis.