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  • DNA  (26)
  • Management
  • 1
    Publication Date: 2021-05-19
    Description: This article has no abstract.
    Description: Published
    Keywords: Acipenser nudiventris ; DNA ; Genetic ; Populations ; Microsatellite
    Repository Name: AquaDocs
    Type: Journal Contribution , Refereed
    Format: pp.229-240
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  • 2
    Publication Date: 2021-05-19
    Description: Molecular comparison of two parasites Lernaea cyprinacea and Lernaea ctenopharyngodoni was carried out using RAPD (Random Amplified Polymorphic DNA) technique. A total of 43 Lernaea specimens belonging to the two species were collected from the Guilan and Khouzestan Provinces. DNA was extracted using the Phenol-chloroform method. The quality and quantity of DNA was assessed using 1% Agarose gel electrophoresis and spectrophotometer. Polymerase Chain Reaction (PCR) was conducted on the target DNA under specific conditions and PCR products were subjected to electrophoresis on polyacrylamide gels (6%). Polyacrylamide gels were stained using silver nitrate and DNA bands were analyzed with BioCapt software. The genetic analysis was conducted using POP GEN 32 software. Forty two primers, 10 nucleotides each were used for PCR reaction. Totally, 397 RAPD loci were counted on polyacrylamide gel where 349 identical loci were polymorphic of which some bands may be used as genetic markers for the identification of both Lernaea species. Data analysis on PCR products showed higher genetic variation (1.15%) of L. Ctenopharyngodon in the Guilan Province as compared to that of the Khouzestan (0.0%). However, genetic variation (27.46%) of L. cyprinacea in the Khouzestan province was 7.26 times higher than that of the Guilan province (3.78%). The two species showed a genetic differentiation of approximately 88%. Based on the observed molecular differences, we state that L. ctenopharyngodoni is a genetically independent species from L. cyprinacea.
    Description: Published
    Keywords: Parasites ; Polymerase chain reaction ; Primers ; Nucleotides ; Lernaea ctenopharyngodoni ; Lernaea cyprinacea ; Molecular structure ; Genetics ; DNA ; Freshwater
    Repository Name: AquaDocs
    Type: Journal Contribution , Refereed
    Format: pp.19-28
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  • 3
    Publication Date: 2021-05-19
    Description: The Persian sturgeon (Acipenser persicus) is more abundant sturgeon species in the South Caspian Sea and consist the highest proportion of Iranian Caviar, meat as well as bringing maximum foreign currency income, however from systematic point of view and differentiation of this species from Russian sturgeon (Acipenser gueldenstadttii) a serious challenging issues remain, where some Russian scientist are believe that the Persian sturgeon is not as an valid species and consider it as a subspecies of Russian sturgeon. This research conducted with the objective of identification and introducing a molecular marker based on specific DNA for differentiation of two species of Persian sturgeon and Russian sturgeon via a proved molecular marker method. For this purposes 8 different molecular approaches such: Microsatellite, AFLP, RAPD, sequencing of Cytb, 16sDNA, ND5, Growth Hormone gene and finally Single Nucleotide Polymorphism (SNP) were investigated. Based on applied methodology, between 5 to 16 caudal fin tissues were sampled for each species from different region of the Caspian Sea, Sefiedrud River, Ural and Volga rivers. Following DNA extraction, its quality and quantity were determined and the PCR experiment has been conducted using 5-110 primers according to various methods and type of gene. The PCR products were electrophoresed on Polyacrilamid or agarose gels and followed by silver and Ethidium Bromide staining. In RAPD method, polymorphic DNA band was cut on the gel followed by purification and then the segments were cloned in vector in Top10 strain of E.coli, and then sequenced. Meanwhile for Growth Hormone gene in Persian and Russian sturgeon the MEGA 4, Gene runner software were used to design the appropriate primers for PCR amplification. The PCR products were cloned in PTZ57R/T vector and transformed in Top10 E.coli strain and sequenced finally. For all other genes, similar methods were applied for PCR amplification and its products were sequenced and statistical analysis as well as phylogenetical tree was performed. In Single Nucleotide Polymorphism (SNP) method, after genomic library construction, in total 14.4 billion nucleotides were sequenced and similarity/ differentiation analysis of two species were investigated using specific bioinformatic software. Results indicated that Microsatellite and AFLP methods showed high level of genetic variation both within and between species. The Cytb gene, when 4 sample sequences from each species were compared two species were differentiated, however when analysis repeated over 15 samples, the sequence comparison couldn't differentiate two above mentioned species. Full sequence comparison of 16sDNA and mtDNA-ND5 gene showed variation in some nucleotide in both species of Persian and Russian sturgeon but no significant. Results of sequences obtained from cloned segment with RAPD method and also specific primer design based on produced sequences could succeed to discover a variable DNA band that able to differentiate two species from each other. Results of the present study also showed that the growth hormone gene (GH) of Persian and Russian sturgeon consists of 645 nucleotide that translate to 214 Amino Acids. The sequence comparison indicated that the gene coding growth hormone in Persian and Russian sturgeon had the highest similarity with GH of Mammals (71%), Anguilaformes (63%) and less similarity with bony fish (37%). Phylogenetic analysis indicates that Persian and Russian sturgeon in compare to other organism are ancient species and this gene is originated from a common ancestor. At present study the most appropriate results obtained from Single Nucleotide Polymorphism (SNP) method by sequencing 14.4 billion nucleotide from genome of two species of Persian and Russian sturgeon from North and the South Caspian Sea could prove that the Persian sturgeon is a valid and independent specie. This excellent results is the biggest scientific achievement for differentiation of two highly commercial important sturgeon species in the Caspian Sea in last two decades.
    Description: Iranian Fisheries Science Research Institute
    Description: Published
    Keywords: 16S rDNA ; Acipenser persicus ; Persian sturgeon ; Acipenser gueldenstadttii ; DNA ; Russian sturgeon ; Species differentiation ; Molecular Marker ; SNP
    Repository Name: AquaDocs
    Type: Report , Refereed
    Format: 239pp.
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  • 4
    Publication Date: 2021-05-19
    Description: Understanding the scale at which wild stocks of Persian sturgeon (Acipenser persicus) are genetically discrete is necessary for effective management of this commercially important species. Disomic DNA microsatellite markers are among the best tools for determining stock structure in fishes. As all sturgeon species have a polyploid ancestry of all sturgeons, most gene loci exhibit more than two alleles per individual, limiting the use of powerful analytical methods that commonly assume disomic inheritance. We scored products from 38 sets of microsatellite primers developed in lake (Acipenser fulvescens) and Atlantic sturgeon (Acipenser oxyrinchus oxyrinchus) to determine whether they would amplify disomic loci in Persian sturgeon. Samples of 45 individuals were detected.Thirty six loci (95%) were amplified successfully in Persian sturgeon. We identified a single monomorphic locus, 12 disomic, 19 tetrasomic, three octosomic, and one locus that was ambiguous. This is the first report on development of disomic single-locus DNA microsatellite markers in Persian sturgeon. These loci could be used to characterize variation in geographically discrete populations of the Persian sturgeon in their native ecosystem including in the Caspian Sea.
    Description: Published
    Keywords: Genetics ; Persian sturgeon ; Acipenser oxyrinchus oxyrinchus ; Acipenser fulvescens ; Acipenser persicus ; Single-locus DNA microsatellite markers ; DNA
    Repository Name: AquaDocs
    Type: Journal Contribution , Refereed
    Format: pp.389-397
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  • 5
    Publication Date: 2021-05-19
    Description: The goal of this study was to analyse the population genetic structure of the Persian sturgeon (Acipenser persicus) between South Caspian Sea and Sefidrud River with mtDNA control region (Dloop gene) and DNA sequencing method during 2010 – 2012 sturgeon stock assessment project. Fish speciemns were collected by bottom trawl net. Extraction of DNA, PCR and DNA sequencing were carried out. Diversity index, the gamma distribution shape parameter for the rate heterogeneity among sites and nucleotide sequence, Fst index, exact test, the historical demographic pattern using neutrality tests and mismatch distribution analysis (D test of Tajima and Fs test of Fu) were analysed. Thirteen haplotypes were obtained, average (±SD) for haplotype diversity was 0.961 ± 0.101, nucleotide diversity was 0.038 ± 0.015, the gamma distribution shape parameter was 0.19, Fst index revealed little genetic structure between populations and the significant Fst value was seen by 10000 permutation only between Sefidrud River and Other Areas (P≤ 0.05) and was confirmed by exact test of population differentiation. Mismatch distribution for Acipenser persicus appeared to be unimodal, which closely matched the expected distributions under the sudden expansion model and supported by the low Harpending’s Raggedness index (0.061). Tajima’s D and Fu’s Fs statistics were -0.84 and - 0.220, respectively, and was not significant. The results of this study showed that the population of Acipenser persicus in Sefidrud River were genetically differentiated from South Caspian Sea and three other areas represented a single panmictic populations. Therefore, fisheries managements of this valuable species should be directed towards conservation of gene pools and increasing different populations.
    Description: Published
    Keywords: Persian Sturgeon ; Acipenser persicus ; Population ; Genetic ; Structure ; DNA
    Repository Name: AquaDocs
    Type: Journal Contribution , Refereed
    Format: pp.11-21
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  • 6
    Publication Date: 2021-05-19
    Description: Population structure of Ship sturgeon, Acipenser nudiventris, from the south coast of Caspian Sea and Ural River was investigated using Microsatellite method. For this reason, 73 specimens of the sturgeon were collected from five locations in two sampling regions the first consisted of Bandar Anzali, SefidRud River, Babolsar, and Gorgan, and the second was Ural River. Four SSR markers were used in this investigation, of which 5 loci produced DNA band, with three of them being polymorph. One primer showed two loci with one of them being polymorph and another was monomorphic). Average expected and observed heterozygosity was 0.86 and 0.75 respectively. Genetic variation was assessed through analysis of molecular variance (AMOVA) that indicated almost all of the variance in data namely %94 (P less than or equal to 0.03) was within locations.
    Description: Published
    Keywords: Rivers ; Anadromous species ; Nucleotide sequence ; Induced breeding ; Primers ; Ships ; Sampling ; Coasts ; Acipenser ; Acipenser nudiventris ; Brackish ; Population Genetics ; DNA ; Genetic diversity ; Population structure ; Genotypes ; Biopolymorphism ; Aquaculture techniques ; Fish ; Sturgeon ; Populations ; Sexual Reproduction
    Repository Name: AquaDocs
    Type: Journal Contribution , Refereed
    Format: pp.99-108
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  • 7
    Publication Date: 2021-05-19
    Description: The objective of this investigation was molecular population study on Penaeus semisulcatus stocks from the Persian Gulf and Oman Sea. Samples were collected using trawling method from Hormuz (40 individuals) and Bushehr (35 individuals) regions. The DNA of samples were extracted using phenol and chloroform method and then were simplified using a pair premier of Cytochrom Oxidase Subunit I (COI) gene sequence by a thermal cycler. Nine restriction enzyme were Used to digest the larger gene region that five of them (Alu I, Hinf I, Hinc I I, Hpa I I and Rca I) appeared Polymorphic patterns. Reap software and X2 test were used to analyses the RFLP data. The average nucleotide diversity arid haplotype diversity among the population were 0.0345720 ± 0.0011952 and 0.28590±0.08174 and nucleotide divergence among population, being studied, is supposed to be 8.5%. Considering the result dispersion of haplotypes in two region showed a significant difference and this is an evidence for proving the variety of the stocks.
    Description: Published
    Keywords: Molecular population ; Penaeus semisulcatus ; Cytochrom Oxidase Subunit I ; COI ; Gene ; RFLP method ; DNA ; Phenol ; Chloroform ; Enzyme ; Polymorphic ; Haplotype ; Nucleotide
    Repository Name: AquaDocs
    Type: Journal Contribution , Refereed
    Format: pp.15-30
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  • 8
    Publication Date: 2021-05-19
    Description: In order to introduce genetic markers of four species of fishes, 80 samples of each species, i.e. Parastromateus niger, Scomberomorus comersoniannus, Trachionotus mookalee and Caranx para were collected. DNA was extracted using phenol- chloroform method . The target gene ( cytochrome b ) was amplified by Thermal cycle (PCR) and the PCR product size estimated 1105 bp. In this research out of 27 DNAase enzymes which were used for PCR product enzyme digesting 8 enzymes(Bam HI, Alw 261, Rsa I, Mbo I, Alu I, Hinf I, Dpn I, Dde I) have cut side on target DNA and three enzymes of them Alu I, Hinf I and Mbo I showed polymorphism genetic differences while other enzymes displayed similar patterns. Variarion of haplotypes from four species are as follows: BAA for P. niger, AAB for T. mookalee, ABA for C. para, and ACA for S. comersonianus. So it is possible to claim that each of the above Haplotypes may be used as genetic markers for each of the species.
    Description: Published
    Keywords: Separation ; Polymerase chain reaction ; Phenotypic variations ; Cytochrome b ; DDE ; Trachionotus mookalee ; Parastromateus niger ; Caranx para ; Carangidae ; Scomberomorus comersoniannus ; Scomberomorus ; Genetics ; DNA ; Enzymes ; Biomarkers ; Identification ; Phenotypes ; Chloroform ; Haplotypes ; Gene polymorphism ; Genetic markers ; Caranx ; Marine
    Repository Name: AquaDocs
    Type: Journal Contribution , Refereed
    Format: pp.1-14
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  • 9
    Publication Date: 2021-05-19
    Description: In this study 60 samples were collected from the southern Caspian Sea and some rivers of Mazandaran and Guilan provinces. Genetic variation and probable population differentiation of Barbus capito were studied based on the mitochondrial cytochrom-b gene. The mitochondrial DNA was extracted from fish fin using phenol-chlorophorm method. The specific primers were designed for B. capito and the PCR experiments were done on 60 samples. 11 restriction endonuclease enzymes were applied for RFLP analysis (ALuI, AvaI, AvaII, HinfI, DdeI, HincI, HpaII, RsaI, Sau3AI, HaeIII, TaqI). PCR products (1062 pb) and DNA digests were subjected to agarose and polyacrilamid gel electrophoresis to seperate fragments according to their molecular weight. These patterns were identified similar fpr all samples. Regarding to this patterns, it can be seen that polymorphysm phenomena cannot be observed by above mentioned enzymes and cytochrome-b gene, and there is no seperate population of B. capito in the southern Caspian Sea.
    Description: Published
    Keywords: mtDNA ; RFLP ; PCR ; Barbus capito ; Genetic variation ; Samples ; Mitochondrial cytochrom-b ; DNA ; Phenol-chlorophorm ; ALuI ; AvaI ; AvaII ; HinfI ; DdeI ; B. capito
    Repository Name: AquaDocs
    Type: Journal Contribution , Refereed
    Format: pp.117-130
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  • 10
    Publication Date: 2021-05-19
    Description: We studied genetic difference and resemblance between Acipenser persicus and Acipenser gueldenstaedtii using Random Amplified Polymorphic DNA (RAPD) technique. The DNA of tail fin tissue of three A. persicus and A. gueldenstaedtii were extracted using phenol-chloroform method. After electrophoresis of the samples by agarose gel, their concentrations were regulated and Polymerase Chain Reaction (PCR) was conducted by 53 primers. PCR products were electrophoresed on polyacrylamide gel and silver staining was done to reveal the DNA bands of the samples. Among 53 primers, 17 had no site on genomic DNA of A. persicus and A. gueldenstaedtii and did not produce any bands while the remaining 36 primers showed band pattern. Analyzing the PCR products data using RAPD PLOT program showed that the maximum and minimum genetic distance between species were 73% and 65% respectively. Also, the mean difference between the species was 70% and the maximum and minimum genetic resemblance between the two species were 35% and 27% respectively. Based on the results, we conclude that A. persicus is an independent species from A. gueldenstaedtii.
    Description: Published
    Keywords: Acipenser persicus ; Acipenser gueldenstaedtii ; RAPD technique ; Genetic ; Tissue ; Polymerase Chain Reaction ; Polyacrylamide ; A. persicus ; A. gueldenstaedtii ; DNA ; Species
    Repository Name: AquaDocs
    Type: Journal Contribution , Refereed
    Format: pp.91-102
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